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(1'S,5'S)-averufin biosynthesis
-
-
PWY-5954
(3R)-N-[(2S)-1-hydroxy-6-[(3R)-3-isocyanobutanamido]hexan-2-yl]-3-isocyanobutanamide biosynthesis
-
-
PWY-8320
(4R)-carvone biosynthesis
-
-
PWY-5928
(4Z,7Z,10Z,13Z,16Z)-docosa-4,7,10,13,16-pentaenoate biosynthesis II (4-desaturase)
-
-
PWY-7728
(4Z,7Z,10Z,13Z,16Z)-docosapentaenoate biosynthesis (6-desaturase)
-
-
PWY-7726
(5Z)-dodecenoate biosynthesis I
-
-
PWY0-862
(5Z)-dodecenoate biosynthesis II
-
-
PWY-7858
(5Z)-icosenoate biosynthesis
-
-
PWY-5361
(8E,10E)-dodeca-8,10-dienol biosynthesis
-
-
PWY-7654
(9Z)-tricosene biosynthesis
-
-
PWY-7035
(aminomethyl)phosphonate degradation
-
-
PWY-7805
(Kdo)2-lipid A modification (H. pylori)
-
-
PWY2DNV-3
(R)- and (S)-3-hydroxybutanoate biosynthesis (engineered)
-
-
PWY-7216
(R)-camphor degradation
-
-
P601-PWY
(R)-cysteate degradation
-
-
PWY-6642
(S)-camphor degradation
-
-
PWY-6989
(S)-lactate fermentation to propanoate, acetate and hydrogen
-
-
PWY-8086
(S)-propane-1,2-diol degradation
-
-
PWY-7013
(S)-reticuline biosynthesis
-
-
(S)-reticuline biosynthesis I
-
-
PWY-3581
(S)-reticuline biosynthesis II
-
-
PWY-6133
1,2-dichloroethane degradation
-
-
12DICHLORETHDEG-PWY
1,3-dimethylbenzene degradation to 3-methylbenzoate
-
-
PWY-5428
1,3-propanediol biosynthesis (engineered)
-
-
PWY-7385
1,4-dichlorobenzene degradation
-
-
14DICHLORBENZDEG-PWY
1,4-dimethylbenzene degradation to 4-methylbenzoate
-
-
PWY-5429
1,5-anhydrofructose degradation
-
-
PWY-6992
1,8-cineole degradation
-
-
6-HYDROXYCINEOLE-DEGRADATION-PWY
1-butanol autotrophic biosynthesis (engineered)
-
-
PWY-6886
1-methylpyrrolinium biosynthesis
-
-
PWY-5315
10-cis-heptadecenoyl-CoA degradation (yeast)
-
-
PWY-7337
10-trans-heptadecenoyl-CoA degradation (MFE-dependent, yeast)
-
-
PWY-7339
10-trans-heptadecenoyl-CoA degradation (reductase-dependent, yeast)
-
-
PWY-7338
11-oxyandrogens biosynthesis
-
-
PWY-8202
15-epi-lipoxin biosynthesis
-
-
PWY66-393
1D-myo-inositol hexakisphosphate biosynthesis I (from Ins(1,4,5)P3)
-
-
PWY-6361
1D-myo-inositol hexakisphosphate biosynthesis II (mammalian)
-
-
PWY-6362
1D-myo-inositol hexakisphosphate biosynthesis III (Spirodela polyrrhiza)
-
-
PWY-4661
1D-myo-inositol hexakisphosphate biosynthesis IV (Dictyostelium)
-
-
PWY-6372
1D-myo-inositol hexakisphosphate biosynthesis V (from Ins(1,3,4)P3)
-
-
PWY-6554
2'-deoxymugineic acid phytosiderophore biosynthesis
-
-
PWY-5912
2,3-dihydroxybenzoate biosynthesis
-
-
PWY-5901
2,4-dinitrotoluene degradation
-
-
PWY-5642
2,5-xylenol and 3,5-xylenol degradation
-
-
PWY-7698
2-amino-3-carboxymuconate semialdehyde degradation to 2-hydroxypentadienoate
-
-
PWY-5654
2-amino-3-carboxymuconate semialdehyde degradation to glutaryl-CoA
-
-
PWY-5652
2-amino-3-hydroxycyclopent-2-enone biosynthesis
-
-
PWY-7536
2-aminophenol degradation
-
-
PWY-6210
2-arachidonoylglycerol biosynthesis
-
-
PWY-8052
2-carboxy-1,4-naphthoquinol biosynthesis
-
-
PWY-5837
2-deoxy-alpha-D-ribose 1-phosphate degradation
-
-
PWY-7180
2-deoxy-D-glucose 6-phosphate degradation
-
-
PWY-8121
2-deoxy-D-ribose degradation I
-
-
PWY-8060
2-deoxy-D-ribose degradation II
-
-
PWY-8058
2-methyl-branched fatty acid beta-oxidation
-
-
PWY-8181
2-methylcitrate cycle I
-
-
PWY0-42
2-methylcitrate cycle II
-
-
PWY-5747
2-methylpropene degradation
-
-
PWY-7778
2-nitrobenzoate degradation I
-
-
PWY-5647
2-nitrotoluene degradation
-
-
PWY-5641
2-oxobutanoate degradation I
-
-
PWY-5130
2-oxobutanoate degradation II
-
-
2OXOBUTYRATECAT-PWY
2-oxoglutarate decarboxylation to succinyl-CoA
-
-
PWY-5084
2-oxoisovalerate decarboxylation to isobutanoyl-CoA
-
-
PWY-5046
24-epi-campesterol, fucosterol, and clionasterol biosynthesis (diatoms)
-
-
PWY-8238
3,3'-disulfanediyldipropannoate degradation
-
-
PWY-7462
3,3'-thiodipropanoate degradation
-
-
PWY-7465
3,4,6-trichlorocatechol degradation
-
-
PWY-6094
3,5-dichlorocatechol degradation
-
-
PWY-6084
3,5-dimethoxytoluene biosynthesis
-
-
PWY-7076
3,8-divinyl-chlorophyllide a biosynthesis I (aerobic, light-dependent)
-
-
CHLOROPHYLL-SYN
3,8-divinyl-chlorophyllide a biosynthesis II (anaerobic)
-
-
PWY-5531
3,8-divinyl-chlorophyllide a biosynthesis III (aerobic, light independent)
-
-
PWY-7159
3-(4-hydroxyphenyl)pyruvate biosynthesis
-
-
PWY-5886
3-chlorocatechol degradation
-
-
3-chlorocatechol degradation I (ortho)
-
-
PWY-6089
3-chlorocatechol degradation II (ortho)
-
-
PWY-6193
3-chlorotoluene degradation II
-
-
PWY-6104
3-dehydroquinate biosynthesis II (archaea)
-
-
PWY-6160
3-hydroxy-4-methyl-anthranilate biosynthesis I
-
-
PWY-7717
3-hydroxy-4-methyl-anthranilate biosynthesis II
-
-
PWY-7765
3-hydroxypropanoate cycle
-
-
PWY-5743
3-hydroxypropanoate/4-hydroxybutanate cycle
-
-
PWY-5789
3-hydroxyquinaldate biosynthesis
-
-
PWY-7733
3-methyl-branched fatty acid alpha-oxidation
-
-
PWY66-387
3-methylbutanol biosynthesis (engineered)
-
-
PWY-6871
3-phenylpropanoate degradation
-
-
P281-PWY
3-phenylpropionate degradation
-
-
3-phosphoinositide biosynthesis
-
-
PWY-6352
3-phosphoinositide degradation
-
-
PWY-6368
4,5-dichlorocatechol degradation
-
-
PWY-6093
4-amino-2-methyl-5-diphosphomethylpyrimidine biosynthesis II
-
-
PWY-7282
4-aminobutanoate degradation I
-
-
PWY-6535
4-aminobutanoate degradation II
-
-
PWY-6537
4-aminobutanoate degradation III
-
-
PWY-6536
4-aminobutanoate degradation IV
-
-
PWY-6473
4-aminobutanoate degradation V
-
-
PWY-5022
4-chlorocatechol degradation
-
-
PWY-6087
4-chloronitrobenzene degradation
-
-
PWY-5645
4-coumarate degradation (aerobic)
-
-
PWY-8002
4-coumarate degradation (anaerobic)
-
-
PWY-7046
4-ethylphenol degradation (anaerobic)
-
-
PWY-6080
4-hydroxy-2-nonenal detoxification
-
-
PWY-7112
4-hydroxy-3-prenylbenzoate biosynthesis
-
-
PWY-7303
4-hydroxybenzoate biosynthesis I (eukaryotes)
-
-
PWY-5754
4-hydroxybenzoate biosynthesis III (plants)
-
-
PWY-6435
4-hydroxymandelate degradation
-
-
4-nitrophenol degradation I
-
-
PWY-5487
4-nitrophenol degradation II
-
-
PWY-5488
4-nitrotoluene degradation II
-
-
PWY-5644
4-oxopentanoate degradation
-
-
PWY-7948
5'-deoxyadenosine degradation I
-
-
PWY-8130
5'-deoxyadenosine degradation II
-
-
PWY-8131
5,6-dimethylbenzimidazole biosynthesis I (aerobic)
-
-
PWY-5523
5-aminoimidazole ribonucleotide biosynthesis I
-
-
PWY-6121
5-aminoimidazole ribonucleotide biosynthesis II
-
-
PWY-6122
5-oxo-L-proline metabolism
-
-
PWY-7942
6-gingerol analog biosynthesis (engineered)
-
-
PWY-6920
6-hydroxymethyl-dihydropterin diphosphate biosynthesis
-
-
6-hydroxymethyl-dihydropterin diphosphate biosynthesis I
-
-
PWY-6147
6-hydroxymethyl-dihydropterin diphosphate biosynthesis IV (Plasmodium)
-
-
PWY-7852
7-dehydroporiferasterol biosynthesis
-
-
PWY-7155
8-amino-7-oxononanoate biosynthesis I
-
-
PWY-6519
8-oxo-(d)GTP detoxification I
-
-
PWY-6502
9-cis, 11-trans-octadecadienoyl-CoA degradation (isomerase-dependent, yeast)
-
-
PWY-7340
9-lipoxygenase and 9-allene oxide synthase pathway
-
-
PWY-5407
ABH and Lewis epitopes biosynthesis from type 1 precursor disaccharide
-
-
PWY-7832
ABH and Lewis epitopes biosynthesis from type 2 precursor disaccharide
-
-
PWY-7831
Ac/N-end rule pathway
-
-
PWY-7800
acetaldehyde biosynthesis I
-
-
PWY-6333
acetaldehyde biosynthesis II
-
-
PWY-6330
acetate and ATP formation from acetyl-CoA I
-
-
PWY0-1312
acetate and ATP formation from acetyl-CoA III
-
-
PWY-8328
acetate conversion to acetyl-CoA
-
-
PWY0-1313
acetoacetate degradation (to acetyl CoA)
-
-
ACETOACETATE-DEG-PWY
acetone degradation I (to methylglyoxal)
-
-
PWY-5451
acetone degradation II (to acetoacetate)
-
-
PWY-5533
acetone degradation III (to propane-1,2-diol)
-
-
PWY-7466
acetyl CoA biosynthesis
-
-
acetyl-CoA biosynthesis from citrate
-
-
PWY-5172
acetyl-CoA fermentation to butanoate
-
-
PWY-5676
acetylene degradation (anaerobic)
-
-
P161-PWY
acrylate degradation I
-
-
PWY-6373
acrylate degradation II
-
-
PWY-8180
acrylonitrile degradation I
-
-
PWY-7308
acyl carrier protein activation
-
-
PWY-6012-1
acyl carrier protein metabolism
-
-
PWY-6012
acyl-CoA hydrolysis
-
-
PWY-5148
adenine and adenosine salvage I
-
-
P121-PWY
adenine and adenosine salvage II
-
-
PWY-6605
adenine and adenosine salvage III
-
-
PWY-6609
adenine and adenosine salvage V
-
-
PWY-6611
adenine and adenosine salvage VI
-
-
PWY-6619
adenine salvage
-
-
PWY-6610
adenosine deoxyribonucleotides de novo biosynthesis I
-
-
PWY-7227
adenosine deoxyribonucleotides de novo biosynthesis II
-
-
PWY-7220
adenosine nucleotides degradation I
-
-
PWY-6596
adenosine nucleotides degradation II
-
-
SALVADEHYPOX-PWY
adenosine ribonucleotides de novo biosynthesis
-
-
PWY-7219
adipate biosynthesis
-
-
PWY-8347
adlupulone and adhumulone biosynthesis
-
-
PWY-7857
aerobic respiration I (cytochrome c)
-
-
PWY-3781
aerobic respiration II (cytochrome c) (yeast)
-
-
PWY-7279
aerobic respiration III (alternative oxidase pathway)
-
-
PWY-4302
aerobic toluene degradation
-
-
Aflatoxin biosynthesis
-
-
aflatoxin biosynthesis
-
-
Alanine, aspartate and glutamate metabolism
-
-
aldoxime degradation
-
-
P345-PWY
alginate degradation
-
-
PWY-6986
alkane biosynthesis II
-
-
PWY-7033
alkane oxidation
-
-
PWY-2724
all-trans-farnesol biosynthesis
-
-
PWY-6859
allantoin degradation
-
-
allantoin degradation to glyoxylate I
-
-
PWY-5694
allantoin degradation to glyoxylate III
-
-
PWY-5705
alliin metabolism
-
-
PWY-5706
allopregnanolone biosynthesis
-
-
PWY-7455
alpha-linolenate biosynthesis I (plants and red algae)
-
-
PWY-5997
alpha-linolenate metabolites biosynthesis
-
-
PWY-8398
alpha-Linolenic acid metabolism
-
-
alpha-tocopherol degradation
-
-
PWY-6377
alpha-tomatine degradation
-
-
PWY18C3-5
Amaryllidacea alkaloids biosynthesis
-
-
PWY-7826
Amino sugar and nucleotide sugar metabolism
-
-
Aminoacyl-tRNA biosynthesis
-
-
Aminobenzoate degradation
-
-
aminopropanol phosphate biosynthesis
-
-
aminopropanol phosphate biosynthesis II
-
-
PWY-7378
ammonia assimilation cycle I
-
-
PWY-6963
ammonia assimilation cycle II
-
-
PWY-6964
ammonia assimilation cycle III
-
-
AMMASSIM-PWY
ammonia oxidation II (anaerobic)
-
-
P303-PWY
amygdalin and prunasin degradation
-
-
PWY-6011
anaerobic aromatic compound degradation (Thauera aromatica)
-
-
BENZCOA-PWY
anaerobic energy metabolism (invertebrates, cytosol)
-
-
PWY-7383
anaerobic energy metabolism (invertebrates, mitochondrial)
-
-
PWY-7384
anandamide biosynthesis I
-
-
PWY-8051
anandamide biosynthesis II
-
-
PWY-8053
anandamide degradation
-
-
PWY6666-1
anandamide lipoxygenation
-
-
PWY-8056
anapleurotic synthesis of oxalacetate
-
-
androgen and estrogen metabolism
-
-
androgen biosynthesis
-
-
PWY66-378
androstenedione degradation I (aerobic)
-
-
PWY-6944
androstenedione degradation II (anaerobic)
-
-
PWY-8152
anteiso-branched-chain fatty acid biosynthesis
-
-
PWY-8173
apratoxin A biosynthesis
-
-
PWY-8361
arachidonate biosynthesis
-
-
arachidonate biosynthesis I (6-desaturase, lower eukaryotes)
-
-
PWY-5353
arachidonate biosynthesis III (6-desaturase, mammals)
-
-
PWY-7592
arachidonate biosynthesis IV (8-detaturase, lower eukaryotes)
-
-
PWY-7601
arachidonate biosynthesis V (8-detaturase, mammals)
-
-
PWY-7725
arachidonate metabolites biosynthesis
-
-
PWY-8397
Arachidonic acid metabolism
-
-
arachidonic acid metabolism
-
-
Arg/N-end rule pathway (eukaryotic)
-
-
PWY-7799
Arginine and proline metabolism
-
-
Arginine biosynthesis
-
-
arginine dependent acid resistance
-
-
PWY0-1299
aromatic glucosinolate activation
-
-
PWY-6684
aromatic biogenic amine degradation (bacteria)
-
-
PWY-7431
aromatic polyketides biosynthesis
-
-
PWY-6316
arsenate detoxification I
-
-
PWY-8264
arsenate detoxification III
-
-
PWY-8263
arsenate detoxification V
-
-
PWY1YI0-1
arsenic detoxification (mammals)
-
-
PWY-4202
arsenic detoxification (plants)
-
-
PWY-8259
arsenic detoxification (yeast)
-
-
PWY-4621
arsenite to oxygen electron transfer
-
-
PWY-4521
arsenite to oxygen electron transfer (via azurin)
-
-
PWY-7429
Ascorbate and aldarate metabolism
-
-
ascorbate glutathione cycle
-
-
PWY-2261
ascorbate recycling (cytosolic)
-
-
PWY-6370
aspartate and asparagine metabolism
-
-
aspirin triggered resolvin D biosynthesis
-
-
PWY66-395
aspirin triggered resolvin E biosynthesis
-
-
PWY66-394
assimilatory sulfate reduction II
-
-
SULFMETII-PWY
assimilatory sulfate reduction III
-
-
PWY-6683
assimilatory sulfate reduction IV
-
-
PWY1ZNC-1
astaxanthin biosynthesis (bacteria, fungi, algae)
-
-
PWY-5288
ATP biosynthesis
-
-
PWY-7980
atromentin biosynthesis
-
-
PWY-7518
avenanthramide biosynthesis
-
-
PWY-8157
backdoor pathway of androgen biosynthesis
-
-
PWY-8200
bacterial bioluminescence
-
-
PWY-7723
baicalein degradation (hydrogen peroxide detoxification)
-
-
PWY-7214
baicalein metabolism
-
-
PWY-7212
benzoate biosynthesis I (CoA-dependent, beta-oxidative)
-
-
PWY-6443
benzoate biosynthesis II (CoA-independent, non-beta-oxidative)
-
-
PWY-6444
benzoate biosynthesis III (CoA-dependent, non-beta-oxidative)
-
-
PWY-6446
benzoate degradation II (aerobic and anaerobic)
-
-
PWY-283
benzoyl-CoA biosynthesis
-
-
PWY-6458
benzoyl-CoA degradation I (aerobic)
-
-
PWY-1361
beta-(1,4)-mannan degradation
-
-
PWY-7456
beta-1,4-D-mannosyl-N-acetyl-D-glucosamine degradation
-
-
PWY-7586
beta-alanine betaine biosynthesis
-
-
PWY-4021
beta-alanine biosynthesis I
-
-
PWY-3981
beta-alanine biosynthesis II
-
-
PWY-3941
beta-alanine biosynthesis IV
-
-
PWY-5760
beta-alanine degradation I
-
-
BETA-ALA-DEGRADATION-I-PWY
beta-alanine degradation II
-
-
PWY-1781
beta-alanine degradation III
-
-
PWY-8120
beta-Alanine metabolism
-
-
beta-carboline biosynthesis
-
-
PWY-5877
beta-D-glucuronide and D-glucuronate degradation
-
-
PWY-7247
Betalain biosynthesis
-
-
betalamic acid biosynthesis
-
-
PWY-5394
betanidin degradation
-
-
PWY-5461
betaxanthin biosynthesis
-
-
PWY-5426
betaxanthin biosynthesis (via dopamine)
-
-
PWY-5403
Bifidobacterium shunt
-
-
P124-PWY
bile acid 7alpha-dehydroxylation
-
-
PWY-7754
bile acid 7beta-dehydroxylation
-
-
PWY-8134
bile acid biosynthesis, neutral pathway
bile acids deconjugation
-
-
PWY-8135
Biosynthesis of ansamycins
-
-
Biosynthesis of enediyne antibiotics
-
-
biosynthesis of Lewis epitopes (H. pylori)
-
-
PWY-7833
Biosynthesis of secondary metabolites
-
-
Biosynthesis of siderophore group nonribosomal peptides
-
-
Biosynthesis of unsaturated fatty acids
-
-
biotin-carboxyl carrier protein assembly
-
-
PWY0-1264
bis(guanylyl molybdopterin) cofactor sulfurylation
-
-
PWY-8164
bisabolene biosynthesis (engineered)
-
-
PWY-7102
Bisphenol degradation
-
-
brassicicene C biosynthesis
-
-
PWY-7517
brassinolide biosynthesis I
-
-
PWY-699
brassinolide biosynthesis II
-
-
PWY-2582
Brassinosteroid biosynthesis
-
-
bryostatin biosynthesis
-
-
PWY-8047
bupropion degradation
-
-
PWY66-241
butachlor degradation
-
-
PWY-7771
butanoate fermentation
-
-
butanol and isobutanol biosynthesis (engineered)
-
-
PWY-7396
C20 prostanoid biosynthesis
-
-
PWY66-374
C25,25 CDP-archaeol biosynthesis
-
-
PWY-8365
C4 and CAM-carbon fixation
-
-
C4 photosynthetic carbon assimilation cycle, NAD-ME type
-
-
PWY-7115
C4 photosynthetic carbon assimilation cycle, NADP-ME type
-
-
PWY-241
C4 photosynthetic carbon assimilation cycle, PEPCK type
-
-
PWY-7117
C5-Branched dibasic acid metabolism
-
-
caffeine biosynthesis I
-
-
PWY-5037
caffeine biosynthesis II (via paraxanthine)
-
-
PWY-5038
caffeine degradation III (bacteria, via demethylation)
-
-
PWY-6538
Calvin-Benson-Bassham cycle
-
-
CALVIN-PWY
camalexin biosynthesis
-
-
CAMALEXIN-SYN
canavanine biosynthesis
-
-
PWY-5
canavanine degradation
-
-
PWY-31
cannabinoid biosynthesis
-
-
PWY-5140
Caprolactam degradation
-
-
capsaicin biosynthesis
-
-
PWY-5710
Carbapenem biosynthesis
-
-
Carbon fixation in photosynthetic organisms
-
-
Carbon fixation pathways in prokaryotes
-
-
cardiolipin and phosphatidylethanolamine biosynthesis (Xanthomonas)
-
-
PWY-7509
cardiolipin biosynthesis
-
-
cardiolipin biosynthesis I
-
-
PWY-5668
cardiolipin biosynthesis II
-
-
PWY-5269
cardiolipin biosynthesis III
-
-
PWY0-1545
carnosine biosynthesis
-
-
PWY66-420
Carotenoid biosynthesis
-
-
carotenoid biosynthesis
-
-
carotenoid cleavage
-
-
PWY-6806
catechol degradation to 2-hydroxypentadienoate I
-
-
P183-PWY
catechol degradation to 2-hydroxypentadienoate II
-
-
PWY-5419
catecholamine biosynthesis
CDP-6-deoxy-D-gulose biosynthesis
-
-
PWY-8139
CDP-diacylglycerol biosynthesis
-
-
CDP-diacylglycerol biosynthesis I
-
-
PWY-5667
CDP-diacylglycerol biosynthesis II
-
-
PWY0-1319
CDP-diacylglycerol biosynthesis III
-
-
PWY-5981
cell-surface glycoconjugate-linked phosphocholine biosynthesis
-
-
PWY-7886
cellulose degradation
-
-
cellulose degradation II (fungi)
-
-
PWY-6788
ceramide and sphingolipid recycling and degradation (yeast)
-
-
PWY-7119
ceramide biosynthesis
-
-
ceramide de novo biosynthesis
-
-
PWY3DJ-12
ceramide degradation (generic)
-
-
PWY-6483
ceramide degradation by alpha-oxidation
-
-
PWY66-388
chitin biosynthesis
-
-
PWY-6981
chitin deacetylation
-
-
PWY-7118
chitin degradation I (archaea)
-
-
PWY-6855
chitin degradation II (Vibrio)
-
-
PWY-6902
chitin degradation III (Serratia)
-
-
PWY-7822
chitin derivatives degradation
-
-
PWY-6906
Chloroalkane and chloroalkene degradation
-
-
Chlorocyclohexane and chlorobenzene degradation
-
-
chlorogenic acid biosynthesis I
-
-
PWY-6039
chlorogenic acid degradation
-
-
PWY-6781
chlorpyrifos degradation
-
-
PWY-8065
cholesterol biosynthesis
-
-
cholesterol biosynthesis (algae, late side-chain reductase)
-
-
PWY-8191
cholesterol biosynthesis (diatoms)
-
-
PWY-8239
cholesterol biosynthesis (plants, early side-chain reductase)
-
-
PWY18C3-1
cholesterol biosynthesis I
-
-
PWY66-341
cholesterol biosynthesis II (via 24,25-dihydrolanosterol)
-
-
PWY66-3
cholesterol biosynthesis III (via desmosterol)
-
-
PWY66-4
cholesterol degradation to androstenedione I (cholesterol oxidase)
-
-
PWY-6945
cholesterol degradation to androstenedione II (cholesterol dehydrogenase)
-
-
PWY-6946
cholesterol degradation to androstenedione III (anaerobic)
-
-
PWY-8151
choline biosynthesis I
-
-
PWY-3385
choline biosynthesis III
-
-
PWY-3561
choline degradation I
-
-
CHOLINE-BETAINE-ANA-PWY
choline degradation IV
-
-
PWY-7494
chondroitin biosynthesis
-
-
PWY-6566
chondroitin sulfate biosynthesis
-
-
PWY-6567
chondroitin sulfate degradation I (bacterial)
-
-
PWY-6572
chorismate biosynthesis from 3-dehydroquinate
-
-
PWY-6163
chorismate metabolism
-
-
cis-geranyl-CoA degradation
-
-
PWY-6672
cis-vaccenate biosynthesis
-
-
Citrate cycle (TCA cycle)
-
-
CMP phosphorylation
-
-
PWY-7205
CMP-legionaminate biosynthesis I
-
-
PWY-6749
CMP-N-acetylneuraminate biosynthesis I (eukaryotes)
-
-
PWY-6138
CMP-N-acetylneuraminate biosynthesis II (bacteria)
-
-
PWY-6139
CMP-N-glycoloylneuraminate biosynthesis
-
-
PWY-6144
CO2 fixation in Crenarchaeota
-
-
CO2 fixation into oxaloacetate (anaplerotic)
-
-
PWYQT-4429
coenzyme A biosynthesis I (bacteria)
-
-
COA-PWY
coenzyme A biosynthesis II (eukaryotic)
-
-
PWY-7851
coenzyme A biosynthesis III (archaea)
-
-
PWY-8342
coenzyme A metabolism
-
-
coenzyme B biosynthesis
-
-
P241-PWY
coenzyme M biosynthesis
-
-
coenzyme M biosynthesis II
-
-
PWY-6643
colupulone and cohumulone biosynthesis
-
-
PWY-5133
complex N-linked glycan biosynthesis (plants)
-
-
PWY-7920
complex N-linked glycan biosynthesis (vertebrates)
-
-
PWY-7426
conversion of succinate to propanoate
-
-
PWY0-43
coumarin biosynthesis (via 2-coumarate)
-
-
PWY-5176
coumarins biosynthesis (engineered)
-
-
PWY-7398
creatine biosynthesis
-
-
GLYCGREAT-PWY
creatine phosphate biosynthesis
-
-
PWY-6158
creatinine degradation
-
-
creatinine degradation I
-
-
CRNFORCAT-PWY
creatinine degradation II
-
-
PWY-4722
cremeomycin biosynthesis
-
-
PWY-8296
crotonate fermentation (to acetate and cyclohexane carboxylate)
-
-
PWY-7401
crotonyl-CoA/ethylmalonyl-CoA/hydroxybutyryl-CoA cycle (engineered)
-
-
PWY-7854
curacin A biosynthesis
-
-
PWY-8358
cutin biosynthesis
-
-
PWY-321
Cutin, suberine and wax biosynthesis
-
-
Cyanoamino acid metabolism
-
-
cyanophycin metabolism
-
-
PWY-7052
cyclic electron flow
-
-
PWY-8270
cylindrospermopsin biosynthesis
-
-
PWY-8045
Cysteine and methionine metabolism
-
-
cytidylyl molybdenum cofactor sulfurylation
-
-
PWY-8165
cytosolic NADPH production (yeast)
-
-
PWY-7268
D-Amino acid metabolism
-
-
D-arabinitol degradation I
-
-
DARABITOLUTIL-PWY
D-arabinose degradation V
-
-
PWY-8334
D-galactosamine and N-acetyl-D-galactosamine degradation
-
-
PWY-7395
D-galactose degradation I (Leloir pathway)
-
-
PWY-6317
D-galactose degradation II
-
-
GALDEG-PWY
D-galactose degradation IV
-
-
PWY-6693
D-galactose detoxification
-
-
PWY-3821
D-glucuronate degradation I
-
-
PWY-5525
d-mannose degradation
-
-
D-mannose degradation I
-
-
MANNCAT-PWY
D-mannose degradation II
-
-
PWY3O-1743
D-myo-inositol (1,3,4)-trisphosphate biosynthesis
-
-
PWY-6364
D-myo-inositol (1,4,5)-trisphosphate biosynthesis
-
-
PWY-6351
D-myo-inositol (1,4,5)-trisphosphate degradation
-
-
PWY-6363
D-myo-inositol (1,4,5,6)-tetrakisphosphate biosynthesis
-
-
PWY-6366
D-myo-inositol (3,4,5,6)-tetrakisphosphate biosynthesis
-
-
PWY-6365
D-myo-inositol-5-phosphate metabolism
-
-
PWY-6367
D-phenylglycine degradation
-
-
PWY-8161
D-sorbitol biosynthesis I
-
-
PWY-5054
D-sorbitol degradation I
-
-
PWY-4101
D-xylose degradation I
-
-
XYLCAT-PWY
D-xylose degradation IV
-
-
PWY-7294
D-xylose degradation to ethylene glycol (engineered)
-
-
PWY-7178
daidzein conjugates interconversion
-
-
PWY-2343
daidzin and daidzein degradation
-
-
PWY-6996
deacetylcephalosporin C biosynthesis
-
-
PWY-5631
degradation of aromatic, nitrogen containing compounds
-
-
degradation of hexoses
-
-
degradation of pentoses
-
-
degradation of sugar acids
-
-
degradation of sugar alcohols
-
-
dermatan sulfate degradation I (bacterial)
-
-
PWY-7646
detoxification of reactive carbonyls in chloroplasts
-
-
PWY-6786
di-homo-gamma-linolenate metabolites biosynthesis
-
-
PWY-8396
di-myo-inositol phosphate biosynthesis
-
-
PWY-6664
diacylglycerol and triacylglycerol biosynthesis
-
-
TRIGLSYN-PWY
diacylglycerol biosynthesis (PUFA enrichment in oilseed)
-
-
PWY-6804
dicranin biosynthesis
-
-
PWY-6603
diethylphosphate degradation
-
-
PWY-5491
digitoxigenin biosynthesis
-
-
PWY-6032
DIMBOA-glucoside activation
-
-
PWY-4441
dimethyl sulfide biosynthesis from methionine
-
-
PWY-7793
dimethylsulfoniopropanoate biosynthesis I (Wollastonia)
-
-
PWY-6054
dimethylsulfoniopropanoate biosynthesis II (Spartina)
-
-
PWY-6055
dimorphecolate biosynthesis
-
-
PWY-5368
dipicolinate biosynthesis
-
-
PWY-8088
dissimilatory sulfate reduction I (to hydrogen sufide))
-
-
DISSULFRED-PWY
divinyl ether biosynthesis II
-
-
PWY-5409
docosahexaenoate biosynthesis I (lower eukaryotes)
-
-
PWY-7053
docosahexaenoate biosynthesis III (6-desaturase, mammals)
-
-
PWY-7606
docosahexaenoate biosynthesis IV (4-desaturase, mammals)
-
-
PWY-7727
docosahexaenoate metabolites biosynthesis
-
-
PWY-8400
dolichol and dolichyl phosphate biosynthesis
dolichyl-diphosphooligosaccharide biosynthesis
-
-
dopamine degradation
-
-
PWY6666-2
drosopterin and aurodrosopterin biosynthesis
-
-
PWY-7442
Drug metabolism - cytochrome P450
-
-
Drug metabolism - other enzymes
-
-
dTDP-beta-L-rhamnose biosynthesis
-
-
DTDPRHAMSYN-PWY
dTMP de novo biosynthesis (mitochondrial)
-
-
PWY66-385
dZTP biosynthesis
-
-
PWY-8289
ectoine biosynthesis
-
-
P101-PWY
enterobactin biosynthesis
Entner Doudoroff pathway
-
-
Entner-Doudoroff pathway I
-
-
PWY-8004
Entner-Doudoroff pathway II (non-phosphorylative)
-
-
NPGLUCAT-PWY
Entner-Doudoroff pathway III (semi-phosphorylative)
-
-
PWY-2221
epoxysqualene biosynthesis
-
-
PWY-5670
ergosterol biosynthesis I
-
-
PWY-6075
ergosterol biosynthesis II
-
-
PWY-7154
ergothioneine biosynthesis I (bacteria)
-
-
PWY-7255
erythritol biosynthesis I
-
-
PWY-8372
erythritol biosynthesis II
-
-
PWY-8373
erythro-tetrahydrobiopterin biosynthesis I
-
-
PWY-5663
Escherichia coli serotype O:127 O antigen biosynthesis
-
-
PWY-8231
Escherichia coli serotype O:1B/Salmonella enterica serotype O:42 O antigen biosynthesis
-
-
PWY-8237
Escherichia coli serotype O:85/Salmonella enterica serotype O:17 O antigen biosynthesis
-
-
PWY-8207
Escherichia coli serotype O:86 O antigen biosynthesis
-
-
PWY-7290
estradiol biosynthesis I (via estrone)
-
-
PWY66-380
ethanol degradation I
-
-
ETOH-ACETYLCOA-ANA-PWY
ethanol degradation II
-
-
PWY66-21
ethanol degradation III
-
-
PWY66-161
ethanol degradation IV
-
-
PWY66-162
ethanolamine utilization
-
-
PWY0-1477
ethene biosynthesis I (plants)
-
-
ETHYL-PWY
ethene biosynthesis II (microbes)
-
-
PWY-6853
ethene biosynthesis III (microbes)
-
-
PWY-6854
ethene biosynthesis IV (engineered)
-
-
PWY-7126
ethene biosynthesis V (engineered)
-
-
PWY-7124
Ether lipid metabolism
-
-
Ethylbenzene degradation
-
-
ethylbenzene degradation (anaerobic)
-
-
PWY-481
ethylene glycol degradation
-
-
PWY0-1280
eumelanin biosynthesis
-
-
PWY-6498
even iso-branched-chain fatty acid biosynthesis
-
-
PWY-8175
farnesylcysteine salvage pathway
-
-
PWY-6577
fatty acid alpha-oxidation I (plants)
-
-
PWY-2501
fatty acid beta-oxidation I (generic)
-
-
FAO-PWY
fatty acid beta-oxidation II (plant peroxisome)
-
-
PWY-5136
fatty acid beta-oxidation III (unsaturated, odd number)
-
-
PWY-5137
fatty acid beta-oxidation IV (unsaturated, even number)
-
-
PWY-5138
fatty acid beta-oxidation V (unsaturated, odd number, di-isomerase-dependent)
-
-
PWY-6837
fatty acid beta-oxidation VI (mammalian peroxisome)
-
-
PWY66-391
fatty acid beta-oxidation VII (yeast peroxisome)
-
-
PWY-7288
Fatty acid biosynthesis
-
-
fatty acid biosynthesis initiation (mitochondria)
-
-
PWY66-429
fatty acid biosynthesis initiation (plant mitochondria)
-
-
PWY-6799
fatty acid biosynthesis initiation (type I)
-
-
PWY-5966-1
fatty acid biosynthesis initiation (type II)
-
-
PWY-4381
Fatty acid degradation
-
-
Fatty acid elongation
-
-
fatty acid elongation -- saturated
-
-
FASYN-ELONG-PWY
fatty acid salvage
-
-
PWY-7094
Fe(II) oxidation
-
-
PWY-6692
felinine and 3-methyl-3-sulfanylbutan-1-ol biosynthesis
-
-
PWY-8001
FeMo cofactor biosynthesis
-
-
PWY-7710
ferrichrome A biosynthesis
-
-
PWY-7571
firefly bioluminescence
-
-
PWY-7913
flavin biosynthesis I (bacteria and plants)
-
-
RIBOSYN2-PWY
flavin biosynthesis II (archaea)
-
-
PWY-6167
flavin biosynthesis III (fungi)
-
-
PWY-6168
flavin salvage
-
-
PWY66-366
Flavone and flavonol biosynthesis
-
-
flavonoid biosynthesis
-
-
PWY1F-FLAVSYN
Flavonoid biosynthesis
-
-
flavonoid biosynthesis
-
-
flavonoid biosynthesis (in equisetum)
-
-
PWY-6787
flavonoid di-C-glucosylation
-
-
PWY-7897
flexixanthin biosynthesis
-
-
PWY-7947
fluoroacetate and fluorothreonine biosynthesis
-
-
PWY-6644
fluoroacetate degradation
-
-
PWY-6646
Fluorobenzoate degradation
-
-
folate transformations I
-
-
PWY-2201
folate transformations II (plants)
-
-
PWY-3841
folate transformations III (E. coli)
-
-
1CMET2-PWY
formaldehyde assimilation I (serine pathway)
-
-
PWY-1622
formaldehyde assimilation II (assimilatory RuMP Cycle)
-
-
PWY-1861
formaldehyde assimilation III (dihydroxyacetone cycle)
-
-
P185-PWY
formaldehyde oxidation
-
-
formaldehyde oxidation I
-
-
RUMP-PWY
formaldehyde oxidation II (glutathione-dependent)
-
-
PWY-1801
formaldehyde oxidation VII (THF pathway)
-
-
PWY-7909
formate assimilation into 5,10-methylenetetrahydrofolate
-
-
PWY-1722
formate oxidation to CO2
-
-
PWY-1881
formate to nitrite electron transfer
-
-
PWY0-1585
formononetin conjugates interconversion
-
-
PWY-2904
fructose 2,6-bisphosphate biosynthesis
-
-
PWY66-423
Fructose and mannose metabolism
-
-
fusicoccin A biosynthesis
-
-
PWY-6659
GABA shunt I
-
-
GLUDEG-I-PWY
GABA shunt II
-
-
PWY-8346
gala-series glycosphingolipids biosynthesis
-
-
PWY-7840
galactolipid biosynthesis I
-
-
PWY-401
gallate degradation III (anaerobic)
-
-
P3-PWY
gamma-butyrobetaine degradation II
-
-
PWY-3621
gamma-glutamyl cycle
-
-
PWY-4041
gamma-linolenate biosynthesis II (animals)
-
-
PWY-6000
gamma-resorcylate degradation I
-
-
PWY-7773
gamma-resorcylate degradation II
-
-
PWY-7772
ganglio-series glycosphingolipids biosynthesis
-
-
PWY-7836
GDP-6-deoxy-D-talose biosynthesis
-
-
PWY-5738
GDP-alpha-D-glucose biosynthesis
-
-
PWY-5661
GDP-D-perosamine biosynthesis
-
-
PWY-5739
GDP-D-rhamnose biosynthesis
-
-
GDPRHAMSYN-PWY
GDP-L-colitose biosynthesis
-
-
PWY-5740
GDP-L-fucose biosynthesis I (from GDP-D-mannose)
-
-
PWY-66
GDP-L-fucose biosynthesis II (from L-fucose)
-
-
PWY-6
GDP-mannose biosynthesis
-
-
PWY-5659
GDP-mycosamine biosynthesis
-
-
PWY-7573
GDP-N-acetyl-alpha-D-perosamine biosynthesis
-
-
PWY-8225
GDP-N-formyl-alpha-D-perosamine biosynthesis
-
-
PWY2B4Q-2
genistein conjugates interconversion
-
-
PWY-2345
geranylgeranyl diphosphate biosynthesis
-
-
PWY-5120
ginkgotoxin biosynthesis
-
-
PWY-8077
ginsenoside metabolism
-
-
ginsenosides biosynthesis
-
-
PWY-5672
gliotoxin biosynthesis
-
-
PWY-7533
globo-series glycosphingolipids biosynthesis
-
-
PWY-7838
glucocorticoid biosynthesis
-
-
PWY66-381
gluconeogenesis I
-
-
GLUCONEO-PWY
gluconeogenesis II (Methanobacterium thermoautotrophicum)
-
-
PWY-6142
gluconeogenesis III
-
-
PWY66-399
glucose and glucose-1-phosphate degradation
-
-
GLUCOSE1PMETAB-PWY
glucose degradation (oxidative)
-
-
DHGLUCONATE-PYR-CAT-PWY
glucosinolate activation
-
-
PWY-5267
Glucosinolate biosynthesis
-
-
glucosinolate biosynthesis from dihomomethionine
-
-
PWYQT-4471
glucosinolate biosynthesis from hexahomomethionine
-
-
PWYQT-4475
glucosinolate biosynthesis from homomethionine
-
-
PWY-1187
glucosinolate biosynthesis from pentahomomethionine
-
-
PWYQT-4474
glucosinolate biosynthesis from phenylalanine
-
-
PWY-2821
glucosinolate biosynthesis from tetrahomomethionine
-
-
PWYQT-4473
glucosinolate biosynthesis from trihomomethionine
-
-
PWYQT-4472
glucosinolate biosynthesis from tryptophan
-
-
PWY-601
glucosinolate biosynthesis from tyrosine
-
-
PWY-7901
glucosylglycerol biosynthesis
-
-
PWY-7902
glutamate and glutamine metabolism
-
-
glutamate removal from folates
-
-
PWY-2161B
glutaminyl-tRNAgln biosynthesis via transamidation
-
-
PWY-5921
glutaryl-CoA degradation
-
-
PWY-5177
glutathione biosynthesis
-
-
GLUTATHIONESYN-PWY
glutathione degradation (DUG pathway)
-
-
PWY-7559
Glutathione metabolism
-
-
glutathione metabolism
-
-
glutathione-mediated detoxification
-
-
glutathione-mediated detoxification I
-
-
PWY-4061
glutathione-mediated detoxification II
-
-
PWY-6842
glutathione-peroxide redox reactions
-
-
PWY-4081
glycerol degradation I
-
-
PWY-4261
glycerol degradation II
-
-
PWY-6131
glycerol degradation to butanol
-
-
PWY-7003
glycerol degradation V
-
-
GLYCEROLMETAB-PWY
glycerol-3-phosphate shuttle
-
-
PWY-6118
glycerol-3-phosphate to cytochrome bo oxidase electron transfer
-
-
PWY0-1561
glycerol-3-phosphate to fumarate electron transfer
-
-
PWY0-1582
glycerol-3-phosphate to hydrogen peroxide electron transport
-
-
PWY0-1591
Glycerolipid metabolism
-
-
glycerophosphodiester degradation
-
-
PWY-6952
Glycerophospholipid metabolism
-
-
glycine betaine biosynthesis
-
-
glycine betaine biosynthesis I (Gram-negative bacteria)
-
-
BETSYN-PWY
glycine betaine biosynthesis II (Gram-positive bacteria)
-
-
PWY-3722
glycine betaine biosynthesis III (plants)
-
-
PWY1F-353
glycine betaine biosynthesis IV (from glycine)
-
-
P541-PWY
glycine betaine biosynthesis V (from glycine)
-
-
PWY-6004
glycine betaine degradation I
-
-
PWY-3661
glycine betaine degradation II (mammalian)
-
-
PWY-3661-1
glycine betaine degradation III
-
-
PWY-8325
glycine biosynthesis I
-
-
GLYSYN-PWY
glycine biosynthesis II
-
-
GLYCINE-SYN2-PWY
glycine biosynthesis III
-
-
GLYSYN-ALA-PWY
glycine biosynthesis IV
-
-
GLYSYN-THR-PWY
glycine cleavage
-
-
GLYCLEAV-PWY
glycine degradation (reductive Stickland reaction)
-
-
PWY-8015
Glycine, serine and threonine metabolism
-
-
glycogen biosynthesis
-
-
glycogen biosynthesis I (from ADP-D-Glucose)
-
-
GLYCOGENSYNTH-PWY
glycogen biosynthesis II (from UDP-D-Glucose)
-
-
PWY-5067
glycogen biosynthesis III (from alpha-maltose 1-phosphate)
-
-
PWY-7900
glycogen degradation I
-
-
GLYCOCAT-PWY
glycogen degradation II
-
-
PWY-5941
glycolate and glyoxylate degradation
-
-
Glycolysis / Gluconeogenesis
-
-
glycolysis I (from glucose 6-phosphate)
-
-
GLYCOLYSIS
glycolysis II (from fructose 6-phosphate)
-
-
PWY-5484
glycolysis III (from glucose)
-
-
ANAGLYCOLYSIS-PWY
glycolysis IV
-
-
PWY-1042
glycolysis V (Pyrococcus)
-
-
P341-PWY
Glycosaminoglycan biosynthesis - chondroitin sulfate / dermatan sulfate
-
-
Glycosaminoglycan biosynthesis - heparan sulfate / heparin
-
-
Glycosaminoglycan biosynthesis - keratan sulfate
-
-
Glycosaminoglycan degradation
-
-
glycosaminoglycan-protein linkage region biosynthesis
-
-
PWY-6557
Glycosphingolipid biosynthesis - ganglio series
-
-
Glycosphingolipid biosynthesis - globo and isoglobo series
-
-
Glycosphingolipid biosynthesis - lacto and neolacto series
-
-
Glycosylphosphatidylinositol (GPI)-anchor biosynthesis
-
-
Glyoxylate and dicarboxylate metabolism
-
-
glyoxylate assimilation
-
-
PWY-5744
glyoxylate cycle
-
-
GLYOXYLATE-BYPASS
glyphosate degradation III
-
-
PWY-7807
gondoate biosynthesis (anaerobic)
-
-
PWY-7663
grixazone biosynthesis
-
-
PWY-7153
guadinomine B biosynthesis
-
-
PWY-7693
guaiacol biosynthesis
-
-
PWY18C3-23
guanine and guanosine salvage I
-
-
PWY-6620
guanine and guanosine salvage II
-
-
PWY-6599
guanosine deoxyribonucleotides de novo biosynthesis I
-
-
PWY-7226
guanosine deoxyribonucleotides de novo biosynthesis II
-
-
PWY-7222
guanosine nucleotides degradation I
-
-
PWY-6607
guanosine nucleotides degradation II
-
-
PWY-6606
guanosine nucleotides degradation III
-
-
PWY-6608
guanosine ribonucleotides de novo biosynthesis
-
-
PWY-7221
H. pylori 26695 O-antigen biosynthesis
-
-
PWY2DNV-5
heme b biosynthesis I (aerobic)
-
-
HEME-BIOSYNTHESIS-II
heme b biosynthesis II (oxygen-independent)
-
-
HEMESYN2-PWY
heme b biosynthesis IV (Gram-positive bacteria)
-
-
PWY-7766
heme b biosynthesis V (aerobic)
-
-
HEME-BIOSYNTHESIS-II-1
heme degradation I
-
-
PWY-5874
heparan sulfate biosynthesis
-
-
PWY-6558
heparan sulfate degradation
-
-
PWY-7651
heparin degradation
-
-
PWY-7644
heterolactic fermentation
-
-
P122-PWY
histamine biosynthesis
-
-
PWY-6173
histamine degradation
-
-
PWY-6181
homocarnosine biosynthesis
-
-
PWY66-421
homocysteine and cysteine interconversion
-
-
PWY-801
homoglutathione biosynthesis
-
-
PWY-6840
homospermidine biosynthesis I
-
-
PWY-5907
homospermidine biosynthesis II
-
-
PWY-8149
hyaluronan degradation
-
-
PWY-7645
hydrogen sulfide biosynthesis II (mammalian)
-
-
PWY66-426
hydrogen to fumarate electron transfer
-
-
PWY0-1576
hydroxycinnamic acid serotonin amides biosynthesis
-
-
PWY-5473
hydroxycinnamic acid tyramine amides biosynthesis
-
-
PWY-5474
hydroxylated fatty acid biosynthesis (plants)
-
-
PWY-6433
hypoglycin biosynthesis
-
-
PWY-5826
hypotaurine degradation
-
-
PWY-7387
hypusine biosynthesis
-
-
PWY-5905
i antigen and I antigen biosynthesis
-
-
PWY-7837
icosapentaenoate biosynthesis I (lower eukaryotes)
-
-
PWY-6958
icosapentaenoate biosynthesis II (6-desaturase, mammals)
-
-
PWY-7049
icosapentaenoate biosynthesis III (8-desaturase, mammals)
-
-
PWY-7724
icosapentaenoate biosynthesis V (8-desaturase, lower eukaryotes)
-
-
PWY-7602
icosapentaenoate biosynthesis VI (fungi)
-
-
PWY-6940
icosapentaenoate metabolites biosynthesis
-
-
PWY-8399
incomplete reductive TCA cycle
-
-
P42-PWY
indole degradation to anthranil and anthranilate
-
-
PWY-7430
indole glucosinolate activation (herbivore attack)
-
-
PWYQT-4476
indole glucosinolate activation (intact plant cell)
-
-
PWYQT-4477
indole-3-acetate biosynthesis II
-
-
PWY-581
indole-3-acetate biosynthesis III (bacteria)
-
-
PWY-3161
indole-3-acetate biosynthesis IV (bacteria)
-
-
PWY-5025
indole-3-acetate biosynthesis VI (bacteria)
-
-
TRPIAACAT-PWY
inosine 5'-phosphate degradation
-
-
PWY-5695
inosine-5'-phosphate biosynthesis I
-
-
PWY-6123
inosine-5'-phosphate biosynthesis II
-
-
PWY-6124
inosine-5'-phosphate biosynthesis III
-
-
PWY-7234
inositol diphosphates biosynthesis
-
-
PWY-6369
Inositol phosphate metabolism
-
-
Insect hormone biosynthesis
-
-
inulin degradation
-
-
PWY-8314
isoleucine metabolism
-
-
isoprene biosynthesis II (engineered)
-
-
PWY-7391
isoprenoid biosynthesis
-
-
isopropanol biosynthesis (engineered)
-
-
PWY-6876
Isoquinoline alkaloid biosynthesis
-
-
itaconate degradation
-
-
PWY-5749
jadomycin biosynthesis
-
-
PWY-6679
jasmonic acid biosynthesis
-
-
PWY-735
juniperonate biosynthesis
-
-
PWY-7619
justicidin B biosynthesis
-
-
PWY-6824
juvenile hormone III biosynthesis II
-
-
PWY-6650
ketogenesis
-
-
PWY66-367
kojibiose degradation
-
-
PWY-7459
L-alanine biosynthesis I
-
-
ALANINE-VALINESYN-PWY
L-alanine biosynthesis II
-
-
ALANINE-SYN2-PWY
L-alanine biosynthesis III
-
-
PWY0-1021
L-alanine degradation II (to D-lactate)
-
-
ALACAT2-PWY
L-alanine degradation III
-
-
ALANINE-DEG3-PWY
L-alanine degradation IV
-
-
PWY1-2
L-alanine degradation V (oxidative Stickland reaction)
-
-
PWY-8189
L-alanine degradation VI (reductive Stickland reaction)
-
-
PWY-8188
L-arabinose degradation II
-
-
PWY-5515
L-arabinose degradation IV
-
-
PWY-7295
L-arginine biosynthesis I (via L-ornithine)
-
-
ARGSYN-PWY
L-arginine biosynthesis II (acetyl cycle)
-
-
ARGSYNBSUB-PWY
L-arginine biosynthesis III (via N-acetyl-L-citrulline)
-
-
PWY-5154
L-arginine biosynthesis IV (archaea)
-
-
PWY-7400
L-arginine degradation I (arginase pathway)
-
-
ARGASEDEG-PWY
L-arginine degradation III (arginine decarboxylase/agmatinase pathway)
-
-
PWY0-823
L-arginine degradation IV (arginine decarboxylase/agmatine deiminase pathway)
-
-
ARGDEG-III-PWY
L-arginine degradation VI (arginase 2 pathway)
-
-
ARG-PRO-PWY
L-arginine degradation VII (arginase 3 pathway)
-
-
ARG-GLU-PWY
L-arginine degradation X (arginine monooxygenase pathway)
-
-
ARGDEG-V-PWY
L-arginine degradation XIII (reductive Stickland reaction)
-
-
PWY-8187
L-arginine degradation XIV (oxidative Stickland reaction)
-
-
PWY-6344
L-ascorbate biosynthesis IV (animals, D-glucuronate pathway)
-
-
PWY3DJ-35471
L-ascorbate biosynthesis VI (plants, myo-inositol pathway)
-
-
PWY-8142
L-ascorbate biosynthesis VIII (engineered pathway)
-
-
PWY-7165
L-ascorbate degradation II (bacterial, aerobic)
-
-
PWY-6961
L-ascorbate degradation III
-
-
PWY-6960
L-asparagine biosynthesis I
-
-
ASPARAGINE-BIOSYNTHESIS
L-asparagine biosynthesis III (tRNA-dependent)
-
-
PWY490-4
L-asparagine degradation I
-
-
ASPARAGINE-DEG1-PWY
L-asparagine degradation II
-
-
PWY-4002
L-asparagine degradation III (mammalian)
-
-
ASPARAGINE-DEG1-PWY-1
L-aspartate biosynthesis
-
-
ASPARTATESYN-PWY
L-aspartate degradation I
-
-
ASPARTATE-DEG1-PWY
L-aspartate degradation II (aerobic)
-
-
PWY-8291
L-aspartate degradation III (anaerobic)
-
-
PWY-8294
L-carnitine biosynthesis
-
-
PWY-6100
L-carnitine degradation II
-
-
PWY-3641
L-citrulline biosynthesis
-
-
CITRULBIO-PWY
L-citrulline degradation
-
-
CITRULLINE-DEG-PWY
L-cysteine biosynthesis I
-
-
CYSTSYN-PWY
L-cysteine biosynthesis II (tRNA-dependent)
-
-
PWY-6308
L-cysteine biosynthesis III (from L-homocysteine)
-
-
HOMOCYSDEGR-PWY
L-cysteine biosynthesis IX (Trichomonas vaginalis)
-
-
PWY-8010
L-cysteine biosynthesis VI (reverse transsulfuration)
-
-
PWY-I9
L-cysteine degradation I
-
-
CYSTEINE-DEG-PWY
L-cysteine degradation III
-
-
PWY-5329
L-dopa and L-dopachrome biosynthesis
-
-
PWY-6481
L-dopa degradation I (mammalian)
-
-
PWY-6334
L-dopa degradation II (bacterial)
-
-
PWY-8110
L-glutamate biosynthesis I
-
-
GLUTSYN-PWY
L-glutamate biosynthesis II
-
-
GLUTAMATE-SYN2-PWY
L-glutamate biosynthesis IV
-
-
GLUGLNSYN-PWY
L-glutamate degradation I
-
-
GLUTAMATE-DEG1-PWY
L-glutamate degradation II
-
-
GLUTDEG-PWY
L-glutamate degradation IX (via 4-aminobutanoate)
-
-
PWY0-1305
L-glutamate degradation V (via hydroxyglutarate)
-
-
P162-PWY
L-glutamate degradation VI (to pyruvate)
-
-
PWY-5087
L-glutamate degradation VII (to butanoate)
-
-
GLUDEG-II-PWY
L-glutamate degradation X
-
-
PWY-5766
L-glutamate degradation XI (reductive Stickland reaction)
-
-
PWY-8190
L-glutamine biosynthesis I
-
-
GLNSYN-PWY
L-glutamine degradation I
-
-
GLUTAMINDEG-PWY
L-histidine biosynthesis
-
-
HISTSYN-PWY
L-histidine degradation I
-
-
HISDEG-PWY
L-histidine degradation II
-
-
PWY-5028
L-histidine degradation III
-
-
PWY-5030
L-histidine degradation V
-
-
PWY-5031
L-histidine degradation VI
-
-
HISHP-PWY
L-homophenylalanine biosynthesis
-
-
PWY-7275
L-homoserine biosynthesis
-
-
HOMOSERSYN-PWY
L-isoleucine biosynthesis I (from threonine)
-
-
ILEUSYN-PWY
L-isoleucine biosynthesis II
-
-
PWY-5101
L-isoleucine biosynthesis III
-
-
PWY-5103
L-isoleucine biosynthesis IV
-
-
PWY-5104
L-isoleucine biosynthesis V
-
-
PWY-5108
L-isoleucine degradation I
-
-
ILEUDEG-PWY
L-isoleucine degradation II
-
-
PWY-5078
L-isoleucine degradation III (oxidative Stickland reaction)
-
-
PWY-8184
L-lactaldehyde degradation
-
-
L-lactaldehyde degradation (anaerobic)
-
-
PWY0-1315
L-leucine biosynthesis
-
-
LEUSYN-PWY
L-leucine degradation I
-
-
LEU-DEG2-PWY
L-leucine degradation II
-
-
PWY-5075
L-leucine degradation III
-
-
PWY-5076
L-leucine degradation IV (reductive Stickland reaction)
-
-
PWY-7767
L-leucine degradation V (oxidative Stickland reaction)
-
-
PWY-8185
L-lysine biosynthesis I
-
-
DAPLYSINESYN-PWY
L-lysine biosynthesis II
-
-
PWY-2941
L-lysine biosynthesis III
-
-
PWY-2942
L-lysine biosynthesis IV
-
-
LYSINE-AMINOAD-PWY
L-lysine biosynthesis V
-
-
PWY-3081
L-lysine biosynthesis VI
-
-
PWY-5097
L-lysine degradation I
-
-
PWY0-461
L-lysine degradation II (L-pipecolate pathway)
-
-
PWY66-425
L-lysine degradation IV
-
-
PWY-5280
L-lysine degradation V
-
-
PWY-5283
L-lysine degradation X
-
-
PWY-6328
L-lysine degradation XI
-
-
LYSINE-DEG1-PWY
L-lysine fermentation to acetate and butanoate
-
-
P163-PWY
L-malate degradation II
-
-
PWY-7686
L-methionine biosynthesis I
-
-
HOMOSER-METSYN-PWY
L-methionine biosynthesis II
-
-
PWY-702
L-methionine biosynthesis III
-
-
HSERMETANA-PWY
L-methionine biosynthesis IV
-
-
PWY-7977
L-methionine degradation I (to L-homocysteine)
-
-
METHIONINE-DEG1-PWY
L-methionine degradation III
-
-
PWY-5082
L-methionine salvage from L-homocysteine
-
-
ADENOSYLHOMOCYSCAT-PWY
L-Ndelta-acetylornithine biosynthesis
-
-
PWY-6922
L-nicotianamine biosynthesis
-
-
PWY-5957
L-ornithine biosynthesis I
-
-
GLUTORN-PWY
L-ornithine biosynthesis II
-
-
ARGININE-SYN4-PWY
L-ornithine degradation I (L-proline biosynthesis)
-
-
ORN-AMINOPENTANOATE-CAT-PWY
L-phenylalanine biosynthesis I
-
-
PHESYN
L-phenylalanine biosynthesis III (cytosolic, plants)
-
-
PWY-7432
L-phenylalanine degradation I (aerobic)
-
-
PHENYLALANINE-DEG1-PWY
L-phenylalanine degradation II (anaerobic)
-
-
ANAPHENOXI-PWY
L-phenylalanine degradation III
-
-
PWY-5079
L-phenylalanine degradation IV (mammalian, via side chain)
-
-
PWY-6318
L-phenylalanine degradation V
-
-
PWY-7158
L-phenylalanine degradation VI (reductive Stickland reaction)
-
-
PWY-8014
L-proline biosynthesis I (from L-glutamate)
-
-
PROSYN-PWY
L-proline biosynthesis II (from arginine)
-
-
PWY-4981
L-proline biosynthesis III (from L-ornithine)
-
-
PWY-3341
L-proline biosynthesis IV
-
-
PWY-4281
L-proline degradation I
-
-
PROUT-PWY
L-selenocysteine biosynthesis I (bacteria)
-
-
PWY0-901
L-selenocysteine biosynthesis II (archaea and eukaryotes)
-
-
PWY-6281
L-serine biosynthesis I
-
-
SERSYN-PWY
L-serine biosynthesis II
-
-
PWY-8011
L-threonine biosynthesis
-
-
HOMOSER-THRESYN-PWY
L-threonine degradation I
-
-
PWY-5437
L-threonine degradation II
-
-
THREONINE-DEG2-PWY
L-threonine degradation III (to methylglyoxal)
-
-
THRDLCTCAT-PWY
L-threonine degradation IV
-
-
PWY-5436
L-threonine degradation V
-
-
PWY66-428
L-tryptophan degradation I (via anthranilate)
-
-
TRPCAT-PWY
L-tryptophan degradation IV (via indole-3-lactate)
-
-
TRPKYNCAT-PWY
L-tryptophan degradation to 2-amino-3-carboxymuconate semialdehyde
-
-
PWY-5651
L-tryptophan degradation V (side chain pathway)
-
-
PWY-3162
L-tryptophan degradation VI (via tryptamine)
-
-
PWY-3181
L-tryptophan degradation VIII (to tryptophol)
-
-
PWY-5081
L-tryptophan degradation X (mammalian, via tryptamine)
-
-
PWY-6307
L-tryptophan degradation XI (mammalian, via kynurenine)
-
-
PWY-6309
L-tryptophan degradation XII (Geobacillus)
-
-
PWY-6505
L-tryptophan degradation XIII (reductive Stickland reaction)
-
-
PWY-8017
L-tyrosine biosynthesis I
-
-
TYRSYN
L-tyrosine biosynthesis IV
-
-
PWY-6134
L-tyrosine degradation I
-
-
TYRFUMCAT-PWY
L-tyrosine degradation II
-
-
PWY-5151
L-tyrosine degradation III
-
-
PWY3O-4108
L-tyrosine degradation IV (to 4-methylphenol)
-
-
PWY-7514
L-tyrosine degradation V (reductive Stickland reaction)
-
-
PWY-8016
L-valine biosynthesis
-
-
VALSYN-PWY
L-valine degradation I
-
-
VALDEG-PWY
L-valine degradation II
-
-
PWY-5057
L-valine degradation III (oxidative Stickland reaction)
-
-
PWY-8183
lactate fermentation to acetate, CO2 and hydrogen (Desulfovibrionales)
-
-
PWY-8377
lacto-series glycosphingolipids biosynthesis
-
-
PWY-7839
lactose degradation III
-
-
BGALACT-PWY
lanosterol biosynthesis
-
-
PWY-6132
leukotriene biosynthesis
-
-
PWY66-375
Limonene and pinene degradation
-
-
limonene degradation IV (anaerobic)
-
-
PWY-8029
linamarin degradation
-
-
PWY-3121
linoleate biosynthesis I (plants)
-
-
PWY-5995
linoleate biosynthesis II (animals)
-
-
PWY-6001
linoleate metabolites biosynthesis
-
-
PWY-8395
Linoleic acid metabolism
-
-
linustatin bioactivation
-
-
PWY-7091
lipid A-core biosynthesis (E. coli K-12)
-
-
LIPA-CORESYN-PWY
lipid IVA biosynthesis (2,3-diamino-2,3-dideoxy-D-glucopyranose-containing)
-
-
PWY2B4Q-4
lipid IVA biosynthesis (E. coli)
-
-
NAGLIPASYN-PWY
lipid IVA biosynthesis (generic)
-
-
PWY-8283
lipid IVA biosynthesis (H. pylori)
-
-
PWYI-14
lipid IVA biosynthesis (P. gingivalis)
-
-
PWY-8245
lipid IVA biosynthesis (P. putida)
-
-
PWY-8073
lipid IVA biosynthesis (Vibrio cholerae serogroup O1 El Tor)
-
-
PWY2G6Z-2
Lipopolysaccharide biosynthesis
-
-
lipoxin biosynthesis
-
-
PWY66-392
long chain fatty acid ester synthesis (engineered)
-
-
PWY-6873
long-chain fatty acid activation
-
-
PWY-5143
lotaustralin degradation
-
-
PWY-6002
lupeol biosynthesis
-
-
PWY-112
lupulone and humulone biosynthesis
-
-
PWY-5132
luteolin triglucuronide degradation
-
-
PWY-7445
m-cresol degradation
-
-
M-CRESOL-DEGRADATION-PWY
malate/L-aspartate shuttle pathway
-
-
MALATE-ASPARTATE-SHUTTLE-PWY
mandelate degradation I
-
-
PWY-1501
manganese oxidation I
-
-
PWY-6591
mangrove triterpenoid biosynthesis
-
-
PWY-6109
mannitol biosynthesis
-
-
PWY-3881
mannitol cycle
-
-
PWY-6531
mannitol degradation II
-
-
PWY-3861
Mannose type O-glycan biosynthesis
-
-
mannosylglycerate biosynthesis
-
-
mannosylglycerate biosynthesis I
-
-
PWY-5656
maresin biosynthesis
-
-
PWY-8356
matairesinol biosynthesis
-
-
PWY-5466
melatonin degradation I
-
-
PWY-6398
melatonin degradation II
-
-
PWY-6399
melibiose degradation
-
-
PWY0-1301
metabolism of amino sugars and derivatives
-
-
metabolism of disaccharids
-
-
Metabolism of xenobiotics by cytochrome P450
-
-
Methanobacterium thermoautotrophicum biosynthetic metabolism
-
-
PWY-6146
methanofuran biosynthesis
-
-
PWY-5254
methanogenesis from acetate
-
-
METH-ACETATE-PWY
methanogenesis from methanol
-
-
CO2FORM-PWY
methanol oxidation to formaldehyde IV
-
-
PWY-5506
methiin metabolism
-
-
PWY-7614
methionine metabolism
-
-
methyl indole-3-acetate interconversion
-
-
PWY-6303
methyl ketone biosynthesis (engineered)
-
-
PWY-7007
methyl parathion degradation
-
-
PWY-5489
methyl phomopsenoate biosynthesis
-
-
PWY-7721
methyl tert-butyl ether degradation
-
-
PWY-7779
methylerythritol phosphate pathway I
-
-
NONMEVIPP-PWY
methylerythritol phosphate pathway II
-
-
PWY-7560
methylgallate degradation
-
-
METHYLGALLATE-DEGRADATION-PWY
methylglyoxal degradation
-
-
methylglyoxal degradation I
-
-
PWY-5386
methylglyoxal degradation II
-
-
PWY-5462
methylglyoxal degradation III
-
-
PWY-5453
methylglyoxal degradation IV
-
-
PWY-5459
methylglyoxal degradation V
-
-
PWY-5458
methylglyoxal degradation VI
-
-
MGLDLCTANA-PWY
methylglyoxal degradation VII
-
-
PWY-5456
methylglyoxal degradation VIII
-
-
PWY-5386-1
methylsalicylate degradation
-
-
PWY18C3-24
mevalonate degradation
-
-
PWY-5074
mevalonate metabolism
-
-
mevalonate pathway I (eukaryotes and bacteria)
-
-
PWY-922
mevalonate pathway II (haloarchaea)
-
-
PWY-6174
mevalonate pathway III (Thermoplasma)
-
-
PWY-7524
mevalonate pathway IV (archaea)
-
-
PWY-8125
Microbial metabolism in diverse environments
-
-
mineralocorticoid biosynthesis
-
-
PWY66-382
mitochondrial L-carnitine shuttle
-
-
PWY-6111
mitochondrial NADPH production (yeast)
-
-
PWY-7269
mixed acid fermentation
-
-
FERMENTATION-PWY
molybdopterin biosynthesis
-
-
PWY-6823
mono-trans, poly-cis decaprenyl phosphate biosynthesis
-
-
PWY-6383
monoacylglycerol metabolism (yeast)
-
-
PWY-7420
Monobactam biosynthesis
-
-
monoterpene biosynthesis
-
-
PWY-3041
Monoterpenoid biosynthesis
mRNA capping I
-
-
PWY-7375
mucin core 1 and core 2 O-glycosylation
-
-
PWY-7433
mucin core 3 and core 4 O-glycosylation
-
-
PWY-7435
Mucin type O-glycan biosynthesis
-
-
mupirocin biosynthesis
-
-
PWY-8012
muropeptide degradation
-
-
PWY0-1546
mycobactin biosynthesis
-
-
PWY185E-1
mycolate biosynthesis
-
-
PWYG-321
mycolyl-arabinogalactan-peptidoglycan complex biosynthesis
-
-
PWY-6397
mycothiol biosynthesis
-
-
PWY1G-0
myo-inositol biosynthesis
myo-inositol degradation I
-
-
P562-PWY
N-acetyl-D-galactosamine degradation
-
-
PWY-7077
N-acetylglucosamine degradation I
-
-
GLUAMCAT-PWY
N-acetylglucosamine degradation II
-
-
PWY-6517
N-acetylneuraminate and N-acetylmannosamine degradation I
-
-
PWY0-1324
N-acetylneuraminate and N-acetylmannosamine degradation II
-
-
PWY-7581
N-Glycan biosynthesis
-
-
N-hydroxy-L-pipecolate biosynthesis
-
-
PWY-7861
N-methylpyrrolidone degradation
-
-
PWY-7978
NAD biosynthesis from 2-amino-3-carboxymuconate semialdehyde
-
-
PWY-5653
NAD biosynthesis from nicotinamide
-
-
NAD-BIOSYNTHESIS-III
NAD de novo biosynthesis I
-
-
PYRIDNUCSYN-PWY
NAD de novo biosynthesis III
-
-
PWY-8352
NAD de novo biosynthesis IV (anaerobic)
-
-
PWY-8277
NAD phosphorylation and dephosphorylation
-
-
NADPHOS-DEPHOS-PWY
NAD phosphorylation and transhydrogenation
-
-
NADPHOS-DEPHOS-PWY-1
NAD salvage (plants)
-
-
PWY-5381
NAD salvage pathway I (PNC VI cycle)
-
-
PYRIDNUCSAL-PWY
NAD salvage pathway II (PNC IV cycle)
-
-
PWY-7761
NAD salvage pathway III (to nicotinamide riboside)
-
-
NAD-BIOSYNTHESIS-II
NAD salvage pathway IV (from nicotinamide riboside)
-
-
PWY3O-4106
NAD salvage pathway V (PNC V cycle)
-
-
PWY3O-4107
NAD(P)/NADPH interconversion
-
-
PWY-5083
NADH repair (eukaryotes)
-
-
PWY-6938
NADH repair (prokaryotes)
-
-
PWY-6938-1
NADH to cytochrome bd oxidase electron transfer I
-
-
PWY0-1334
NADH to cytochrome bo oxidase electron transfer I
-
-
PWY0-1335
NADH to fumarate electron transfer
-
-
PWY0-1336
NADP biosynthesis
-
-
PWY-8148
NADPH repair (eukaryotes)
-
-
PWY-8137
NADPH repair (prokaryotes)
-
-
PWY-8136
NADPH to cytochrome c oxidase via plastocyanin
-
-
PWY-8271
Naphthalene degradation
-
-
naringenin biosynthesis (engineered)
-
-
PWY-7397
neolacto-series glycosphingolipids biosynthesis
-
-
PWY-7841
neolinustatin bioactivation
-
-
PWY-7092
Neomycin, kanamycin and gentamicin biosynthesis
-
-
Nicotinate and nicotinamide metabolism
-
-
nicotine biosynthesis
-
-
PWY-5316
nicotine degradation I (pyridine pathway)
-
-
P181-PWY
nicotine degradation III (VPP pathway)
-
-
PWY-7128
nicotine degradation IV
-
-
PWY66-201
nicotine degradation V
-
-
PWY66-221
nitrate reduction I (denitrification)
-
-
DENITRIFICATION-PWY
nitrate reduction II (assimilatory)
-
-
PWY-381
nitrate reduction IX (dissimilatory)
-
-
PWY0-1581
nitrate reduction VII (denitrification)
-
-
PWY-6748
nitrate reduction X (dissimilatory, periplasmic)
-
-
PWY0-1584
nitric oxide biosynthesis II (mammals)
-
-
PWY-4983
nitrifier denitrification
-
-
PWY-7084
nitrite-dependent anaerobic methane oxidation
-
-
PWY-6523
nitroethane degradation
-
-
PWY-5355
nitrogen remobilization from senescing leaves
-
-
PWY-6549
Nitrotoluene degradation
-
-
nocardicin A biosynthesis
-
-
PWY-7797
nonaprenyl diphosphate biosynthesis I
-
-
PWY-5805
noradrenaline and adrenaline degradation
-
-
PWY-6342
norspermidine biosynthesis
-
-
PWY-6562
Novobiocin biosynthesis
-
-
nucleoside and nucleotide degradation (archaea)
-
-
PWY-5532
nylon-6 oligomer degradation
-
-
P621-PWY
O-antigen biosynthesis
-
-
O-antigen building blocks biosynthesis (E. coli)
-
-
OANTIGEN-PWY
O-Antigen nucleotide sugar biosynthesis
-
-
o-diquinones biosynthesis
-
-
PWY-6752
octanoyl-[acyl-carrier protein] biosynthesis (mitochondria, yeast)
-
-
PWY-7388
octopamine biosynthesis
-
-
PWY-7297
odd iso-branched-chain fatty acid biosynthesis
-
-
PWY-8174
oleandomycin activation/inactivation
-
-
PWY-6972
oleate beta-oxidation
-
-
PWY0-1337
oleate beta-oxidation (isomerase-dependent, yeast)
-
-
PWY-7291
oleate beta-oxidation (reductase-dependent, yeast)
-
-
PWY-7307
oleate beta-oxidation (thioesterase-dependent, yeast)
-
-
PWY-7292
oleate biosynthesis I (plants)
-
-
PWY-5147
oleate biosynthesis II (animals and fungi)
-
-
PWY-5996
oleate biosynthesis III (cyanobacteria)
-
-
PWY-7587
oleate biosynthesis IV (anaerobic)
-
-
PWY-7664
One carbon pool by folate
-
-
ophiobolin F biosynthesis
-
-
PWY-7720
ophthalmate biosynthesis
-
-
PWY-8043
Other glycan degradation
-
-
Other types of O-glycan biosynthesis
-
-
oxalate degradation III
-
-
PWY-6696
oxalate degradation VI
-
-
PWY-7985
oxidative decarboxylation of pyruvate
-
-
Oxidative phosphorylation
-
-
oxidative phosphorylation
-
-
palmitate biosynthesis
-
-
palmitate biosynthesis I (type I fatty acid synthase)
-
-
PWY-5994
palmitate biosynthesis II (type II fatty acid synthase)
-
-
PWY-5971
palmitate biosynthesis III
-
-
PWY-8279
palmitoleate biosynthesis I (from (5Z)-dodec-5-enoate)
-
-
PWY-6282
palmitoleate biosynthesis III (cyanobacteria)
-
-
PWY-7589
palmitoleate biosynthesis IV (fungi and animals)
-
-
PWY3O-1801
palmitoyl ethanolamide biosynthesis
-
-
PWY-8055
Pantothenate and CoA biosynthesis
-
-
pantothenate biosynthesis
-
-
paraoxon degradation
-
-
PWY-5490
parathion degradation
-
-
PARATHION-DEGRADATION-PWY
partial TCA cycle (obligate autotrophs)
-
-
PWY-5913
paspaline biosynthesis
-
-
PWY-7492
patulin biosynthesis
-
-
PWY-7490
pederin biosynthesis
-
-
PWY-8049
Penicillin and cephalosporin biosynthesis
-
-
pentachlorophenol degradation
-
-
PCPDEG-PWY
pentacyclic triterpene biosynthesis
-
-
PWY-7251
Pentose and glucuronate interconversions
-
-
Pentose phosphate pathway
-
-
pentose phosphate pathway
-
-
pentose phosphate pathway (non-oxidative branch) I
-
-
NONOXIPENT-PWY
pentose phosphate pathway (non-oxidative branch) II
-
-
PWY-8178
pentose phosphate pathway (oxidative branch) I
-
-
OXIDATIVEPENT-PWY
pentose phosphate pathway (partial)
-
-
P21-PWY
peptido-conjugates in tissue regeneration biosynthesis
-
-
PWY-8355
Peptidoglycan biosynthesis
-
-
peptidoglycan biosynthesis
-
-
peptidoglycan biosynthesis I (meso-diaminopimelate containing)
-
-
PEPTIDOGLYCANSYN-PWY
peptidoglycan biosynthesis II (staphylococci)
-
-
PWY-5265
peptidoglycan biosynthesis III (mycobacteria)
-
-
PWY-6385
peptidoglycan biosynthesis IV (Enterococcus faecium)
-
-
PWY-6471
peptidoglycan biosynthesis V (beta-lactam resistance)
-
-
PWY-6470
peptidoglycan maturation (meso-diaminopimelate containing)
-
-
PWY0-1586
peptidoglycan recycling I
-
-
PWY0-1261
peptidoglycan recycling II
-
-
PWY-7883
petrobactin biosynthesis
-
-
PWY-6289
phenylacetate degradation (aerobic)
-
-
phenylacetate degradation I (aerobic)
-
-
PWY0-321
Phenylalanine metabolism
-
-
phenylalanine metabolism
-
-
Phenylalanine, tyrosine and tryptophan biosynthesis
-
-
phenylethanol biosynthesis
-
-
PWY-5751
phenylethylamine degradation I
-
-
2PHENDEG-PWY
phenylpropanoid biosynthesis
-
-
PWY-361
Phenylpropanoid biosynthesis
-
-
phenylpropanoid biosynthesis
-
-
phenylpropanoids methylation (ice plant)
-
-
PWY-7498
pheomelanin biosynthesis
-
-
PWY-7917
phloridzin biosynthesis
-
-
PWY-6515
phosphate acquisition
-
-
PWY-6348
phosphatidate biosynthesis (yeast)
-
-
PWY-7411
phosphatidate metabolism, as a signaling molecule
-
-
PWY-7039
phosphatidylcholine acyl editing
-
-
PWY-6803
phosphatidylcholine biosynthesis I
-
-
PWY3O-450
phosphatidylcholine biosynthesis II
-
-
PWY4FS-2
phosphatidylcholine biosynthesis III
-
-
PWY4FS-3
phosphatidylcholine biosynthesis IV
-
-
PWY4FS-4
phosphatidylcholine biosynthesis V
-
-
PWY-6825
phosphatidylcholine biosynthesis VII
-
-
PWY-7470
phosphatidylcholine resynthesis via glycerophosphocholine
-
-
PWY-7367
phosphatidylethanolamine biosynthesis II
-
-
PWY4FS-6
phosphatidylethanolamine biosynthesis III
-
-
PWY-6273
phosphatidylethanolamine bioynthesis
-
-
phosphatidylglycerol biosynthesis I
-
-
PWY4FS-7
phosphatidylglycerol biosynthesis II
-
-
PWY4FS-8
phosphatidylinositol biosynthesis I (bacteria)
-
-
PWY-6580
phosphatidylinositol biosynthesis II (eukaryotes)
-
-
PWY-7625
phosphatidylserine and phosphatidylethanolamine biosynthesis I
-
-
PWY-5669
phosphatidylserine biosynthesis I
-
-
PWY-7501
phosphatidylserine biosynthesis II
-
-
PWY-7506
phospholipases
-
-
LIPASYN-PWY
phospholipid desaturation
-
-
PWY-762
phospholipid remodeling (phosphatidate, yeast)
-
-
PWY-7417
phospholipid remodeling (phosphatidylcholine, yeast)
-
-
PWY-7416
phospholipid remodeling (phosphatidylethanolamine, yeast)
-
-
PWY-7409
Phosphonate and phosphinate metabolism
-
-
phosphopantothenate biosynthesis I
-
-
PANTO-PWY
phosphopantothenate biosynthesis II
-
-
PWY-3961
photorespiration I
-
-
PWY-181
photorespiration II
-
-
PWY-8362
photorespiration III
-
-
PWY-8363
photosynthesis light reactions
-
-
PWY-101
photosynthetic 3-hydroxybutanoate biosynthesis (engineered)
-
-
PWY-7218
phytate degradation I
-
-
PWY-4702
phytate degradation II
-
-
PWY-4781
phytochelatins biosynthesis
-
-
PWY-6745
phytol degradation
-
-
PWY66-389
phytosterol biosynthesis (plants)
-
-
PWY-2541
pinitol biosynthesis I
-
-
PWY-6738
pinoresinol degradation
-
-
PWY-7982
plasmalogen biosynthesis I (aerobic)
-
-
PWY-7782
plasmalogen degradation
-
-
PWY-7783
plastoquinol-9 biosynthesis I
-
-
PWY-1581
plastoquinol-9 biosynthesis II
-
-
PWY-6978
platensimycin biosynthesis
-
-
PWY-8179
plaunotol biosynthesis
-
-
PWY-6691
poly(3-O-beta-D-glucopyranosyl-N-acetylgalactosamine 1-phosphate) wall teichoic acid biosynthesis
-
-
PWY-7819
poly(glycerol phosphate) wall teichoic acid biosynthesis
-
-
TEICHOICACID-PWY
poly(ribitol phosphate) wall teichoic acid biosynthesis I (B. subtilis)
-
-
PWY-7815
poly(ribitol phosphate) wall teichoic acid biosynthesis II (S. aureus)
-
-
PWY-7816
poly-hydroxy fatty acids biosynthesis
-
-
PWY-6710
Polycyclic aromatic hydrocarbon degradation
-
-
polyhydroxybutanoate biosynthesis
-
-
PWY1-3
polyhydroxydecanoate biosynthesis
-
-
PWY-6657
Porphyrin and chlorophyll metabolism
-
-
ppGpp metabolism
-
-
PPGPPMET-PWY
preQ0 biosynthesis
-
-
PWY-6703
Primary bile acid biosynthesis
-
-
procollagen hydroxylation and glycosylation
-
-
PWY-7894
progesterone biosynthesis
-
-
PWY-7299
propanethial S-oxide biosynthesis
-
-
PWY-5707
propanoate fermentation to 2-methylbutanoate
-
-
PWY-5109
Propanoate metabolism
-
-
propanoyl CoA degradation I
-
-
PROPIONMET-PWY
propanoyl-CoA degradation II
-
-
PWY-7574
propionate fermentation
-
-
protectin biosynthesis
-
-
PWY-8357
protein citrullination
-
-
PWY-4921
protein N-glycosylation (Haloferax volcanii)
-
-
PWY-7661
protein N-glycosylation initial phase (eukaryotic)
-
-
MANNOSYL-CHITO-DOLICHOL-BIOSYNTHESIS
protein N-glycosylation processing phase (endoplasmic reticulum, yeast)
-
-
PWY-7918
protein N-glycosylation processing phase (plants and animals)
-
-
PWY-7919
protein NEDDylation
-
-
PWY-7899
protein O-mannosylation I (yeast)
-
-
PWY-7921
protein O-mannosylation II (mammals, core M1 and core M2)
-
-
PWY-7922
protein O-mannosylation III (mammals, core M3)
-
-
PWY-7979
protein O-[N-acetyl]-glucosylation
-
-
PWY-7437
protein S-nitrosylation and denitrosylation
-
-
PWY-7798
protein ubiquitination
-
-
PWY-7511
protocatechuate degradation I (meta-cleavage pathway)
-
-
P184-PWY
PRPP biosynthesis
-
-
PWY0-662
psilocybin biosynthesis
-
-
PWY-7936
purine deoxyribonucleosides degradation I
-
-
PWY-7179
purine deoxyribonucleosides degradation II
-
-
PWY-7179-1
purine deoxyribonucleosides salvage
-
-
PWY-7224
purine nucleobases degradation I (anaerobic)
-
-
P164-PWY
purine nucleobases degradation II (anaerobic)
-
-
PWY-5497
purine ribonucleosides degradation
-
-
PWY0-1296
putrescine biosynthesis I
-
-
PWY-40
putrescine biosynthesis II
-
-
PWY-43
putrescine biosynthesis III
-
-
PWY-46
putrescine degradation I
-
-
PUTDEG-PWY
putrescine degradation III
-
-
PWY-0
putrescine degradation IV
-
-
PWY-2
putrescine degradation V
-
-
PWY-3
pyridoxal 5'-phosphate biosynthesis I
-
-
PYRIDOXSYN-PWY
pyridoxal 5'-phosphate salvage I
-
-
PLPSAL-PWY
pyridoxal 5'-phosphate salvage II (plants)
-
-
PWY-7204
pyrimidine deoxyribonucleosides degradation
-
-
PWY-7181
pyrimidine deoxyribonucleosides salvage
-
-
PWY-7199
pyrimidine deoxyribonucleotide phosphorylation
-
-
PWY-7197
pyrimidine deoxyribonucleotides biosynthesis from CTP
-
-
PWY-7210
pyrimidine deoxyribonucleotides de novo biosynthesis I
-
-
PWY-7184
pyrimidine deoxyribonucleotides de novo biosynthesis II
-
-
PWY-7187
pyrimidine deoxyribonucleotides de novo biosynthesis III
-
-
PWY-6545
pyrimidine deoxyribonucleotides de novo biosynthesis IV
-
-
PWY-7198
pyrimidine deoxyribonucleotides dephosphorylation
-
-
PWY-7206
Pyrimidine metabolism
-
-
pyrimidine metabolism
-
-
pyrimidine ribonucleosides degradation
-
-
PWY0-1295
pyrimidine ribonucleosides salvage I
-
-
PWY-7193
pyrimidine ribonucleosides salvage II
-
-
PWY-6556
pyruvate decarboxylation to acetyl CoA I
-
-
PYRUVDEHYD-PWY
pyruvate decarboxylation to acetyl CoA II
-
-
PWY-6970
pyruvate decarboxylation to acetyl CoA III
-
-
PWY-8275
pyruvate fermentation to (R)-lactate
-
-
PWY-8274
pyruvate fermentation to (S)-lactate
-
-
PWY-5481
pyruvate fermentation to acetate I
-
-
P142-PWY
pyruvate fermentation to acetate II
-
-
PWY-5482
pyruvate fermentation to acetate III
-
-
PWY-5483
pyruvate fermentation to acetate IV
-
-
PWY-5485
pyruvate fermentation to acetate V
-
-
PWY-5537
pyruvate fermentation to acetate VI
-
-
PWY-5538
pyruvate fermentation to acetate VII
-
-
PWY-5600
pyruvate fermentation to acetate VIII
-
-
PWY-5768
pyruvate fermentation to acetoin III
-
-
PWY3O-440
pyruvate fermentation to acetone
-
-
PWY-6588
pyruvate fermentation to butanoate
-
-
CENTFERM-PWY
pyruvate fermentation to butanol I
-
-
PWY-6583
pyruvate fermentation to butanol II (engineered)
-
-
PWY-6883
pyruvate fermentation to ethanol I
-
-
PWY-5480
pyruvate fermentation to ethanol II
-
-
PWY-5486
pyruvate fermentation to ethanol III
-
-
PWY-6587
pyruvate fermentation to hexanol (engineered)
-
-
PWY-6863
pyruvate fermentation to isobutanol (engineered)
-
-
PWY-7111
pyruvate fermentation to propanoate I
-
-
P108-PWY
quercetin glucoside degradation (Allium)
-
-
PWY-7133
queuosine biosynthesis II (queuine salvage)
-
-
PWY-8105
quinoxaline-2-carboxylate biosynthesis
-
-
PWY-7734
Rapoport-Luebering glycolytic shunt
-
-
PWY-6405
reactive oxygen species degradation
-
-
DETOX1-PWY-1
reductive acetyl coenzyme A pathway
-
-
reductive acetyl coenzyme A pathway I (homoacetogenic bacteria)
-
-
CODH-PWY
reductive glycine pathway of autotrophic CO2 fixation
-
-
PWY-8303
reductive monocarboxylic acid cycle
-
-
PWY-5493
reductive TCA cycle I
-
-
P23-PWY
reductive TCA cycle II
-
-
PWY-5392
resolvin D biosynthesis
-
-
PWY66-397
retinoate biosynthesis I
-
-
PWY-6872
retinol biosynthesis
-
-
PWY-6857
Riboflavin metabolism
-
-
ricinoleate biosynthesis
-
-
PWY-7618
roseoflavin biosynthesis
-
-
PWY-7863
rosmarinic acid biosynthesis I
-
-
PWY-5048
rosmarinic acid biosynthesis II
-
-
PWY-5049
Rubisco shunt
-
-
PWY-5723
rutin degradation (plants)
-
-
PWY-7134
S-(6-hydroxy-4-methylhexan-4-yl)-L-cysteinylglycine biosynthesis
-
-
PWY-8301
S-(6-hydroxy-4-methylhexan-4-yl)-L-cysteinylglycine degradation
-
-
PWY-8302
S-adenosyl-L-methionine biosynthesis
-
-
SAM-PWY
S-adenosyl-L-methionine salvage I
-
-
PWY-6151
S-adenosyl-L-methionine salvage II
-
-
PWY-5041
S-methyl-5'-thioadenosine degradation II
-
-
PWY-6756
S-methyl-5-thio-alpha-D-ribose 1-phosphate degradation I
-
-
PWY-4361
S-methyl-5-thio-alpha-D-ribose 1-phosphate degradation II
-
-
PWY-7174
S-methyl-5-thio-alpha-D-ribose 1-phosphate degradation III
-
-
PWY-8132
S-methyl-L-methionine cycle
-
-
PWY-5441
salicin biosynthesis
-
-
PWY-6766
salicortin biosynthesis
-
-
PWY-6763
salicylate biosynthesis I
-
-
PWY-6406
salicylate biosynthesis II
-
-
PWY-8321
salidroside biosynthesis
-
-
PWY-6802
salinosporamide A biosynthesis
-
-
PWY-6627
Salmonella enterica serotype O:13 O antigen biosynthesis
-
-
PWY-8230
Salmonella enterica serotype O:54 O antigen biosynthesis
-
-
PWY-8204
sapienate biosynthesis
-
-
PWY-5362
saponin biosynthesis II
-
-
PWY-5756
sciadonate biosynthesis
-
-
PWY-6598
scopoletin biosynthesis
-
-
PWY-6792
secologanin and strictosidine biosynthesis
-
-
PWY-5290
Secondary bile acid biosynthesis
-
-
sedoheptulose bisphosphate bypass
-
-
PWY0-1517
selenate reduction
-
-
PWY-6932
seleno-amino acid biosynthesis (plants)
-
-
PWY-6936
seleno-amino acid detoxification and volatilization I
-
-
PWY-6931
seleno-amino acid detoxification and volatilization III
-
-
PWY-6933
Selenocompound metabolism
-
-
selenocysteine biosynthesis
-
-
serine racemization
-
-
PWY-8140
serotonin and melatonin biosynthesis
-
-
PWY-6030
serotonin degradation
-
-
PWY-6313
sesamin biosynthesis
-
-
PWY-5469
Sesquiterpenoid and triterpenoid biosynthesis
-
-
sitosterol degradation to androstenedione
-
-
PWY-6948
sophorolipid biosynthesis
-
-
SOPHOROSYLOXYDOCOSANOATE-SYN-PWY
sorbitol biosynthesis II
-
-
PWY-5530
sorgoleone biosynthesis
-
-
PWY-5987
spermidine biosynthesis I
-
-
BSUBPOLYAMSYN-PWY
spermidine biosynthesis II
-
-
PWY-6559
spermidine biosynthesis III
-
-
PWY-6834
spermine and spermidine degradation I
-
-
PWY-6117
spermine and spermidine degradation III
-
-
PWY-6441
spermine biosynthesis
-
-
ARGSPECAT-PWY
sphingolipid biosynthesis (mammals)
-
-
PWY-7277
sphingolipid biosynthesis (plants)
-
-
PWY-5129
sphingolipid biosynthesis (yeast)
-
-
SPHINGOLIPID-SYN-PWY
Sphingolipid metabolism
-
-
sphingomyelin metabolism
-
-
PWY3DJ-11281
sphingosine and sphingosine-1-phosphate metabolism
-
-
PWY3DJ-11470
sphingosine metabolism
-
-
Spodoptera littoralis pheromone biosynthesis
-
-
PWY-7656
sporopollenin precursors biosynthesis
-
-
PWY-6733
stachyose degradation
-
-
PWY-6527
Starch and sucrose metabolism
-
-
starch biosynthesis
-
-
PWY-622
starch degradation I
-
-
PWY-842
starch degradation II
-
-
PWY-6724
starch degradation III
-
-
PWY-6731
starch degradation V
-
-
PWY-6737
stearate biosynthesis I (animals)
-
-
PWY-5972
stearate biosynthesis II (bacteria and plants)
-
-
PWY-5989
stearate biosynthesis III (fungi)
-
-
PWY3O-355
stearate biosynthesis IV
-
-
PWY-8280
stellatic acid biosynthesis
-
-
PWY-7736
Steroid hormone biosynthesis
-
-
sterol biosynthesis (methylotrophs)
-
-
PWY-8026
sterol:steryl ester interconversion (yeast)
-
-
PWY-7424
stigma estolide biosynthesis
-
-
PWY-6453
Stilbenoid, diarylheptanoid and gingerol biosynthesis
-
-
streptomycin biosynthesis
-
-
PWY-5940
Streptomycin biosynthesis
-
-
streptorubin B biosynthesis
-
-
PWY1A0-6120
suberin monomers biosynthesis
succinate to chytochrome c oxidase via cytochrome c6
-
-
PWY1YI0-2
succinate to cytochrome bd oxidase electron transfer
-
-
PWY0-1353
succinate to cytochrome bo oxidase electron transfer
-
-
PWY0-1329
succinate to cytochrome c oxidase via plastocyanin
-
-
PWY1YI0-3
succinate to plastoquinol oxidase
-
-
PWY1YI0-8
sucrose biosynthesis I (from photosynthesis)
-
-
SUCSYN-PWY
sucrose biosynthesis II
-
-
PWY-7238
sucrose biosynthesis III
-
-
PWY-7347
sucrose degradation I (sucrose phosphotransferase)
-
-
SUCUTIL-PWY
sucrose degradation II (sucrose synthase)
-
-
PWY-3801
sucrose degradation III (sucrose invertase)
-
-
PWY-621
sucrose degradation IV (sucrose phosphorylase)
-
-
PWY-5384
sucrose degradation V (sucrose alpha-glucosidase)
-
-
PWY66-373
sucrose degradation VII (sucrose 3-dehydrogenase)
-
-
SUCROSEUTIL2-PWY
sulfate activation for sulfonation
-
-
PWY-5340
sulfated glycosaminoglycan metabolism
-
-
sulfide oxidation I (to sulfur globules)
-
-
P222-PWY
sulfide oxidation III (to sulfite)
-
-
PWY-5285
sulfide oxidation IV (mitochondria)
-
-
PWY-7927
sulfite oxidation II
-
-
PWY-5279
sulfite oxidation III
-
-
PWY-5278
sulfite oxidation IV (sulfite oxidase)
-
-
PWY-5326
sulfolactate degradation III
-
-
PWY-6638
sulfopterin metabolism
-
-
sulfur volatiles biosynthesis
-
-
PWY-6736
superoxide radicals degradation
-
-
DETOX1-PWY
superpathway of 5-aminoimidazole ribonucleotide biosynthesis
-
-
PWY-6277
superpathway of coenzyme A biosynthesis III (mammals)
-
-
COA-PWY-1
superpathway of fatty acid biosynthesis initiation
-
-
FASYN-INITIAL-PWY
superpathway of fermentation (Chlamydomonas reinhardtii)
-
-
PWY4LZ-257
superpathway of glucose and xylose degradation
-
-
PWY-6901
superpathway of glycolysis and the Entner-Doudoroff pathway
-
-
GLYCOLYSIS-E-D
superpathway of glycolysis, pyruvate dehydrogenase, TCA, and glyoxylate bypass
-
-
GLYCOLYSIS-TCA-GLYOX-BYPASS
superpathway of glyoxylate cycle and fatty acid degradation
-
-
PWY-561
superpathway of L-aspartate and L-asparagine biosynthesis
-
-
ASPASN-PWY
superpathway of methylsalicylate metabolism
-
-
PWY18C3-25
superpathway of nicotine biosynthesis
-
-
PWY-7342
superpathway of ornithine degradation
-
-
ORNDEG-PWY
superpathway of phospholipid biosynthesis II (plants)
-
-
PHOSLIPSYN2-PWY
superpathway of photosynthetic hydrogen production
-
-
PWY-7731
superpathway of polyamine biosynthesis II
-
-
POLYAMINSYN3-PWY
superpathway of pyrimidine deoxyribonucleotides de novo biosynthesis (E. coli)
-
-
PWY0-166
superpathway of UDP-glucose-derived O-antigen building blocks biosynthesis
-
-
PWY-7328
syringate degradation
-
-
PWY-6339
Taurine and hypotaurine metabolism
-
-
taurine biosynthesis I
-
-
PWY-5331
taurine biosynthesis II
-
-
PWY-7850
taurine biosynthesis III
-
-
PWY-8359
TCA cycle I (prokaryotic)
-
-
TCA
TCA cycle II (plants and fungi)
-
-
PWY-5690
TCA cycle III (animals)
-
-
PWY66-398
TCA cycle IV (2-oxoglutarate decarboxylase)
-
-
P105-PWY
TCA cycle V (2-oxoglutarate synthase)
-
-
PWY-6969
TCA cycle VI (Helicobacter)
-
-
REDCITCYC
TCA cycle VII (acetate-producers)
-
-
PWY-7254
TCA cycle VIII (Chlamydia)
-
-
TCA-1
tea aroma glycosidic precursor bioactivation
-
-
PWY-7114
teichuronic acid biosynthesis (B. subtilis 168)
-
-
PWY-7820
terminal O-glycans residues modification (via type 2 precursor disaccharide)
-
-
PWY-7434
Terpenoid backbone biosynthesis
-
-
testosterone and androsterone degradation to androstendione (aerobic)
-
-
PWY-6943
tetracenomycin C biosynthesis
-
-
PWY-7485
tetradecanoate biosynthesis (mitochondria)
-
-
PWY66-430
tetrahydrofolate biosynthesis I
-
-
PWY-6614
tetrahydrofolate metabolism
-
-
tetrahydrofolate salvage from 5,10-methenyltetrahydrofolate
-
-
PWY-6613
tetrahydromonapterin biosynthesis
-
-
PWY0-1433
tetrahydropteridine recycling
-
-
PWY-8099
tetrahydroxyxanthone biosynthesis (from benzoate)
-
-
PWY-5001
tetrapyrrole biosynthesis I (from glutamate)
-
-
PWY-5188
tetrapyrrole biosynthesis II (from glycine)
-
-
PWY-5189
the visual cycle I (vertebrates)
-
-
PWY-6861
theobromine biosynthesis I
-
-
PWY-5039
theophylline degradation
-
-
PWY-6999
thiamine diphosphate biosynthesis III (Staphylococcus)
-
-
PWY-6907
thiamine diphosphate biosynthesis IV (eukaryotes)
-
-
PWY-6908
thiamine diphosphate salvage III
-
-
PWY-6898
thiamine diphosphate salvage IV (yeast)
-
-
PWY-7356
thiamine triphosphate metabolism
-
-
PWY-7369
thiazole component of thiamine diphosphate biosynthesis I
-
-
PWY-6892
thioredoxin pathway
-
-
THIOREDOX-PWY
thiosulfate disproportionation IV (rhodanese)
-
-
PWY-5350
threo-tetrahydrobiopterin biosynthesis
-
-
PWY-6983
thymine degradation
-
-
PWY-6430
thyroid hormone biosynthesis
thyroid hormone metabolism I (via deiodination)
-
-
PWY-6260
thyroid hormone metabolism II (via conjugation and/or degradation)
-
-
PWY-6261
toluene degradation II (aerobic) (via 4-methylcatechol)
-
-
TOLUENE-DEG-3-OH-PWY
toluene degradation to 2-hydroxypentadienoate (via toluene-cis-diol)
-
-
TOLUENE-DEG-DIOL-PWY
toluene degradation to 2-hydroxypentadienoate I (via o-cresol)
-
-
TOLUENE-DEG-2-OH-PWY
toluene degradation to benzoate
-
-
TOLUENE-DEG-CATECHOL-PWY
trans, trans-farnesyl diphosphate biosynthesis
-
-
PWY-5123
trans-3-hydroxy-L-proline degradation
-
-
PWY-7515
trans-4-hydroxy-L-proline degradation I
-
-
HYDROXYPRODEG-PWY
trans-caffeate degradation (aerobic)
-
-
PWY-8003
traumatin and (Z)-3-hexen-1-yl acetate biosynthesis
-
-
PWY-5410
trehalose biosynthesis V
-
-
PWY-2661
trehalose degradation I (low osmolarity)
-
-
TREDEGLOW-PWY
trehalose degradation II (cytosolic)
-
-
PWY0-1182
trehalose degradation IV
-
-
PWY-2722
trehalose degradation V
-
-
PWY-2723
trehalose degradation VI (periplasmic)
-
-
PWY0-1466
triacylglycerol degradation
-
-
LIPAS-PWY
trimethylamine degradation
-
-
PWY-6968
trimethylamine N-oxide biosynthesis
-
-
PWY-8292
tRNA charging
-
-
TRNA-CHARGING-PWY
tRNA processing
-
-
PWY0-1479
tRNA splicing I
-
-
PWY-6689
tRNA-uridine 2-thiolation and selenation (bacteria)
-
-
PWY-7892
tropane alkaloid biosynthesis
-
-
tropane alkaloids biosynthesis
-
-
PWY-5317
Tropane, piperidine and pyridine alkaloid biosynthesis
-
-
Tryptophan metabolism
-
-
tryptophan metabolism
-
-
tunicamycin biosynthesis
-
-
PWY-7821
type I lipoteichoic acid biosynthesis (S. aureus)
-
-
PWY-7817
type IV lipoteichoic acid biosynthesis (S. pneumoniae)
-
-
PWY-7818
ubiquinol-10 biosynthesis (early decarboxylation)
-
-
PWY-5857
ubiquinol-10 biosynthesis (late decarboxylation)
-
-
PWY-5872
ubiquinol-6 biosynthesis (late decarboxylation)
-
-
PWY3O-19
ubiquinol-6 biosynthesis from 4-aminobenzoate (yeast)
-
-
PWY-7230
ubiquinol-7 biosynthesis (early decarboxylation)
-
-
PWY-5855
ubiquinol-7 biosynthesis (late decarboxylation)
-
-
PWY-5873
ubiquinol-8 biosynthesis (early decarboxylation)
-
-
PWY-6708
ubiquinol-8 biosynthesis (late decarboxylation)
-
-
PWY-5870
ubiquinol-9 biosynthesis (early decarboxylation)
-
-
PWY-5856
ubiquinol-9 biosynthesis (late decarboxylation)
-
-
PWY-5871
Ubiquinone and other terpenoid-quinone biosynthesis
-
-
ubiquinone biosynthesis
-
-
UDP-alpha-D-galactofuranose biosynthesis
-
-
PWY-7622
UDP-alpha-D-glucose biosynthesis
-
-
PWY-7343
UDP-alpha-D-glucuronate biosynthesis (from myo-inositol)
-
-
PWY-4841
UDP-alpha-D-glucuronate biosynthesis (from UDP-glucose)
-
-
PWY-7346
UDP-alpha-D-xylose biosynthesis
-
-
PWY-4821
UDP-GlcNAc biosynthesis
-
-
UDP-N-acetyl-alpha-D-mannosaminouronate biosynthesis
-
-
PWY-7335
UDP-N-acetyl-D-galactosamine biosynthesis I
-
-
PWY-5512
UDP-N-acetyl-D-galactosamine biosynthesis II
-
-
PWY-5514
UDP-N-acetyl-D-galactosamine biosynthesis III
-
-
PWY-8013
UDP-N-acetyl-D-glucosamine biosynthesis I
-
-
UDPNAGSYN-PWY
UDP-N-acetyl-D-glucosamine biosynthesis II
-
-
UDPNACETYLGALSYN-PWY
UDP-N-acetylmuramoyl-pentapeptide biosynthesis I (meso-diaminopimelate containing)
-
-
PWY-6387
UDP-N-acetylmuramoyl-pentapeptide biosynthesis II (lysine-containing)
-
-
PWY-6386
UDP-N-acetylmuramoyl-pentapeptide biosynthesis III (meso-diaminopimelate containing)
-
-
PWY-7953
ultra-long-chain fatty acid biosynthesis
-
-
PWY-8041
UMP biosynthesis I
-
-
PWY-5686
UMP biosynthesis II
-
-
PWY-7790
UMP biosynthesis III
-
-
PWY-7791
uracil degradation I (reductive)
-
-
PWY-3982
urate conversion to allantoin I
-
-
PWY-5691
urate conversion to allantoin II
-
-
PWY-7394
urate conversion to allantoin III
-
-
PWY-7849
urea degradation II
-
-
PWY-5704
UTP and CTP de novo biosynthesis
-
-
PWY-7176
UTP and CTP dephosphorylation I
-
-
PWY-7185
UTP and CTP dephosphorylation II
-
-
PWY-7177
Valine, leucine and isoleucine biosynthesis
-
-
Valine, leucine and isoleucine degradation
-
-
valproate beta-oxidation
-
-
PWY-8182
vancomycin resistance I
-
-
PWY-6454
vancomycin resistance II
-
-
PWY-6455
vanillin and vanillate degradation I
-
-
PWY-7097
vanillin and vanillate degradation II
-
-
PWY-7098
vanillin biosynthesis I
-
-
PWY-5665
Various types of N-glycan biosynthesis
-
-
vernolate biosynthesis III
-
-
PWY-6917
very long chain fatty acid biosynthesis I
-
-
PWY-5080
very long chain fatty acid biosynthesis II
-
-
PWY-7036
vitamin B1 metabolism
-
-
vitamin B6 degradation I
-
-
PWY-5499
Vitamin B6 metabolism
-
-
vitamin B6 metabolism
-
-
vitamin D3 biosynthesis
-
-
PWY-6076
vitamin D3 metabolism
-
-
vitamin E biosynthesis (tocopherols)
-
-
PWY-1422
wax esters biosynthesis II
-
-
PWY-5885
wogonin metabolism
-
-
PWY-7213
xanthine and xanthosine salvage
-
-
SALVPURINE2-PWY
xanthohumol biosynthesis
-
-
PWY-5135
xanthommatin biosynthesis
-
-
PWY-8249
xylitol degradation I
-
-
LARABITOLUTIL-PWY
xyloglucan degradation II (exoglucanase)
-
-
PWY-6807
zymosterol biosynthesis
-
-
PWY-6074
[2Fe-2S] iron-sulfur cluster biosynthesis
-
-
PWY-7250
adipate degradation

-
-
PWY-8354
bile acid biosynthesis, neutral pathway

-
-
PWY-6061
bile acid biosynthesis, neutral pathway
-
-
catecholamine biosynthesis

-
-
PWY66-301
catecholamine biosynthesis
-
-
curcuminoid biosynthesis

-
-
PWY-6432
curcuminoid biosynthesis
-
-
cyanate degradation

-
-
CYANCAT-PWY
dolichol and dolichyl phosphate biosynthesis

-
-
PWY-6129
dolichol and dolichyl phosphate biosynthesis
-
-
enterobactin biosynthesis

-
-
ENTBACSYN-PWY
enterobactin biosynthesis
-
-
ethylmalonyl-CoA pathway

-
-
PWY-5741
ethylmalonyl-CoA pathway
-
-
folate polyglutamylation

-
-
PWY-2161
folate polyglutamylation
-
-
methylaspartate cycle

-
-
PWY-6728
methylaspartate cycle
-
-
Monoterpenoid biosynthesis

-
-
Monoterpenoid biosynthesis
-
-
morphine biosynthesis

-
-
PWY-5270
morphine biosynthesis
-
-
myo-inositol biosynthesis

-
-
PWY-2301
myo-inositol biosynthesis
-
-
octane oxidation

-
-
P221-PWY
suberin monomers biosynthesis

-
-
PWY-1121
suberin monomers biosynthesis
-
-
thyroid hormone biosynthesis

-
-
PWY-6241
thyroid hormone biosynthesis
-
-
urea cycle

-
-
PWY-4984
vitamin K-epoxide cycle

-
-
PWY-7999
vitamin K-epoxide cycle
-
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
-
1, 25, 26, 27, 51, 60, 86, 127, 133, 163, 165, 168, 169, 192, 193, 281, 288, 297, 377, 381, 395, 396, 403, 404, 405, 411, 470, 488, 494, 495, 497, 498, 500, 501, 503, 504, 505, 516, 519, 530, 562, 563, 572, 584, 585, 586, 587, 635, 644, 647, 648, 650, 651, 652, 654, 658, 661, 670, 675, 681, 701, 704, 729, 732, 733, 734, 736, 737, 738, 748, 749, 750, 752, 754, 755, 756, 757, 758, 760, 762, 763, 764, 765, 782, 787, 818, 819, 828, 832, 833, 834, 838, 839, 840, 841, 843, 858, 988, 989, 993, 996, 997, 1065, 1068, 1070, 1076, 1080, 1099, 1100, 1118, 1119, 1121, 1122, 1123, 1124, 1125, 1129, 1130, 1132, 1133, 1134, 1135, 1136, 1138, 1139, 1144, 1147, 1150, 1174, 1191, 1194, 1213, 1222, 1327, 1354, 1384, 1390, 1391, 1394, 1448, 1449, 1450, 1451, 1452, 1453, 1454, 1455, 1456, 1458, 1459, 1460, 1461, 1462, 1466, 1467, 1468, 1469, 1471, 1472, 1475, 1476, 1504, 1535, 1539, 1546, 1574, 1575, 1576, 1580, 1582, 1584, 1586, 1591, 1592, 1594, 1597, 1627, 1664, 1673, 1677, 1685, 1688, 1710, 1715, 1718, 1719, 1735, 1737, 1739, 1743, 1745, 1747, 1758, 1769, 1770, 1773, 1774, 1775, 1779, 1783, 1784, 1788, 1885, 1906, 1912, 1925, 2211, 2212, 2215, 2228, 2233, 2257, 2258, 2259, 2260, 2261, 2266, 2267, 2269, 2271, 2277, 2278, 2279, 2280, 2287, 2373, 2376, 2420, 2421, 2422, 2423, 2434, 2442, 2443, 2446, 2447, 2449, 2497, 2520, 2532, 2537, 2624, 2654, 2656, 2659, 2777, 2812, 2868, 2875, 2933, 2983, 2984, 2985, 2997, 2998, 3000, 3002, 3005, 3008, 3009, 3013, 3014, 3021, 3022, 3024, 3026, 3028, 3029, 3030, 3032, 3034, 3038, 3039, 3041, 3043, 3047, 3054, 3059, 3066, 3067, 3075, 3077, 3079, 3080, 3087, 3093, 3094, 3095, 3097, 3098, 3099, 3100, 3102, 3105, 3106, 3107, 3108, 3109, 3112, 3113, 3117, 3118, 3120, 3121, 3122, 3124, 3125, 3133, 3134, 3135, 3189, 3227, 3232, 3236, 3346, 3359, 3407, 3411, 3413, 3415, 3416, 3588, 3594, 3598, 3608, 3609, 3610, 3611, 3612, 3613, 3614, 3616, 3617, 3679, 3681, 3682, 3683, 3684, 3688, 3693, 3697, 3704, 3706, 3711, 3800, 3807, 3811, 3813, 3840, 3868, 3901, 3960, 3961, 3962, 3971, 3974, 3981, 3995, 3996, 4002, 4008, 4009, 4010, 4013, 4016, 4022, 4024, 4025, 4027, 4035, 4045, 4051, 4097, 4100, 4142, 4144, 4145, 4149, 4160, 4161, 4162, 4176, 4200, 4204, 4217, 4220, 4222, 4224, 4231, 4236, 4237, 4238, 4239, 4241, 4242, 4244, 4245, 4246, 4247, 4248, 4249, 4250, 4251, 4252, 4254, 4255, 4347, 4356, 4361, 4364, 4365, 4366, 4367, 4375, 4382, 4383, 4386, 4387, 4390, 4391, 4406, 4407, 4408, 4409, 4413, 4422, 4423, 4424, 4433, 4437, 4542, 4543, 4555, 4556, 4564, 4566, 4569, 4571, 4572, 4573, 4667, 4668, 4669, 4670, 4673, 4677, 4678, 4679, 4682, 4692, 4697, 4698, 4711, 4761, 4763, 4771, 4776, 4777, 4787, 4788, 4791, 4843, 4844, 4846, 4849, 4851, 4854, 4860, 4862, 4945, 5077, 5111, 5112, 5114, 5115, 5116, 5117, 5118, 5119, 5129, 5168, 5169, 5175, 5181, 5200, 5203, 5360, 5584, 5585, 5589, 5590, 5594, 5595, 5598, 5751, 5776, 5870, 5877, 5878, 5880, 5889, 5893, 5925, 5931, 5933, 5934, 5935, 5938, 5939, 5975, 5997, 6034, 6042, 6866, 6870, 6871, 6873, 7019, 7021, 14078, 14080, 16276, 16278, 23917, 26853, 26855, 26858, 26862, 26863, 26864, 26866, 26868, 28967, 28971, 29060, 29061, 29341, 29355, 29360, 29361, 29374, 29378, 29380, 29381, 29385, 29386, 29389, 29390, 29395, 29401, 29573, 29596, 29674, 29677, 29716, 29815, 29874, 30137, 30138, 30140, 30141, 30160, 30549, 30553, 30778, 30780, 30781, 30785, 30798, 30803, 31017, 31020, 31025, 31029, 31030, 31031, 31064, 31068, 31069, 31079, 31080, 31084, 31312, 31313, 31315, 31317, 31318, 31319, 31320, 31321, 31322, 31323, 31324, 31325, 31326, 31327, 31328, 31330, 31331, 31333, 31335, 31336, 31337, 31339, 31340, 31341, 31353, 31354, 31356, 31357, 31367, 31368, 31370, 31380, 31382, 31386, 31392, 31401, 31408, 31468, 31469, 33151, 33330, 33352, 33535, 33547, 33551, 33604, 33612, 33629, 33732, 33754, 33757, 33797, 33808, 33810, 33815, 34283, 34287, 34321, 34325, 34326, 34432, 34439, 34449, 34450, 34455, 34456, 34457, 34477, 34478, 34486, 34488, 34489, 34490, 34491, 34492, 34493, 34494, 34495, 34496, 34497, 34498, 34500, 34501, 34541, 34542, 34544, 34546, 34547, 34548, 34549, 34554, 34555, 34556, 34557, 34558, 34559, 34561, 34562, 34769, 34774, 34775, 34779, 34785, 34792, 34800, 34807, 34808, 34809, 34816, 34820, 34821, 34831, 34834, 34835, 34837, 34838, 34839, 34840, 34843, 34846, 34848, 34851, 34854, 34856, 34864, 34871, 34877, 34878, 34933, 34935, 34939, 34942, 34943, 34945, 34964, 34994, 35011, 35209, 35217, 35347, 35870, 35871, 35873, 35874, 35880, 35883, 35887, 35889, 35892, 35908, 35916, 35922, 35923, 35926, 35937, 35955, 35966, 35971, 35974, 35980, 35981, 35982, 35986, 35987, 35988, 35989, 35990, 35991, 35993, 35994, 35995, 35996, 35997, 35998, 35999, 36000, 36004, 36025, 36028, 36042, 36043, 36054, 36057, 36062, 36063, 36064, 36122, 36124, 36125, 36127, 36133, 36137, 36138, 36139, 36140, 36141, 36142, 36143, 36144, 36146, 36179, 36182, 36183, 36188, 36199, 36201, 36202, 36203, 36204, 36206, 36208, 36210, 36211, 36213, 36222, 36223, 36224, 36227, 36229, 36259, 36264, 36265, 36321, 36325, 36337, 36417, 36443, 36444, 36445, 36503, 36522, 36558, 36619, 36634, 36636, 36637, 36642, 36655, 36661, 36663, 36664, 36666, 36717, 36748, 36850, 36855, 36867, 36909, 36910, 36913, 36915, 36921, 36933, 36948, 37053, 37056, 37057, 37059, 37063, 37064, 37067, 37068, 37069, 37071, 37078, 37079, 37080, 37082, 37083, 37085, 37086, 37087, 37405, 37413, 37420, 37421, 37422, 37427, 37435, 37436, 37438, 37481, 37496, 37498, 37528, 37571, 37579, 37584, 37585, 37586, 37590, 37591, 37592, 37593, 37599, 37603, 37607, 37609, 37612, 80775, 80782, 80783, 80785, 80787, 80788, 80790, 80791, 80819, 80839, 80843, 80851, 80865, 80866, 80869, 80870, 80874, 80887, 80889, 80891, 80892, 80895, 80901, 80903, 80906, 80915, 80916, 80917, 80921, 80937, 80941, 80955, 80964, 80973, 80975, 80976, 80980, 80992, 80993, 81014, 81016, 81040, 81041, 81046, 81048, 81049, 81055, 81056, 81075, 81076, 81083, 81107, 81113, 81114, 81116, 81210, 81211, 81216, 81219, 81220, 81223, 81241, 81243, 81244, 81251, 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711452, 711455, 711469, 711474, 711490, 711555, 711621, 711626, 711636, 711637, 711638, 711639, 711640, 711645, 711651, 711687, 711688, 711695, 711707, 711719, 711720, 711722, 711731, 711736, 711772, 711773, 711792, 711794, 711829, 711856, 711858, 711859, 711920, 711921, 711923, 711924, 711927, 711929, 711941, 711966, 712006, 712007, 712020, 712050, 712062, 712072, 712119, 712120, 712168, 712174, 712184, 712188, 712190, 712201, 712324, 712325, 712326, 712388, 712399, 712415, 712446, 712495, 712498, 712559, 712560, 712594, 712615, 712621, 712633, 712690, 712699, 712700, 712795, 712814, 712815, 712817, 712826, 712829, 712840, 712851, 712873, 712881, 712884, 712923, 712925, 712933, 712934, 712942, 712943, 712944, 713008, 713067, 713089, 713110, 713120, 713122, 713123, 713150, 713186, 713196, 713199, 713203, 713204, 713217, 713241, 713366, 713468, 713491, 713519, 713542, 713546, 713547, 713549, 713582, 713591, 713688, 713713, 713716, 713722, 713727, 713737, 713743, 713752, 713944, 713952, 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723652, 723699, 723788, 723811, 723958, 724104, 724127, 724170, 724191, 724198, 724313, 724326, 724336, 724430, 724435, 724526, 724535, 724555, 724682, 724707, 724715, 724747, 724779, 724796, 724830, 724911, 724921, 724965, 725056, 725062, 725073, 725082, 725171, 725173, 725303, 725427, 725456, 725461, 725469, 725531, 725633, 725651, 725652, 725656, 725675, 725736, 725765, 725766, 725768, 725818, 725859, 725962, 726046, 726047, 726048, 726092, 726125, 726308, 726334, 726368, 726472, 726542, 726668, 726673, 726809, 726856, 726888, 727011, 727056, 727094, 727109, 727140, 727148, 727151, 727153, 727198, 727322, 727424, 727633, 727650, 727808, 727884, 727931, 727944, 727969, 727993, 728029, 728034, 728156, 728179, 728227, 728431, 728614, 728682, 728930, 728938, 729021, 729114, 729185, 729207, 729307, 729333, 729349, 729378, 729516, 729541, 729542, 729553, 729558, 729681, 729721, 729779, 729782, 729805, 729834, 729947, 729954, 730008, 730038, 730103, 730120, 730158, 730236, 730237, 730239, 730241, 730242, 730243, 730378, 730420, 730475, 730476, 730811, 730994, 730995, 731015, 731092, 731093, 731094, 731103, 731105, 731109, 731110, 731219, 731296, 731339, 731364, 731369, 731377, 731385, 731403, 731424, 731441, 731453, 731487, 731566, 731569, 731589, 731627, 731629, 731674, 731702, 731719, 731757, 731891, 731959, 731960, 731972, 732147, 732205, 732312, 732314, 732364, 732367, 732368, 732375, 732550, 732575, 732576, 732583, 732609, 732697, 732716, 732724, 732751, 732762, 732777, 732896, 732912, 732944, 732945, 732968, 732991, 732996, 733062, 733064, 733205, 733368, 733383, 733399, 733404, 733420, 733491, 733517, 733661, 733688, 733708, 733709, 733790, 733906, 734114, 734115, 734121, 734131, 734235, 734325, 734431, 734432, 734529, 734530, 734532, 734538, 734600, 734662, 734677, 734744, 734859, 734865, 735029, 735047, 735089, 735119, 735134, 735146, 735203, 735302, 735342, 735409, 735423, 735458, 735626, 735627, 735644, 735917, 735966, 736014, 736097, 736269, 736319, 736429, 736550, 736607, 736728, 736793, 736885, 737125, 737438, 737572, 737644, 737733, 737962, 738007, 738016, 738017, 738064, 738101, 738173, 738176, 738177, 738224, 738284, 738420, 738620, 738639, 738674, 738896, 738911, 738914, 739070, 739071, 739072, 739176, 739214, 739248, 739499, 739574, 739647, 739686, 739745, 739837, 739952, 740092, 740108, 740143, 740146, 740194, 740247, 740248, 740279, 740376, 740478, 740535, 740537, 740634, 740635, 740806, 740834, 740883, 740888, 740911, 741010, 741079, 741104, 741117, 741248, 741273, 741564, 741580, 741796, 741817, 742031, 742055, 742219, 742246, 742248, 742257, 742271, 742308, 742315, 742356, 742439, 742448, 742452, 742457, 742507, 742555, 742557, 742561, 742564, 742567, 742735, 742811, 742814, 742816, 742817, 742818, 742857, 742886, 743135, 743151, 743188, 743217, 743353, 743357, 743359, 743360, 743361, 743362, 743434, 743622, 743634, 744206, 744210, 744290, 744301, 744332, 744450, 744478, 744498, 744508, 744569, 744767, 744829, 744852, 744863, 744869, 745257, 745258, 745267, 745528, 745587, 745602, 745616, 745617, 745839, 745891, 745971, 746327, 746721, 746970, 747036, 747229, 747233, 747280, 747479, 747727, 748220, 748245, 748626, 749111, 749176, 749270, 749342, 749371, 749399, 749402, 749433, 749533, 749543, 749758, 749861, 749862, 750035, 750213, 750281, 750336, 750479, 750619, 750661, 750868, 750993, 750996, 751019, 751383, 751698, 751791, 751813, 751816, 751969, 752167, 752408, 752435, 752439, 752609, 752655, 752687, 752688, 752691, 752695, 752792, 752835, 752845, 752912, 753289, 753757, 754040, 754341, 754396, 755130, 755327, 755393, 755785, 755866, 755939, 756096, 756282, 756511, 756579, 756635, 756998, 757467, 757560, 757808, 758628, 758695, 758771, 758774, 758963, 758982, 758983, 759587, 759685, 759698, 759721, 759850, 760135, 760684, 760690, 760901, 760946, 761014, 761025, 761125, 761360, 761409, 761459, 761605, 761734, 761735, 761950, 762017, 762101, 762105, 762392, 762496, 762517, 762740, 762758, 762781, 762959, 763027, 763378, 763379, 763514, 763515, 763517, 764026, 764079, 764190, 764629, 764644, 764771, 764822, 764825, 765028, 765299, 765331, 765742, 765859, 766080, 766115, 766154, 766268, 766288, 766306, 766595, 766649, 766721, 766748, 767206, 767211, 767269, 767534, 767548, 768070, 768081, 768082, 768237, 768447, 768456, 768943, 769436, 769481, 769539, 769655, 770000, 770583, 770663, 770669, 770703, 770793, 770921, 770991, 771311, 771452, 771569, 771585, 771592, 771599, 771616, 771625, 771943, 772054, 772190, 772201, 772210, 772373, 772436, 773131, 773248, 773310, 773428, 773610, 773620, 773649, 773763, 773845, 774211, 774213, 774303, 774376, 774712, 774724, 774726, 774822, 775302, 775694, 775830, 776030, 776083, 776089, 776097, 776212, 776381, 777011, 777067, 777368, 777716, 777832, 778606, 778623, 779111, 779365, 779370, 779401, 779444
-
brenda
-
AF333982, DQ978330
GenBank
brenda
-
37000, 94912, 94927, 288681, 349039, 390273, 390274, 392524, 393063, 395498, 439168, 439169, 485140, 485208, 485210, 485508, 486386, 487641, 489419, 489421, 489423, 489611, 490038, 490134, 490135, 490136, 490145, 490199, 490200, 490201, 490202, 490203, 490254, 490283, 490284, 490341, 490343, 490344, 490382, 490383, 490392, 490393, 490428, 490459, 490485, 490486, 490492, 490493, 490494, 490504, 490505, 490506, 490507, 490508, 490509, 490514, 490548, 490549, 490550, 490558, 490573, 490637, 490638, 490639, 490640, 490641, 490642, 490643, 490644, 490646, 490665, 490676, 490760, 490947, 490992, 490993, 490995, 491015, 491017, 491018, 491073, 491080, 491081, 491092, 491093, 491094, 491095, 491096, 491097, 491098, 491116, 491117, 491118, 491119, 491157, 491168, 491177, 491178, 491179, 491180, 491190, 491200, 491201, 491202, 491203, 491204, 491227, 491231, 491232, 491233, 491234, 491235, 491236, 491247, 491248, 491249, 491250, 491251, 491252, 491253, 491257, 491258, 491259, 491270, 491297, 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SwissProt
brenda
-
TREMBL
brenda
-
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756652, 756974, 757014, 757064, 757069, 757169, 757321, 757567, 757697, 758876, 758981, 759138, 759407, 759852, 760034, 760044, 760109, 760486, 760639, 760752, 760780, 761000, 761130, 761166, 761408, 761466, 761802, 761874, 761908, 762009, 762014, 762356, 762494, 762503, 762597, 762716, 762748, 762762, 762805, 763065, 763067, 763377, 763769, 763849, 763866, 763918, 763929, 764034, 764172, 764408, 764443, 764520, 764551, 764565, 764592, 764672, 764821, 764894, 764913, 764935, 765230, 765779, 765858, 766115, 766162, 766247, 766566, 766792, 766899, 767070, 767383, 767385, 767622, 768204, 768254, 768448, 768934, 769041, 769136, 769293, 769310, 769545, 769656, 769994, 770018, 770039, 770228, 770981, 770988, 771610, 771613, 771614, 771615, 771744, 771801, 772188, 772390, 772703, 772981, 772985, 773249, 773418, 773735, 773783, 773803, 774366, 774379, 774717, 775334, 775377, 775745, 775988, 776100, 776272, 776381, 776533, 776708, 776754, 777023, 777086, 777456, 777589, 777652, 777716, 777718, 777814, 778325, 778543, 778606, 778668, 778765, 779415
A0A068FP44, A0A0G2K047, A0A0G2K1W9, A0A0G2K502, A0A0G2K6D8, A0A0G2K8N8, A0A0G2K9T1, A0A1B0GWP2, A1L1J2, A3KN98, B0BMT9, B1H230, B2GV06, B3GSH5, B5DEJ6, B5DFD5, D1MCF1, D3ZDM7, D3ZFU9, D3ZI76, D3ZKD3, D3ZKT0, D3ZN15, D3ZNG3, D3ZTF6, D3ZTX4, D3ZU86, D3ZUA0, D3ZW08, D4A0E8, D4A2S8, D4A488, D4A4P4, D4A5Q9, D4A5S6, D4A7X5, D4AA31, D4AA47, D4AAT7, F1LRE1, F1M4T7, F1M5N4, F7EXV6, G3V6E6, G3V6L4, G3V7N1, G3V7S5, M0R401, M0RC77, O08557, O09175, O10743, O35052, O35078, O35186, O35303, O35331, O35543, O35760, O35795, O35952, O54735, O54939, O70177, O70196, O70199, O70282, O70467, O88484, O88496, O88618, O88813, O88846, O88867, P00388, P00684, P00731, P00770, P00786, P00884, P04041, P04176, P04177, P04182, P04762, P04785, P04797, P04799, P04800, P04903, P04904, P04905, P05182, P05982, P06686, P06762, P07154, P07338, P07379, P07632, P07687, P07824, P07861, P07872, P07895, P07896, P07943, P08010, P08011, P08289, P08516, P08683, P09034, P09367, P09606, P09811, P09812, P0C1T0, P10111, P10860, P10959, P11497, P11506, P12007, P12527, P13233, P13255, P13444, P13635, P14137, P14173, P14408, P14604, P14650, P14882, P15304, P15651, P15684, P16067, P16228, P16232, P16636, P17105, P17256, P17712, P18125, P18163, P18297, P18298, P18424, P18666, P18886, P18910, P19112, P19356, P20070, P20595, P20717, P20816, P20817, P21588, P21816, P22057, P22071, P22288, P22734, P22789, P22985, P23457, P23711, P24268, P24329, P24464, P27158, P28841, P29476, P30099, P32738, P33124, P33436, P35559, P35571, P35738, P37136, P38062, P38659, P40146, P40329, P41516, P42893, P43428, P45479, P46462, P46844, P47820, P48450, P49621, P49864, P50123, P50233, P50282, P50430, P50554, P51590, P51635, P52844, P52873, P53817, P54316, P54318, P59722, P61459, P69478, P70473, P70496, P70498, P70551, P70618, P70627, P80067, P80225, P80299, P81563, P83645, P85973, P97532, P97535, P97687, P97697, Q00972, Q01062, Q02293, Q02353, Q02401, Q02759, Q02765, Q03238, Q04631, Q05683, Q06518, Q07523, Q08201, Q08877, Q10728, Q10739, Q10743, Q10836, Q10980, Q10984, Q14TE9, Q1HGK5, Q2KMM4, Q2THW7, Q3L7L9, Q3L7M0, Q3ZAU5, Q499V1, Q4FZY2, Q4G056, Q4G064, Q4KLP0, Q4KLZ0, Q4QQV7, Q4V8B9, Q561S0, Q5BJZ6, Q5BQE6, Q5DRK1, Q5EGZ1, Q5I0C3, Q5M819, Q5M886, Q5PPH0, Q5RKL4, Q5U2W9, Q5U367, Q5XI55, Q5XI78, Q5XI85, Q5XIF5, Q62600, Q62651, Q62696, Q62967, Q63009, Q63120, Q63424, Q63619, Q63707, Q63716, Q64230, Q64232, Q64536, Q64560, Q64565, Q64591, Q64604, Q64610, Q64654, Q68FT9, Q6AYB9, Q6AYK3, Q6F596, Q6IN16, Q6J1Y9, Q6MG60, Q6P7D7, Q6P7S1, Q6QMG6, Q6TEK4, Q6TY19, Q76HM9, Q76HN1, Q78EH2, Q7TP52, Q80W57, Q80Z26, Q80ZG2, Q811Q1, Q88563, Q8CGU9, Q8CGV7, Q8CHN8, Q8K1P9, Q8R2H5, Q8R5G2, Q8VHE9, Q91XT5, Q920D2, Q920D5, Q920F5, Q920L2, Q923M1, Q924C3, Q924I2, Q924N5, Q924V1, Q925R7, Q925U2, Q92887, Q99MA2, Q99MI5, Q99NA5, Q99NI4, Q9EQV6, Q9EQV9, Q9ER34, Q9ERM3, Q9ESP7, Q9ESV6, Q9JHE5, Q9JHK1, Q9JI61, Q9JJ46, Q9JKC1, Q9JLJ3, Q9JMI1, Q9P1X0, Q9QYU4, Q9R0C5, Q9R1T5, Q9WTZ3, Q9Z0U5, Q9Z0V5, Q9Z2Q3, Q9Z2Q4, Q9Z330
Uniprot
brenda
(SPF/VAF)-strain albino rats
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1 month old
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1- to 3-day old Sprague-Dawley rat pups
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12-14 days old
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15 days old albino
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15-16 days old
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15-20 days old
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18-day old embryos
SwissProt
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18-days-pregnant Sprague-Dawley rats
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brenda
180 female Hanover Wistar rats
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brenda
2 components: I, II
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2 different phosphatidate phosphatidases: PAP-1 and PAP-2
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brenda
2 different splice variants
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brenda
2 enzyme forms NI and NII from nucleus and 2 enzyme forms CI and CII from cytoplasm
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brenda
2 enzyme forms: A and B
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brenda
2 forms of enzyme: PEMT1 and PEMT2
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brenda
2 forms of liver uridine kinase in foetus
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2 forms: A and B
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2 forms: high-MW form and low-MW form
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2 forms: type A and B
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2 isoenzymes of 46 and 48 kDa
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2 isoenzymes: A and B
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2 isoforms
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2 isoforms in cytosol and mitochondria
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2 isoforms L-CPT I and M-CPT I
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brenda
2 isoforms of CPT I in heart mitochondria, liver L-CPT I, skeletal muscle M-CPT I
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2 isoforms XT-I and XT-II
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brenda
2 isoforms: CNP1 and CNP2 differing by a 20-amino acid extension at the N-terminus
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brenda
2 isoforms: CNP1 and CNP2, encoded by a single gene
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2 isoforms: heme oxygenase-1, inducible
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brenda
2 isozymes 5alpha-R1 and 5alpha-R2
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brenda
2 isozymes I and II
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brenda
2 isozymes II and Ib of platelet-activating factor acetylhydrolase PAF-AH
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brenda
2 isozymes of MsrA
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2 isozymic forms: acidic type L, and basic type M
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2 subunits encoded by 2 genes
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2-3 days old, isoform B
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2-days-old Sprague-Dawley rats
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2-days-old Wistar rats
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20 days old
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21-day-old Wistar rats
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250-300 g
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2fold increase in enzyme activity on diet of total parenteral nutrition plus choline
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3 aconitases
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3 charge variant forms
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3 enzyme forms: 1, 2, and 3
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3 enzyme forms: A, B1, B2
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brenda
3 enzyme forms: APcI, APcII, APcIII
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brenda
3 forms of the enzyme: enolase I, enolase II and enolase III
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3 forms: 1. inducible fatty acyl-CoA oxidase, 2. noninducible fatty acyl-CoA oxidase, 3. noninducible trihydroxycoprostanoyl-CoA oxidase
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3 isoenzymes: 1, 2.1, 2.2
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3 isoenzymes: MAT-I, MAT-II, MAT-III
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3 isoforms TR1, TR2, TR3
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3 isozymes alpha, beta, and gamma
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3 isozymes LH1-3
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brenda
3 isozymes PDHK1, PDHK2, PDHK4
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3 months old Wistar rats
SwissProt
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3 to 4fold induction by 3-methylcholanthrene
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4 different isozymes: PDK1, PDK2, PDK3, PDK4
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4 enzyme forms from kidney, heart and brain
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4 forms, one of them is probably identical to mitochondrial L-aspartate aminotransferase EC 2.6.1.1
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4 independent lipolytic carboxylesterases
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4.5fold higher specific activity in starved than in fed rats
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5 cellular DNA template-dependent DNA polymerases are encoded by distinct genes: polymerase alpha, i.e. pol I, polymerase beta, only in vertebrates, polymerase gamma, required for mitochondrial DNA replication but encoded in the nucleus, polymerase delta. Enzymes in mammalian cell contain tightly associated 3'-5'-exonuclease activities, 2 forms: proliferating cell nuclear antigen-dependent and a proliferating cell nuclear antigen-independent polymerase, also called DNA polymerase delta II, now named DNA polymerase epsilon, polymerase epsilon, tightly associated 3'-5'-exonuclease activity, formerly named DNA polymerase delta II
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5-7 days old Wistar rats
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brenda
5-weeks-old male Wistar rats
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brenda
6-OHDA-unilaterally-lesioned Wistar Kyoto and spontaneously hypertensive rats
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6-weeks-old BBDR rats
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7 days old
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7, 14 and 21 days old
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7- to 10-day old rats
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7-day-old Sprague-Dawley rat
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brenda
7-week-old Wistar rats
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72.5 kDa N-terminal fragment of the 110 kDa subunit
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76 male Sprague-Dawley rats (200-250 g), 96 different age rats (from 1 month to 12 months old) and insulin-resistant animals
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8-12 months and 32-38 months old
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8-week-old Sprague-Dawley rats
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a Ca2+-dependent enzyme and a Mg2+-dependent enzyme
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a novel enzyme form different from DNA ligase I
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a nuclear and a mitochondrial form
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a single enzyme may function as diacylglycerol kinase and as monoacylglycerol kinase
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brenda
a single protein possesses both N-deacetylase and N-sulfotransferase activity
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a two-hybrid interaction assay is performed, using as bait the mouse Kir6.2 C terminus, for the screening a rat heart cDNA library is used
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A-type Abo gene A1; at least 4 different A-type Abo genes
SwissProt
brenda
A-type Abo gene A2; at least 4 different A-type Abo genes
SwissProt
brenda
A-type Abo gene A3; at least 4 different A-type Abo genes
SwissProt
brenda
A-type Abo gene A4; at least 4 different A-type Abo genes
SwissProt
brenda
aconitase 2; Wistar rats, aconitase 2 encoded by gene Aco2
UniProt
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ACS3, one of multiple form of the enzyme in brain
SwissProt
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activity in male rats is higher than in female rats
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brenda
activity increases during development
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brenda
adenine phosphorylase activity and a distinct inosine-guanosine phosphorylase activity
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brenda
adult
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adult albino
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adult albino Wistar rats of both sexes
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adult and newborn
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adult femal Sprague-Dawley rats
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brenda
adult female and male rats
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brenda
adult female and male Wistar rats
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brenda
adult female Sprague Dawley rats
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-
brenda
adult female Sprague-Dawley rat
-
-
brenda
adult female Sprague-Dawley rat
SwissProt
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adult female Sprague-Dawley rats
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brenda
adult female Wistar rats
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brenda
adult male
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brenda
adult male albino rats of Charles-Foster strain
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brenda
adult male and female Sprague Dawley rats
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brenda
adult male and female Wistar rats
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brenda
adult male Fischer 344 rats, gene arsM
SwissProt
brenda
adult male Sprague-Dawley and Wistar rats
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-
brenda
adult male Sprague-Dawley rat
SwissProt
brenda
adult male Sprague-Dawley rats
-
-
brenda
adult male Sprague-Dawley rats
SwissProt
brenda
adult male Sprague-Dawley rats, fed a Purina lab chow diet
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brenda
adult male Wilstar
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-
brenda
adult male Wistar
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-
brenda
adult male Wistar
SwissProt
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adult male Wistar rat
-
-
brenda
adult male Wistar rats
640254, 686054, 689159, 689353, 695207, 697585, 700652, 703566, 709630, 710532, 712828
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adult male Wistar rats, gene spdS
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brenda
adult or neonatal
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brenda
adult Sprague-Dawley rat
-
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brenda
adult Sprague-Dawley rats
-
-
brenda
adult Sprague-Dawley rats
SwissProt
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adult Wistar
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adult Wistar female ovariectomized rats
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brenda
adult Wistar rats
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-
brenda
adult, female, Sprague-Dawley
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brenda
adult, i.e. 4-month-old, and aged, i.e. 30-month-old
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brenda
adult, male
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brenda
adults
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brenda
after carbon monoxide induced hypoxia
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after induction of acid reflux oesophagitis. Expression of COX-2 and enzyme isoform mPGES-1 are markedly increased in oesophagitis and co-localize in epithelial cells of the basal layer, as well as inflammatory and mesenchymal cells in the lamina propria and submucosa
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-
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aged 3 to 15 weeks, fed on a 25% casein diet for one week
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-
brenda
albino
-
-
brenda
albino
SwissProt
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albino animals
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-
brenda
albino male Holtzman rats
-
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brenda
albino male Sprague-Dawley rats
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-
brenda
albino rat
-
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brenda
albino rats
-
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brenda
albino Sprague Dawley
-
-
brenda
albino Wistar rats
-
-
brenda
albinus
-
-
brenda
alpha and beta subunits of complex component E1 (BCKD), a tetramer (alpha2beta2), cf. EC 1.2.4.4
UniProt
brenda
alpha class isozymes GSTA2-2, GSTA1-2 and GSTA1-1
-
-
brenda
alpha subunit of the skeletal muscle enzyme
SwissProt
brenda
alpha(1,3)GT
-
-
brenda
alpha- and beta-enzyme form
-
-
brenda
alpha-1 subunit
SwissProt
brenda
alpha-chain
SwissProt
brenda
alpha-subunit
UniProt
brenda
alpha-subunit and beta-subunit
UniProt
brenda
alpha-subunit; alpha-subunit
UniProt
brenda
alpha1 subunit
SwissProt
brenda
alpha2 subunit
SwissProt
brenda
alternative splicing generates long RING finger protein March10a, i.e. G3XDV3, and is a short RING finger-less protein March10b
UniProt
brenda
alternative splicing produces 3 isoforms: PTPxi-A, the full-length form, PTPxi-B, the short form and PTPxi-S an extracellular variant
-
-
brenda
alternatively spliced variant 1, i.e. Dhcr7-AS-1; 5 isozymes of enzyme Dhcr7 through alternative splicing of gene Dhcr7
SwissProt
brenda
alternatively spliced variant 2, i.e. Dhcr7-AS-2; 5 isozymes of enzyme Dhcr7 through alternative splicing of gene Dhcr7
SwissProt
brenda
alternatively spliced variant 4, i.e. Dhcr7-AS-4; 5 isozymes of enzyme Dhcr7 through alternative splicing of gene Dhcr7
SwissProt
brenda
AMPD1,2 and 3
-
-
brenda
and strain BB/OK
-
-
brenda
angiotensin type 1 receptor-blocked rats
-
-
brenda
animals fed with semipurified diets containing either 1% w/w corn oil or 10% each of beef tallow, corn oil, perilla oil, and fish oil. Enzyme activity is reduced in the polyunsaturated fat-fed group in the order of fish oil, perilla oil, and corn oil
-
-
brenda
animals infected with Trypanosoma evansi
-
-
brenda
animals with free access to sucrose solution
-
-
brenda
antibodies against the liver enzyme activate NADH 5-alpha reductase
-
-
brenda
aromatic amino acid-pyruvate transaminase and aromatic amino acid-2-oxoglutarate transaminase
-
-
brenda
aryl sulfotransferase IV
-
-
brenda
ascites fluid of Novikoff tumor cells maintained in rat
-
-
brenda
AST IV
-
-
brenda
at least 3 DELTA3,DELTA2-enoyl-CoA isomerases: 1.mitochondrial clofibrate-inducible short-chain isomerase, 2.mitochondrial non-inducible long-chain isomerase, 3.peroxisomal isoenzyme, which is a part of a multifunctional protein
-
-
brenda
at least 3 different isozymes PKNalpha/PKN-1/PAK-1, PKNbeta, and PRK2/PKNgamma/PAK-2
-
-
brenda
at least 7 forms
-
-
brenda
at least three isoenzymes in liver: 1. mitochondrial short-chain preferring isomerase, 2. mitochondrial long-chain preferring isomerase, 3. peroxisomal isoenzyme, which is part of a multifunctional protein
-
-
brenda
B-type creatine kinase; gene Ckb
UniProt
brenda
B-type gene Abo2
SwissProt
brenda
bearing Walker 256 carcinosarcoma
-
-
brenda
beta-1,4 galactosyltransferase I
UniProt
brenda
beta-ARK 1
-
-
brenda
beta-ARK 1, 2 isoenzymes beta-ARK 1 and 2, adult Sprague-Dawley rats
SwissProt
brenda
beta-ARK 2, 2 isoenzymes beta-ARK 1 and 2, adult Sprague-Dawley rats
SwissProt
brenda
beta-isoform
Swissprot
brenda
beta-subunit
UniProt
brenda
beta-subunit; male Wistar-Han rats
UniProt
brenda
beta-subunit; Sprague-Dawley rats
UniProt
brenda
beta1 subunit
UniProt
brenda
beta2 subunit
UniProt
brenda
bifunctional 6-phosphofructo-2-kinase/fructose 2,6-bisphosphatase
SwissProt
brenda
bifunctional 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase
-
-
brenda
bifunctional 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase, recombinant enzyme
-
-
brenda
bifunctional 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase, recombinant enzyme expressed in Mv1Lu cell line
-
-
brenda
bifunctional 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase, recombinant enzyme expressed in Mv1Lu cells
-
-
brenda
bifunctional 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase, recombinant enzyme, liver and muscle isoform
-
-
brenda
bifunctional alpha-AE
-
-
brenda
bifunctional alpha-AE
SwissProt
brenda
bifunctional amylo-1,6-glucosidase and oligo-1,4-1,4 glucanotransferase
-
-
brenda
bifunctional copper- and zinc-dependent enzyme
-
-
brenda
bifunctional enzyme EC 5.1.3.14/EC 2.7.1.60
-
-
brenda
bifunctional enzyme EC 5.1.3.14/EC 2.7.1.60
Uniprot
brenda
bifunctional enzyme showing peptidylglycine alpha-hydroxylating monooxygenase, PHM, EC 1.14.17.3, and peptidylamidoglycolate lyase, PAL, EC 4.3.2.5, activities
-
-
brenda
bifunctional enzyme, cf. EC 2.7.1.60
Uniprot
brenda
bifunctional enzyme, cf. EC 3.2.1.183
Uniprot
brenda
bifunctional kynurenine aminotransferase/glutamine transaminase, 4 isoforms, expression in COS1-cells
-
-
brenda
bifunctional Mn2+-dependent ADP-ribose/CDP-alcohol diphosphatase
UniProt
brenda
bifunctional peptidylglycine alpha-amidating enzyme
SwissProt
brenda
bifunctional serine pyruvate/alanine:glyoxylate aminotransferase
-
-
brenda
bilirubin UDP-glucuronosyltransferase not in Gunn strain
-
-
brenda
biotin-deficient animals
-
-
brenda
both alcohol:NAD+ oxidoreductase activity, EC 1.1.1.1, and 5beta-cholestane-3alpha,7alpha,12alpha,26-tetraol:NAD+ 26-oxidoreductase activity, EC 1.1.1.161, are catalyzed by the same active side of the same enzyme protein
-
-
brenda
both S-COMT and MB-COMT
-
-
brenda
brain isoform
UniProt
brenda
brain isozyme PFKFB2; genes PFKFB1-4, four isozymes
SwissProt
brenda
brain KAT I
-
-
brenda
brain KAT I
SwissProt
brenda
Brown Norway rats
-
-
brenda
buffalo
-
-
brenda
buffalo rat
-
-
brenda
C-mannosylating enzyme
-
-
brenda
Ca2+-dependent isozyme
-
-
brenda
calpain-1 catalytic subunit
SwissProt
brenda
calpain-2 catalytic subunit
SwissProt
brenda
CaM-KII is encoded by four different genes encoding isozymes alpha-delta, alternative splicing results in 24 different enzyme variants
-
-
brenda
CaMKII isozymes alpha, beta, gamma, and delta, each with a number of splicing variants
-
-
brenda
carbohydrate sulfotransferase 3; gene C6st1
SwissProt
brenda
carbonic anhydrase III
-
-
brenda
carbonic anhydrase IV
-
-
brenda
carboxypeptidase A 2, evolutionary relationships between rat carboxypeptidases
-
-
brenda
carboxypeptidase A1
-
-
brenda
carcinoma Walker 256
-
-
brenda
casein-treated male Wistar
-
-
brenda
CAT-1 partially purified, obtained with isoenzymes CAT-IIA, CAT-IIB
-
-
brenda
catalytic subunit
SwissProt
brenda
catalytic subunit 1
UniProt
brenda
catalytic subunit p110alpha; isozyme PI3Kalpha
UniProt
brenda
catalytic subunit p110beta; isozyme PI3Kbeta
Swissprot
brenda
Cavbeta2a
UniProt
brenda
CCl4-treated rats
-
-
brenda
CD-strain
-
-
brenda
cDNA sequence, EMBL accession number
SwissProt
brenda
CDR Fisher, male
-
-
brenda
cell line PC C-13
-
-
brenda
cerebral hemodynamic modifications induce decreases in SSAO activity resulting in cell dedifferentiation and inducing dysregulation of glucose transport
-
-
brenda
cf. EC 1.17.3.2
UniProt
brenda
cf. EC 1.5.1.20
UniProt
brenda
cf. EC 3.1.3.76
UniProt
brenda
cf. EC 3.1.4.11
SwissProt
brenda
cf. ECs 3.4.11.1, 3.4.11.5
UniProt
brenda
Charles River adult rats, strain CD
-
-
brenda
Charles River albino
-
-
brenda
Charles River CD strain
-
-
brenda
Charles River male rats, strain CDF
-
-
brenda
chimeric lipase constructed of the N-terminal 329 residues of hepatic lipase and the C-terminal 136 residues of human lipoprotein lipase
-
-
brenda
chimeric lipase from lipoprotein lipase and hepatic lipase
-
-
brenda
chymases with Val199 are found only in animals expressing multiple chymases, consistent with the premise that their substrate specificity differs from that of chymases with Gly199
-
-
brenda
class I enzyme
-
-
brenda
class II alcohol dehydrogenase
-
-
brenda
class II enzyme
-
-
brenda
class IV enzyme
-
-
brenda
clone 9 cells express higher amounts of the enzyme after insulin treatment
-
-
brenda
cloned and expressed in Escherichia coli
-
-
brenda
cloned in Escherichia coli
-
-
brenda
coagulation factor XII precursor; Brown Norway strain, male rats injected with the activated beta-fragment of human beta-FXIIa
SwissProt
brenda
Cohen diabetic-sensitive rat
-
-
brenda
Colworth-Wistar, male
-
-
brenda
commercial product
-
-
brenda
comparison of the mouse, rat, and human ogt genes
-
-
brenda
comparison with hepatic 5'-deiodinase EC 1.97.1.10
-
-
brenda
comparison with placental 5-deiodinase EC 1.97.1.11
-
-
brenda
constitutive isozyme HO-2
-
-
brenda
contains isozymic forms, mitochondrial and cytosolic, of omega-amidase
-
-
brenda
control and B-6-deficient rats
-
-
brenda
control group and diabetes group
-
-
brenda
conventional, novel, and atypical isozyme types, overview
-
-
brenda
conversion of oxidoreductatse to oxidase
UniProt
brenda
conversion of xanthine oxidoreductase to oxidase
UniProt
brenda
cortisone 5beta-reductase and reduction of androstenedione (3-oxo-5beta-steroid:NADP+ DELTA4-oxidoreductase activity, EC 1.3.1.23) catalyzed by the same catalytic site of a single protein
-
-
brenda
cortisone 5beta-reduction (EC 1.3.1.3) and androstenedione reduction (EC 1.3.1.23) are catalyzed by the same catalytic site of a single protein
-
-
brenda
Cu,Zn-SOD
-
-
brenda
cultured BRL cells
-
-
brenda
cultured C-6 glial cells
-
-
brenda
cultured H9c2 cells
-
-
brenda
cyclic, pregnant, and pseudopregnant rats
-
-
brenda
cytochrome b5/cytochrome b5 reductase fusion protein, exists also as a variant where the whole exon 12 is deleted
SwissProt
brenda
cytokine-inducible isoform CPD-N with incomplete N-terminal domain and intact domains II and III
-
-
brenda
cytoplasm: dihydrodiol dehydrogenase EC 1.3.1.20 and 3alpha-hydroxysteroid dehydrogenase EC 1.1.1.5 are undistinguishable
-
-
brenda
cytosolic and mitochondrial enzyme
-
-
brenda
cytosolic and mitochondrial isozyme
-
-
brenda
cytosolic isoform
-
-
brenda
cytosolic isozyme; 1 cytosolic and 1 mitochondrial isozyme
SwissProt
brenda
cytosolic KAT I
SwissProt
brenda
DAHl salt-sensitive and -resistant rats
-
-
brenda
Dahl salt-sensitive rats
-
-
brenda
Dahl salt-sensitive rats
SwissProt
brenda
definite classification as EC 1.13.11.11 based on protein sequence
SwissProt
brenda
DGK-I, DGK-II and DGK-III
-
-
brenda
DGK-theta
-
-
brenda
DGKbeta
-
-
brenda
diabetic Goto-Kakizaki
-
-
brenda
diabetic hypertensive rats
-
-
brenda
diabetic rat
-
-
brenda
diabetic rats
-
-
brenda
diaphorase activity of nitric oxide synthase
-
-
brenda
different enzyme forms, i.e. Radical Fringe, Lunatic Fringe, and Manic Fringe
-
-
brenda
different isoforms in different tissues
-
-
brenda
different splice isoforms of nNOS, e.g. splicing variant nNOSalpha
-
-
brenda
dihydrolipoamide dehydrogenase E3
-
-
brenda
distribution
-
-
brenda
distribution in Wistar and Gunn strain
-
-
brenda
DNA ligase I and II
-
-
brenda
DNA ligase I and III
-
-
brenda
DNA ligase III
-
-
brenda
Donryu
-
-
brenda
Donryu strain
-
-
brenda
Donryu strain rats
-
-
brenda
drug-induced
-
-
brenda
dual specificity: phloretin hydrolase and pyridoxine-5'-beta-D-glucoside hydrolase activity
-
-
brenda
E15.5-18.5 embryos from Sprague-Dawley rats
-
-
brenda
ecto-5'-nucleotidase
-
-
brenda
ecto-5-nucleosidase isoform
-
-
brenda
ecto-5-nucleotidase isoform
-
-
brenda
ecto-nucleotide diphosphatase/phosphodiesterase
-
-
brenda
encoded by Blmh gene; Wistar rats
SwissProt
brenda
endopeptidase-2, male Wistar
-
-
brenda
entry name QSCN6_RAT
SwissProt
brenda
enzyme activity increases during lactation
-
-
brenda
enzyme activity is about 2.5 to 3 times higher in male than in female
-
-
brenda
enzyme additionally acts as an aldehyde isomerase converting malondialdehyde to methylglyoxal
-
-
brenda
enzyme also has DNA 3'-phosphatase activity
-
-
brenda
enzyme also is polynucleotide 5'-hydroxyl kinase
-
-
brenda
enzyme complex of sucrase and isomaltase integrated into the intestinal alpha-glucosidase function with the complex of maltase-glucoamylase
-
-
brenda
enzyme complex reconstituted from cytochrome P-450 and NADPH-cytochrome P-450 reductase
-
-
brenda
enzyme concentration decreases from fed over fasted to diabetic animals
-
-
brenda
enzyme exists as a 72000 MW component of the multienzyme aminoacyl-tRNA synthetase complex or as 60000 MW free enzyme form
-
-
brenda
enzyme expressed in COS cells
-
-
brenda
enzyme expression and activity is regulated by circadian rhythm
-
-
brenda
enzyme form AAA-1 and AAA-2
-
-
brenda
enzyme form CN1 and CN2
-
-
brenda
enzyme form CPT I
486309, 486539, 486544, 486546, 486558, 486560, 486571, 486572, 486576, 486589, 486591
-
-
brenda
enzyme form CPT II
-
-
brenda
enzyme form PIPKIIgamma
-
-
brenda
enzyme forms cGKI, in 2 isoforms cGKIalpha and cGKIbeta, and cGKII
-
-
brenda
enzyme forms CPTo and CPTi from outer and inner mitochondrial membrane
-
-
brenda
enzyme forms the core of the pyruvate dehydrogenase multienzyme complex
-
-
brenda
enzyme from the promotion phase of hepatocarcinogenesis and phenobabital-inducible enzyme
-
-
brenda
enzyme has additional activity of 3-phosphoadenosine 5-phosphate phosphatase
SwissProt
brenda
enzyme I
-
-
brenda
enzyme is a bifunctional selenoprotein
-
-
brenda
enzyme is different from long chain acyl-CoA ligase, EC 6.2.1.3
-
-
brenda
enzyme is expressed through the use of at least 4 different promotors
-
-
brenda
enzyme is in complex with alpha-ketoglutarate dehydrogenase
-
-
brenda
enzyme is in complex with pyruvate dehydrogenase
-
-
brenda
enzyme isoform PMCA 1, PMCA 2 and PMCA3
-
-
brenda
enzyme isoforms I, II, and III
-
-
brenda
enzyme level in developing rat tissues
-
-
brenda
enzyme may be a component of an enzyme complex named alpha-ketoisocaproate:alpha-keto-beta-methylvalerate dehydrogenase
-
-
brenda
enzyme produced in Sf9cells using baculovirus system
-
-
brenda
enzyme transfected to RC12 cells, a pheochromocytoma cell line
-
-
brenda
enzymes PTP-I, PTP-II, PTP-III
-
-
brenda
enzymes xanthine oxidase and xanthine dehydrogenase catalyze NADH oxidation, generating superoxide radicals
-
-
brenda
Erk1
SwissProt
brenda
ERK2
SwissProt
brenda
ERK2; Sprague-Dawley rats
SwissProt
brenda
estrogenized female rats and castrated male and female rats
-
-
brenda
EtOH-treated rats
-
-
brenda
eukaryotic elongation factor EF-2
-
-
brenda
eukaryotic initiaton factor eIF-2
-
-
brenda
evaluation of heterogeneity
-
-
brenda
exposed to thinner fumes
-
-
brenda
expressed in Escherichia coli
-
-
brenda
expressed in Pichia pastoris strain KM71
SwissProt
brenda
expression in COS-7 cells
-
-
brenda
expression in COS-7 cells, the two enzymes EC 1.14.17.3 and EC 4.3.2.5 are generated from a common precursor protein encoded by a single mRNA
-
-
brenda
expression in Escherichia coli
SwissProt
brenda
expression in Escherichia coli BL21 (DE3)
UniProt
brenda
expression in hBRIe 380i cells. Both peptide YY and neuropeptide Y increase expression of enzyme to a level sufficient to induce cell migration by activating the Rho GTPase Cdc42. Peptide YY and neuropeptide Y modulate synchronously enzyme, CD63 and Cdc42
-
-
brenda
expression in MCF-7 human breast cancer cell
-
-
brenda
expression in Mus musculus
SwissProt
brenda
expression in Nicotiana tabacum
-
-
brenda
expression in wild type and in vitamin-C-deficient Arabidopsis thaliana
-
-
brenda
expression of enzyme in baculovirus-insect cell system, yields a mixture of native dimeric, demolydbo-dimeric and monomeric forms. All forms contain flavin, the monomeric forms lack molybdopterin and the iron-sulfur centers. Monomeric forms require only three electrons for complete reduction
-
-
brenda
expression of GMD is higher in macrophages than in endothelial cells
-
-
brenda
expression of GMD was higher in macrophages than in endothelial cells
-
-
brenda
exprsssion in Sacchaoromyces cerevisiae
-
-
brenda
fawn-hooded hypertensive (FHH) rats
-
-
brenda
FBNxKGH, AugxWF, BNLr-1, LEW, KGH, DA
-
-
brenda
fed a biotin deficient and normal diet
-
-
brenda
fed a high-fat diet
-
-
brenda
fed with vitamin B6 deficient diet
-
-
brenda
fed with vitamin E-replete and -defcient diet
-
-
brenda
femal Wistar rats
-
-
brenda
female
-
-
brenda
female adult Wistar rats
-
-
brenda
female albino rats
-
-
brenda
female and male Sprague Dawley rats
UniProt
brenda
female and male Sprague-Dawley rats
-
-
brenda
female and male Sprague-Dawley rats, isozyme PLD1
-
-
brenda
female and male Wistar rats
-
-
brenda
female Charles River CD
-
-
brenda
female Charles River CD-strain
-
-
brenda
female Fischer or male Buffalo rats
-
-
brenda
female LOng-Evans rats, isozymes CaMKIIalpha and beta
-
-
brenda
female rat
-
-
brenda
female Spargue-Dawley
-
-
brenda
female Spargue-Dawley rats
-
-
brenda
female Spargue-Dawley rats
UniProt
brenda
female Sprague Dawley rat
-
-
brenda
female Sprague Dawley rats
-
-
brenda
female Sprague-Dawley
-
-
brenda
female Sprague-Dawley CD rats
-
-
brenda
female Sprague-Dawley rat
-
-
brenda
female Sprague-Dawley rat
SwissProt
brenda
female Sprague-Dawley rat of the U and H substrain
-
-
brenda
female Sprague-Dawley rats
285218, 487258, 639090, 659656, 690669, 693787, 694485, 694562, 695473, 698332, 704633, 706689, 707642
-
-
brenda
female Sprague-Dawley rats
SwissProt
brenda
female Sprague-Dawley rats with spinal cord injury
-
-
brenda
female Sprague-Dawley rats, gene CYP17
-
-
brenda
female Sprague-Dawley rats, young and middle-aged Otsuka Long-Evans Tokushima Fatty rats, isozymes PDK2 and PDK4
-
-
brenda
female wild-type Kyoto-Wistar and tremor rats
Uniprot
brenda
female Wistar
-
-
brenda
female wistar rat
-
-
brenda
female Wistar rats
441635, 441636, 642156, 642163, 654466, 656639, 657284, 657329, 661025, 668863, 684676, 686836, 691058, 692265, 699742, 708192
-
-
brenda
female Wistar rats
SwissProt
brenda
female Wistar rats
UniProt
brenda
female Zucker rats
-
-
brenda
female, Lewis
-
-
brenda
female, nonpregnant, DUB:(SD)
-
-
brenda
female, normale and diabetic mal Wistar rats
-
-
brenda
female, oestradiol-treated
-
-
brenda
female, pregnant, Sprague-Dawley
-
-
brenda
female, Sprague-Dawley strain
-
-
brenda
female, Sprague-Dawley, 2 weeks
-
-
brenda
female, strain Sprague-Dawley
-
-
brenda
female, Wistar-Imamichi strain
-
-
brenda
fenofibrate-fed Otsuka Long-Evans Tokushima fatty rats
-
-
brenda
fetal Sprague-Dawley rats
-
-
brenda
fetus, dual-specificity enzyme, activity of EC 2.7.8.1 and EC 2.7.8.2
-
-
brenda
Fischer
-
-
brenda
Fischer
SwissProt
brenda
Fischer 344
-
-
brenda
Fischer 344 male rats
-
-
brenda
Fischer 344 rat
-
-
brenda
Fischer 344 rats
-
-
brenda
Fischer F344
-
-
brenda
Fischer rats
-
-
brenda
Fischer-344 rats
-
-
brenda
Fischer-344, especially male rats
-
-
brenda
Fisher 344 male and female
-
-
brenda
Fisher 344 x Brown Norway, male, 8-month old or 30-month old
-
-
brenda
Fisher344 rats
-
-
brenda
FKBP12
UniProt
brenda
flavoprotein subunit of thr succinate dehydrogenase; gene sdhA
UniProt
brenda
FMOs exist as a multi-gene family consisting of individual members that are expressed in a tissue-, developmental-, and sex-specific fashion
-
-
brenda
foetal and adult
-
-
brenda
foetuses, newborn, suckling, weaning and adult rats
UniProt
brenda
form I and II
-
-
brenda
four CaMKII isozymes alpha, beta, gamma, delta
-
-
brenda
four PLC delta isoenzymes: PLC delta1-4
-
-
brenda
free and myosin-bound form
-
-
brenda
from heart
SwissProt
brenda
full-length gene, genomic DNA; 5 isozymes of enzyme Dhcr7 through alternative splicing of gene Dhcr7, i.e. splicing variants Dhcr7-AS-1-5
SwissProt
brenda
GalNAc-T1
-
-
brenda
GalNAc-T1
SwissProt
brenda
gamma1 subunit
UniProt
brenda
gene 147CC514
UniProt
brenda
gene aacl
-
-
brenda
gene ADAMTS2; gene ADAMTS2
UniProt
brenda
gene Aibp
UniProt
brenda
gene ATP7A, three splicing variants
-
-
brenda
gene Capn5
SwissProt
brenda
gene CERK
UniProt
brenda
gene CHSY1
-
-
brenda
gene contains three highly similar variable exons and two constant exons, each variable exon is preceded by a distinct promoter and is separately spliced to a set of two constant exons to generate functional Gcnt2 mRNA
-
-
brenda
gene Ctsk; male Wistar rats, gene Ctsk
UniProt
brenda
gene CYP24A1
-
-
brenda
gene CYP24A1
UniProt
brenda
gene CYP27A1
UniProt
brenda
gene CYP46A1
UniProt
brenda
gene EPHX2
UniProt
brenda
gene expression in Escherichia coli
-
-
brenda
gene Ggh
SwissProt
brenda
gene Itpka
UniProt
brenda
gene Itpkb
SwissProt
brenda
gene Itpkc
UniProt
brenda
gene KLK1, pancreatic glandular kallikrein 1 precursor
SwissProt
brenda
gene KLK3
SwissProt
brenda
gene KLK8
-
-
brenda
gene KLK8
SwissProt
brenda
gene KLK8 or PRSS19 or NRPN or BSP1
SwissProt
brenda
gene KLK9, submandibular glandular kallikrein 9 precursor
SwissProt
brenda
gene KLKB1 or PK, plasma kallikrein precursor
SwissProt
brenda
gene MGAT5
UniProt
brenda
gene Pdk1
-
-
brenda
gene Pfkfb1
SwissProt
brenda
gene PIKfyve
UniProt
brenda
gene ppt
-
-
brenda
gene QSOX1
SwissProt
brenda
gene Rc1
-
-
brenda
gene rVkorc1
UniProt
brenda
gene TPH2
UniProt
brenda
gene VKORC1
-
-
brenda
gene VKORC1, mutant Y139F
-
-
brenda
gene Vkorc1, VKORC1 mutant Y137F
-
-
brenda
gene/isozyme PFKFB2
SwissProt
brenda
genes CCT1-5, 6A, 7, and 8 encoding subunits CCT-alpha, CCT-beta, CCT-gamma, CCT-delta, CCT-epsilon, CCT-zeta, CCT-eta, and CCT-theta
P28480, Q5XIM9, Q6P502, Q7TPB1, Q68FQ0, Q3MHS9, D4AC23, D4ACB8
UniProt
brenda
genes GCLC and GCLM encoding heavy and light chain subunits
UniProt
brenda
genes gclC and gclM encoding the two subunits of the enzyme
-
-
brenda
genetically obese, fa/fa, Zucker rats
-
-
brenda
GH3 pituitary cells
-
-
brenda
GH31 module subject to phylogenetic analysis
SwissProt
brenda
Gi1alpha, Gi2alpha anf Gi3alpha
-
-
brenda
Gialpha1
-
-
brenda
glandular kallikrein 3 fragment
SwissProt
brenda
glutathione-insulin transhydrogenase and protein disulfide-isomerase are both not catalyzed by a single enzyme species
-
-
brenda
glyceraldehyde-3-phosphate dehydrogenase working as arsenate reductase
-
-
brenda
Goto-Kakizaki rat
-
-
brenda
GRK2; male Wistar rats
SwissProt
brenda
Gunn strain
-
-
brenda
H35 hepatoma cells
-
-
brenda
Harlan Sprague-Dawley
SwissProt
brenda
healthy and diabetic Sprague-Dawley rats
-
-
brenda
healthy and endotoxemic rats, plasma type enzyme
-
-
brenda
healthy and heart-failure rats
-
-
brenda
healthy and permanently bile diverted male Wistar rats
-
-
brenda
healthy and streptozotocin-induced diabetic rats
-
-
brenda
healthy and type 2 diabetic GK rats
-
-
brenda
heart isozyme PFKFB2; genes PFKFB1-4, four isozymes
SwissProt
brenda
heavy, catalytic subunit
SwissProt
brenda
heme oxygenase-1 is a heat shock protein that is inducible by numerous stimuli, including heavy metals, oxidative stress and injury, and cytokines, a 3 isomer, heme oxygenase-3, exhibits 90% homology to heme oxygenase-2, its mRNA has been detected in several tissues including kidney
-
-
brenda
heme oxygenase-2, constitutive
-
-
brenda
hepatocyte primary culture
-
-
brenda
hepatoma
-
-
brenda
hepatoma 3924A
-
-
brenda
hepatoma 7777
-
-
brenda
hexokinase IV or D
-
-
brenda
hexokinase type I
-
-
brenda
hexokinase type II
-
-
brenda
high expression
-
-
brenda
high fat-fed rats
-
-
brenda
high-salt diet-fed
-
-
brenda
histidase activity is induced in pair-fed rats
-
-
brenda
histone demethylases Ndy1
-
-
brenda
HK I+, a modified form of HK I
-
-
brenda
Holtzman
-
-
brenda
Holtzman albion rat
-
-
brenda
Holtzman rats, copper-deficient rats via copper-deficient diet
-
-
brenda
Holtzman rats, postnatal day 24 male rats and day 26 male rats
-
-
brenda
Holtzman Sprague-Dawley, Harlan Sprague-Dawley
-
-
brenda
Holtzman strain
-
-
brenda
Holtzman strain, male rats
-
-
brenda
homozygous warfarin-resistent rats
-
-
brenda
HTC and Phi-1 tumour cells
-
-
brenda
HTC cells and liver acetone powder
-
-
brenda
hydrolases A and B
-
-
brenda
hyper- and hypothyroid adult rats
-
-
brenda
hypertensive DOCA-salt rat, for the on vitro activity assay recombinant mouse APA is used
-
-
brenda
hypoxia can stimulate enzyme mRNA and protein expression involving binding of hypoxia-induced factor 1 to a specific hypoxia responsive element in the enzyme's promoter
-
brenda
identical to kidney soluble cysteine conjugate beta-lyase also referred to as glutamine transaminase K, K stands for kidney
-
-
brenda
identification of a novel rat mRNA sequence that is highly homologous to human ribonuclease III by differential display
SwissProt
brenda
iGb3 synthase
-
-
brenda
iisoform CPT1a
SwissProt
brenda
immature 12-day-old male Wistar albino rats
-
-
brenda
immature female Sprague-Dawley rats
-
-
brenda
immature female Wistar rats
-
-
brenda
immature Sprague Dawley
-
-
brenda
immunological differentiation from rat liver cathepsin B, human and rabbit liver cathepsin H
-
-
brenda
IMPDH2
UniProt
brenda
inbred Lewis strain euthyroid, hyperthyroid and hypothyroid male and female rats
-
-
brenda
inbred strains, recombinant inbred strains
-
-
brenda
includes 4.3.1.17 and 4.3.1.19; male Sprague-Dawley rat
UniProt
brenda
indoleamine 2,3-dioxygenase from small intestine
-
-
brenda
inducible by growth on di-(2-ethylhexyl)phthalate
-
-
brenda
inducible enzyme
-
-
brenda
inducible isozyme HO-1
-
-
brenda
inducible isozyme HO-1, constitutive isozyme HO-2
UniProt
brenda
induction of enzyme by dexamethasone
-
-
brenda
injection of glucagon elevates activity
-
-
brenda
inositol polyphosphate 4-phosphatase type II
SwissProt
brenda
INS-1 beta-cells
-
-
brenda
insulin resistant strain JCR:LA-cp and wild type rats
-
-
brenda
insulin-resistant
-
-
brenda
insulin-resistant Zucker fa/fa and Fa/? strains
-
-
brenda
insulin-resistent ZDF rats, Zucker diabetic fatty rats
-
-
brenda
insulinoma cell line RINm5F
-
-
brenda
IRP1
UniProt
brenda
isoenzyme 1, 2, 3 and 4
-
-
brenda
isoenzyme 2
-
-
brenda
isoenzyme A
-
-
brenda
isoenzyme ACS1
UniProt
brenda
isoenzyme ACS2
UniProt
brenda
isoenzyme ACSL3
UniProt
brenda
isoenzyme ACSL6_v1
UniProt
brenda
isoenzyme ACSL6_v2
UniProt
brenda
isoenzyme I and II
-
-
brenda
isoenzymes AC6, AC5, AC4, AC 7 and AC 9
-
-
brenda
isoenzymes PD I and PD II
-
-
brenda
isoform 11beta-HSD1
-
-
brenda
isoform 2
-
-
brenda
isoform 5alpha reductase type 1
SwissProt
brenda
isoform 5alpha reductase type 2
UniProt
brenda
isoform alpha
UniProt
brenda
isoform B; isoform B
SwissProt
brenda
isoform beta
UniProt
brenda
isoform BRE1B
SwissProt
brenda
isoform C
-
-
brenda
isoform CNP2 fused to GFP
-
-
brenda
isoform CPT1a
SwissProt
brenda
isoform CPT1b
UniProt
brenda
isoform CPT2
UniProt
brenda
isoform CRA_a
SwissProt
brenda
isoform Decr2
UniProt
brenda
isoform E-NPP1
UniProt
brenda
isoform E-NPP3
SwissProt
brenda
isoform ecto-adenylate kinase
-
-
brenda
isoform ecto-nucleotide pyrophosphatase/phosphodiesterase
-
-
brenda
isoform Ephx2
UniProt
brenda
isoform GalT-1, expression in CHOlec8 cells
-
-
brenda
isoform Gpx4
SwissProt
brenda
isoform HAS2
SwissProt
brenda
isoform I and II
-
-
brenda
isoform inositol 1,4,5-trisphosphate 3-kinase A
UniProt
brenda
isoform Kdm6a
UniProt
brenda
isoform Kf-1
UniProt
brenda
isoform KIF5C
-
-
brenda
isoform lipocalin-type prostaglandin D synthase
-
-
brenda
isoform MnSOD
-
-
brenda
isoform NAT1
SwissProt
brenda
isoform NAT2
SwissProt
brenda
isoform NDPK B
-
-
brenda
isoform NT5E
UniProt
brenda
isoform paraoxonase 1
-
-
brenda
isoform PDE1
-
-
brenda
isoform PDE1A
-
-
brenda
isoform PDE2
-
-
brenda
isoform PDE4D, short variants PDE4D1 and PDE4D2 are transcriptionally regulated by follicle-stimulating hormone
-
-
brenda
isoform PDE5
-
-
brenda
isoform PLC-beta3
-
-
brenda
isoform PLCbeta1, two subtypes
-
-
brenda
isoform RBCK1
UniProt
brenda
isoform RNase9
SwissProt
brenda
isoform Shp2
-
-
brenda
isoform STcys
-
-
brenda
isoform STtyr
-
-
brenda
isoform SULT2B1a
SwissProt
brenda
isoform SULT2B1b
SwissProt
brenda
isoform TPP1
UniProt
brenda
isoform TR1
SwissProt
brenda
isoform TrxR1
SwissProt
brenda
isoform TrxR2
UniProt
brenda
isoform type III of 3beta-hydroxysteroid dehydrogenase/DELTA5-DELTA4 isomerase with almost exclusive 3-ketosteroid reductase activity
-
-
brenda
isoform UCHL1
SwissProt
brenda
isoform zeta
SwissProt
brenda
isoforms 1 and 2
-
-
brenda
isoforms alpha, beta
-
-
brenda
isoforms ART2a and ART2b, expression in rat mammary adenocarcinoma cells
-
-
brenda
isoforms GAD65 and GAD67
-
-
brenda
isoforms GAD65 and GAD67, expression in Sf9/baculovirus system
-
-
brenda
isoforms gamma, epsilon
-
-
brenda
isoforms I and II
-
-
brenda
isoforms II, III, IV, V, VI and VII in liver
-
-
brenda
isoforms KAT I and KAT II
-
-
brenda
isoforms MAT1A, MAT2A
-
-
brenda
isoforms of enzyme targeting subunit 1, MYPT 1
-
-
brenda
isoforms PDE1, PDE2, PDE3, PDE10, PDe11
-
-
brenda
isoforms PDE5, PDE9
UniProt
brenda
isozyme 11beta-HSD1
-
-
brenda
isozyme 11beta-HSD2
-
-
brenda
isozyme 5alpha-R1
SwissProt
brenda
isozyme 5alpha-R2
UniProt
brenda
isozyme A
-
-
brenda
isozyme ACC1; gene ACACA, encoding isozyme ACC1 or ACC-alpha
Uniprot
brenda
isozyme ACC2; gene ACACB, encoding isozyme ACC2 or ACC-beta
Uniprot
brenda
isozyme ACSL5
UniProt
brenda
isozyme AKR1C9
-
-
brenda
isozyme beta
-
-
brenda
isozyme beta; isozyme beta
UniProt
brenda
isozyme CaM kinase IIalpha
-
-
brenda
isozyme CaMKIgamma; two alternative splicing isoforms of CaMKIgamma
SwissProt
brenda
isozyme CaMKIIa
SwissProt
brenda
isozyme CaMKIIalpha
-
-
brenda
isozyme CaMKIIdelta exists in two splicing variants deltaB and deltaC in the heart
-
-
brenda
isozyme CES2
SwissProt
brenda
isozyme cPLA2alpha
-
-
brenda
isozyme CYP4A1
-
-
brenda
isozyme FMO1-FMO5
-
-
brenda
isozyme GRK6 A and GRK6 B
-
-
brenda
isozyme HAS1; 3 isozymes HAS1, HAS2, and HAS3
SwissProt
brenda
isozyme HAS2; isozyme HAS2
SwissProt
brenda
isozyme HAS3
SwissProt
brenda
isozyme HO-1
-
-
brenda
isozyme HO-1
UniProt
brenda
isozyme HO2
-
-
brenda
isozyme IP3K-C
-
-
brenda
isozyme L1
-
-
brenda
isozyme LH2b; 3 isozymes LH1-3
SwissProt
brenda
isozyme ME2
-
-
brenda
isozyme Nat3; inbred strains F344, WKY, and SPRD, isozymes Nat1, Nat2, and Nat3
SwissProt
brenda
isozyme NDPKB
-
-
brenda
isozyme nNOS
UniProt
brenda
isozyme OST-PTP
-
-
brenda
isozyme PAD6
-
-
brenda
isozyme PAP-2
-
-
brenda
isozyme PDE11A
-
-
brenda
isozyme PDK1
SwissProt
brenda
isozyme PDK2
-
-
brenda
isozyme PDK2
SwissProt
brenda
isozyme PDK2, Protein Data Bank: 1JM6
-
-
brenda
isozyme PI3Kdelta
-
-
brenda
isozyme pKCalpha
-
-
brenda
isozyme PKCdelta
-
-
brenda
isozyme PLD1
-
-
brenda
isozyme PLD2
-
-
brenda
isozyme RSK1, i.e. p90 ribosomal S6 kinase or 14-3-3
-
-
brenda
isozyme SMS1
-
-
brenda
isozyme SPT2
-
-
brenda
isozyme topo IIbeta
-
-
brenda
isozyme type I
-
-
brenda
isozyme type II
-
-
brenda
isozyme type III
-
-
brenda
isozyme type III
SwissProt
brenda
isozymes 11beta-HSD1 and 11beta-HSD2, male WAG rats, male hypertensive NISAG rats, i.e. rat strain with hereditary stress-induced arterial hypertension
-
-
brenda
isozymes alpha, betaI, betaII, and gamma
-
-
brenda
isozymes alpha, betaI, betaII, gamma, delta, epsilon, lambda, eta, theta, and zeta
-
-
brenda
isozymes alpha1 and alpha2
-
-
brenda
isozymes CaMKII alpha, beta, gamma, and delta
-
-
brenda
isozymes colonic HKalpha2, showing 3 splicing variants, and gastric HKalpha1
-
-
brenda
isozymes DGKalpha, DGKzeta, and DGKepsilon
-
-
brenda
isozymes GAD67 and GAD65, encoded by different genes
-
-
brenda
isozymes GSTA1-1, GSTM1-1, and GSTP1-1
-
-
brenda
isozymes IP33K-A, IP33K-B, and IP33K-C
-
-
brenda
isozymes L-CPT1 and M-CPT1
-
-
brenda
isozymes LOX1, LOXL2, LOXL3, and LOXL4
Uniprot
brenda
isozymes LPP1, LPP-2, and LPP-3
-
-
brenda
isozymes LPP1-3, several splicing variants of LPP1
-
-
brenda
isozymes NDP kinase alpha and NDP kinase beta
-
-
brenda
isozymes NMT1 and NMT2
-
-
brenda
isozymes PAP-1 and PAP-2
-
-
brenda
isozymes PDE1C and PDE1A
-
-
brenda
isozymes PDK1 and PDK2
-
-
brenda
isozymes PDK1, PDK2, and PDK4
-
-
brenda
isozymes PDK1, PDK2, PDK3, and PDK4
-
-
brenda
isozymes PDK2 and PDK4
-
-
brenda
isozymes PKG-Ialpha and PKG-Ibeta
-
-
brenda
isozymes PLD1 and PLD2
-
-
brenda
isozymes PLD1 and PLD2, and two splice variants of PLD1, PLD1a and PLD1b
-
-
brenda
isozymes SRD5alpha1, SRD5alpha2, and SRD5alpha3
-
-
brenda
isozymes: 1 soluble not-inducible and 1 membraneous inducible by lipopolysaccharides
-
-
brenda
KAT I and KAT II
-
-
brenda
KAT II accounts for more than 70% of kynurenate production under physiological conditiones
-
-
brenda
katanin p60 ATPase-containing subunit A1; gene Katna1
SwissProt
brenda
L-CPT I
-
-
brenda
lactating postpartum female rats
-
-
brenda
lang-Evans hooded rats, male, 6-8 month old
-
-
brenda
lean and obese Wistar rats
-
-
brenda
LES rat
-
-
brenda
LEW.1A and LEW.1W rats
SwissProt
brenda
Lewis rat
-
-
brenda
Lewis1WR1
-
-
brenda
light, regulatory subunit
SwissProt
brenda
Like the yeast enzyme, mammalian, plant and fly orthologs share the capacity for the conversion of Ins(1,4,5)P3 to Ins(1,3,4,5,6)P5. Plant and fly IPMKs recapitulate the yeast enzyme's preference for D6-hydroxyl phoshorylation followed by D3-hydroxylphosphorylation, mammalian IPMKs appear to prefer the reverse order.
-
-
brenda
liver isozyme PFKFB1; genes PFKFB1-4, four isozymes
SwissProt
brenda
liver regeneration protein induced during partial heparectomy. Insulin plays a key role in activation of enzyme. Activation occurs by conformational change in protein structure in the 1-pyrroline-5-carboxylate docking site due to sugars binding in the atrial natriuretic factor receptor region of the enzyme
-
-
brenda
liver, contains isozymic forms, mitochondrial and cytosolic, of omega-amidase
-
-
brenda
Lobund-Wistar rat with transplanted PA-3 prostate tumors
-
-
brenda
Lon protease homolog 2, peroxisomal; gene Lonp2
UniProt
brenda
long chain acyl-CoA synthetase 1
-
-
brenda
long chain acyl-CoA synthetase 2
-
-
brenda
long chain acyl-CoA synthetase 3
SwissProt
brenda
long chain acyl-CoA synthetase 4
-
-
brenda
long chain acyl-CoA synthetase 5
-
-
brenda
Long Evans cinnamon
SwissProt
brenda
Long Evans rats
-
-
brenda
Long-Evans
-
-
brenda
Long-Evans female rats
-
-
brenda
Long-Evans rat pups, several isozymes
-
-
brenda
Long-Evans Tokushima Otsuka (LETO) rat
-
-
brenda
Long-Evans Tokushima Otsuka, Otsuka Long-Evans Tokushima Fatty and rosiglitazone-treated Otsuka Long-Evans Tokushima Fatty rats, all male and 4 weeks old.
-
-
brenda
LOU and Brown-Norway rats, male inbred BN/Rij rats, two inbred strains with different susceptibilities to arterial fragility, genes and isozymes LOXL1 and LOX
-
-
brenda
low activity
-
-
brenda
low molecular weight angiotensin I converting enzyme
-
-
brenda
lysophospholipase and beta-subunit and gamma-subunit; male Wistar
SwissProt
brenda
lysyl oxidase LO and several lysyloxidase-like proteins LOXL
-
-
brenda
M.R.C. hooded rat
-
-
brenda
male
575, 135998, 347985, 486245, 486352, 486354, 486369, 636620, 642881, 644818, 644832, 646570, 684811, 711646, 712595, 715153, 715663, 715984, 718007, 720117, 725072
-
-
brenda
male
SwissProt
brenda
male 6-months-old Fisher 344 rats
-
-
brenda
male 9-weeks-old Wistar rats
-
-
brenda
male adult Buffalo
-
-
brenda
male adult Wistar
-
-
brenda
male adult Wistar rats
-
-
brenda
male adult Wistar rats, 3 splicing forms CK1epsilon-1 - CK1epsilon-3
SwissProt
brenda
male Albino Charles Foster rats
-
-
brenda
male albino rat Charles River CD strain
-
-
brenda
male albino rats
-
-
brenda
male albino Sprague-Dawley
-
-
brenda
male albino Wistar rats
-
-
brenda
male albino, normal and alloxan diabetic rats, no change of enzyme activity and CoASSG content in diabetic rats
-
-
brenda
male and femal Wistar rats, age 1-20 months
-
-
brenda
male and female
-
-
brenda
male and female August-Copenhagen Irish, ACI, rats
SwissProt
brenda
male and female Crj:CD(SD)IGS rats and male Sprague-Dawley rats
-
-
brenda
male and female WAG/Rij rats
-
-
brenda
male and female Wistar rats
-
-
brenda
male and pregnant female Wistar rats
SwissProt
brenda
male animals, under starvation, isoforms AlaAT I and AlaAT II
-
-
brenda
male CD strain rats
-
-
brenda
male CDR Fisher rats
-
-
brenda
male Charles River Sprague-Dawley rats
-
-
brenda
male Chbb Thom rat
-
-
brenda
male Donryu
-
-
brenda
male Donryu
SwissProt
brenda
male Donryu rats
-
-
brenda
male E14 Fisher 344 rats
-
-
brenda
male F344 Fischer, Wistar, and Sprague-Dawley rats
-
-
brenda
male F344 rats
-
-
brenda
male Fischer 344 rats
-
-
brenda
male Fischer rats
-
-
brenda
male Fisher 344 rats
-
-
brenda
male Fisher F344 rat
-
-
brenda
Male Fisher rats of different ages
-
-
brenda
male Harlan Sprague-Dawley rats
-
-
brenda
male Holtzman rats
-
-
brenda
male Hooded Lister rats of the Rowett strain
SwissProt
brenda
male inbred WKAH/HkmSlc rats
UniProt
brenda
male Lewis rats
-
-
brenda
male Long Evans rats
-
-
brenda
male Long-Evans rats
-
-
brenda
male Long-Evans, Turku strain
-
-
brenda
male M.R.C. hooded rat
-
-
brenda
male rat
-
-
brenda
male rats
-
-
brenda
male rats
SwissProt
brenda
male rats
UniProt
brenda
male Sasco/King (SD)BR strain
-
-
brenda
male Spague-Dawley rats
-
-
brenda
male Spargue-Dawley rats
-
-
brenda
male specific-pathogen-free Sprague Dawley
-
-
brenda
male spontaneously hypertensive rats and normotensive Wistar-Kyoto rats
-
-
brenda
male Sprague Dawley
-
-
brenda
male Sprague Dawley rat
-
-
brenda
male Sprague Dawley rats
-
-
brenda
male Sprague Dawley rats
SwissProt
brenda
male Sprague Dawley rats
UniProt
brenda
male Sprague Dawley rats, gene CK2alpha
-
-
brenda
male Sprague Dawley strain
-
-
brenda
male Sprague Dawley, cholestryamine-treated rats
-
-
brenda
male Sprague-Daley rats
-
-
brenda
male Sprague-Dawley
31387, 31395, 392111, 392115, 486350, 486354, 487596, 488023, 489741, 636998, 637004, 639897, 639898, 639901, 642551, 643860, 645048, 645807, 645819, 645820, 645824, 645825, 645826, 645828, 645994, 649570, 653421, 653859, 657394, 658222, 658529, 661435, 674079, 688524
-
-
brenda
male Sprague-Dawley
SwissProt
brenda
male Sprague-Dawley
Uniprot
brenda
male Sprague-Dawley albino rats
-
-
brenda
male Sprague-Dawley and Wistar rats
SwissProt
brenda
male Sprague-Dawley IGS rats
-
-
brenda
male Sprague-Dawley or Han-Wistar rats
-
-
brenda
male Sprague-Dawley rat
-
-
brenda
male Sprague-Dawley rat
SwissProt
brenda
male Sprague-Dawley rat
UniProt
brenda
male Sprague-Dawley rat, isoenzyme ES10, belonging to the nonspecific carboxylesterase family
SwissProt
brenda
male Sprague-Dawley rat, isoenzyme ES3, belonging to the nonspecific carboxylesterase family
SwissProt
brenda
male Sprague-Dawley rat, isoenzyme ES4, belonging to the nonspecific carboxylesterase family
SwissProt
brenda
male Sprague-Dawley rat, isoenzyme termed AB010635, belonging to the nonspecific carboxylesterase CES2 family
SwissProt
brenda
male Sprague-Dawley rat, isoenzyme termed AY034877, belonging to the nonspecific carboxylesterase CES2 family
SwissProt
brenda
male Sprague-Dawley rat, isoenzyme termed D50580 or CE21p, belonging to the nonspecific carboxylesterase family
O35535
SwissProt
brenda
male sprague-dawley rats
135971, 247008, 285345, 286023, 286024, 286472, 286473, 288490, 288491, 288496, 392339, 392366, 392473, 395107, 487368, 489616, 640731, 640737, 640738, 640756, 640773, 640774, 644967, 645728, 646078, 646114, 646432, 646435, 646631, 646640, 649690, 649761, 650330, 653232, 654887, 655495, 657523, 657876, 658432, 659757, 659760, 661275, 661458, 661658, 661848, 662084, 662148, 662397, 662491, 662563, 664479, 665836, 666131, 666459, 666460, 667025, 667163, 667365, 667477, 668486, 669455, 669606, 669626, 669635, 669904, 669937, 669962, 671005, 671237, 671657, 673034, 674065, 674136, 675097, 676737, 677433, 677498, 678983, 681089, 682806, 683051, 684367, 686553, 687078, 688062, 688137, 688523, 688671, 689164, 689314, 689699, 689994, 689999, 690360, 690680, 690886, 691132, 691165, 691828, 692005, 692195, 692200, 692232, 692277, 693075, 693356, 693803, 693847, 694355, 694394, 695088, 695205, 699464, 699831, 699936, 700470, 701687, 701919, 702529, 703239, 703244, 703381, 703591, 703698, 704688, 705395, 705804, 705930, 706769, 709039, 709719, 709742, 710616, 711036, 711328
-
-
brenda
male sprague-dawley rats
SwissProt
brenda
male sprague-dawley rats
UniProt
brenda
male Sprague-Dawley rats of 125-149 g. Diabetes and all-trans-retinoic acid administration decrease the hepatic phosphatidylethanolamine:phosphatidylcholine ratio by 37% compared to control values
-
-
brenda
male Sprague-Dawley rats, 10 weeks old
-
-
brenda
male Sprague-Dawley rats, 260-320 g, approximately 12 weeks old
-
-
brenda
male Sprague-Dawley rats, 7 weeks old
-
-
brenda
male Sprague-Dawley rats, cytosolic isozyme
SwissProt
brenda
male Sprague-Dawley rats, dietary manipulated
-
-
brenda
male Sprague-Dawley rats, inducible isozyme HO-1
UniProt
brenda
male Sprague-Dawley rats, isozyme iNOS
UniProt
brenda
male Sprague-Dawley rats, isozymes nNOS and iNOS
-
-
brenda
male Sprague-Dawley rats, low enzyme level in rats fed a low protein diet, high enzyme level when low protein diet is supplemented with cysteine, homocystine, or methionine
-
-
brenda
male Sprague-Dawley rats, mitochondrial isozyme
SwissProt
brenda
male Sprague-Dawley rats, potassium oxonate-induced hyperuricemic rats
-
-
brenda
male Sprague-Dawley rats, repeated lung injury model
-
-
brenda
male Sprague-Dawley rats, streptozotocin diabetic rats perfused in the presence or absence of insulin, under either diabetic or control conditions
-
-
brenda
male Sprague-Dawley rats, tissue-specific isozymes L-CPT I and M-CPT I
-
-
brenda
male Sprague-Dawley rats, very low activity in animals fed a low protein diet, high level of enzyme in animals fed a protein, methionine, or cysteine rich diet
-
-
brenda
male Sprague-Dawley strain
-
-
brenda
male SpragueDawley rats
-
-
brenda
male SpragueDawley rats, type I and IV isozymes
-
-
brenda
male Sprangue-Dawley rats
-
-
brenda
male Spreague-Dawley
-
-
brenda
male Winstar rats
-
-
brenda
male Wistar
31365, 31366, 31369, 80872, 285406, 486521, 486631, 486637, 486640, 486641, 486671, 488281, 492105, 636623, 640599, 641387, 641390, 642601, 642833, 643179, 643180, 645976, 650884, 653349, 677455, 677499, 682244, 685413, 685674, 690194
-
-
brenda
male Wistar
Q6IMX8
UniProt
brenda
male Wistar albino rats
-
-
brenda
male Wistar albino, fed a standard diet or fasted for three days
-
-
brenda
male Wistar and Wistar Kyoto rats
-
-
brenda
male Wistar Hannover rats
-
-
brenda
male Wistar Kyoto rats
-
-
brenda
male Wistar LAT1
-
-
brenda
male wistar rat
348526, 439023, 489933, 667459, 673486, 677454, 679695, 685343, 686180, 686560, 690352, 693934, 696511, 696995, 700461, 701040, 704909
-
-
brenda
male Wistar rat, 9-11 weeks
-
-
brenda
male Wistar rats
135998, 136013, 391993, 486435, 488979, 639868, 639872, 645024, 646618, 649721, 650339, 650432, 651195, 651983, 653008, 653094, 655139, 657277, 658716, 660006, 660037, 660568, 660949, 661442, 661495, 661569, 661606, 662146, 662592, 662673, 662841, 664246, 664474, 664764, 666114, 666534, 667984, 669943, 671244, 671341, 671678, 672439, 673101, 673929, 675697, 676101, 679249, 679661, 679670, 681090, 681494, 682110, 682112, 682252, 682902, 683217, 683322, 683441, 683708, 683791, 683838, 685900, 686054, 686487, 686548, 686892, 687055, 687064, 687989, 688006, 688765, 689159, 689171, 689173, 689202, 689210, 689285, 689991, 690145, 690358, 691036, 692128, 692207, 692267, 693720, 694353, 694363, 694386, 694392, 694399, 695151, 695203, 695968, 695972, 696596, 697060, 697223, 697420, 699395, 699744, 699751, 699758, 699761, 700610, 701186, 703135, 703626, 703977, 704822, 705350, 705505, 705905, 705922, 707376, 707719, 708195, 708569, 709705, 710250, 710645, 711690, 714034
-
-
brenda
male Wistar rats
O55171, O88267, P11884, P19643, P21396, P21643, P80254, Q07014, Q6AYS7, Q9ES71, Q9QX71
SwissProt
brenda
male Wistar rats
UniProt
brenda
male Wistar rats 7-(P7) and 60-day-old (P60)
-
-
brenda
male Wistar rats weighing 180-200 g. 30-40% less phosphatidylcholine is generated in hepatocytes from ethanol-fed rats as compared to controls. Hepatocytes isolated from rats fed the betaine-supplemented ethanol diet have significantly higher phosphatidylcholine generation compared to hepatocytes from ethanol-fed rats.
-
-
brenda
male Wistar rats with heart failure induced by coronary artery ligation and sham-operated controls, stroke-prone spontaneously hypertensive rats and Wistar Kyoto rats as controls, cyp1a1Ren-2 transgenic rats and Fischer controls, and adult Sprague-Dawley rats
-
-
brenda
male Wistar rats, 2 isozymes 5alpha-R1 and 5alpha-R2
-
-
brenda
male Wistar rats, 2 isozymes, ICD1 and ICD2
-
-
brenda
male Wistar rats, 4 weeks old
-
-
brenda
male Wistar rats, enzyme activity is stimulated by intravenous doses of methylprednisolone
-
-
brenda
male Wistar rats, genes GCLC and GCLM
-
-
brenda
male Wistar rats, healthy and subjected to myocardial infarction
-
-
brenda
male Wistar rats, isozyme NDPK-D
-
-
brenda
male Wistar rats, isozymes CTE-I, MTE-I, and PTE-I
-
-
brenda
male Wistar rats, isozymes PD I and PD II
-
-
brenda
male Wistar rats, neuropathic rats
-
-
brenda
male Wistar rats, SAST124, a splice variant of SAST
-
-
brenda
male Wistar rats, six-months-old, develop diet-induced hyperphagia and obesity, male obese (fa/fa) Zucker rats, three-months-old, display genetic obesity due to deficit in leptin receptors, and male lean Zucker rats, three-month-old
SWissProt
brenda
male Wistar rats, strain HSdCpB: WU
-
-
brenda
male Wistar strain
-
-
brenda
male Wistar-Han rats
UniProt
brenda
male Wistar-Imamichi, showing very low enzyme amount, and Sprague-Dawley rats
-
-
brenda
male Wistar-Kyoto rats
-
-
brenda
male Wistar-Kyoto rats
UniProt
brenda
male Wister rat
UniProt
brenda
male Wister strain albino rats
-
-
brenda
male Zucker diabetic rats
-
-
brenda
male, adult
-
-
brenda
male, Donryu
-
-
brenda
male, Sprague-Dawley
-
-
brenda
male, Sprague-Dawley, low sodium, high potassium treated
-
-
brenda
male, Wistar
-
-
brenda
male, Wistar background, primary culture of hepatocytes
SwissProt
brenda
male, Wistar strain
-
-
brenda
male, Wistar, hypothyroidism and hyperthyroidism is induced by diet
-
-
brenda
male, Zur:SIV low sodium, high potassium or high sodium, low potassium treated for stimulation or supprssion, respectively
-
-
brenda
male-specific hepatic microsomal vitamin D 25-hydroxlase CYP2C11
UniProt
brenda
maleWistar rats
-
-
brenda
malonyl transferase domain of EC 2.3.1.85
-
-
brenda
MAO A and MAO B are encoded by separate genes
-
-
brenda
MAO-A
-
-
brenda
MAO-A; male albino rats, isozyme MAO-A
SwissProt
brenda
MAO-B; male albino rats, isozyme MAO-B
SwissProt
brenda
MAOA
SwissProt
brenda
MAOB
SwissProt
brenda
marked variations in enzyme activity of different strains
-
-
brenda
mast-cell line RBL-2H3
-
-
brenda
mature male Wistar
-
-
brenda
mature mitochondrial isozyme mAAT
SwissProt
brenda
maximal activity in 14-18 days old rats
-
-
brenda
membrane-bound ALDH, ALDH-I: soluble high Km ALDH, and ALDH-II: low Km ALDH
-
-
brenda
methods of enzyme determination
-
-
brenda
MGAT3 gene is a pseudogene in mice but functional in rats
-
-
brenda
microsomes: dihydrodiol dehydrogenase and 3alpha-hydroxysteroid dehydrogenase are different enzymes, cytosol: dihydrodiol dehydrogenase and 3alpha-hydroxysteroid dehydrogenase activity is unseparable
-
-
brenda
Milan hypertensive and normotensive rats
-
-
brenda
mitochondrial and cytosolic enzyme, distinct
-
-
brenda
mitochondrial enzyme inducible by glucagon or cAMP, peroxisomal enzyme inducible by clofibrate
-
-
brenda
mitochondrial isoform
-
-
brenda
mitochondrial isozyme mAspAT
-
-
brenda
Mn-SOD
-
-
brenda
monofunctional DELTA3-DELTA2-enoyl-CoA isomerase
SwissProt
brenda
Morris hepatoma 9618A2, 7777, 5123TC, 7800, 5123B, 7787
-
-
brenda
Morris hepatoma cells
-
-
brenda
mouse neuroblastoma * rat glioma hybrid cell line
-
-
brenda
mRNA increases 30fold in brown adipose tissue within 6 h of cold exposure
SwissProt
brenda
MRP6
-
-
brenda
mu class isozyme M1-1, GST-M1-1
-
-
brenda
multienzyme complex
UniProt
brenda
multienzyme system
-
-
brenda
multifunctional enzyme type 2, i.e. MFE-2
-
-
brenda
multiparous rats
-
-
brenda
multiple enzymes
-
-
brenda
multiple forms
-
-
brenda
multiple forms of mitochondrial topoisomerase I: 66000 MW form, 77000 ME form and 100000 MW form
-
-
brenda
multiple forms: cathepsin CI, CII, and CIII are immunologically closely related if not identical
-
-
brenda
multiple forms: I, II, II
-
-
brenda
myoblastic cell line H9c2
-
-
brenda
myosin-binding subunit of MLCP
-
-
brenda
N-acylethanolamine-specific phospholipase D, NAPE-PLD
-
-
brenda
NADPH- and NADH-linked 5alpha-dihydroprogesterone 3alpha-hydroxysteroid oxidoreductase activity
-
-
brenda
native and selenomethionine-substituted cysteine dioxygnease
Uniprot
brenda
native recombinant AspRS from rat and the N-terminal truncated derivatives AspRS-DELTA20 and AspRS-DELTA36, expressed in yeast
-
-
brenda
neonatal
-
-
brenda
neonatal and adult
-
-
brenda
neonatal rats
-
-
brenda
neonatal Sprague-Dawley rats
-
-
brenda
neonatal Wistar rats
-
-
brenda
neuron-specific isozymes DGKbeta and DGKgamma
-
-
brenda
neuronal enzyme
UniProt
brenda
neuropsin precursor
SwissProt
brenda
neutral beta-galactosidase
-
-
brenda
neutral lipase and acid lipase
-
-
brenda
newborn and adults
-
-
brenda
newborn rats
-
-
brenda
nine-week-old male Wistar rats
SwissProt
brenda
nine-week-old male Wistar rats
UniProt
brenda
no activity detected in rat liver homogenate
-
-
brenda
no activity detected in rat liver using capilarry gas chromatography-mass spectrometry
-
-
brenda
no activity in Morris hepatoma 7777 cells
-
-
brenda
no information in the literature concerning reduction of cis-2-enoyl-CoA substrates, thus classification of rat enzyme according to EC 1.3.1.8 or EC 1.3.1.38 impossible
390751, 390752, 390753, 390754, 390755, 390756, 390757, 390758, 390759, 390855, 390856, 390857, 390858
-
-
brenda
no information in the literature concerning reduction of cis-2-enoyl-CoA substrates, thus classification of rat enzyme according to EC 1.3.1.8 or EC 1.3.1.38 not yet possible
-
-
brenda
non-proliferating cells inactivate 88000-90000 Da M1 subunit by degradation into 40000 Da fragments
-
-
brenda
non-specific, housekeeping isoform ALAS-N and erythroid-specific isoform ALAS-E
-
-
brenda
normal and diabetic
-
-
brenda
normal animals and animals with hexachlorobenzene-induced porphyria
-
-
brenda
normotensive and angiotensin-hypertensive rats, two isoforms cGKIalpha and cGKIbeta of enzyme form cGKI
-
-
brenda
normotensive male Wistar-Han rats
-
-
brenda
not a full length clone
SwissProt
brenda
Novikoff hepatoma cells
-
-
brenda
NPP3, recombinant
SwissProt
brenda
NPR-A; adult male Wistar rats
UniProt
brenda
NPR-B; adult male Wistar rats
UniProt
brenda
NTPDase1
UniProt
brenda
NTPDase2
UniProt
brenda
NTPDase8
UniProt
brenda
OAS1A
UniProt
brenda
obese Zucker rat
-
-
brenda
obese Zucker rats
-
-
brenda
on normal or clofibrate enriched diet
-
-
brenda
one isoenzyme in kidney
-
-
brenda
only minute amounts of heme oxygenase-1 in testis
-
-
brenda
only one isoform in rats
-
-
brenda
only one isoform in rats
UniProt
brenda
Osborne-Mendel strain
-
-
brenda
ospzyme LH2a; 3 isozymes LH1-3
SwissProt
brenda
Otsuka Long Evans Tokushima Fatty rats, model of type II Diabetes mellitus
-
-
brenda
Otsuka Long-Evans Tokushima Fatty (OLETF) rat, spontaneously diabetic
-
-
brenda
ovalbumin-induced rat model of asthma
-
-
brenda
ovarectomised animal
-
-
brenda
ovariectomised female Wistar rats
-
-
brenda
ovariectomized female rats with and without estradiol replacement undergoing 2-h middle cerebral artery occlusion. Estradiol reduces basal and post-ischemic soluble epoxide hydrolase expression. Middle cerebral artery occlusion strongly induces mRNA levels of tumor necrosis factor-alpha, interleukin 6, and interleukin 1beta, which is attenuated in enzyme knock-outs, but not by enzyme inhibitors
-
-
brenda
over-expression in mice
-
-
brenda
overexpressed in CHO cells
-
-
brenda
overexpression in transgenic Mus musculus
-
-
brenda
overview
-
-
brenda
P11960 i.e. E1 subunit alpha, P35738 i.e. E1 subunit beta
UniProt
brenda
P60 katanin, enzyme expression changes during development of the nervous system and correlates with axonal growth
SwissProt
brenda
PAD1; isozyme PAD1
UniProt
brenda
PAD2; isozyme PAD2
UniProt
brenda
PAD3; isozyme PAD3
UniProt
brenda
PAD4; isozyme PAD4
UniProt
brenda
PAM-1 and PAM-2
-
-
brenda
particulate enzyme
-
-
brenda
PC-1, nucleotide pyrophosphatase/phosphodiesterase I
-
-
brenda
PC-12 pheochromocytoma cells
-
-
brenda
PC12 cells
-
-
brenda
PDE3
-
-
brenda
PH-PLCdelta1 residues 11-140
-
-
brenda
phenobarbital-treated
-
-
brenda
pheochromacytoma PC-12 cells
-
-
brenda
PI3-C2gamma
SwissProt
brenda
PI3KC2alpha
-
-
brenda
PLC-delta1
-
-
brenda
PLCbeta1a and PLCbeta1b
SwissProt
brenda
PLCepsilon
SwissProt
brenda
ppGaNTase-T9
Uniprot
brenda
precursor
SwissProt
brenda
precursor
UniProt
brenda
precursor fragment
SwissProt
brenda
precursor; comparative and phylogenetic analysis of alpha-L-fucosidase genes
SwissProt
brenda
pregnant and nonpregnant Sprague-Dawley rats
-
-
brenda
pregnant female Wistar
-
-
brenda
pregnant rat
-
-
brenda
pregnant Sprague-Dawley
-
-
brenda
pregnant Sprague-Dawley rats
-
-
brenda
pregnant Sprague-Dawley rats
SwissProt
brenda
pregnant Wistar rats
-
-
brenda
primary hepatocytes
-
-
brenda
procathepsin L
UniProt
brenda
prostatic glandular kallikrein 8 precursor
SwissProt
brenda
purified cytosolic isozyme
-
-
brenda
purified enzyme
-
-
brenda
purified premature mitochondrial isozyme pmAAT
-
-
brenda
Q04631 i.e. alpha-subunit, Q02293 i.e. beta-subunit
UniProt
brenda
Q04631 i.e. alpha-subunit, Q02293 i.e. beta-subunit, cf. EC 2.5.1.58
UniProt
brenda
R/A Pfd strain
-
-
brenda
rapid increase of enzyme level during development
-
-
brenda
rat
2159, 2423, 4231, 4270, 4271, 4705, 5237, 5252, 5253, 5360, 5364, 81039, 135465, 136606, 171965, 171966, 172058, 208998, 209214, 209215, 209284, 209286, 209287, 209292, 209370, 209371, 209372, 209373, 209374, 209375, 209376, 209377, 209378, 209379, 209380, 209381, 209382, 209383, 209384, 209385, 209386, 209387, 209390, 209393, 209394, 209539, 209584, 209585, 209586, 209589, 209590, 209593, 209594, 209595, 209596, 209598, 209648, 209779, 209799, 209828, 210134, 210151, 210158, 210160, 210161, 210163, 210166, 210516, 210581, 210584, 210585, 210588, 210589, 210590, 210591, 210596, 210597, 210599, 210600, 285262, 285264, 285268, 285271, 285272, 285273, 285329, 286146, 286164, 286165, 286166, 286170, 286172, 286173, 286174, 286175, 286176, 286177, 286181, 286182, 286183, 286190, 286192, 286196, 286204, 286214, 286215, 286629, 286645, 286647, 286650, 286665, 286672, 286826, 286827, 286829, 286833, 286836, 286838, 286840, 286846, 286849, 286850, 286859, 286863, 286868, 286877, 286882, 286886, 286892, 286895, 287801, 349356, 390762, 395924, 395928, 395931, 395933, 395936, 438005, 438006, 438010, 438015, 438027, 439944, 439946, 439989, 441440, 485193, 485398, 485554, 485555, 485557, 485559, 485711, 485961, 485965, 485966, 485967, 485968, 485969, 485970, 485971, 485972, 485974, 485975, 485976, 485978, 486290, 486291, 486292, 486293, 486294, 486295, 486296, 486297, 486298, 486299, 486300, 486301, 486304, 486308, 486309, 486864, 487005, 487016, 487403, 487404, 487406, 487407, 487408, 487410, 487414, 487416, 487417, 487418, 487421, 487422, 487423, 487424, 487429, 487430, 487432, 488093, 488094, 488096, 488099, 488102, 488106, 488108, 488109, 488110, 488111, 488112, 488113, 488114, 488115, 488122, 488482, 637814, 637820, 638980, 639000, 639904, 639905, 639907, 639908, 639912, 639919, 639924, 640391, 640393, 641075, 641080, 641239, 642710, 642712, 642715, 642716, 642721, 642722, 642724, 642726, 642728, 642731, 642994, 642995, 642996, 643002, 644208, 645294, 645296, 645307, 645313, 645316, 645318, 645321, 645383, 645386, 645387, 645388, 645390, 645418, 645708, 645709, 645712, 645713, 645717, 645718, 645719, 645722, 645726, 645727, 645728, 645730, 645733, 645773, 645774, 645776, 645784, 645785, 645792, 645890, 645906, 646880, 646885, 648785, 648786, 648787, 648788, 648789, 648790, 648791, 648792, 649264, 649273, 649325, 649420, 649576, 650462, 650868, 651520, 651797, 651908, 652066, 652234, 652245, 652337, 652393, 652414, 652488, 652608, 652709, 653220, 653314, 653595, 653696, 653816, 654006, 658227, 665199, 667429, 667893, 670820
-
-
brenda
rat
SwissProt
brenda
rat
Uniprot
brenda
rat fibrosis model
-
-
brenda
rat hepatic microsomal trans-2-enoyl-CoA reductases with cofactor requirement (NADH or NADPH) depending on chain length of substrates are characterized. Since no cis-2-enoyl-CoA compounds are tested as substrates a classification according to EC 1.3.1.8, EC 1.3.1.38 or EC 1.3.1.44 is impossible
-
-
brenda
rat hepatoma H-4-II-E cells
-
-
brenda
rat liver long-chain acyl-CoA synthetase activity and phytanoyl-CoA synthetase activity are catalyzed by one enzyme protein
-
-
brenda
rat model of permanent ischemia
-
-
brenda
rat SPC3 cDNA expressed in a mouse L cell line
-
-
brenda
rat theta-class glutathione transferase T2-2 (rGST T2-2) presents an ideal scaffold for the design of a novel glutathione peroxidase catalyst because it binds GSH and contains a serine close to substrate binding site, which can be chemically modified to bind selenium. The modified Se-rGST T2-2 efficiently catalyzes the reduction of hydrogen peroxide, and the glutathione peroxidase activity surpasses the activities of some natural glutathione peroxidases
-
-
brenda
rat, albino
-
-
brenda
rat, cytosolic isoform
SwissProt
brenda
rat, female Wistar
-
-
brenda
rat, Holtzman
-
-
brenda
rat, male Sprague-Dawley
-
-
brenda
rat, male Wistar
-
-
brenda
rat, male Wistar albino
-
-
brenda
rat, mitochondrial isoform
SwissProt
brenda
rat, pheochromocytoma PC-12 line
-
-
brenda
rat, Sprague-Dawley
392077, 392084, 485515, 485517, 643819, 646495, 649299, 651913, 652058, 652071, 653223, 653858
-
-
brenda
rat, strain F344
-
-
brenda
rat, strain Wistar
-
-
brenda
rat, trifunctional cytoplasmic enzyme
-
-
brenda
rat, Wistar
-
-
brenda
rat, Wistar
SwissProt
brenda
rat, Wistar AF/Han
-
-
brenda
rats of a Sprague-Dawley-derived strain, 8-10 weeks old male and female rats
-
-
brenda
rats with common bile duct ligation and obstructive jaundice respectively
-
-
brenda
Rattus norvegicus
-
-
brenda
recombinant
650113, 658974, 661210, 664085, 669315, 669383, 671712, 674672, 685099, 686640, 686876, 693530
-
-
brenda
recombinant
SwissProt
brenda
recombinant
UniProt
brenda
recombinant enzyme
489824, 489825, 650417, 651567, 657940, 658070, 658279, 661282, 667327, 667412, 669042, 669298, 674998
-
-
brenda
recombinant enzyme
SwissProt
brenda
recombinant enzyme expressed in Xenopus laevis oocyte
-
-
brenda
recombinant enzyme truncated at amino acid 37 from N-terminus
-
-
brenda
recombinant enzyme, isoform MAT I, tetramer, and MAT III, dimer
UniProt
brenda
recombinant hexokinase type I
SwissProt
brenda
recombinant hexokinases II and III
-
-
brenda
recombinant IP3K overexpressed in Escherichia coli
-
-
brenda
recombinant isoenzyme B expressed in HeLa cells
-
-
brenda
recombinant liver CPT I
-
-
brenda
recombinant mutant L192F/F194Y/A377T/S435N/I491V/V495M, a humanized version of the rat FAAH
SwissProt
brenda
recombinant protein
-
-
brenda
recombinant protein
SwissProt
brenda
recombinant wild-type enzyme and N-terminally truncated form
-
-
brenda
recombinantly expressed in Escherichia coli
-
-
brenda
recombinat enzyme
-
-
brenda
regucalcin-expressing transgenic Sprague-Dawley rats and wild-type male Wistar rats
-
-
brenda
regulation by circadian clock at posttranscriptional level
-
-
brenda
response to 24 h starvation and high fat feeding
-
-
brenda
review
-
-
brenda
RN5CATOMT
-
-
brenda
S-adenosylhomocysteine-synthetic activity significantly increases in animals fed a vitamin B6-free diet, while S-adenosylhomocysteine hydrolytic activity shows no significant difference in animals fed a vitamin B6-free diet or control diet. Enzyme mRNA in the liver does not show changes due to diet
-
-
brenda
S-COMT
-
-
brenda
sand rat, i.e. Psammomys obesus
-
-
brenda
SCD1
SwissProt
brenda
SCD2
UniProt
brenda
SD rats
-
-
brenda
SDH activity and its gene expression are induced in both growing and mature rats when their protein intake exceeds their nutrintional requirements
-
-
brenda
Sea:SD rats
-
-
brenda
selective increase in amount of PDHK4 protein in both hyperthyroidism and high-fat feeding
-
-
brenda
selenoprotein
-
-
brenda
selenoprotein
SwissProt
brenda
separation in NADPH-specific short-chain enoyl-CoA reductase and NAD(P)H-dependent long-chain enoyl-CoA reductase
-
-
brenda
seven-week-old, male, Wistar
-
-
brenda
several intestinal isozymes
-
-
brenda
several isozymes
-
-
brenda
several isozymes, e.g. CYP4F and CYP4A, 9-week-old, male Sprague-Dawley rats
-
-
brenda
several isozymes, UGT1A isozyme occur in Wistar rats, not in Gunn rats
-
-
brenda
several PKC isozymes
-
-
brenda
several strains
UniProt
brenda
sexually mature, female, albino
-
-
brenda
sGC alpha1 subunit; female Wistar rats
UniProt
brenda
sGC beta1 subunit; female Wistar rats
UniProt
brenda
SHR and Wistar-Kyoto rats
-
-
brenda
Shumixy cataract animals
-
-
brenda
Shumiya cataract rat
Uniprot
brenda
six-week-old male Sprague-Dawley rats
-
-
brenda
SMP30, gene rgn; gene rgn
SwissProt
brenda
sodium/potassium-transporting ATPase subunit alpha-1
SwissProt
brenda
sodium/potassium-transporting ATPase subunit alpha-2
UniProt
brenda
sodium/potassium-transporting ATPase subunit alpha-3
SwissProt
brenda
soluble, bifunctional form PAM-3, expression in a human embryonic kidney cell line that lacks regulated secretory granules, EC 1.14.17.3 and EC 4.3.2.5 are contained within the bifunctional peptidylglycine alpha-amidation monooxygenase, PAM
-
-
brenda
Spargue-Dawley rats
-
-
brenda
spleen heme oxygenase-1 is not induced by hematin
-
-
brenda
splice variant
SwissProt
brenda
splice variant
UniProt
brenda
splicing form CKIepsilon-2; male adult Wistar rats, 3 splicing forms CKIepsilon-1 - CKIepsilon-3
SwissProt
brenda
splicing form CKIepsilon-3; male adult Wistar rats, 3 splicing forms CKIepsilon-1 - CKIepsilon-3
SwissProt
brenda
spontaneous hypertension rats
-
-
brenda
spontaneous hypertensive rats
-
-
brenda
spontaneously hypertensive model rats
-
-
brenda
spontaneously hypertensive rat
-
-
brenda
spontaneously hypertensive rat (SHR) and age-matched Wistar Kyoto rats (WKY/Izm)
UniProt
brenda
spontaneously hypertensive rats
-
-
brenda
spontaneously hypertensive rats
UniProt
brenda
spontaneously hypertensive rats (SHR) and Wistar Kyoto (WKY) rats
SwissProt
brenda
spontaneously hypertensive rats and Wistar Kyoto rats
-
-
brenda
spontaneously hypertensive rats of various ages and age-matched normotensive Wistar-Kyoto rats
-
-
brenda
spontaneously hypertensive rats, SHR
Uniprot
brenda
spontaneously hypertensive, SHR, rats and Wistar Kyoto, WKY, rats
-
-
brenda
Sprague Dawley
31026, 395466, 438636, 439372, 439373, 439374, 486673, 638898, 663910, 666540, 675951, 681533
-
-
brenda
Sprague Dawley
SwissProt
brenda
Sprague Dawley and August Copenhagen x Irish strains
-
-
brenda
Sprague Dawley rat
-
-
brenda
Sprague Dawley rats
-
-
brenda
Sprague Dawley rats, spontaneously hypertensive rats and age-matched Wistar-Kyoto rats
-
-
brenda
Sprague Dawley strain
-
-
brenda
Sprague Dawley, rat
-
-
brenda
Sprague-Dawley
2271, 2423, 135460, 135465, 137135, 137149, 208432, 285217, 285357, 286014, 286023, 286647, 286665, 286827, 287336, 389979, 389981, 391706, 438005, 440196, 440197, 440203, 440228, 440230, 440236, 485053, 485054, 485559, 485599, 485605, 486295, 486297, 486298, 486323, 486489, 486490, 486502, 487123, 487429, 487488, 487492, 487493, 487494, 487570, 487978, 488102, 488120, 489307, 489405, 489421, 489870, 489934, 636612, 636888, 637267, 637288, 639901, 639979, 640017, 640393, 640395, 640399, 640585, 640592, 640830, 641391, 641392, 644829, 644832, 644955, 644958, 644967, 644973, 644980, 644985, 645390, 645717, 645726, 645727, 645728, 646406, 646570, 653657, 667146, 667150, 669600, 669911, 677467, 677489, 677945, 678098, 679127, 679298, 682272, 683003, 684981, 687757, 691394, 776030
-
-
brenda
Sprague-Dawley
Uniprot
brenda
Sprague-Dawley albino
-
-
brenda
Sprague-Dawley albino rats, hexokinases B and C
-
-
brenda
Sprague-Dawley and Nagase analbuminemic rats
-
-
brenda
Sprague-Dawley CD strain
-
-
brenda
Sprague-Dawley female rats
-
-
brenda
Sprague-Dawley male rat
-
-
brenda
Sprague-Dawley male rats
-
-
brenda
Sprague-Dawley male rats. GlcN (30 micromol/kg/min) or physiological saline (control) is intravenously infused into the rats for 2 h
-
-
brenda
Sprague-Dawley or Lewis rats
-
-
brenda
Sprague-Dawley rat
5113, 285349, 288891, 485243, 488700, 488718, 488725, 488727, 488738, 488773, 639731, 655140, 660677, 668500, 671273, 672503, 673231, 675574, 675725, 675880, 676093, 676108, 679137, 681000, 683231, 691620, 693885, 695457, 696053, 696542, 697806, 698163, 699936, 703568, 703574, 704802, 709252, 710227, 710615
-
-
brenda
Sprague-Dawley rat
UniProt
brenda
Sprague-Dawley rat pups
-
-
brenda
Sprague-Dawley rat, female animals
-
-
brenda
Sprague-Dawley rat, fetus, newborn, adult
UniProt
brenda
Sprague-Dawley rats
34326, 286122, 392340, 392355, 439299, 486267, 639069, 642881, 642888, 644798, 644799, 645680, 650833, 651514, 653344, 654699, 659105, 659578, 659666, 660665, 661256, 661600, 663766, 663883, 663988, 664469, 665568, 666130, 666707, 666929, 667361, 667685, 667847, 668339, 668871, 671227, 672835, 673965, 674683, 675105, 675549, 675565, 676189, 677482, 678083, 679355, 681543, 683045, 683802, 683845, 684353, 684505, 688220, 688555, 688606, 688717, 689074, 690007, 690357, 692000, 692039, 692058, 693451, 693532, 693781, 694874, 698943, 698948, 700431, 701244, 701571, 702430, 702624, 705286, 705524, 705935, 707071, 707363, 707731, 709064, 709661, 711965, 712849, 712899, 713111, 713242, 713552
-
-
brenda
Sprague-Dawley rats
SwissProt
brenda
Sprague-Dawley rats
Uniprot
brenda
Sprague-Dawley rats, 1-2 days old, 2 isoforms: CNP1 and CNP2 differing by a 20-amino acid extension exclusive to CNP2
-
-
brenda
Sprague-Dawley rats, 18-25 days old
-
-
brenda
Sprague-Dawley rats, adult, 2 isoforms: CNP1 and CNP2, produced by ribosome initiation at different AUG codons
-
-
brenda
Sprague-Dawley rats, female
-
-
brenda
Sprague-Dawley rats, female
SwissProt
brenda
Sprague-Dawley rats, female
UniProt
brenda
Sprague-Dawley rats, isozyme PKCalpha
-
-
brenda
Sprague-Dawley rats, several isozymes
-
-
brenda
Sprague-Dawley rats, tissue-specific isozymes L-CPT1 and M-CPT1
-
-
brenda
Sprague-Dawley strain
285685, 287797, 288048, 288546, 288549, 288560, 288565, 288577, 288578, 288585, 288606, 288607, 288616, 439200, 439201, 439247, 486158, 486164, 486350, 486352, 486354, 637738, 640813, 640971, 650484
-
-
brenda
Sprague-Dawley strain male rats
-
-
brenda
Sprague-Dawley strain, albino rats, 15 days old
-
-
brenda
Sprague-Dawley strain, fasted male rats, 250 - 350 g
-
-
brenda
Sprague-Dawley, 12.5, 15.5 and 18.5 days of gestation
SwissProt
brenda
Sprague-Dawley, at least 3 different splicing variants PAM-1, PAM-2, and PAM-3
-
-
brenda
Sprague-Dawley, BR strain
-
-
brenda
Sprague-Dawley, Buffalo strain
-
-
brenda
Sprague-Dawley, EC 1.14.17.3 (PHM) and EC 4.3.2.5 (PAL) are part of a bifunctional, integral membrane protein precursor, peptidylglycine alpha-amidating monooxygenase, PAM, which consists of independent catalytic domains separated from each other and from the putative transmembrane domain by flexible regions accessible to attack by a wide variety of endoproteinases
-
-
brenda
Sprague-Dawley, especially male rats
-
-
brenda
Sprague-Dawley, female
-
-
brenda
Sprague-Dawley, male
-
-
brenda
Sprague-Dawley, male
SwissProt
brenda
Sprague-Dawley, rats switched from a high protein diet to a low protein diet or to a low protein diet supplemented with cysteamine do not demonstrate a change in tissue cysteamine dioxygenase activity over the course of 10 h.
-
-
brenda
Sprague-Dawley, virgin rat, pregnant rat, in pregnant rats with hypertension
-
-
brenda
SpragueDawley
-
-
brenda
SpragueDawley or Fisher 344. Rats carrying the Tsc2 gene (Eker rats) in a Fisher 344 background
-
-
brenda
SpragueDawley rats
-
-
brenda
SpragueDawley rats
Uniprot
brenda
SpragueDawley rats of ages 1 week, 23, 12 and 18 months
-
-
brenda
Sprangue Dawley rats
-
-
brenda
Sprangue-Dawley
-
-
brenda
Spraque-Dawley rats
-
-
brenda
SRC
SwissProt
brenda
ST1A1
-
-
brenda
ST1B1
SwissProt
brenda
ST1C1
SwissProt
brenda
ST6GAL1
SwissProt
brenda
ST6GAL2, fragment
SwissProt
brenda
stably expressed in CHO cells
-
-
brenda
strains WKY and SHR
-
-
brenda
strains: F344, Sprague-Dawley and F344/Brown-Norway hybrid
-
-
brenda
streptozotocin-induced diabetic rat
-
-
brenda
streptozotocin-induced diabetic rats
-
-
brenda
streptozotocin-induced diabetic, female and male
-
-
brenda
stroke-prone spontaneously hypertensive rat
-
-
brenda
stroke-prone spontaneously hypertensive rats, SHRSPs, and their ancestral hypertensive but stroke-resistant spontaneously hypertensive rats, SHRs
SwissProt
brenda
study on ten different strains
UniProt
brenda
subunit alpha
UniProt
brenda
subunit alpha-3 of sodium/potassium-transporting ATPase; Sprague-Dawley
SwissProt
brenda
subunit AMPKbeta-1
UniProt
brenda
subunit AMPKbeta-2
UniProt
brenda
subunit beta
UniProt
brenda
subunit SPTLC1 and SPTLC2
UniProt
brenda
subunit UQCRC1
UniProt
brenda
subunits alpha1 and beta1
UniProt
brenda
subunits TAP1 and TAP2
UniProt
brenda
suffering chronic dietary iron overload
-
-
brenda
SULT1C2 or ST1C6
SwissProt
brenda
SULT1C2A or ST1C7
SwissProt
brenda
SULT2B1; Sprague-Dawley rats, gene SULT2B1, isozymes SULT2B1a and SULT2B1b as a result of an alternative exon I
SwissProt
brenda
SwissProt accession number U26033
SwissProt
brenda
TAP1 and TAP2 subunits
UniProt
brenda
ten 10-week-old Sprague-Dawley
-
-
brenda
testis isozyme PFKFB4; genes PFKFB1-4, four isozymes
SwissProt
brenda
tetrameric form MAT I
UniProt
brenda
the classification is ambiguous because the stereochemistry is not exactly determined
UniProt
brenda
The enzyme may be a 3-phytase (EC 3.1.3.8), or a 4-phytase (synonym 6-phytase, EC 3.1.3.26). The product of the hydrolysis of myo-inositol hexakisphosphate to 1D-myo-inositol 1,2,4,5,6-pentakisphosphate or alternatively 1D-myo-inositol 1,2,3,5,6-pentakisphosphate has not been identified.
-
-
brenda
the rats are divided into the follwing age groups: 0.5, 1,2.4.8.12.20 and 28 month of age
-
-
brenda
the xanthine dehydrogenase form can be obtained through incubation of xanthine oxidase with sulphydryl reducing reagents
-
-
brenda
thermophilic enzyme
-
-
brenda
theta class isozyme GST T2-2
-
-
brenda
three alpha1,2-fucosyltransferase genes: FTA, FTB and FTC
-
-
brenda
three dynamin isoforms, dynamin1-dynamin3, and multiple splice variants for each of the three dynamins
-
-
brenda
three Fringe homologues Lfng, Mfng, and Rfng
-
-
brenda
three isoforms
-
-
brenda
three subforms: 1, 2 and 3
-
-
brenda
three-week-old male Crl:CD (SD) IGS rats
-
-
brenda
tissue distribution
SwissProt
brenda
tissue-type transglutaminase, abbrevation TGC
-
-
brenda
topoiomerase IIalpha
-
-
brenda
transferases A and B
-
-
brenda
transgenic mice overexpressing the galactosylceramide synthesizing enzyme UDP-galactose:ceramide galactosyltransferase in oligodendrocytes
-
-
brenda
transgenic rats harboring the mouse renin transgene and exhibiting elevated tissue angiotensin II levels
-
-
brenda
treated by oral intake of thioacetamide
-
-
brenda
treated for 7 days with cocaine, or cocaine with a NADPH oxidase inhibitor apocynin, or cocaine with a xanthine oxidoreductase inhibitor allopurinol
-
-
brenda
treated with streptozocin, representing a model of type 1 diabetes mellitus
-
-
brenda
treatment with single injection or for one week with daily injection of saline or L-Arg plus Nomega-nitro-L-arginine methyl ester or alpha-tocopherol plus ascorbic acid
-
-
brenda
treatment with testosterone and estradiol
-
-
brenda
trifunctional enzyme which exhibits the activities of EC 5.3.3.8, EC 4.2.1.17 and EC 1.1.1.35
-
-
brenda
truncated type A enzyme which catalyzes a two-step reaction involving an initial hydroxylation of peptidyl-Gly followed by conversion of the peptidyl-alpha-hydroxyglycine intermediate to the amidated product, enzyme is secreted into the medium from mouse C127 cells transfected with the rat MTC cDNA encoding the truncated type A enzyme
-
-
brenda
truncated, soluble form
-
-
brenda
tryptophan 2,3-dioxygenase from liver
-
-
brenda
two enzyme forms
-
-
brenda
two enzyme forms: DPP II-M and DPP II-S
-
-
brenda
two enzyme forms: type I and type II 3-phosphatase
-
-
brenda
two isoenzymes: skeletal muscle type and erythrocyte type
-
-
brenda
two isoforms
-
-
brenda
two isoforms derived by alternative spicing, isofoms 2 contains a 22 amino acid insert
-
-
brenda
two isoforms, an inducible HO-1 and a constitutive HO-2
UniProt
brenda
two isoforms: ACO-I, ACO-II
-
-
brenda
two isozymes
-
-
brenda
two isozymes Acc1 and Acc2
-
-
brenda
two isozymes CTalpha and CTbeta2
-
-
brenda
two isozymes in lung and liver
-
-
brenda
two isozymes, lung-type and liver-type
-
-
brenda
two kinases: pyruvate dehydrogenase-intrinsic activity and free pyruvate dehydrogenase kinase
-
-
brenda
two MAT III isoforms
-
-
brenda
two PDE3 isoforms
-
-
brenda
two splicing isozymes Pcyt2alpha and Pcyt2beta
-
-
brenda
two splicing variants, peripheral-type pChAT and common-type cChAT
-
-
brenda
type 1 enzyme
-
-
brenda
type I and type II enzyme isoforms
-
-
brenda
type I enzyme
-
-
brenda
type I enzyme isoform, bifunctional 3beta-hydroxysteroid dehydrogenase/D5-D4 isomerase
UniProt
brenda
type I phosphatidylinositol 4-phosphate 5-kinase isozyme gamma, 3 splicing forms a-c
-
-
brenda
UCH-L1, SwissProt: Q00981
-
-
brenda
V-type proton ATPase 116 kDa subunit a1
UniProt
brenda
various isoenzymes
-
-
brenda
vitamin A deficient and sufficient diet fed
-
-
brenda
vitamin A deficient and sufficient diet fed
Uniprot
brenda
vitamin A depleted diet fed
-
-
brenda
vitamin B6-deficient strain
-
-
brenda
Walker 256 tumour rat
-
-
brenda
warfarin-resistant rat
-
-
brenda
warfarin-susceptible rats; gene VKORC1
UniProt
brenda
weanling
-
-
brenda
weanling male wistar
SwissProt
brenda
white rats
-
-
brenda
white Sprague-Dawley
-
-
brenda
whole-body hypothermia increases the degree of substrate inhibition of enzyme, its maximum rate and its Km-value
-
-
brenda
wild-type and mutant
-
-
brenda
wild-type and mutant enzyme with a deletion of 34 amino acids from its N-terminus
-
-
brenda
wild-type and two truncated forms lacking 20 or 36 amino acid residues from their amino-terminal polypeptide extension, overexpressed in Saccharomyces cerevisiae
-
-
brenda
wild-type Ren-2 and transgenic hypertensive (mRen2)27 rats
-
-
brenda
wild-type Sprague-Dawley rats and iron-deficient Belgrade rats, three isozymes: platelet, leukocyte, and epidermis isozyme, Alox15 is a leukocyte-type isozyme
UniProt
brenda
wild-type Wistar and spontaneously hypertensive rats (SHR) derived thereof
Uniprot
brenda
Wistar
2269, 2280, 134176, 135459, 135464, 135467, 135472, 135998, 209222, 209224, 286287, 286565, 287071, 287073, 288681, 389978, 390714, 394700, 486296, 487120, 487915, 487916, 487919, 489225, 489862, 489872, 490912, 586940, 636623, 637118, 637552, 640051, 640053, 640060, 640062, 640174, 640175, 640391, 640826, 640834, 641735, 641740, 645554, 645564, 645713, 646725, 646732, 648109, 658533, 661910, 668750, 673922, 677241, 678087, 678416, 678634, 686856, 688814, 689220, 695686, 699949
-
-
brenda
Wistar
SwissProt
brenda
Wistar (male)
-
-
brenda
Wistar albino
-
-
brenda
Wistar albino female rats
-
-
brenda
Wistar albino rat
-
-
brenda
Wistar albino rats
-
-
brenda
Wistar and Lister strains, age ranging from postnatal day 3 to 60
-
-
brenda
Wistar and Wistar-Kyoto rats, and 1 month-old, prehypertensive/spontaneously hypertensive rats
-
-
brenda
Wistar BB/E n=12, Wistar BB/E n=6
-
-
brenda
Wistar Imamichi, male
-
-
brenda
Wistar Kyoto and spontaneously hypertensive rats
-
-
brenda
Wistar rat
5129, 33732, 288884, 394824, 649668, 660674, 664165, 666971, 671179, 681319, 686182, 688449, 693318, 695147, 697749
-
-
brenda
Wistar rat
SwissProt
brenda
Wistar rat
UniProt
brenda
Wistar rat embryos
-
-
brenda
Wistar rats
137131, 137132, 137148, 488967, 489223, 489225, 640207, 640764, 640765, 640766, 640767, 640775, 644795, 644809, 646167, 646182, 661662, 662952, 664240, 666120, 667165, 668540, 675535, 680258, 681575, 682128, 683383, 684952, 685867, 686015, 686258, 688515, 692562, 693722, 693830, 694251, 695063, 698165, 699129, 701944, 702810, 706775, 707910, 708098, 710112, 710453, 711354, 712794, 713129, 713518
-
-
brenda
Wistar rats
SwissProt
brenda
Wistar rats
UniProt
brenda
Wistar rats and Donryu rats
-
-
brenda
Wistar rats and Donryu rats
UniProt
brenda
wistar rats and GK rats
UniProt
brenda
Wistar rats and OXYS rats, the latter showing inherited overgeneration of free radicals
-
-
brenda
Wistar rats weighing 300-400 g
-
-
brenda
Wistar rats, 2 days old
-
-
brenda
Wistar rats, 2 isozymes 5alpha-R1 and 5alpha-R2
-
-
brenda
Wistar rats, 2 months old
-
-
brenda
Wistar rats, 6-12 weeks, either sex. In the immunohistochemistry experiment phenylethanolamine N-methyltransferase demonstrate strong staining in the majority of cells, representing the adrenergic cell population.
-
-
brenda
Wistar rats, adult
-
-
brenda
Wistar rats, both sexes, 6 month
Uniprot
brenda
Wistar rats, four isoforms alpha, beta2, gamma, and delta, of CaMKI
-
-
brenda
Wistar rats, from post-natal days 5 to 90, hypothyroid and controls
-
-
brenda
Wistar rats, gene ACY1
SwissProt
brenda
Wistar rats, gene Ap-B
Uniprot
brenda
Wistar rats, isozymes PDHK1, PDHK2, PDHK3, and PDHK4
-
-
brenda
Wistar rats, peroxisomal ABC transporters are encoded by the ABCD genes, ABCD1-ABCD3
-
-
brenda
Wistar rats, ppGaNTase-T6, -T1 and -T4
Uniprot
brenda
Wistar rats, several isozymes
-
-
brenda
Wistar strain
80971, 81039, 209589, 246998, 286886, 286895, 287708, 287712, 288049, 288050, 288554, 288580, 288605, 288612, 390263, 392363, 437741, 440190, 440202, 440232, 441399, 486349, 486369, 488695, 488697, 488698, 488701, 488703, 488706, 488707, 488711, 488712, 488715, 488717, 488719, 488720, 488721, 488723, 488724, 488730, 488734, 488735, 488736, 488737, 488739, 488740, 488746, 488750, 488752, 488762, 488792, 489872, 639701, 639709, 642643, 650483, 650890, 651201, 651976, 652968, 675782, 681612
-
-
brenda
Wistar strain
SwissProt
brenda
Wistar strain
UniProt
brenda
Wistar strain and Sprague Dawley strain
-
-
brenda
Wistar strain male albino rats
-
-
brenda
Wistar strain male albino rats, vitamin K-deficient or warfarin-treated
UniProt
brenda
Wistar strain male rats
-
-
brenda
Wistar strain rats
-
-
brenda
Wistar strain, male
-
-
brenda
Wistar strain, pregnant female
-
-
brenda
Wistar, 7-13 weeks old
-
-
brenda
Wistar, cloned
SwissProt
brenda
Wistar, female
-
-
brenda
Wistar, male
-
-
brenda
Wistar, male albino
-
-
brenda
Wistar, male, H18H
-
-
brenda
Wistar, subjected to 40% food restriction
-
-
brenda
Wistar, Wistar Kyoto, and spontaneously hypertensive rats, isozyme soluble guanylate cyclase beta1, sGC-beta1
-
-
brenda
Wistar-Furth, citrate synthase deficient strain, 28% decreased activity compared to wild-type
-
-
brenda
Wistar-Kyoto and spontaneously hypertensive rats
-
-
brenda
Wistar-Kyoto and Sprague-Dawley rat
-
-
brenda
Wistar-Kyoto rats
-
-
brenda
Wistar-Kyoto rats and Dahl salt-sensitive and salt-resistant rats, isozymes 11beta-HSD1 and 11beta-HSD2
-
-
brenda
Wistar-Kyoto rats and spontaneously hypertensive rats
-
-
brenda
Wistar-Kyoto rats and Sprague-Dawley rats
UniProt
brenda
Wistar-strain
-
-
brenda
Wistar/Moell
-
-
brenda
Wister, male
-
-
brenda
Wister-Kyoto rat and spontaneously hyptertensive rat
-
-
brenda
with experimental chronic heart failure
-
-
brenda
with folate-deficiency induced hyperhomocysteinemia
-
-
brenda
with induced neonatal hypothyroidism
-
-
brenda
with spinal cord injury
SwissProt
brenda
WKY rats
-
-
brenda
WKY rats and spontaneously hypertensive rats
-
-
brenda
xanthine oxidoreductase can exists in a dehydrogenase form, XD, and in an oxidase form, XO
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Yoshida sarcoma ascites cells
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young adult female Sprague-Dawley rats
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young male Sprague-Dawley
Uniprot
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young rats of 3-4 months and aged rats of 20-22 months
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young, male Wistar rats
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young, pregnant, female
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Z1-81
UniProt
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Zivic Miller SD-strain
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Zucker diabetic fatty rats
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Zucker diabetic fatty rats, comparison with Zucker fatty and Zucker lean rats
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Zucker fa/fa rats
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Zucker fatty and Zucker lean rats
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Zucker rat
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Zucker rats
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Zucker rats and Sprague-Dawley rats
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Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
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hepatoma cell line
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vascular smooth muscle cell line
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abdominal skin
brenda
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brenda
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brenda
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brenda
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-
brenda
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brenda
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mesencephalic-derived cell line
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forebrain and cerebral cortex
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mainly expressed in airway and vascular smooth muscle cells in rat lung tissue
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glutathione-requiring enzyme
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from spinal cord
brenda
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-
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i.e. AT1 cells, from transdifferentiation of AT2 cells
brenda
type 1 alveolar epithelial (R3/1) cell
brenda
-
brenda
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-
brenda
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-
brenda
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higher expression than in corpus cavernosum
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high expression of beta1 and moderate to low expression of both alpha subunits
brenda
-
brenda
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brenda
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tissue distribution of CPE
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brenda
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brenda
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brenda
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brenda
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brenda
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nontumorigenic cell line, low level of gamma-glutamyltranspeptidase
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tumorigenic cell line, high level of gamma-glutamyl transpeptidase
brenda
-
-
brenda
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-
brenda
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grown in the abdomen of swiss white mice
brenda
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PI-PLC expression pattern, overview
brenda
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-
brenda
metastatic prostate cancer cells
brenda
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from neonatal rats
brenda
-
primary, forebrain and cerebral cortex
brenda
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-
brenda
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-
brenda
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initial expression of mAPase occurs as cells progressed into S phase
brenda
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neuroblastoma cell line
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brenda
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brenda
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brenda
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brenda
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brenda
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brenda
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brenda
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brenda
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12 weeks after initiation of BBN treatment: higher PyNpase level in superficial cancer and hyperplasia compared to controls, 16 and 20 weeks after initiation of BBN treatment: higher PyNpase level in superficial cancer but not in hyperplasia compared to controls
brenda
in the blastomeres, Gpx4 granules are formed, and in the blastocysts, even clusters are present mainly around the cell nuclei
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in the blastomeres, Gpx4 granules are formed, and in the blastocysts, even clusters are present mainly around the cell nuclei
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adult bone marrow-derived insulin-producing cells, presence of transketolase protein under high-glucose conditions
brenda
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brenda
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plasma membrane vesicles from brain microvessel endothelial cells
brenda
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labeled product also found in vitro in brain tissue slices
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brenda
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carcinoma
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brenda
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brenda
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brenda
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brenda
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brenda
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brenda
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brenda
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brenda
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brenda
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brenda
Q4FZY2
-
brenda
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-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
presence of enzyme immunoreactive material at birth, progressive reduction with age with complete loss at postnatal day 18
brenda
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a rat hepatoma cell line established from N-nitrosodiethyla-mine-induced Wistar rat hepatoma
brenda
-
brenda
-
brenda
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-
brenda
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688660, 691554, 692085, 693721, 693777, 693779, 694359, 694395, 697348, 699690, 701003, 702959, 704524, 704782, 708434, 713549, 717193, 718019, 734538, 774712
brenda
compared to the canonical AChE-S splice variant, the readthrough splice variant AChE-R is expressed at much lower levels but presents distinct regulation patterns in PC-12 cells and rat primary cerebral granule cells following exposure to pesticide chlorpyrifos
brenda
-
-
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enriched in GRK2 and GRK5
brenda
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FAEES activity is increased 4fold in the choroid of alcohol-treated rats compared with controls
brenda
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brenda
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brenda
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brenda
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gamma-glutamyltransferase is upregulated after oxidative stress through the Ras signal transduction pathway in rat colon carcinoma cells
brenda
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brenda
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brenda
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brenda
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7th cranial nerve
brenda
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pulmonary artery smooth muscle cell line
brenda
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-
brenda
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secretion of active enzyme is stimulated by thyrotropin, insulin, and/or somatostatin
brenda
-
-
brenda
-
brenda
dental papilla cells (DPCs) are mesenchymal cells that are surrounded by the enamel organ during tooth development
brenda
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incisor
brenda
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-
brenda
-
brenda
-
brenda
mRNA of FTA and FTC
brenda
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brenda
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-
brenda
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high activity at pH 4.5
brenda
-
brenda
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-
brenda
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brenda
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brenda
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NRP and GRP-neuronal and glial restricted precursors are isolated from embryonic day 13.5 rats and transplantated into rats.
brenda
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in healthy hearts, DDAHI is absent, and DDAHII is localized to endothelium and endocardium with a similar distribution to that of eNOS
brenda
-
endocrine islets of Langerhans
brenda
-
-
brenda
-
enzyme is found in luminal and glandular epithelial cells and in stroma during late pregnancy
brenda
-
isozyme PGF synthase II
brenda
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brain
brenda
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-
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ER-1-24h, ER-1-1M cell produced
brenda
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brenda
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-
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isoenzyme CA3 is depressed, message levels of isoenzyme CA2 and CA4 are higher in extraocular muscle than in extensor digitorum longus, expression of isoenzyme CA5 is equivalent in extraocular muscle and extensor digitorum longus
brenda
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brenda
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brenda
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glycolytic fiber
brenda
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hepatoma cell line
brenda
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-
brenda
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-
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mainly
brenda
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primary fiber cells
brenda
FTC133 and FTC236
brenda
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brenda
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brenda
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from spinal cord
brenda
relationship between expression level of the enzyme and mucosal proliferation, overview
brenda
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brenda
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external
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important role for Rho-GTPases in the morphology and function of glomerular epithelial cells. Activation of RhoA appears to be protective against complement-mediated injury
brenda
age-related changes in immunoreactivity for dopamine beta-hydroxylase in carotid body glomus cells in spontaneously hypertensive rats
brenda
-
northern blot
brenda
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-
brenda
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-
brenda
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-
brenda
-
myosin ATPase isoenzymes show different temperature sensivities
brenda
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forebrain and cerebral cortex
brenda
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-
brenda
inguinal white adipose tissue
brenda
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-
brenda
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brenda
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-
brenda
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Reuber hepatoma cell line
brenda
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brenda
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brenda
-
a derivative of the H4-IIE-C3 rat hepatoma cell line
brenda
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brenda
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brenda
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a microglial cell line
brenda
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brenda
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brenda
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brenda
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-
brenda
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brenda
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brenda
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R-type isozyme
brenda
-
brenda
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brenda
in embryos at 12.5 days of gestation guanidinoacetate N-methyltransferase is detectable in the hepatic primordium only, with all other tissues being negative. Non-radioactive in situ hybridization (58°C for 40 h in 5 x SSC, 50% formamide and 40 microg/ml salmon sperm DNA) with digoxigenin-labeled antisense and sense riboprobes (400 ng/ml) for rat guanidinoacetate N-methyltransferase. guanidinoacetate N-methyltransferase proteins are detected with rabbit polyclonal antibodies
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somatostatin-sensitive enzyme form
brenda
-
brenda
-
glutathione-requiring enzyme
brenda
-
-
brenda
-
brenda
tumorigenic cell line, 3-5fold higher hyaluronan accumulation than in the parental cell line 3Y1
brenda
-
brenda
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treatment with ascorbate in a hypoxic condition for 24 h results in the maximal increase of hydroxyproline by 1.8-fold. The presence of cobalt chloride can substitute for hypoxic condition
brenda
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brenda
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intestinal cell line
brenda
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-
brenda
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-
brenda
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brenda
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forebrain and cerebral cortex
brenda
inguinal adipose tissue
brenda
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brenda
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brenda
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brenda
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-
brenda
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brenda
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brenda
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brenda
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brenda
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brenda
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brenda
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brenda
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-
brenda
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brenda
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brenda
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-
brenda
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-
brenda
-
acini
brenda
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-
brenda
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forebrain and cerebral cortex
brenda
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thalamus and hypothalamus
brenda
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-
brenda
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-
brenda
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thalamus and hypothalamus
brenda
-
the active caspase-3 expression is higher in the anterior pole of the lens
brenda
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cultivated rat leptomeningeal cells
brenda
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-
brenda
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diethylnitrosamine-induced liver tumor
brenda
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rat liver cell line
brenda
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-
brenda
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brenda
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brenda
shows HSL staining in cytoplasm during proestrus and estrus, in the nucleus during metestrus, and in cytoplasm and the nucleus during diestrus
brenda
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-
brenda
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brenda
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tumorigenic cell line derived from OC22 by reiterated treatment with N-methyl-N-nitro-N-nitrosoguanidine
brenda
NOX2 and NOX4 are the main isoforms present in macula densa cells
brenda
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-
brenda
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-
brenda
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no statistically significant difference in the amount of enzyme between tumors with and without activated H1-ras oncogene
brenda
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brenda
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brenda
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brenda
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brenda
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a prostate cancer cell line
brenda
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1710, 4771, 36122, 654375, 662463, 680820, 690298, 693822, 704909, 714316, 717762, 748626
brenda
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12 to 14% of cell profiles express pyroglutamyl peptidase II mRNA in the medial septum-diagonal band of Broca, in this region the specific activity of the enzyme is relatively high. Injection of the pyroglutamyl peptidase II inhibitor p-Glu-Asn-Pro-7-amido-4-methylcoumarin into the medial septum enhances the effect of thyrotropin-releasing hormone. The injection of a phosphinic thyrotropin-releasing hormone analog, a higher affinity inhibitor of pyroglutamyl peptidase II, diminishes the duration of ethanol-induced loss of righting reflex by itself
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DGKbeta is expressed in medium spiny neurons constituting the striatonigral and striatopallidal pathways, whereas striatal interneurons are below the detection threshold
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mouse embryonic fibroblast
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primary embryonic metanephric mesenchymal cells
brenda
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from bone marrow
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macula densa cell line, significantly lower enzyme levels than in a proximal tubule cell line. Treatment with an inhibitor of cyclooxygenase-2 increases enzyme level
brenda
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brenda
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brenda
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Morris hepatoma tumors 9618A2, 7777, 5123TC, 7800, 5123B, 7787
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primary, different layers
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primary
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stomach
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soleus muscle
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EDL muscle
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amplified by PCR from
brenda
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GRK2
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neuropil, tyrosine hydroxylase-immunoreactive nerve terminals are distributed throughout the ganglia and contained exclusively pleomorphic clear synaptic vesicles
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phosphodiesterase 5
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-
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neuroblastoma cell
brenda
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T-lymphoma cell, exclusive synthesis of isoform SPD-N
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lymphoma cell, exclusive synthesis of isoform SPD-N
brenda
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brenda
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-
brenda
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enzyme activity is well-maintained in the dissociated neostriatal neurons
brenda
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preganglionic
brenda
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brenda
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-
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neurons from wild-type embryos are co-cultured with oligodendrocytes prepared from either wild-type or tremor rats
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fibroblast cells
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brenda
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brenda
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brenda
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brenda
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brenda
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a pivotal region in reflex regulation of arterial pressure in the brain stem. Quantitative determination of expression levels of specific class I PI3K subunits, p85alpha, p85beta, p110alpha, p110beta, p110delta, and p110gamma, in the nucleus tractus solitarii of spontaneously hypertensive rats, overview
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transformed fibroblast cell line
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a non-tumorigenic cell line of oval cells established from livers of rats undergoing carcinogenesis by the choline deficient/ethionine-supplemented diet for 12 weeks
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on the dental root side, expression pattern of cathepsin K, high expression level in the age of 4-5 weeks, when physiological root resorption occurs actively, co-expression with matrix metalloproteinase-9
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brenda
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brenda
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the olfactory receptor neurones (replaceable) appear to be strongly immunoreactive as do the principal neurones (mitral and mitral/tufted cells), while in the olfactory bulb the replaceable periglomerular and granule cells appear to be non-reactive, distribution in cellular compartments, overview
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NTPDase1
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rhabdomyosarcoma cell
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aldosterone-insensitive, NADP+ specificity
brenda
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brenda
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brenda
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brenda
clonal derivative of PC12 cell line
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neuronal cell line, derived from PC12 cell line
brenda
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brenda
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brenda
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PNN
brenda
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-
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from heart and abdominal aorta
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NMT activity is observed to be 3fold higher in peripheral blood mononuclear cells from rats with colonic cancer than in controls, and shows also differential localization
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significantly increased agmatine levels in the prefrontal, entorhinal, and perirhinal cortices in a T-maze training group relative to the control group
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brenda
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brenda
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the selective distribution of isozyme DAGKepsilon in photoreceptor cells is a light-dependent mechanism that promotes increased 1-stearoyl, 2-arachidonoylglycerol removal and synthesis of 1-stearoyl, 2-arachidonoyl phosphatidic acid in the sensorial portion of this cell
brenda
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shows high levels of expression for beta1 mRNA and moderate for alpha1 and alpha2 mRNAs
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GH3 tumour
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originated from kidney
brenda
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brenda
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immortalized rat granulosa cell line
brenda
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brenda
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brenda
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brenda
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brenda
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AC2
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thalamus and hypothalamus
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brenda
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brenda
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mixed neuron-glial cultures prepared from the brains of embryonic days 16-17 rats
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cerebellar
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brenda
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prostate tumor
brenda
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mRNA of FTA, FTB and FTC
brenda
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-
brenda
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-
brenda
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-
brenda
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brenda
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heat stress enhances ALP activity in pulp cells
brenda
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Cornu Ammonis 1 pyramidal cells
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renal cortical collecting duct cell line
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in distal tubular cells, adiponectin through luminal ADIPOR1 activates AMPK, leading to the inhibition of glycogen synthase. During hyperglycemia, this regulation is altered, which may explain, at least in part, the accumulation of large glycogen deposits
brenda
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brenda
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brenda
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brenda
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brenda
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ischemic retinal ganglion cells
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gastric mucosal cell
brenda
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brenda
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brenda
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brenda
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liver cell line
brenda
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a retinal Mueller cell line, enzyme expression analysis, uptake of D-serine in Mueller cells is specific for neutral amino acids and excludes anionic and cationic amino acids, specificity and activity of transporters, overview
brenda
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raphe cell line
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rat osteosarcoma cell line
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in neonatal animals, small, moderately stained NADPH-d-positive cells are identified in the vertical arm and in the elbowv of the rostral migratory stream. In adult and aging rats a few labeled cells could be also detected in the RMS horizontal arm. The number of NADPH-d-positive cells increases with advancing age
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virus-transformed and normal
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brenda
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brenda
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brenda
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brenda
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brenda
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-
brenda
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brenda
-
layers III and V
brenda
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brenda
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brenda
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brenda
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brenda
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-
brenda
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brenda
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in culture
brenda
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brenda
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-
brenda
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brenda
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primary, different layers
brenda
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brenda
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brenda
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brenda
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brenda
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metastatic cell line, 3-5fold higher hyaluronan accumulation than in the parental cell line 3Y1
brenda
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higher levels of phenylethanolamine N-methyltransferase in stellate ganglia of mice compared with rats. Phenylethanolamine N-methyltransferase mRNA is present in stellate ganglia. Immobilization stress increases the gene expression of phenylethanolamine N-methyltransferase in stellate ganglia of rats, the highest levels of phenylethanolamine N-methyltransferase mRNA are immediatetly after and 3 h after the end of a stressful stimulus, while recovery to control levels occurs 6 h after the termination of immobilization. Immobilization repeated seven times further increases mRNA levels of phenylethanolamine N-methyltransferase in stellate ganglia of rats. There is no change in phenylethanol N-methyltransferase protein levels in stellate ganglia after a single immobilization, but protein levels are increased after repeated immobilization stress exposure.
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the paraventricular nucleus of the hypothalamus and the central amygdala
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-
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A-type enzyme expression
brenda
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-
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marrow stromal cell-brain microvascular endothelial cell contact coculture and indirect co-culture of marrow stromal cell and brain microvascular endothelial cell
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-
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shows high expression of beta1, moderate of alpha2, and low of alpha1
brenda
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L-COMT is the predominant enzyme form
brenda
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-
brenda
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brenda
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brenda
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brenda
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brenda
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brenda
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human TAP-deficient lymphoblastoid cell, expressing rat wild-type TAP or single rat TAP1 or TAP2 chains
brenda
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-
brenda
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highest levels of expression in nucleus accumbens, taenia tecta, cerebellar cortex, cerebral cortical layer I, hippocampus, hypothalamus, mesencephalic raphe nuclei, central and lateral amygdala, and the circumventricular organs
brenda
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brenda
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brenda
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brenda
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-
brenda
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brenda
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-
brenda
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-
brenda
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Tpl-2 isolated from Moloney leukemia virus-induced thymoma cells
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
a variety of mammalian cell lines in tissue culture
brenda
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at the later secretory stage mostly in the outer part of the forming enamel, weakly in inner forming enamel associated with the holes located near the DEJ
brenda
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brenda
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-
brenda
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-
brenda
-
-
brenda
invasive bladder cancer cell
brenda
-
brenda
-
brenda
-
brenda
-
-
brenda
-
brenda
-
order of hydrogen sulfide production rates for different tissues are: liver (777 nM/min/g), followed by uterus (168 nM/min/g), fetal membranes (22.3 nM/min/g), placenta (11.1 nM/min/g), compared to human placenta (200 nM/min/g)
brenda
-
constitutively present. No change in PDE-5 protein expression throughout pregnancy
brenda
-
-
brenda
-
dorsal motor nucleus of the vagus nerve, contains a peripheral-type pChAT, a splice variant that lacks exons 6-9 of the common-type ChAT, cChAT
brenda
-
-
brenda
-
brenda
-
VSMC culture
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
thalamus and hypothalamus
brenda
-
-
brenda
-
D-amino acid oxidase is localized in the transitional cells, which are parasensory cells located between the sensory epithelium and the dark cells
brenda
-
-
brenda
-
primary
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
increased expresison of isozyme PKCtheta in insulin-resistant rats
brenda
-
newborn
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
fibroblast, expression of isozymes HAS1 and HAS2 is increased after oncogenic malignant transformation with v-sre and/or v-fos, while only the expression of isozyme HAS2 is increased by transformation with v-HA-ras
brenda
fibroblast, oncogenic malignant transformation with v-sre and/or v-fos, and v-HA-ras
brenda
-
-
brenda
-
fibroblast cell line
brenda
-
brenda
an embryonic thoracic aorta cell line
brenda
-
CRL 1444 (ATCC)
brenda
hypoxic atmosphere upregulates P4ha1 mRNA
brenda
hypoxic atmosphere upregulates P4ha2 mRNA
brenda
smooth muscle cells
brenda
-
brenda
-
Go-alpha subunit
brenda
-
in addition to gonadotropes the enzyme is observed in a subpopulation of corticotropes and tyrotropes
brenda
-
80891, 94261, 94269, 486338, 486485, 486487, 486489, 486495, 486560, 486577, 486955, 486974, 640583, 640905, 640908, 641796, 644323, 644806, 648771, 648772, 652081, 653094, 661039, 661684, 662994, 665562, 665964, 666926, 668760, 669504, 671353, 671678, 676029, 689376, 690781, 691540, 692365, 693043, 694251, 695529, 699840, 701623, 702011, 710639, 712594, 714034, 723027, 740806, 753943, 754445, 771400, 771625
brenda
-
3T3-L1
brenda
-
AACS mRNA is preferentially detected in mature adipocytes but not in preadipocytes. AACS mRNA expression in primary preadipocytes increases during the adipocyte differentiation
brenda
-
cell culture
brenda
-
differentiated from 3T3-L1 fibroblasts
brenda
-
during differentiation of 3T3-L1 cells into adipocytes, isoform p110b is up-regulated approximately 10-fold, expression of p110a is unaltered
brenda
-
epididymal fat, presence of a functional glucose-6-phosphate-transporter hexose-6-phosphate dehydrogenase 11beta-hydroxysteroid dehydrogenase type 1 system
brenda
-
Go-alpha subunit
brenda
-
hormone-sensitive lipase, lipolysis of storage triacylglycerides
brenda
-
isolated from parametrial adipose
brenda
-
isozyme type III
brenda
-
methionine restriction induces isoform 11beta-HSD1 activity in all types of adipose tissue examined, correlating with increased tissue corticosterone. Inverse relationship between 11beta-HSD1 activity and adipocyte size is observed. Methionine restriction additionally increases adipose triglyceride lipase and acetyl-coenzyme A carboxylase protein levels
brenda
-
primary
brenda
-
rodent adipocyte
brenda
-
SSAO inhibition is not sufficient to impair fat deposition. Combined MAO and SSAO inhibition limits adiposity in non-obese as well as in obese rats
brenda
-
SSAO inhibition is not sufficient to impair fat deposition. However, combined monoamine oxidase (EC 1.4.3.4) inhibition and SSAO inhibition limits adiposity in non-obese as well as in obese rats
brenda
-
-
80870, 80874, 94883, 94885, 94892, 94898, 94899, 94906, 94907, 673313, 705266
brenda
-
brown fat of hypothyroid and hyperthyroid rats. Hypothyroidism increases MAO activity. T3 increased content of uncoupling protein 1 decreases activity of MAO
brenda
-
epididymal
brenda
epididymal fat, increased activity upon cessation of wheel running. Increase in mtGPAT protein might contribute to the overshoot in triacylglycerol synthesis
brenda
-
glycerol kinase mRNA tends to increase by 2.5fold in the mesenteric fat from Otsuka Long-Evans Tokushima Fatty rats compared to Long-Evans Tokushima Otsuka rats. A small increase in glycerol kinase mRNA expression is detected in the epididymal fat from Otsuka Long-Evans Tokushima Fatty rats compared with Long-Evans Tokushima Otsuka rats (124.5%). Rosiglitazone treatment markebly increases glycerol kinase mRNA expression in both the mesenteric and epididymal adipose tissues (1085.9% and 523.8% of the abundance in Long-Evans Tokushima Otsuka rats, respectively). The magnitude of glycerol kinase induced by rosiglitazone is significantly greater in the mesenteric fat than in the epididymal fat.
brenda
-
563, 572, 648, 675, 702, 733, 1354, 1444, 1445, 80889, 80891, 80895, 80901, 80921, 94263, 94271, 94935, 95049, 95057, 134638, 134861, 134867, 134871, 134882, 170806, 285684, 286615, 286826, 389395, 394810, 394812, 394817, 395105, 486489, 487574, 488192, 488193, 488197, 640421, 640772, 640775, 641572, 643748, 643979, 644967, 646068, 652069, 652173, 654401, 654572, 654792, 655415, 655960, 656598, 668323, 669504, 673444, 673510, 676029, 677471, 686052, 690828, 692187, 693792, 694170, 695529, 701423, 702619, 704840, 706844, 707910, 710682, 711346, 716200, 718751, 740146, 740806, 743142, 762713
brenda
-
36% of liver activity
brenda
-
decrease of enzyme activity in mesenteric and epididymal white adipose tissue upon chronic stress, accompanied by weight reduction of tissue. Decrease of enzyme activity upon acute stress only in retroperitoneal white adipose tissue
brenda
-
enolase I
brenda
epicardial
brenda
-
epididymal
brenda
-
epididymal adipose tissue
brenda
-
epididymal fat pads
brenda
-
equal amounts of isozyme L and M
brenda
expression of rat vitamin K-dependent carboxylase in adult and embryonic tissues
brenda
gonadal and inguinal adipose tissue
brenda
-
high-fat fed animals overexpress 11beta-hydroxysteroid dehydrogenase type 2 in subcutaneous but not in retroperitoneal fat. Enzyme mRNA levels strongly correlate in both tissues with different parameters related to obesity, such as body weight, adiposity, and insulin resistance
brenda
-
isoenzymes PRSI and PRSII
brenda
-
isozyme Acc1
brenda
-
lipin-1 accounts for all of the PAP1 activity in adipose tissue and skeletal muscle
brenda
-
mainly isozyme PDK2
brenda
-
range of enzyme activity differs up to 4fold among mink, mice, chinese hamster, rat and guinea pig
brenda
-
reduced acitvity in diabetic animals
brenda
-
SSAO activity regulates NO availability in white adipose tissue
brenda
-
sucrose can promote increased 11beta-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase message in mesenteric fat while concomitantly decreasing 11beta-dehydroxysteroid dehydrogenase message and increasing hexose-6-phosphate dehydrogenase message in liver
brenda
-
the activity of 11beta-HSD1 is increased in adipose tissue of obese Zucker rats
brenda
-
very low expression level of WNK1
brenda
-
visceral adipose tissue, the predominant AMPK subunit in adipose tissue is AMPKalpha1
brenda
-
visceral and epididymal
brenda
-
white adipose tissue
brenda
-
white and brown
brenda
-
-
34308, 36025, 134673, 285410, 285411, 286698, 347830, 392084, 392085, 673345, 673910, 673924
brenda
-
both 15-hydroxyprostaglandin dehydrogenase mRNA and protein levels are significantly higher in kidney cortex than in papilla. Enzyme is mainly localized to the tubular epithelial cells in kidney cortex and outer medulla
brenda
-
capsular portion in zona glomerulosa cells, decapsular in zonae fasciculata and reticularis
brenda
-
constitutive expression of HO-2
brenda
O35547, O88813, P13233, P14270, P14646, P17178, P18163, P33124, P54748, Q63151, Q6T861, Q8VHT6, Q9E2H5, Q9WTZ3, Q9Z2Z8
-
648, 3134, 4222, 4555, 4556, 28967, 31365, 34477, 36043, 37064, 94261, 95241, 95774, 134942, 137183, 208687, 208880, 208881, 208892, 208899, 285406, 285547, 285604, 286024, 286263, 287071, 287362, 289278, 389377, 389378, 389395, 389464, 390826, 391044, 392734, 392745, 394033, 438598, 438655, 438698, 438706, 440203, 486677, 486688, 486689, 486706, 488111, 488114, 488192, 488698, 488790, 488794, 639430, 639433, 643812, 646025, 647183, 648740, 648948, 649328, 651007, 653621, 653857, 654401, 654830, 657526, 659168, 659354, 664566, 665562, 666534, 668309, 672503, 675267, 675554, 676131, 680069, 682114, 685021, 687125, 688009, 695380, 696484, 697266, 702945, 706014, 706689, 710682, 711719, 727633, 735969, 740248, 745891, 750212
brenda
-
about 5% of the activity in aorta
brenda
-
adrenal corrtex
brenda
-
adrenalectomy elevates enzyme levels
brenda
-
brain natriuretic peptide stimulated membrane-bound GC
brenda
-
cortex, PKGI
brenda
-
DGK-Ibeta
brenda
-
dietary copper deficiency is associated with increased formation of enzyme
brenda
-
enzyme mRNA is only found in the inner zones of adrenal cortex, not the glomerulosa. Enzyme activity in the inner zone mitochondria is enhaced by corticotrophin and by a low-sodium diet, but suppressed by betamethasone
brenda
-
ganglion cells in medulla
brenda
-
highest activity and highest mRNA level, significant immunohistochemical reactivity
brenda
-
highest hydrolytic activity
brenda
-
isoenzyme PRSI
brenda
-
isoform I
brenda
-
less than 0.002 mg Prx I per mg of soluble protein Prx I, 0.002 mg Prx II per mg of soluble protein, less than 0.004 mg Prx III per mg of soluble protein, 0.0003 mg Prx V per mg of soluble protein and 0.0003 mg Prx VI per mg of soluble protein
brenda
-
limb muscle, increase of enzyme activity and mRNA level upon chronic stress
brenda
-
low ACE mRNA expression
brenda
low activity
brenda
mRNA expression
brenda
-
only isoform SPCA1
brenda
-
only isozyme II
brenda
-
relative high level of mRNA
brenda
-
tissue containing a 62 kDa fragment of ADAMTS-1
brenda
-
tyrosine hydroxylase in hypertensive rats shows 35% lower expression and a reduced Vmax due to a decreased phosphorylation at Ser40
brenda
-
81289, 81295, 81302, 392084, 438654, 438683, 438688, 681522, 695599, 697765, 745402
brenda
-
2fold activity under cold stress. Injection of the angiotensin converting enzyme inhibitor enalapril malate prevented the increase of tyrosine hydroxylase under cold stress
brenda
-
-
brenda
-
2-4 months old
brenda
-
-
brenda
-
type II cell
brenda
-
type II cell, L- and H-form
brenda
-
brenda
-
i.e. AT2 cells, primary cells, transdifferentiation to AT1 cells
brenda
-
PAP-2
brenda
Q9QX71
pneumocyte type II
brenda
-
brenda
-
from Pneumocystis carinii infected rats
brenda
-
brenda
-
isozymes DGKalpha and DGKzeta
brenda
-
-
brenda
-
corners of, highest enzyme content
brenda
-
brenda
central nucleus of amygdala
brenda
-
highest levels of expression in nucleus accumbens, taenia tecta, cerebellar cortex, cerebral cortical layer I, hippocampus, hypothalamus, mesencephalic raphe nuclei, central and lateral amygdala, and the circumventricular organs
brenda
immunoreactive cells are found in 3 days old but not in 1-month-old male rats
brenda
-
lateral
brenda
-
low activity
brenda
neprilysin is the predominant peptidase responsible for degrading enkephalins in the intercalated cells of the amygdala
brenda
-
prominent for beta1 and to a lesser extent for the other subunits
brenda
-
the posterodorsal medial amygdala has high levels of histidine decarboxylase
brenda
-
-
brenda
-
AC2
brenda
-
-
brenda
developing pituitary gland
brenda
-
no expression of GRK3
brenda
O35920, P11884, P14270, P14644, P14646, P15791, P19686, P20689, P33436, P47820, P54748, P70705, P97711, Q80WY4
-
246966, 288616, 288970, 391742, 485560, 486688, 486703, 491168, 491257, 491258, 642371, 647027, 651779, 664555, 665184, 668120, 668380, 670113, 671227, 674575, 679248, 684802, 685021, 687732, 688446, 688758, 689994, 690352, 690360, 691656, 692207, 693075, 693826, 695461, 695968, 697357, 698049, 699781, 699875, 699878, 701239, 703977, 707783, 709149, 709653, 711166, 711859, 711920, 711923, 713366, 722222, 731569, 735119, 749535, 750336, 754999, 771311, 772258
brenda
-
3MST and cytosolic and mitochondrial cysteine aminotransferases are localized to endothelial cells of the thoracic aorta
brenda
-
and large capacitance vessels, predominantly expression of 3-exon-out/leucine-zipper positive MYPT 1 isoform
brenda
-
aortas of transgenic rats harboring the mouse renin transgene exhibit greater NADPH oxidase activity, reactive oxygen species levels, C-reactive protein, tumor necrosis factor-alpha expression, apoptosis, and wall thickness, which are significantly attenuated by in vivo treatment with angiotensin type 1 receptor blockade by valsartan or the superoxide dismutase/catalase mimetic tempol
brenda
-
aortic homogenate, neointima
brenda
-
aortic intima of both spontaneously hypertensive rats and rats infused with angiotensin II exhibits an elevated level of soluble epoxide hydrolase
brenda
-
aortic ring
brenda
-
aortic smooth muscle cells
brenda
-
arteries from hypertensive rats, vascular PDE1A, PDE1B, PDE1C, and PDE5 isoforms
brenda
-
cultured aortic smooth muscle cell
brenda
-
different spatial and temporal expression of LOX and LOXL1 during growth and aging, expression analysis of LOXL1 and LOX in the aorta during the development, growth, and aging of LOU rats, overview
brenda
distribution of OGTase in the aorta is examined by immunofluorescence microscopy
brenda
-
electrogenic Na+K+-ATPase partially contributes to the ustained hyperpolarization of endothelial cells in response to acetylcholine
brenda
-
expression is not significantly different between diabetic and control rats. Activation of the 5-lipoxygenase previously reported in streptozotocin-induced diabetic rats can be explained by an augmented sensitivity to cysteinyl leukotrienes in the diabetic aorta
brenda
-
expression of leucine-zipper positive isoform of MYPT 1 predominantes in healthy animal
brenda
-
extremely low activity
brenda
-
fragments of the 110 kDa subunit
brenda
-
healthy and elastase-perfused aortas. Increased MMP-13 in experimental abdominal aortic aneurysms in males compared with females, while there are no differences in aortic diameter, collagen, and MMP-13 levels in baseline males versus females, MMP-13 expression analysis, overview
brenda
-
highest activity of all tissues tested
brenda
lower enzyme activity compared to vena cava
brenda
-
normal aortic endothelium. Co-distribution of prostaglandin cyclase and cyclooxygenase COX-1, with only minor expression of cyclooxygenase COX-2 in endothelium
brenda
-
PDE1
brenda
-
PDE10
brenda
-
PDE11
brenda
-
PDE2
brenda
-
PDE3
brenda
-
PDE4
brenda
-
PDE5
brenda
-
PDE6
brenda
-
PDE7
brenda
-
PDE8
brenda
-
PDE9
brenda
-
PLC delta3 and delta4
brenda
rat abdominal aortas
brenda
-
the direct antioxidative and anti-inflammatory effects of peroxisome proliferator-activated receptors ligands are associated with the inhibition of angiotensin converting enzyme expression in streptozotocin-induced diabetic rat aorta
brenda
-
thoracic, muscle
brenda
-
tissue NEP activity and its protein and mRNA expression are lower in the late phase of the septic shock compared to the early phase of the shock and the control
brenda
-
vascular smooth muscle cells
brenda
vascular smooth muscle cells. UCH-L1 is up-regulated in injured arteries
brenda
-
vascular wall and smooth muscle cells
brenda
-
wall
brenda
-
-
brenda
-
chronic treatment with the AT1R antagonist almesartan induces a fivefold increase in ACE2 mRNA in the aorta which leads to a significant increase in aortic angiotensin(1-7) protein expression
brenda
-
brenda
-
thorax
brenda
-
brenda
-
commercial preparation
brenda
-
-
brenda
-
AR4-2J pancreatic tumor cells, which show increased phosphorylation of the eIF4E regulatory protein 4E-BP1 and high levels of eIF4E compared to normal cells, also exhibit increased translational initiation of ODC mRNA
brenda
-
a pancreatic acinar cell line
brenda
-
pancreatic tumor cell
brenda
-
rat pancreatic tumor cell line
brenda
-
cerebral, microvascular, isolated from cortical vessels
brenda
-
coronary
brenda
-
brenda
-
aged arterial wall, colocalization of activated enzyme and transforming growth factor TGF-beta1. Treatment of young aortic rings with activated enzyme enhances active transforming growth factor TGF-beta-1, collagen, and fibronectin expression to the level of untreated old counterparts
brenda
-
cerebral arterial walls
brenda
-
first-order mesenteric resistance artery, high expression of enzyme with predominance of 3-exon-excluded, leucine-zipper negative MYPT 1 isoform
brenda
-
highly expressed in vascular lesions
brenda
-
iliac artery, expression of leucine-zipper positive isoform of MYPT 1 predominates in healthy animal
brenda
-
intrapulmonary arterial tissue, enzyme protein increases with age and is highest in adult rat. In contrast, enzyme specific activity is significantly higher in fetal compared with adult tissue
brenda
-
intrapulmonary arteries
brenda
-
intrapulmonary smooth muscle
brenda
-
mesenteric arterial bed, enzyme is identical with its pancreatic counterpart
brenda
mesenteric artery
brenda
-
middle cerebral
brenda
-
PDE 1 vascular expression is increased in arteries from angiotensin II hypertensive rats
brenda
-
PDE5 vascular expression is decreased in arteries from angiotensin II hypertensive rats compared to control rats
brenda
-
pulmonary
brenda
-
pulmonary artery, predominantly expression of 3-exon-out/leucine-zipper positive MYPT 1 isoform
brenda
-
pulmonary, but not aorta
brenda
small resistance mesenteric artery
brenda
-
smoking impaires acetylcholine-induced relaxations of carotid arteries, which can be improved by the NAD(P)H oxidase inhibitor apocynin. Both smoking and in vitro cigarette smoke extract exposure significantly increase vascular superoxide anion production
brenda
-
study on enzyme activity, function, and expression in cerebral and systemic arteries. Superoxide production from enzyme is 10- to 100fold greater in intracranial arteries, basilar and middle cerebral arteries than in aorta, carotid, renal or mesenteric arteries. Isoform Nox4 shows 10fold higher expression in the basilar arteries versus aorta, carotid and mesenteric arteries
brenda
-
153-306 times higher overexpression in rat AS-30D hepatoma cells than in normal freshly isolated rat hepatocytes. The enhanced glycolytic flux in fast-growth tumor cells is controlled by an overproduced, but glucose 6-phosphate-inhibited hexokinase
brenda
-
hepatocarcinoma cell line
brenda
-
hepatoma cell, expresses only mitochondrial isoform
brenda
-
-
brenda
-
Ehrlich cells
brenda
D4A0E8, P07379, P10686, P10687, P10688, P20717, P23457, P29476, P41562, P50430, P50442, P50554, P80254, P97532, P97629, Q03351, Q62711, Q8QZV1, Q91XW7, Q920P6, Q99JE6, Q99P84, Q9QW07, Q9QYU4, Q9Z330
-
37080, 37082, 288890, 439372, 439373, 490550, 640019, 640025, 650743, 652975, 656588, 664925, 668117, 669962, 672959, 673797, 673803, 675523, 675554, 681021, 681523, 681931, 686537, 686856, 686868, 690828, 692519, 693314, 694136, 695162, 696995, 697491, 697804, 699685, 699996, 702961, 704009, 705902, 707930, 709623, 710106, 710108, 711354, 711720, 712120, 713111, 715124, 715713, 715743, 715987, 719592, 721077, 721714, 725461, 725768, 728179, 729806, 731627, 734170, 739470, 743355, 750661, 751384, 753121, 755785, 757808, 758628, 763094, 764565, 770136, 770703, 772436, 774366, 777716
brenda
-
adult brain
brenda
-
adult brain, PLC-delta1 is concentrated in astroglial cells, much lower levels in neurons
brenda
-
astrocyte-specific glutamine synthetase
brenda
astrocytes in the substantia nigra express KAT-I under normal conditions. The amount of this enzyme increases after administration of 6-hydroxydopamine
brenda
-
cell culture
brenda
cell culture, expression of aggrecanase-1 mRNA is induced if cells are treated with beta-amyloid
brenda
-
cerebral cortex astrocytes, isoform B
brenda
cortical
brenda
-
cultured cell
brenda
-
cultured cortical astrocytes maintained with endothelins show an almost complete loss of glutamine synthetase
brenda
DDT is inducibly expressed within astrocytes and neurons, rather than in microglia following spinal cord contusion
brenda
-
expression of both muscle isoform and phosphorylase BB
brenda
-
hexokinase I: predominant in normal brain, hexokinase II: increased in brain tumors, ethylnitrosourea-induced 36B-10 astrocytic F-344 rat brain tumor cell line
brenda
-
highest expression of recombinant isoenzyme A in astrocytes of hippocampal cultures transfected with isoenzyme A
brenda
hypothalamic
brenda
-
in lower brain stem and cerebellum, as well as type-1 astrocytes from cerebral cortex and the cerebellum
brenda
-
in rat brain, the P-protein is confined to astrocytes. The intensity of astrocyte staining varies with regions, with the strongest staining in the hippocampus, the cerebellar cortex, the Bergmann glia in the cerebellum and the Muller cells in the retina
brenda
-
in the lesion site after spinal cord injury
brenda
-
increased SPT enzyme activity in reactive astrocytes of the hippocampus at 2 weeks post-kainate injection
brenda
-
insulin-like growth factor-I, epidermal growth factor, and insulin markedly increase TG-2 expression and activity. This effect is reduced when glial cultures are primed with both dexamethasone and estradiol. The regulation of TG-2 in astrocytes is signal- and hormone dependent
brenda
-
involvement of reactive oxygen species from NADPH oxidase in cytokine induction of secretory phospholipase A2-IIA in astrocytes
brenda
isoforms CPT1a and CPT2 are expressed exclusively by astrocytes
brenda
-
isoforms NOX2 and NOX4
brenda
-
isozyme type III
brenda
-
low expression
brenda
-
major site for expression
brenda
-
molar ratios of P-, T-, and H-protein mRNA in cerebrocortical astrocyte culture are 5.7:1.0:2.4
brenda
-
of cortex
brenda
of optic nerve
brenda
-
omega-amidase activity is significantly higher in astrocytes than in neurons
brenda
-
only expresses PDE7
brenda
-
perivascular
brenda
PI-PLC delta3
brenda
primary
brenda
-
primary astrocyte
brenda
-
primary astrocytes express different sterol hydroxylases and are able to uptake exogenous 27-hydroxycholesterol
brenda
-
primary cell culture
brenda
-
primary cells
brenda
-
primary cortical
brenda
-
primary cortical astrocyte cultures
brenda
-
primary culture. Proliferation induced by fibrillar beta-amyloid peptide Abeta1-40 is mediated both by microglial release of TNF-alpha and by production of hydrogen peroxide by enzyme
brenda
-
primary rat cortical astrocytes
brenda
primary type 2
brenda
-
primary, cortical
brenda
-
secretion, induced by interleukin-1beta
brenda
-
similar level of expression of AMPD2, but greater expression of AMPD3 than in neurons
brenda
-
transcriptional regulation of ACE2 mRNA in astrocytes is dependent on the relative concentrations of both angiotensin II and angiotensin(17) as well as on interaction with their respective receptors
brenda
-
-
brenda
-
astroglia-rich primary culture from neonatal rats
brenda
-
primary astroglial cultures prepared from newborn rat cerebral cortices
brenda
-
brenda
coexpression of mineralocorticoid receptor with its protecting enzyme 11beta-HSD2 as well as aldosterone with its processing enzyme CYP11beta2 in cardiac neurons within rat atria
brenda
-
-
brenda
-
neuronal cell line
brenda
-
-
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precursor
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-
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immature B-lineage cell
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in rat brain, the P-protein is confined to astrocytes. The intensity of astrocyte staining varies with regions, with the strongest staining in the hippocampus, the cerebellar cortex, the Bergmann glia in the cerebellum and the Muller cells in the retina
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P-protein mRNA is expressed mainly in glia-like cells, including Bergmann glias in the cerebellum, while T- and H-protein mRNAs are detected in both glial-like cells and neurons
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-
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in bile of albendazole-treated animals, only albendazole S-oxide, but not the sulfone, is present
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-
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surface membrane
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-
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80-90% of activity
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36043, 37080, 94574, 134758, 208880, 208881, 668120, 688137, 698343, 732583, 733064, 752242
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high level
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N-butyl-N-(4-hydoxybutyl) nitrosamine (BBN) treatment for 12 weeks induces superficial cancer development in rats
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vascular endothelium and muscle fibers, castration decreases and T supplementation restores PDE5 gene expression
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2269, 2654, 30798, 134945, 135474, 286013, 286014, 286024, 439290, 485595, 485605, 485609, 485615, 487246, 488023, 640037, 645722, 647141, 650933, 651189, 651191, 666181, 667159, 669780, 675591, 681018, 682101, 682915, 683726, 686598, 701287, 705320, 707725, 709320, 777419
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activity increases between birth and 40 days of age
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enolase I
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hypophysial portal blood
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lysate contains carbonic anhydrase I, II and III
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maximal expression level of MsrA in kidney and liver, followed by heart, lung, brain, skeletal muscle, retina, testis, bone marrow, and blood
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one electrophorectic form
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plasma isozyme
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postheparin lipoprotein lipase increases by about 200%
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trace amount
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-
-
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bound to
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-
3028, 3029, 35209, 94285, 94286, 646508, 646513, 653008, 653145, 653580, 653977, 660336, 664313, 664847, 665836, 666927, 667885, 670957, 677500, 678597, 678634, 678658, 679471, 679670, 681178, 681319, 681325, 686933, 688758, 691169, 691193, 691671, 693485, 694937, 695446, 696112, 696134, 696136, 696668, 696746, 697044, 697764, 697774, 697821, 697822, 698423, 699445, 699748, 701687, 702514, 702623, 703233, 703898, 703947, 704840, 707456, 707644, 710575, 710609, 710690, 712050, 714002, 714637, 714925, 718282, 729349, 731424, 731674, 732147, 732968, 744508, 751792, 752912, 755449, 756305, 770942, 771569, 773649, 773763
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-
amitriptyline at 0.03, 0.05, 0.1 and 0.5 mM concentrations lower enzyme activity in the plasma of the heparinised rat by 14, 22, 23 and 28%, respectively
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Cysteamine levels in plasma of rats fed the cysteamine supplemented diet are significantly higher than those in tissues of rats fed basal diet. Rats fed the cysteamine-supplemented diet have no markedly elevated levels of hypotaurine in plasma.
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dopamine beta-hydroxyase is reduced in rats subjected to chronic mild stress for 5 weeks. Imipramine treatment minimizes these chronic mild stress-induced reductions
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in vivo administration of adrenaline and acute stress causes an increase in plasma lipoprotein lipase activity
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increased plasma biotinidase activity in rats with paracetamol-induced acute liver injury. The increase may serve as an indicator of paracetamol-induced acute liver injury in the rat
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limb muscle, increase of enzyme activity and mRNA level upon chronic and acute stress
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lipoyllysine hydrolase activity is highest in kidney, liver and blood plasma
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plasma ALA level of the fatigued rats is slightly higher (approximately 1.4fold) than that of the control or food-restricted animals
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plasma estradiol levels are stimulated 3 days ahead of inhibitor application with pregnant mare's serum gonadotropin (PMSG)
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the high plasma titer of factor XII observed in estrogen-treated and prolactin-treated rats is caused by enhanced hepatic expression of both transcriptional and translational levels, as well as by increased secretion of factor XII
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while hyperthyroid rats exhibit lower levels of plasma AP A activity than controls, the kidney of hyperthyroid animals expresses significantly higher AP A than controls and hypothyroid animals. A discrepancy between the high expression of AP A in kidney of hyperthyroid rats and the low activity of AP A measured in plasma and kidney of hyperthyroid animals is found. The posttranslational influence of environmental biochemical factors may be in part responsible for that divergence
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210163, 210166, 287910, 663994, 681897, 684342, 690148, 696924, 737402, 754048, 774211
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colocalization of enzyme with an ecto-nucleoside triphosphate diphosphohydrolase and an ecto-5-nucleotidase on platelet surface
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colocalization with ecto-nucleoside triphosphate diphosphohydrolase and ecto-5'-nuleotidase on platelet surface
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exogenous oxidative stress, thrombin activation, progression of ageing and type 2 diabetes lead to protein carbonyls formation in platelets, and this modification can be attenuated by antioxidant enzymes
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high activity in intact platetelts
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isozyme PS-PLA1 or PLA1A
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very little expression
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-
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activity is greatly increased in rats with mammary tumors. The activity may be involved in the promotion and progression of breast cancer through oxytocin, vasopressin and/or renin-angiotensin system misregulation
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activity is highest in 5-day-old rats, it decreases till the age of 14 days and increases mainly in 14-day to 35-day-old animals, significant decrease in activity in rats between 35 to 40 days, adult rats aged 90-120 days show a stable activity of dopamine bet-hydroxylase
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sedentary diabetic rats have higher circulating GPLD1 compared to controls, which can be reversed by exercise training and is associated with modifying in glycemic and insulin profile
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similar mRNA expression levels in (fa/fa) Zucker rats (obese) compared to lean Zucker rats (control) as well as in cafeteria diet-fed Wistar rats (diet-induced obesity) compared to standard chow diet-fed Wistar rats (control)
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treatment with benzylamine + vanadate reduces the elevated serum SSAO activity, decreases the accumulation of advanced-glycation end products and increases the bioavailability of nitric oxide in diabetic animals, similarly to insulin
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-
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arterial pulmonary
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basal membrane
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DDAH-2 is strongly expressed in blood vessels
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DDAHII immunoreactivity is localized to infiltrating inflammatory cells and blood vessels in the healing infarct
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endothel, isozymes PGF synthase I and II
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oviductal and uterine, endothelium, NTPDase1 is located especially in the lamina propria mucosae and uterine blood vessel endothelium
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PKGI
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pulmonary arterial, smooth msucle
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wall
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-
34774, 94567, 94625, 95818, 134711, 135474, 209799, 209936, 652449, 652666, 653621, 663766, 668120, 691134, 695615, 695899, 711688, 745431, 753882
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activities in adult tissues are only 10-40% of those found in newborn
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adult
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embryo bone
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surfaces under the ruffled borders and some clear zones of osteoclasts. MMP-13 may play an important role in the degradation of type I collagen in bone matrix, acting in concert with cathepsin K and MMP-9 produced by osteoclasts
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-
1327, 1384, 4142, 30779, 134945, 135126, 392077, 392084, 392085, 487379, 642685, 645147, 645150, 658264, 663609, 669619, 712050, 737733
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184% of liver activity
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activity is significantly higher in bone marrow of rats treated with N-nitro-L-arginine methylester
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glutathione-requiring enzyme
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maximal expression level of MsrA in kidney and liver, followed by heart, lung, brain, skeletal muscle, retina, testis, bone marrow, and blood
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stem marrow cell, no expression of isozymes LH3 and LH2b
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-
-
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NMT activity is observed to be 5fold higher in bone marrow cells from rats with colonic cancer than in controls, and shows also differential localization
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cholinergic neuron-like cells
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GluAP is upregulated in osteogenic differentiated BMSC cells in vitro
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PC1/PC3 is absent in undifferentiated bone marrow stromal stem cells, its expression is initiated upon the induction of differentiation. PC1 is expressed at a relatively lower level as compared to enzymes functioning in the constitutive pathway
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PC2 is absent in undifferentiated bone marrow stromal stem cells, its expression is initiated upon the induction of differentiation. PC2 is expressed at a relatively lower level as compared to enzymes functioning in the constitutive pathway
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B5DEJ6, D3ZKT0, D4A2H2 AND Q3B7D2, D4AAT7, F7EN52, M0RC77, O08560, O08680, O09175, O10743, O35052, O35078, O35547, O42123, O55171, O70196, O88267, O88422, O88806, O88807, O88813, O88867, O89049, P00787, P04177, P05696, P05708, P06687, P06762, P07154, P07335, P07379, P07861, P08413, P08430, P08542, P09215, P09216, P09217, P09759, P09875, P0C1T0, P0C644, P10111, P10687, P11275, P11884, P13233, P13234, P14270, P14646, P14882, P15791, P16259, P16453, P17105, P17712, P18163, P18266, P19139, P19468, P19643, P20717, P21396, P21816, P21936, P22734, P23457, P23711, P24008, P24155, P29476, P31214, P32577, P32738, P33124, P35465, P35559, P36511, P36970, P37136, P40329, P41562, P42335, P42676, P48508, P49621, P50123, P50282, P50442, P50554, P51556, P51650, P53610, P53669, P54645, P54748, P54757, P55213, P56558, P63086, P70627, P70708, P80201, P80202, P80203, P80204, P83006, P97532, P97564, P97608, P97612, P97629, P97675, P97711, P97756, Q00972, Q02527, Q03114, Q04400, Q04589, Q04631, Q05683, Q07014, Q08201, Q08415, Q4V8J4, Q58FK9, Q5BQE6, Q5EGZ1, Q5GF25, Q5KTC7, Q5PPH0, Q62761, Q62762, Q62763, Q62784, Q62829, Q62915, Q62967, Q63009, Q63151, Q63415, Q63450, Q63470, Q63484, Q63604, Q63793, Q64244, Q64428, Q64550, Q64559, Q64595, Q64633, Q64637, Q67B98, Q68EJ0, Q6AYB9, Q6E0V2, Q6IUU3, Q6P7S1, Q769K2, Q76EQ0, Q76IC5, Q80ZG2, Q811A3, Q8K4Y7, Q8QZV1, Q8R431, Q8R4C0, Q8VHT6, Q91V26, Q91XT9, Q920L2, Q924C3, Q925R7, Q96EB6, Q99NA5, Q99NB2, Q99P39, Q9E2H5, Q9EQV6, Q9ESP7, Q9JKC1, Q9JMI1, Q9QXJ0, Q9QYU4, Q9QZC4, Q9QZL2, Q9R0C5, Q9R0E0, Q9WTZ3, Q9Z2Z8
-
562, 563, 572, 658, 755, 786, 819, 988, 989, 995, 996, 997, 1174, 1354, 1384, 1504, 1537, 1594, 1664, 1743, 1774, 2269, 2532, 2933, 3098, 3100, 3105, 3108, 3118, 3124, 3134, 3236, 3411, 3413, 3415, 3706, 3971, 3974, 3981, 3995, 3996, 4097, 4144, 4160, 4161, 4162, 4200, 4222, 4224, 4236, 4238, 4239, 4270, 4542, 4705, 4776, 4844, 4846, 5112, 5119, 23917, 28967, 31366, 31367, 31369, 31370, 33330, 33352, 33612, 33629, 33808, 34477, 34561, 34816, 34834, 34840, 35871, 35916, 35923, 35966, 36043, 36057, 36138, 36179, 36456, 36921, 37053, 37064, 37067, 37068, 37069, 37079, 37080, 37083, 37086, 37413, 37427, 37496, 37498, 80941, 80973, 80976, 80992, 81039, 81116, 81210, 81289, 81302, 81307, 81618, 81620, 94261, 94314, 94319, 94322, 94340, 94389, 94418, 94468, 94558, 94906, 94935, 94961, 94973, 94990, 95067, 95068, 95069, 95144, 95164, 95165, 95229, 95241, 95254, 95300, 95310, 95312, 95314, 95315, 114150, 114159, 114160, 114184, 114214, 114215, 114217, 114223, 114233, 114234, 114236, 114243, 114245, 133865, 134162, 134176, 134180, 134638, 134671, 134813, 134885, 134888, 134923, 134927, 134942, 134945, 135125, 135126, 135136, 135139, 135171, 135172, 135175, 135183, 135236, 135290, 135380, 135381, 135399, 135401, 135404, 135407, 135418, 135419, 135422, 135429, 135433, 135447, 135474, 135595, 135623, 136451, 136490, 136606, 136607, 137040, 137041, 137042, 137046, 137047, 137048, 137161, 137180, 137183, 137210, 137217, 137221, 137222, 137223, 137224, 137225, 137342, 137363, 170806, 171148, 171187, 171271, 171319, 171509, 171513, 171965, 171987, 171988, 207968, 208399, 208402, 208432, 208687, 208880, 208881, 208975, 208984, 208987, 208998, 208999, 209000, 209001, 209002, 209010, 209012, 209018, 209292, 209381, 209384, 209387, 209388, 209393, 209413, 209414, 209535, 209539, 209542, 209545, 209546, 209584, 209588, 209589, 209593, 209594, 209596, 209598, 209625, 209701, 209837, 209898, 209943, 210006, 210007, 210008, 210009, 210010, 210011, 210013, 210014, 210015, 210016, 210017, 210018, 210161, 210202, 210206, 210568, 210571, 246682, 246950, 246958, 246962, 246964, 246969, 246972, 285214, 285221, 285222, 285224, 285231, 285349, 285410, 285604, 285684, 285699, 285720, 285879, 286013, 286020, 286023, 286024, 286147, 286164, 286166, 286172, 286174, 286175, 286176, 286177, 286181, 286182, 286183, 286184, 286190, 286214, 286215, 286269, 286308, 286518, 286520, 287014, 287308, 287336, 287380, 287526, 287797, 287888, 288048, 288049, 288050, 288064, 288158, 288161, 288166, 288172, 288174, 288554, 288884, 288890, 288893, 288971, 289055, 289059, 289068, 289069, 289158, 289253, 289268, 289278, 289280, 289281, 289282, 326411, 348503, 348521, 349034, 349035, 349037, 349266, 389525, 389559, 389980, 389981, 390346, 390826, 391541, 391626, 391706, 391716, 391879, 391898, 392038, 392161, 392545, 392734, 392789, 393080, 393796, 393971, 394026, 394366, 394559, 394699, 394810, 394812, 394817, 394866, 394867, 394871, 395011, 395105, 395466, 395924, 395928, 438197, 438244, 438316, 438317, 438318, 438319, 438421, 438422, 438636, 438654, 438659, 438683, 439373, 439378, 439477, 440190, 440191, 440192, 440196, 440197, 440198, 440203, 440210, 440212, 440213, 440220, 440228, 440232, 440236, 441313, 441314, 441315, 441317, 441353, 441356, 441507, 441508, 441514, 441536, 441543, 441556, 441560, 441575, 441577, 485030, 485035, 485053, 485054, 485188, 485191, 485592, 485595, 485596, 485600, 485605, 485606, 485612, 485615, 485965, 485967, 485968, 485971, 485972, 486027, 486103, 486296, 486352, 486403, 486456, 486458, 486521, 486618, 486621, 486645, 486955, 486960, 486974, 487163, 487246, 487277, 487278, 487279, 487288, 487297, 487305, 487310, 487407, 487416, 487432, 487554, 487742, 487744, 487754, 487756, 487771, 487836, 487964, 487978, 487982, 487989, 487990, 488023, 488193, 488405, 488794, 488990, 489215, 489216, 489217, 489218, 489219, 489220, 489225, 489226, 489240, 489303, 489304, 489305, 489307, 489309, 489310, 489333, 489334, 489339, 489404, 489405, 489407, 489418, 489419, 489495, 489573, 489574, 489581, 489611, 489616, 489741, 489862, 489867, 489868, 489872, 489876, 489878, 489885, 490038, 490200, 490382, 490485, 490492, 490558, 490643, 490757, 490758, 490759, 491017, 491018, 491080, 491096, 491098, 491168, 491202, 491227, 491232, 491247, 491257, 491258, 491403, 491431, 491630, 491869, 491870, 491984, 492160, 532653, 636548, 636626, 636734, 636888, 636964, 637038, 637040, 637041, 637045, 637050, 637052, 637114, 637126, 637308, 637504, 637517, 637616, 637619, 637738, 637741, 637745, 637746, 637814, 638026, 638223, 638228, 638232, 638234, 638235, 638395, 638587, 638597, 638771, 638783, 638784, 638791, 638959, 639693, 639705, 639829, 639901, 639946, 640009, 640019, 640025, 640031, 640037, 640039, 640171, 640172, 640173, 640174, 640175, 640221, 640359, 640364, 640366, 640372, 640375, 640395, 640399, 640421, 640732, 640735, 640736, 640737, 640738, 640748, 640749, 640814, 640822, 640824, 640826, 640828, 640829, 640834, 640835, 640853, 640965, 640973, 641090, 641202, 641346, 641359, 641371, 641392, 641403, 641404, 641564, 641769, 641770, 641802, 641806, 641812, 641822, 641824, 641829, 641830, 641833, 641852, 642128, 642159, 642371, 642421, 642551, 642558, 642641, 642661, 642685, 642688, 642747, 642750, 642888, 642893, 643312, 643319, 643325, 643681, 643979, 643989, 644099, 644105, 644183, 644187, 644188, 644195, 644196, 644208, 644323, 644328, 644338, 644343, 644345, 644349, 644355, 644360, 644385, 644401, 644406, 644409, 644806, 644958, 645037, 645044, 645048, 645083, 645164, 645219, 645269, 645316, 645383, 645387, 645484, 645561, 645562, 645648, 645650, 645654, 645689, 645690, 645691, 645692, 645695, 645730, 645804, 645805, 645807, 645828, 645972, 645973, 645974, 645975, 645977, 645987, 646024, 646025, 646046, 646118, 646121, 646131, 646158, 646161, 646164, 646165, 646167, 646171, 646376, 646389, 646395, 646418, 646449, 646454, 646725, 647025, 647026, 647258, 647262, 647265, 647271, 647283, 647286, 647288, 647304, 647604, 647982, 648109, 648700, 648788, 648789, 648790, 648791, 648792, 648947, 648949, 649263, 649426, 649531, 649789, 649803, 650326, 650486, 650495, 650743, 650814, 650849, 650943, 651004, 651265, 651315, 651443, 651540, 651779, 652975, 653120, 653121, 653127, 653243, 653345, 653349, 653367, 653416, 653621, 653676, 653859, 653873, 653994, 654021, 654614, 654830, 654852, 654858, 655133, 655198, 655234, 655290, 655346, 655998, 656021, 656079, 656251, 656588, 656589, 656593, 656596, 656607, 656639, 656651, 656868, 657262, 657263, 657523, 657701, 657738, 657744, 657761, 658200, 658240, 658562, 658832, 658837, 659111, 659168, 659354, 659381, 659578, 659757, 660007, 660008, 660014, 660038, 660669, 660815, 660965, 660978, 661256, 661334, 661404, 661406, 661683, 661850, 662185, 662302, 662308, 662501, 662592, 662673, 662693, 662959, 663274, 663275, 663813, 663883, 664165, 664179, 664469, 664474, 664477, 664564, 664566, 664721, 664865, 664935, 665064, 665110, 665484, 665488, 665491, 665505, 665568, 665608, 665833, 665849, 666120, 666122, 666130, 666131, 666132, 666213, 666241, 666460, 666463, 666467, 666719, 667114, 667366, 667505, 667523, 667729, 667791, 667821, 667841, 667847, 667884, 668117, 668229, 668410, 668542, 668816, 668828, 669164, 669295, 669332, 669635, 669636, 669904, 669940, 669943, 669962, 670003, 670329, 670342, 670363, 670381, 670392, 670394, 671177, 671278, 671322, 671679, 671705, 671799, 672227, 672598, 672792, 672835, 672841, 672847, 672851, 673005, 673201, 673232, 673287, 673313, 673352, 673460, 673480, 673654, 673829, 673910, 673911, 673929, 674052, 674380, 674558, 674603, 674713, 675008, 675099, 675105, 675240, 675267, 675304, 675509, 675510, 675514, 675524, 675541, 675549, 675550, 675554, 675555, 675556, 675688, 675951, 676029, 676088, 676157, 676161, 676162, 676164, 676175, 676178, 676179, 676187, 676189, 676808, 676849, 677529, 677986, 678070, 678326, 678362, 678375, 678393, 678441, 678984, 679129, 679165, 679180, 679288, 679513, 679514, 679659, 679661, 679665, 679670, 679695, 680122, 680257, 680759, 680835, 681285, 681516, 681522, 681523, 681527, 681587, 681632, 682110, 682111, 682114, 682117, 682118, 682119, 682128, 682252, 682284, 682568, 682902, 682957, 683087, 683088, 683319, 683322, 683342, 683344, 683369, 683469, 683490, 683509, 683520, 683708, 683791, 683799, 683932, 683958, 684954, 685021, 685433, 685556, 685873, 685888, 685891, 686015, 686020, 686040, 686054, 686058, 686194, 686293, 686367, 686537, 686724, 686749, 687055, 687536, 687793, 687935, 688220, 688257, 688492, 688496, 688507, 688515, 688530, 688556, 688606, 688608, 688660, 689134, 689159, 689170, 689182, 689202, 689224, 689944, 689999, 690097, 690099, 690170, 690174, 690374, 690680, 690703, 690723, 690798, 690828, 690846, 690858, 690880, 691139, 691169, 691545, 691556, 691558, 691561, 691775, 692000, 692058, 692060, 692162, 692200, 692232, 692516, 692517, 692519, 692560, 693528, 693733, 693758, 693774, 693830, 693868, 693989, 694170, 694359, 694360, 694370, 694379, 694386, 694592, 694874, 695063, 695151, 695205, 695599, 695972, 696115, 696124, 696139, 696484, 696596, 696995, 697042, 697045, 697046, 697048, 697348, 698035, 698337, 698738, 698999, 699099, 699670, 699685, 699687, 699968, 700077, 700110, 700411, 700416, 700423, 700429, 700450, 700456, 700461, 700470, 700475, 701042, 701186, 701245, 701715, 701984, 702352, 702387, 702504, 702632, 702696, 702955, 702963, 703129, 703133, 703135, 703199, 703351, 703993, 704154, 704377, 704449, 704493, 704657, 704704, 704804, 704927, 704976, 705250, 705270, 705278, 705284, 705286, 705454, 705910, 705915, 705918, 705922, 705930, 705936, 705939, 706140, 706540, 706688, 706844, 707056, 707107, 707118, 707553, 707661, 708134, 708263, 708300, 708437, 708464, 708501, 708576, 708595, 708981, 708982, 709247, 709257, 709296, 709595, 709605, 709664, 709817, 710078, 710084, 710085, 710112, 710123, 710451, 710539, 710575, 710682, 710833, 710899, 711146, 711354, 711447, 711449, 711688, 711707, 711720, 712006, 712119, 712174, 712324, 712690, 712699, 712815, 712943, 713007, 713120, 713150, 714001, 714107, 714114, 714699, 714819, 715124, 715425, 715433, 715713, 715787, 715984, 716049, 716346, 717173, 717528, 717679, 718294, 718751, 718981, 719302, 719421, 720443, 720547, 720554, 720555, 720858, 721249, 721701, 721714, 721741, 721929, 722788, 723027, 723585, 724210, 724682, 725073, 725456, 725675, 726043, 726048, 726917, 727167, 728034, 729185, 729516, 729681, 729954, 730238, 730475, 730962, 731403, 731627, 731702, 732139, 732368, 732576, 732583, 733064, 733404, 733661, 733662, 733732, 733751, 733776, 733794, 733906, 733958, 734134, 735256, 735302, 735602, 735627, 736550, 736678, 737402, 737427, 738674, 738756, 738895, 738988, 739470, 740102, 740108, 740146, 740194, 740247, 740410, 740438, 740702, 740888, 741440, 741458, 741796, 742219, 742253, 742349, 742443, 742816, 742853, 742857, 743126, 743353, 743355, 743358, 744767, 744852, 745347, 745485, 745617, 745890, 745891, 745971, 747036, 748220, 748445, 748691, 749082, 749758, 749862, 749869, 749958, 750479, 750619, 750658, 751285, 751698, 752408, 752416, 752835, 753277, 753487, 754291, 754341, 754458, 754463, 754571, 754615, 754898, 754903, 757382, 757567, 758983, 759445, 759850, 759852, 760639, 761409, 761459, 761598, 761735, 762009, 762211, 762503, 762517, 762740, 763094, 763378, 763517, 764034, 764079, 765028, 765252, 765297, 765742, 765779, 766288, 767269, 767378, 767622, 768081, 768237, 770004, 770018, 770583, 770663, 771452, 771585, 771599, 771613, 772054, 772181, 772190, 772210, 772703, 772985, 773245, 773249, 773428, 773648, 774211, 774303, 774366, 774379, 774724, 776089, 778606, 778765, 779365, 779370, 779444
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0.0013 mg Prx I per mg of soluble protein Prx I, 0.0013 mg Prx II per mg of soluble protein, 0.0005 mg Prx III per mg of soluble protein, 0.001 mg Prx V per mg of soluble protein and 0.0017 mg Prx VI per mg of soluble protein
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11beta-HSD2 in the adult brain is thought to protect mineralocorticoid receptors from inactivation by corticosterone
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11HSD1 is highly expressed in various brain structures, including the hippocampus
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2 isoenzymes
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2 isozymes from alternative slicing
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248% of liver activity
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30% increase in DLDH expression in rats between 10 and 20 days of age, whereas there is no further increase during the period from 20 to 60 days. Diaphorase activity shows a 46% increase in rats between 10 and 20 days of age, but there is also no further increase between 20 and 60 days. DLDH dehydrogenase activity increases progressively over the period from 10 to 60 days of age (63% between 10 and 20 days, 30% between 20 and 30 days, and 25% between 30 and 60 days of age)
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4-hydroxybenzoate transferase activity is high during birth and 18 months of age in rat brain
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6-week-old rats, tissue amounts of bleomycin hydrolase determined
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A-type enzyme expression
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about 40% of the activity in aorta
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abundantly expressed
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aconitase-specific activity increases by 42% at 2% O2 compared to 21% O2
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ACSL3 and ACSL6 are the predominant isoforms in brain
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activities in adult tissues are only 10-40% of those found in newborn
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activity is 4 times lower in adult than in embryonic brain
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activity is enhanced following portacaval anastomosis
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activity measurement over a 6-week period in rats fed pyridoxine-sufficient and pyridoxine-deficient diets
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adult
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adult cortex, activity is enriched 5fold higher in the white matter than in the gray matter of the young adult brain
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adult, isozymes 5alpha-R1 and 5alpha-R2
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adult, PLC-gamma1 is diffusely distributed, expression pattern of PLC-gamma1 and PLC-delta1 during development, expression pattern of PLC-gamma2
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all parts of brain, neurons and glia, very low levels in astrocytes
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almost exclusively the nonglycosylated form of the enzyme
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amoeboid microglial cells in the postnatal rat brain
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amygdala, caudate-putamen, central gray, dorsal raphe, globus pallidus, hippocampus, hypothalamus, locus coerulus, medial and lateral geniculate, olfactory bulb, periaqueductal gray, solitary nucleus, spinal trigeminal nucleus, substantia nigra, superior colliculus, thalamus, corpus callosum, fornix, habenular commissure, solitary tract, stria medularis, stria therminalis
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analysis of the levels of ECE-1 expression and distribution under normal and pathologic conditions of Alzheimer disease, overview
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areas expressing high levels of trkB or trkC mRNAs included olfactory formations, neocortex, hippocampus, thalamic and hypothalamic nuclei, brainstem nuclei, cerebellum and spinal cord motoneurons
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arginine decarboxylase and arginase are both constitutively and widely expressed in rat brain neurons
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astrocytes and tanycytes express type 2 deiodinase
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astrocytes in the cerebellum and hippocampus
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at the protein level, but not at the mRNA level, the content of brain isoform of glycogen phosphorylase is similar in heart and brain. Muscle isoform of glycogen phosphorylase is more abundant in the heart than in the brain
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AT4 receptor/IRAP is found in neurons in the cortex, hippocampus and basal ganglia
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atlas on distribution of eleven histone deacetylase isoforms in the brain
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based on immunohistochemistry, PLD is detected in some neurons and glial cells in the cerebrum
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beta-ARK mRNA is expressed intensely in the cerebellar granule cell layer and moderately in the hippocampal pyramidal cells and dentate granule cells. The neocortex and piriform cortex express it moderately to weakly, whereas the thalamus and hypothalamus express it weakly to faintly. No significant expression of the mRNA is detected in the caudate-putamen. Weak expression of beta-ARK mRNA in several nuclei of the brainstem and in the spinal gray matter
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bilateral distribution of aminopeptidases in stress-related areas, overview
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brain isoform CPT1a RNA and total protein expression are unchanged throughout post-natal development (PND0, PND7, PND14, PND21 and PND50). Acylcarnitines, generated by CPT1a, significantly increase with age and peak at PND21 in all brain regions, concurrent with the increased expression of enzymes involved in mitochondrial beta-oxidation
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brain isoform CPT2 RNA peaks at post-natal day 21 and remains unchanged through post-natal day 50 in all regions studied. CPT2 transcript abundance is highly developmentally regulated in the cortex, midbrain, and cerebellum, and significantly increases with age. The peak of acylcarnitine abundance in all brain regions profiled at post-natal day 21 corresponds to the maximal expression of CPT2 mRNA
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brain specific transglutaminases NI and NII
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brain tissue of thermally injured rats displays an increase in the brain water content and the presence of Evans blue, temporally associated with an increased expression of endogenous tPA and uPA. Peripheral thermal injury does induce an increase in the permeability of the blood brain barrier
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brains-specific isozymes CaMKII alpha and CaMKIIbeta
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brainstem, midbrain
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Ca2+-dependent isoform
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CaMKII is the main isozyme in the brain
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capillary endothelium
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carbonic anhydrase IV
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caspase-3 is increased in ischemic brain, in penumbra and core
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cathepsin B is expressed in induced cerebral aneurysms and aneurysmal walls, and promotes the progression of cerebral aneurysms
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cChAT and pChAt expression analysis in brain, overview
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cellular localization of the enzyme changes postnatally. The enzyme is distributed in most neurons of the brain of 1-2 week old rats, whereas it is localized in the oligodendrocytes of adult animals
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cellular localization reveals age-related pattern of expression of the reductase in selected regions such as cortex, substantia nigra, hippocampus and in the cerebellum
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central nervous system myelin
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cerebellum and cortex
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cerebellum excluded
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cerebellum, medulla oblongata, pons, hypothalamus, striatum, midbrain, hippocampus, cerebral cortex
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cerebral cortex
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cerebral cortex, enzyme is catalytically and immunologically related to testis enzyme
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cerebral cortex, lowest activity
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cerebral hemisphere
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cerebral, ipsilateral cortex
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cerebrum
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cerebrum, cerebellum and brain stem of 14 and 21 days old rats, whole brain of 7 days old rats
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changes in enzyme activity caused by kindling relate to regulation of the expression of TRH receptors and degrading enzyme
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changes in the mRNA expression of the SMS1 gene occur in rats after focal cerebral ischemia. In damaged ipsilateral cortex in the ischemic cortex, the level of SMS1 transcripts is decreased, overview
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chronic ethanol consumption down-regulates CMP-NeuAc:GM3 alpha 2,8-sialyltransferase gene in the rat brain
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circadian expression of TPH in dorsal and median raphe in correlation to glucocorticoid fluctuations, e.g. corticosterone, expression pattern, overview
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CNP is associated with tubulin from brain
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CNPase expression pattern of brain tissues in hypothyroid and control rats from post-natal days 5 to 90, hypothyroidism impairs transiently the CNPase gene expression, effect on oligodendrocyte differentiation and myelination
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co-expression with heme oxygenases HO-1 and HO-2, BVR expression patterns, overview
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COMT is not present in presynaptic dopaminergic and noradrenergic neurons
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corpus striatum
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cortex
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cortex and anterior brain, striatum and middle brain, posterior brain
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cortex and anterior brain, striatum and middle brain, posterior brain, low enzyme activity
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cortex and striatum
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cortex, striatum, hippocampus
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cortical astrocytes, isoform B
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CTbeta2 mRNA is highly expressed in the brain
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Cyp27a1 is expressed in all the cell types but at highest levels in microglia
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Cysteamine levels in brain of rats fed the cysteamine supplemented diet are significantly higher than those in tissues of rats fed basal diet. Rats fed the cysteamine-supplemented diet have markedly elevated levels of hypotaurine in brain.
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cytosolic brain isozyme
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cytosolic OGT activity is 10times more abundant in brain tissue compared with muscle, adipose, heart, and liver tissue
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detectable levels of expression demonstrated at the RNA and protein level
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developing brain
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developing rat brain
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developmental regulation of auzotaxin shown by mRNA expression in the brain, analyzed by quanitative RT-PCR, using recombined ATX-green fluorescent protein (GFP), immunocytochemistry visualized with 3,3'-diaminobenzidine as a chromogen, for double-labeling immunofluorescence several markers used
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DGK-IVksi
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distinct and highly regionalized patterns of expression in the adult brain
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distributed throughout the brain, with high expression in the retrosplenial cortex and in hippocampal neurons
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distribution in brain areas
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distribution in brain regions of cytosolic and particulate 5alpha-dihydroprogesterone 3alpha-hydroxysteroid oxidoreductase activity
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distribution in brain tissues
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distribution in brain tissues, immunohistochemic analysis, overview
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distribution in the brain
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distribution in tissues, brain most active source
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distribution of BB-type MB-type and MM-type iszozymes
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distribution of NAPE-PLD in various brain regions and its age-dependent expression
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distribution of POP immunoreactivity in the rat brain and its colocalizations with IP3R1 and SP markers shown
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distribution of sPLa2-IIe, sPLA2-V, and sPLA2-X is mainly neuronal with highest abundance in cerebral cortex and hippocampus. Enzymes are differentially induced by kainic acid
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dopamine-producing cells in the substantia nigra
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dorsal and median raphe
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dorsal raphe nuclei
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dorsal raphe nucleus, expression analysis and enzyme levels of TPH2, quantitative immunoautoradiography and in situ hybridization histochemistry, overview, activity occurs also in striatum, nucleus accumbens and cingulate cortex
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during embryonic development GCDH is predominantly expressed in neurons of the central and peripheral nervous system. Significant expression in brain of adult animals
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embryonic
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embryonic brain
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embryonic brain cells, the enzyme is present at relatively low levels for the first 9 days in culture, but it increases steadily between days 9 and 30
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embryonic, D-Asp initially emerges in the hindbrain and then spreads into the forebrain. Within nerve cells of the rat embryonic brain, D-Asp first occurs in the cell bodies of neuroblasts in the outer layer of the neuronal epithelium, and then it appears in the processes of the cells
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embryonic. PLD2 immunoreactivity is first observed in the chotoid plexus and in the most ventricular zone of the lateral and third ventricles at embryonic day 15, followed by gradual restriction to the limited zone of the ventricles at embryonic day 20. PLD2 expression is high in the developing cerebral cortex and hippocampus. In der cortex, PLD2 expression is observed in the marginal zone from the earliest stage and then declines and completely disappears by embryonic day 20
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enolase I (alpha,alpha-enolase), enolase II (alpha,gamma-enolase), enolase III (gamma,gamma-enolase)
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entire ventricular zone and tegmentum, ciliarly ganglion, inferior olive, interpeduncular nucleus, red nucleus, dorsal tegmental nucleus and nuclues of the lateral lemniscus
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enzyme activity expressed only in oligodendrocytes
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enzyme activity remains low during all stages of development
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enzyme expression analysis in male and pseudopregnant female rat brain, in situ hybridization, overview, strong expression in olfactory bulb, striatum, cortex, thalamus, hypothalamus, septum, habenula, hippocampus and cerebellum, pseudopregnancy has no effect on enzyme expression in brain, effect of lesions, overview
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enzyme form AAA-1 shows highest specific activity in corpus striatum and lowest activity in cerebellum, enzyme form AAA-2 shows highest specific activity in cerebellum and lowest acticity in corpus striatum
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enzyme in sustantia nigra and globus pallidus is localized on nerve terminals originating from neurones in the caudate putamen
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enzyme levels in healthy and injured brain, primary rat microglia, overview
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enzyme type L and enzyme type B
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epithelial cells of brain
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equally distributed in all areas of the brain
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especially in frontal and temporal cortex, the level of L-pipecolate is highest in the cerebellum
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especially midbrain and cerebellum, quantitative detection of GCPII content in the brain by labeling with [125I]-N-[N-((S)-1,3-dicarboxypropyl)carbamoyl]-S-3-iodo-L-tyrosine is a potent antagonist of the enzyme activity
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estrogen regulates neprilysin activity in brain. Ovariectomy leads to a 30% decrease in neprilysin activity at 45 or 85 days, but not 21 days, post surgery
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ethanol induces a transitory increase in NEP activities in the frontal cortex and ventral tegmental area, and in the nucleus accumbens
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expression analysis for CaMKI
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expression analysis in brain after implantation of 9L glioma cells, overview
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expression analysis of TPH2
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expression at different developmental stages, highest specific activities of DOHH occur in the parietal cortex during the first 5 days of life. After this period, DOHH activity declines to less than 50% of the level in the newborn within 15 days
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expression level of 1a-type mRNA, encoding the active enzyme form is higher than that of 1b-type mRNA, encoding an inactive enzyme form
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expression of both isozymes, the isozyme KGA/LGA ratio is very high in brain
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expression of CK1epsilon-1, CK1epsilon-2, CK1epsilon-3
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expression of enzyme is developmentally regulated, with increasing expression during maturation of the CNS, reaching the maximum in young adulthood
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expression of long-rSK1 mRNA
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expression of soluble epoxide hydrolase is significantly lower in stroke-prone than in stroke-resitant rats. Identification of 3 polymorphisms that significantly influence promoter transcriptional activity in vitro
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expression pattern of sGC in tissue form wild-type and spontaneously hypertensive rats, e.g. in rostral ventrolateral medulla, overview
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expression profile of Cyp46 in the brains of intact, sham-operated, and lesioned animals, overview. Ablation of the sensorimotor cortex induces increase of Cyp46 immunoreactivity in the ipsilateral cortex
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extrapineal distribution
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fetal
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fetal and adult
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fetal brain
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fetal brain: GAD67, adult brain: GAD67 and GAD65
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fetal, low ACE mRNA expression
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forebrain
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from male rats
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from rats fed on different, e.g. alpha-linolenic acid-deficient, diets
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from rats with unilateral depletion of dopamine in the substantia nigra compacta treated with L-DOPA at 30 mg/kg body weight for 34 days, nNOS expression is restricted to neurons
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frontal cortex
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gene is expressed by all neurons of the adult brain, but mostly in the hippocampus, cerebral cortex and large neurons of the deep cerebellar nuclei, as well as the Purkinje and granular cells of the cerebellum
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glial localization in cerebellum
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glutathione-independent enzyme
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grey and white matter
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healthy and ischemic
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heparanase protein is mainly detected in neurons. Heparanase transcript and protein reach their greatest levels at early postnatal stages, in particular within the neocortex. At adulthood the increased heparanase transcript level correlates in the hippocampus with enhanced angiogenesis following repeated hypoxia exposures. Potential importance of heparanase in brain homeostasis
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heterogenous expression of spermidine synthase, which primarily localizes to neurons and neuropil. Highest levels of expression in accumbens nucleus, taenia tecta, cerebellar cortx, cerebral cortical layer I, hippocamppus, hippothalamus, mesencephalic raphe nuclei, central and lateral amygdala, and the circumventricular organs
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hexokinase I
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high activity
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high amounts of TPPII mRNA are detected in neocortex, especially in the frontal region and the hippocampus
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high basal expression with 2.3-fold increase in mRNA after 6 h of hypoxia
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high CaM kinase II expression, highly regulated activity in brain development, distribution overview
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high CDase expression
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-
high enzyme activity
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high enzyme activity. GGTI expression and activity are particularly enriched in the adult brain and developmentally regulated after birth in various mammalian tissues
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high enzyme content
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high expression
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high expression level of neutral ceramidase
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high expression level, increased expression level during development
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high level of isoform PDP1 and PDP2
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high levels in adenohypophysis
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higher activity in cerebral cortex and hippocampus than in hypothalamus, pons, medulla and olfactory bulbs
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-
highest activity
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highest activity in cerebellum, distribution in various brain regions
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highest activity in choroid plexus, substantia nigra, caudate putamen, globus pallidus, olfactory tubercle, nucleus accumbens. Moderate activity in amygdala, interpenducular nucleus, molecular layer of the cerebellum, periaqueductal gray matter, and the hippocampus
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highest activity in fetal and young rat brains
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highest activity in hippocampal pyramidal neurons, as well as cerbellar granule cells and Purkinje cells. Some interneurons are also labeled and many thiamine triphosphatase mRNA-positive and immunoreactive cells are distributed thoughout cerebral cortical gray matter and the thalamus. No significant activity in white matter
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highest activity in hippocampus. In all brain areas membrane-bound enzyme activity is lower than soluble enzyme activity
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-
highest activity in the cortex, lowest activity in the striatum and hippocampus
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-
highest activity in the synaptosomal and myelinic fractions
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-
highest concentration in striatum and midbrain
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-
highest enzyme activity
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highest expression in cerebellum, lowest in hippocampus, intermediate in cerebral cortex
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-
highest in cerebellum, lowest in telencephalic structures
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highest level of expression in young rats
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-
highest levels in brain and spinal cord
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highest mRNA contents in cerebellum and diencephalons
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-
highly expressed
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highly expressed in selected olfactory regions, in septal and hypothalamic nuclei, throughout the hippocampal formation and cerebral cortex, and in motor and motor associated nuclei. IRAP is expressed exclusively in neurons in these regions
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hippocampus
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hippocampus and parietal cortex
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hippocampus, cerebellum and neocortex
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-
HO-2
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hypothalamic paraventricular nucleus and tanycytes
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-
immuno-chemical localization of biliverdin reductase protein in normal brain correlates well with the presence of HO-1 and HO-2 throughout the forebrain, diencephalon, cerebellum and brainstem regions
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immunocytochemical visualization of sulfinoalanine decarboxylase with a specific antiserum
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immunohistochemical study on distribution
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immunoreactive enzyme detected exclusively in neurons, primarily in axon-like structures and presynaptic elements. No enzyme in noradrenaline cells or terminals. Enzyme immunopositive cells mostly also express hypocretin-1/orexin-A
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immunoreactivity of APA in the medulla oblongata, the rostral ventrolateral medulla, and ambiguous nucleus
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in adult brain, the relative activities of alpha-, beta I-, beta II-, and gamma-subspecies are roughly 16%, 8%, 55%, and 21%
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in adults primarily expressed in neurons, including those of the hippocampus and cortex. Embryos have markedly decreased expression levels. Batk may be upregulated at birth throughout the brain except in the cerebellum
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-
in all parts of the brain
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in all regions of the adult rat brain
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in choroid plexus epithelial cells, glial cells of pons, medulla oblongata, and especially in Bergmann glia of cerebellum
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in embryos at 15.5 days of gestation guanidinoacetate N-methyltransferase is detectable in pons and striatum. In embryos at 18.5 days of gestation guanidinoacetate N-methyltransferase is detectable in neocortex, hippocampus, striatum, pallidum and spinal cord. Non-radioactive in situ hybridization (58°C for 40 h in 5 x SSC, 50% formamide and 40 microg/ml salmon sperm DNA) with digoxigenin-labeled antisense and sense riboprobes (400 ng/ml) for rat guanidinoacetate N-methyltransferase. guanidinoacetate N-methyltransferase proteins are detected with rabbit polyclonal antibodies
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-
in global cerebral ischemia STEP mRNA is selectively down-regulated in brain areas susceptible to ischemic damage, while in regions of the brain that are relatively resistant to ischemic damage STEP mRNA levels are increased
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-
in globus pallidus and substantia nigra much of the enzyme is associated with presynaptic nerve terminals originating from efferent striatal neurons
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in internal structures of cerebellum, hippocampus, and corpus callosum
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in raphe nuclei, in lateral hypothalamic nuclei and in pineal body
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-
in rat brain, the P-protein is confined to astrocytes. The intensity of astrocyte staining varies with regions, with the strongest staining in the hippocampus, the cerebellar cortex, the Bergmann glia in the cerebellum and the Muller cells in the retina
brenda
in situ and in vitro enzymatic activity of transglutaminase isoforms on brain tissue sections and brain extract, monitoring of differences in post-translational protein modifications during neurodegeneration, overview. TG6 shows only a faint vascular signal as compared to a prominent cellular staining in rat tissue
brenda
in situ hybridization, quantitative expression analysis in brain of wild-type and tremor rats, overview
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in striatum, THOP1 activity decreases following sleep deprivation and a recovery period
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-
in the cortex, activity of soluble PGP I and particulate PGP I decreases 5fold and 4fold, respectively, from the embryo to the adult
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in the gray matter, AADC neurons are not only found in the region around the central canal but also in the dorsal horn, intermediate zone, and ventral horn. In the white matter a large number of glial cells are AADC-immunopositive in different spinal segments and the vast majority of these cells express oligodendrocyte and radial glial phenotypes. Additionally, a small number of AADC neurons are found in the white matter along the ventral median fissure
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-
in the group of rats aged 12 months, the highest specific activity is found in the small intestine
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inactive isozyme mAH multimers occur in rat brain in a model of Huntingtons disease
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increased expression of 12/15-LOX, predominantly in neurons, and elevated production of 12(S)-hydroperoxyicosatetraenoate and 15(S)-hydroperoxyicosatetraenoate in ischemic brain
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-
ingestion of lower quantity and quality of dietary protein are likely to control the mRNA level and concentration of NGF, and cause a decline in the activity of choline acetyltransferase in the brains of young rats
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-
inhibition of caspase-1 in rat brain reduces spontaneous nonrapid eye movement sleep and nonrapid eye movement sleep enhancement induced by lipopolysaccharide
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-
inhibition of phosphoglucomutase activity by chronic treatment with Li+ causes alterations of glucose-phosphate level with compensatory elevation of phosphoglucomutase activity
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-
InsP3 3-kinase A and B mRNA
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-
intensely detected in neuronal cells of the hippocampal formation, olfactory bulbs, cerebellum, cerebral cortex and nuclei in the brainstem
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-
involvement of brain phosphatidylinositol-specific phospholipase C in the centrally administered histamine-induced activation of the adrenomedullary outflow in rats
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-
iPLA2
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-
is colocalized with tau protein and GSK3beta in brain cortex
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-
ischemic cortex, ipsilateral penumbra area, pyriform cortex, hippocampus, leptomeninges
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-
isoenzyme A is the major isoform present in neuronal cells
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isoenzyme MEK5 beta
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-
isoenzyme PRSI
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-
isoenzymes PD I and PD II. PD II activity is highest in the hippocampus, followed by the cerebellum, cerebral cortex, caudatum, and the midbrain. Age-related alterations in PD I and PD II
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-
isoform A
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-
isoform C
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-
isoform I
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-
isoform PDE5A shows an age-related increase or decrease in mRNA expression in at least 1 of the 4 brain regions examined (hippocampus, cortex, striatum, and cerebellum). mRNA expression of isoform PDE9A does not change with age. Age-related increases in PDE11A4, and PDE1C1 protein expression are confirmed in hippocampus of old versus young rodents, as are age-related increases in PDE8A3 protein expression in the striatum
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isoform SULT2B1a
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-
isoforms PDE1B, PDE1C, PDE2A, PDE10A, and PDE11A show an age-related increase or decrease in mRNA expression in at least 1 of the 4 brain regions examined (hippocampus, cortex, striatum, and cerebellum). mRNA expression of isoforms PDE1A, PDE3A, PDE3B, PDE4B, and PDE9A does not change with age. Age-related increases in PDE11A4, and PDE1C1 protein expression are confirmed in hippocampus of old versus young rodents, as are age-related increases in PDE8A3 protein expression in the striatum
brenda
-
isoforms PDE4A, PDE4D, PDE7A, PDE8A, PDE8B show an age-related increase or decrease in mRNA expression in at least 1 of the 4 brain regions examined (hippocampus, cortex, striatum, and cerebellum). mRNA expression of isoforms PDE7A, PDE7B does not change with age. Age-related increases in PDE11A4, PDE8A3, PDE8A4/5, and PDE1C1 protein expression are confirmed in hippocampus of old versus young rodents, as are age-related increases in PDE8A3 protein expression in the striatum
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-
isozyme 2-oxoglutarate dehydrogenase-like protein
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-
isozyme HO-2
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-
isozyme PKNalpha
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-
isozyme topoisomerase IIbeta
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-
isozyme type III
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-
isozyme-specific and developmental stage-specific alterations in brain PKC following exposure to a polychlorinated biphenyl mixture
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-
isozymes dymain 1, dymanin 2, and dynamin 3
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-
isozymes IP33K-A, IP33K-B, and IP33K-C
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-
isozymes LGA and KGA
brenda
Itpka is particularly active in neurons of the hippocampus and cerebellum
brenda
-
KAT I activity in glial cells of striatum, in astrocytes of the hippocampus and in glial cells of the temporal lobe
brenda
-
KAT I and KAT II
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-
L-COMT is the predominant enzyme form
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-
left and right dorsolateral prefrontal cortex, immunohistochemic IDE expression analysis, overview
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-
lesioned and contralateral striatum
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-
levels of thyroid hormone binding capacity for cytosolic NADPH-dependent T3 binding are noticeably lower in the cerebellum than in the cerebrum of adult rat brain at all stages of development. NADPH-dependent T3 binding is only detected in kidney, liver, heart and spleen after birth, increasing over the next 6 weeks. NADPH-dependent T3 binding is detected in cerebrum and cerebellum 5 days before birth, increasing with a sharp transient spike at the time of birth, that is specific for the brain, particularly in cerebrum, and cannot be seen in other tissues. The NADPH-dependent T3 binding in cerebrum decreases after birth, but begins to increase again 2 weeks after birth. The level in cerebellum does not show this increase. The brain may contain at least two distinct P2C reductases/ketimine reductase, one of which is predominant in the fore-brain and another that is prominent in the cerebellum
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-
limbic system and cerebellum
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-
limbic system, induced and uninduced enzyme activity in different structures, overview
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-
lipoyl-p-aminobenzoic acid hydrolase activity is highest in liver, brain and kidney
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-
located mainly in astrocytes
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long-term aluminium feeding results in activation of monoamine oxidase A up to 1.9fold
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long-term aluminium feeding results in activation of monoamine oxidase B up to 3.8fold
brenda
-
low
brenda
-
low activity
brenda
-
low activity in female and male rats, constant at age 2 months to age 9 months
brenda
-
low content
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-
low content L-CPT I and CPT II
brenda
-
low enzyme activity
brenda
low expression level
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-
low level
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-
lower activity in cortex than in whole brain
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-
lower level than in liver
brenda
-
lowest activity of the tissues tested
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-
lowest specific activity
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-
lysed synaptosomes
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-
M-type, i.e. muscle-type, C-type, i.e. fibroplast-type, and L-type, i.e. liver-type, PFK isoforms
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-
M1-type isozyme
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mainly expressed in
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-
major activity
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maximal expression level of MsrA in kidney and liver, followed by heart, lung, brain, skeletal muscle, retina, testis, bone marrow, and blood
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-
measurement of creatine kinase activity (hippocampus, striatum, cerebellum, cerebral cortex and prefrontal cortex) in brain if rats are submitted to renal ischemia and the effect of administration of antioxidants (N-acetylcysteine, N-acetylcysteine and deferoxamine, deferoxamine) on this enzyme. Creatine kinase activity is not altered in cerebellum and striatum of rats. Creatine kinase activity is inhibited in prefrontal cortex and hippocampus of rats 12 h after renal ischemia. The treatment with antioxidants prevents such effect. In cerebral cortex creatine kinase activity is inhibited 6 and 12 h after renal ischemia. Only N-acetylcysteine or N-acetylcysteine plus deferoxamine are able to prevent the inhibition on the enzyme. Although it is difficult to extrapolate the findings to the human condition, the inhibition of brain creatine kinase activity after renal failure may be associated to neuronal loss and may be involved in the pathogenesis of uremic encephalopathy
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-
membrane-bound COMT activities in the cerebral cortex are significantly reduced in high-salt loaded Dahl salt-sensitive rats compared with normal-salt loaded Dahl salt-sensitive rats
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-
membrane-bound isoform MB-COMT is predominant
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-
mercury decreases porphobilinogen-synthase activity
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-
methylmalonyl-CoA mutase and propionyl-CoA carboxylase enzymes are co-expressed in neurons and found in all regions of the central nervous system except in astrocytes and oligodendrocytes. The highest expression in the developing brain is in the periventricular zones of telencephalon, midbrain, and rhombencephalon. The highest expression levels of MCM in adult rat CNS are in neocortex and hippocampal formation, thalamic and hypothalamic nuclei, midbrain nuclei such as the red nucleus and substantia nigra, as well as pons, medulla and the Purkinje and granular layers of cerebellum
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-
MGL is localized to axon terminals throughout the brain
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-
microvessel
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-
microvessel of endothelial cells, immortalized cell line
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-
microvessels
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-
midbrain
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moderately high expression
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-
more abundant in fetal than in adult rat brain
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most abundant in
brenda
mostly in the hippocampus and cerebellum
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-
MsrA
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-
muscle isozyme
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-
myelin
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-
NADH-linked 5alpha-dihydroprogesterone 3alpha-hydroxysteroid oxidoreductase activity is decreased by 40-50% in lactating rats
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-
native enzyme, insulysin is able to form a stable complex with amyloid beta
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-
negative correlation between locomotion of rats in the open field and activity of G-6-PDH in the sensorimotor cortex, especially in efferent layer V neurons and neurons of the caudate nucleus and nucleus accumbens, which attests to different capacity of the brain in Wistar rats with high and low open-field locomotion to regeneration of phosphopyridine nucleotides (NADP(+)) and production of pentoses via the pentose phosphate shunt. No correlation between enzyme activity in the hippocampus and locomotion
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-
neocortex
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neonatal male rat brain
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NEPII is expressed heterogeneously among several neuronal populations
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-
nerve cells of the cerebral cortex, microglia, Golgi epithelial cells, Bergmann glia cells. Activity in brain is low, but steadily increases after birth. No activity in neurons of the cerebellar cortex
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-
nerve endings from forebrain
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-
nerve endings from forebrains
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-
nerve terminals
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-
neuron, DGK-Ibeta
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-
neuron, including the pyramidal cells of the hippocampus and the Purkinje cells of the cerebellum, the regional localization varies, with high levels of expression in the hippocampus, the dentate gyrus, the outer cortices of the brain, and the substantia nigra
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-
neuronal AMPK
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-
neuronal enzyme
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-
neurons and astrocytes
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-
nNOS
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nNOS is the predominant isozyme in brain
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-
no activity in liver
brenda
-
no difference in enzyme activity between young and adult animals
brenda
-
no significant changes in the enzyme activity between morphine-treated and control samples
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-
normal brain aging is associated with significant increases in the activity of monoamine oxidase. Dehydroepiandrosterone treatment significantly decreases monoamine oxidase activity, lipid peroxidation and lipofuscin accumulation in brain regions of aging rats
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-
nuclear accumbens shell and core, prefrontal cortex
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-
nucleus accumbens and dorsal striatum
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-
of adult
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-
of embryo
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-
of fetus
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-
of fully or partially kindled rats. Aminopeptidase N mRNA levels are decreased at stage II and increased at stage V of kindling, in frontal cortex-olfactory tubercle, and hippocampus. Neprilysin and aminopeptidase N enzymatic activities, follow similar variations to their respective mRNA levels. The coordinated changes of neprilysin and aminopeptidase N expression are opposite to those previously observed for pyroglutamyl peptidaseII mRNA and activity levels in limbic regions
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-
of normal and triethyltin-intoxicated rats
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-
of wild-type and striatal 6-hydroxydopamine lesioned rats
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-
oligodendrocyte, DGK-Ialpha
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-
paranigral lipopolysaccharide infusion to rats results in intense microglial activation around the lesion area followed by a delayed injury in nigrostriatal pathway in 2 weeks. Simultaneously, catechol-O-methyltransferase activity in the substantia nigra is gradually increased up to 213%. Soluble COMT and membrane bound COMT proteins are increased by 255% and 86%, respectively. Increased catechol-O-methyltransferase immunoreactivity is located primarily into the activated microglial cells in the lesion area
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-
paraventricular nucleus, lateral hypothalamus and ventromedial nucleus
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parietal cortex
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particularly enriched in cerebellar granule cells
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-
PC2 is the most abundant PC in the brain
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PCTAIRE 2 is concentrated in the neuronal layers of the hippocampus and olfactory bulb, which mostly consist of post-mitotic neurons. PCTAIRE 2 is detected in the cell bodies and extended neurites of neurons, but not in astrocytes
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-
PDE10A is strongly expressed in the brain, highly expressed in striatal complex including caudate putamen, nucleus accumbens, and olfacory tubercle
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-
penumbra
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-
pericyte
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-
pericyte and almost all structures, hyperactive in RAS and SHR, distribution overview
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-
phosphatidylinositol 4-phosphate 5-kinase Igamma_v6 is not a major brain variant
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-
PIPP enzyme
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-
PLC delta1, delta3 and delta4
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Pomt1 and Pomt2 mRNA are coexpressed in neurons (dentate gyrus and CA1-CA3 region of the hippocampus and cerebellar Purkinje cells)
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-
poor activity
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-
post-natal, developing, neuron-specific isozymes DGKbeta and DGKgamma, and isozyme DGKalpha, isozymes alpha and gamma appear at birth and then decline, while isozyme beta appears about 14 days after birth and reaches a maximum at day 28, overview
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-
postnatal increase of activity
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ppGaNTase-T9, less amount
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-
predominantly located in the dendrides
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preferentially expressed in brain and pancreas
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-
presence of 2 isoforms
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-
presence of enzymatically active DHODH in many regions of the central nervous system, albeit at different intensities. High levels of both DHODH activity and immunoreactivity are observed in the neocortex, hippocampus, spinal cord and choroid plexus. Lower levels are seen in the cerebellum, and only marginal expression in brain stem
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presence of mRNA as well as protein of both subunits of 3-methylcrotonyl-CoA carboxylase in ependymocyte, microglial cell and oligodendrocyte cultures derived from the brains of newborn rats
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-
presence of the enzyme in the membranes surrounding neuronal somata and apical dendrites and less frequently in astrocytes
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-
primary hippocampal and corical cultures
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primary hippocampal neuron
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PRMT5 expression gradually increases throughout postnatal brain development, coinciding with the period of active myelination
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-
prostaglandin-H2 D-isomerase is produced in the membrane system surrounding the brain and is secreted into the cerebrospinal fluid to become beta-trace
brenda
-
proteasome composition in brain, overview
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-
Purkinje cells, DGK-Igamma
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raphe nuclei
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-
region of the raphe nucleus of rat midbrain
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-
regional activities in brain
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regional and cellular distribution of beta-ARK 1 and 2 in brain
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-
regional distribution
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-
relatively small amounts
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repeated nandrolone decanoate administration reduces activity of monoamine oxidase A
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repeated nandrolone decanoate administration reduces activity of monoamine oxidase B
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-
sGC beta1 is the most abundant and ubiquitous subunit
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-
silencing of choline acetyltransferase expression by lentivirus-mediated RNA interference
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six-week intermittent hypoxia increases NEP expression and activity, selectively in temporal cortex, but not in the hippocampus and frontal cortex. The increase in NEP activity and expression is reverted followed by two weeks recovery in normoxia
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Sky receptor may play an important role in development, function, and maintenance of specific neuronal populations in the central nervous system
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-
slight activity
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-
smMLCK expresses in almost every tissue, including brain
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-
soma
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-
spatiotemporal expression of four isoforms of CaMKI in brain, isozyme CaMKIbeta2 is a brain-specific splicing variant, overview
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-
specific expression of UCH-L1
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specific isozyme PFKFB2
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-
stem
brenda
-
striatal neurons
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-
striatum
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-
striatum and olfactory tubercle
brenda
-
strictly localized in astrocytes in the cerebellum and in the hippocampus
brenda
strong expression
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-
substantia nigra and ventral tegmental areas
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-
subventricular zone rostral extension, CNPase expression pattern during development from postnatal day 3 to 60
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SULT1A1, mainly striatum, lower contents in cortex, hippocampus, and cerebellum
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SULT2B1a is only expressed in brain and testis
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-
suprachiasmatic nucleus
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synapses
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synaptic junctions
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-
synaptic membrane
brenda
-
synaptosomal fraction
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-
synaptosomes
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-
temporal cortex of amyloid beta(25-35)-infused and healthy rats
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-
testis enzyme is about 4fold more active than brain enzyme
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-
testosterone concentrations during postnatal sexual differentiation of the rat Ccentral nervous system, among other sex-dependent factors, influence brain levels of 5alpha-reductase isozymes in adulthood and the pattern of their regulation by androgen hormones
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-
thalamus, hypothalamus and pons, mRNA expression in the subiculum, the pyramidal cell layer of cornus ammonis and the granular cell layer of dentate gyrus, mRNA expression is discretely focussed in a cortex-side layer of Purkinje cells, streptozotocin-induced diabetes does not change the localization profile of SCOT mRNA
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-
the brain enzyme is regionally and developmentally regulated
brenda
the cells which strongly express the sgk gene are in the deep layers of the cortex and in the corpus callosum. It is likely that the sgk transcript is expressed by oligodendrocytes after brain injury. Neurons in layers I and II of the cortex, lateroposterior and laterodorsal thalamic nucleus, and ventral posterolateral and posteromedial thalamic nucleus strongly express sgk mRNA at postnatal day 1 and day 7, but these neurons show no expression in fetal or adult brain. Induction of sgk gene may be associated with a series of axonal regenerations after brain injury, and in addition, the sgk gene may also play important roles in the development of particular groups of neurons in the postnatal brain
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-
the distributions of H3-K4 mono-, di-, and tri-methylated histones exhibit exactly the same pattern as the LSD1 protein, immunofluoresecence histochemic analysis, overview
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-
the enzyme from brain is similar or identical to that present in liver
brenda
-
the enzyme is distributed in most brain regions of rat with higher activity in soluble proteins extracted from striatum and substantia nigra
brenda
-
the enzyme is found in all parts of the brain in the membraneous subcellular fractions of neurons
brenda
-
the enzyme is lowly expressed in the molecular layer of the cerebral cortex and hippocampal layers, and highly expressed in other areas of the brain
brenda
-
the enzyme is not expressed after ischemic infarct
brenda
-
the enzyme is prominently expressed in the striatal patch compartment and in putative interneurones of the matrix compartment
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-
the expression of TACE is increased in intermittent and prolonged hyperoxia
brenda
-
the highest activity
brenda
-
the level of PLD2 in both the cerebrum and hindbrain is minimal compared to that of PLD1
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-
the majority of the SULT1E1 activity is observed in the frontal cortical area, superior cortical areas, subcortical areas, and brain stem
brenda
the number of Sqrdl transcripts in the brain increases with increasing age
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-
the presence of glucokinase phosphorylating activity is detected in different brain areas of 21-day-old foetuses with a contribution to the total glucose-phosphorylating activity of between 17.2% and 12.4%
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-
the type IIalpha enzyme is concentrated both at the synapse and in the region of the Golgi complex in neuronal perikarya
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-
there is little CNP2 in the forebrain postsynaptic density fraction, CNP1 is the major isoform in the neural and non-neural rat tissues, with the exception of myelinating cells in the adult brain, in which both isoforms are highly expressed, CNP2 is barely detectable in embryonic brain
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-
third ventricle of the brain
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-
transcriptional regulation of ACE2 mRNA in astrocytes is dependent on the relative concentrations of both angiotensin II and angiotensin(17) as well as on interaction with their respective receptors
brenda
-
transcripts of L, X and Y mRNAs are detected
brenda
-
treated with pentylenentetrazol, an antagonist of GABAa receptor ion channel binding site. Significant decrease of enzyme activity and protein in the hippocampus after administration of pentylenentetrazol, pretreatment with MK-801 recovered the change of activity
brenda
-
treatment with 1,2,3,4-tetrahydroisoquinolone affects the enzymatic activity of gamma-glutamyl transpeptidase in the dopaminergic structures of brain
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-
triatum
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twenty-four hours after bilateral contusion of the medial prefrontal cortex, similar levels of 3beta-hydroxysteroid dehydrogenase mRNA expression are observed in males and pseudopregnant females in the non-injured group, with a significant decrease in the 3beta-hydroxysteroid dehydrogenase mRNA expression in the contusion site within the frontal cortex in both males and pseudopregnant females. In all other regions analyzed, 3beta-hydroxysteroid dehydrogenase mRNA expression is not affected by traumatic brain injury and there is no difference between males and pseudopregnant females
brenda
two alternative splicing isoforms of CaMKIgamma, expression patterns in brain regions, such as the olfactory bulb, hippocampal pyramidal cell layer of CA3, central amygdaloid nuclei, ventromedial hypothalamic nucleus, and pineal gland, overview
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-
two electrophorectic forms
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-
upregulation of active MMP-13 in rat brains after 90 min of cerebral ischemia
brenda
ventral striatum, hippocampus, and frontal cortex
brenda
-
very low activity
brenda
-
very low expression level of WNK1
brenda
-
very low level
brenda
visual cortex, use of the NADPH-d histochemistry technique to evaluate the expression of NOS across the nervous system
brenda
-
weakly expressed
brenda
-
Western blot analysis of PLD in the cerebrum shows that PLD1, a major PLD isoform in the brain, is detected weakly in the cerebrum at day 17 embryonic stage and its levels gradually increase until postnatal day 35 and remain unaltered thereafter
brenda
-
white matter contains a more than 2-fold higher activity than cortex
brenda
widely distributed in various brain regions of rat, with the highest activity in the brain stem. The enzyme activity in rat brain changes during development, and infant rats show a several-fold higher activity than adult rats
brenda
-
widespread in brain
brenda
-
widespread in the gray matter, not found in the white matter
brenda
-
642888, 651540, 661901, 663925, 665836, 666460, 672503, 673705, 679665, 681643, 681935, 683389, 683926, 685334, 686570, 688608, 688814, 691231, 692179, 694394, 697491, 699606, 699685, 700426, 700477, 704640, 705259, 705503, 706831, 707801, 707929, 708399, 711731, 711794, 712829, 716639, 723787, 730120, 739470, 741580, 753121
brenda
-
frontal cortex, single inescapable shock reduces PI-PLC activity in the frontal cortex and hippocampus of learned helplessness rats. Repeated inescapable shock not only reduced PI-PLC activity but also selectively decreases the expression of PLCbeta1 and PLCgamma1 isozymes
brenda
-
high expression of QC in neurons of several cell layers of the cortex and hippocampus
brenda
-
prefrontal
brenda
prefrontal cortex
brenda
SULT1A1
brenda
-
-
brenda
-
medial prefrontal brain cortex
brenda
-
439477, 640746, 659578, 661683, 664474, 669636, 675509, 688009, 691561, 698532, 708319, 708686, 727633, 762740, 765779
brenda
-
about 20% of the ACE2 gene expression in kidney cortex
brenda
-
alpha and beta isozymes
brenda
-
cerebrum shows higher activity than cerebellum
brenda
-
cerebrum, cerebellum and brain stem of 14 and 21 days old rats
brenda
-
pChAT+ nerve fibers are found exclusively in the trigeminal and solitary systems. The ventral portion of the principal sensory nucleus contains many pChAT+ fibers
brenda
-
the contribution of glucokinase to total glucose-phosphorylating activity is of 12.4% in the brainstem
brenda
TPH2 mRNA expression in the midbrain part of the dorsal raphe nucleus and in the brainstem containing the rest of the raphe complex
brenda
-
very low enzyme level
brenda
-
very low level both of expression and activity
brenda
-
brenda
N-methyl nitrosourea (NMU)-induced breast cancer
brenda
-
BRL3A cell line
brenda
-
liver cell line served as host for vesicular stomatitis virus
brenda
O35547, O55171, O88267, O88813, P12694 AND P21953, P14882, P18163, P33124, P35571, Q63151, Q64559, Q9Z244
-
80992, 95805, 394293, 487416, 487418, 646112, 646161, 651443, 656431, 664215, 666181, 675267, 705936, 706844, 714050, 714316, 722713, 740537, 762713, 763434
brenda
-
cell culture
brenda
-
contains carbonic anhydrase I, III and III
brenda
-
CPT II, M-CPT I, L-CPT I
brenda
-
di-(2-ethylhexyl)phthalate-inducible acetyl-CoA hydrolase activity
brenda
embryo, high level
brenda
-
high activity in female and male rats, decreasing from age 2 months to age 9 months
brenda
-
interscapular
brenda
-
interscapular brown adipose tissue
brenda
isozyme Acc2
brenda
-
isozyme type II
brenda
-
isozyme type III
brenda
-
M-CPT1 isozyme
brenda
-
644002, 671608, 677215, 679669, 680257, 682121, 682285, 687604, 688759, 690140, 690143, 690846, 692085, 693933, 694138, 705283, 705322, 707558, 709276, 710078, 714913, 715713, 760646
brenda
astrocytoma
brenda
astrocytoma, PI-PLC delta3
brenda
-
cell line expresses aromatase mRNA and shows a cytoplasmic pattern of aromatase immunoreactivity. In addition, the cell line expresses estrogen receptor alpha
brenda
-
glioma C6 cell line
brenda
-
glioma cell line
brenda
-
glioma cells
brenda
-
lower level of expression of both AMPD2 and AMPD3 than neurons, and a lower expression of AMPD3 than astrocytes
brenda
-
upreglation of gamma-glutamyl transpeptidase is induced by suboptimal concentrations of the serum and modification of intracellular cAMP level by dibutyryl cAMP. Up-regulation of gamma-glutamyl transpeptidase can contribute to adaption of astrocytic cells to metabolic and/or oxidative perturbances occuring under various pathological conditions, including radiation- and drug-induced toxicity
brenda
-
-
brenda
-
weak enzyme expression
brenda
-
brenda
-
mammary adenocarcinoma cell, expression of high levels of enzyme
brenda
-
-
brenda
-
Walker rat 256 cell
brenda
-
34477, 80870, 134613, 134638, 209387, 209388, 209393, 246966, 285699, 286726, 287888, 639901, 642279, 643979, 647271, 653282, 664537, 665243, 692267, 741580, 752440
brenda
5fold lower than in unstimulated brown adipose tisssue, no increase during cold-stress
brenda
-
cMLCK is exclusively expressed in cardic muscle, smMLCK expresses in almost every tissue, including cardiac muscles
brenda
-
heart ventricle
brenda
-
high activity
brenda
-
hypoxia activates glycogen synthase in fed rat myocardium through a combination of rapid glycogenolysis, elevated local glucose 6-phosphate content, and increased protein phosphatase 1 activity, and fasting attenuates this action independent of local glucose 6-phosphate content. Activation of glycogen synthase in myocardium induced by intermittent hypoxia is much lower in fasted than in fed rats
brenda
-
PLC delta3 and delta4
brenda
-
756086, 760135, 760466, 761466, 761515, 762615, 762716, 766946, 770227, 772308, 776083
brenda
ventricular
brenda
-
661498, 668269, 672635, 673104, 676101, 676316, 677930, 693696, 694346, 697356, 704433, 712794, 716279, 716810, 720447, 722774, 743576
brenda
-
colocalized with cyclooxygenase-2
brenda
-
expressed both at transcript and protein levels
brenda
-
expression of several isozymes
brenda
neonatal
brenda
-
NRCM
brenda
-
primary cell culture
brenda
-
ventricle
brenda
-
WY-14643 causes a significant induction of cte1 in isolated adult rat cardiomyocytes
brenda
-
brenda
-
H9c2 cardiomyolbasts, ATCC CRL 1446
brenda
-
670034, 672941, 673104, 673668, 674683, 676101, 683354, 685974, 687975, 688449, 690344, 690926, 691840, 692271, 693123, 694143, 698208, 700511, 700512, 703143, 703234, 707036, 708015, 708016, 709213, 711965, 712415, 721982, 730008, 735146, 736319, 738284, 738639, 739053, 739745, 740279, 742457, 743188, 743634, 747446, 754128, 754244
brenda
-
adult ventricular
brenda
-
both DDAHI and DDAHII proteins are detected in peri-infarct cardiomyocytes, while DDAHII immunoreactivity is additionally localized to infiltrating inflammatory cells and blood vessels in the healing infarct. Both plasma and left ventricular concentrations of the DDAH substrate, ADMA, are increased post-myocardial infarction
brenda
cardiomyocyzes cultured in vitro
brenda
cultured neonatal rat cardiomyocytes (NRCMs)
brenda
-
inhibition of creatine kinase blunts high extracellular Ca2+-induced increases in cardiomyocyte contractile response
brenda
-
neonatal
brenda
-
neonatal and posterior ventricular cardiac myocytes
brenda
-
PLD1
brenda
primary
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primary cardiomyocyte
brenda
ventricular
brenda
ventricular myocyte
brenda
-
-
brenda
-
hypoxic conditions
brenda
-
-
brenda
-
PDE4
brenda
-
standard model of the balloon catheter injury of the carotid. Periadventitial application of recombinant uPA significantly reduces lumen size and vessel area encompassed by the external lamina both 1 and 4 days after treatment.In fallatory cells accumulate in the arterial adventitia at both 1 and 4 days after uPA treatment. Four days after injury in uPA-treated arteries, 3 proinflammatory and 2 oxidation-related genes are differentially expressed
brenda
-
brenda
-
enzyme histochemistry show high activity of TPP I in carotid body glomeruli. The glomus cells contain many TPP I-positive granules, while the glial-like sustentacular cells display a slightly fainter reaction
brenda
-
PDE4
brenda
-
brenda
-
ear
brenda
-
from ear
brenda
-
matrix, articular, of proximal tibiae, highest activity in the hypertrophic zone
brenda
-
of knee meniscus
brenda
presence of PACE4 protein is restricted to chondrocytes of healthy cartilage, whereas the expression is increased in osteoarthritis cartilage
brenda
zyphoid
brenda
-
-
brenda
-
two forms of beta 2-N-acetylglucosaminyltransferase I in rat testicular and epididymal fluids
brenda
-
weak enzyme expression, in the tubular epithelial cells of the caput and cauda
brenda
-
-
brenda
-
substantial portion of ATP-hydrolyzing activity depends on enzyme, enzyme is coexpressed with ecto-ATPase
brenda
-
-
brenda
-
a large fraction of the enzyme is localized on intrinsic striatal neurons
brenda
-
highest levels of mRNA for beta1, alpha1 and alpha2 subunits
brenda
-
neuron, DGK-II
brenda
-
-
brenda
A-type enzyme expression
brenda
B-type enzyme expression in the surface epithelium
brenda
-
microbiol azoreductase activity
brenda
-
487958, 487960, 641572, 645977, 656588, 661112, 661569, 663233, 668484, 672059, 672401, 674739, 676184, 676976, 688533, 697570, 709250, 710616, 715070, 740888, 770262, 771184, 771400
brenda
-
astrocyte, primary
brenda
astrocytes
brenda
-
astroglia-rich primary culture from neonatal rats
brenda
-
brown adipocytes
brenda
-
cerebral ischemia cell culture model
brenda
-
chondrosarcoma cell line
brenda
Con8.hd6 rat mammary tumor cell line
brenda
-
cortical cells
brenda
-
derived from anterior pituitary gland gonadotropin-producing cells in different stages of the estrous cycle: proestrus, estrus, metestrus, and diestrus
brenda
Enzymes and their fragments expressed in Escherichia coli.
brenda
-
Fao hepatoma cells
brenda
-
fibroblast
brenda
-
from submandibular salivary glands
brenda
-
from superior cervical ganglia
brenda
-
glial-neuronal coculture
brenda
-
hepatocyte
brenda
-
hepatocyte primary culture
brenda
-
in vitro model of the blood-brain barrier, primary rat astrocyte-enriched cultures are co-cultured with primary adult rat brain microvascular endothelial cells on opposite sides of a transwell membrane
brenda
-
insulin-secreting
brenda
insulin-treated rat 1 HIRc B cells
brenda
-
KRC-7 hepatoma cells
brenda
mammary gland-derived epithelial cell line
brenda
myoblast L6 cell line
brenda
-
neonatal cardiac myofibroblasts
brenda
neurons
brenda
-
NIH/hIR/rIRS1cells
brenda
-
of isolated ventricular myocytes
brenda
-
PC 12 cells
brenda
PC12 cells
brenda
pituitary tumor cell line GH3
brenda
-
priary neuronal cell culture derived from cerebral cortex of fetal rats
brenda
-
primary
brenda
primary anterior pituitary cells
brenda
-
primary cardiac cell culture of neonatal rats, increase in enzyme activity by interaction of enzyme subunit IV with protein kinase Cepsilon upon hypoxia
brenda
-
primary from brain cortical neurons
brenda
-
primary hypothalamic or adipose cells
brenda
-
primary midbrain mesencephalonic cells
brenda
RBL-2H3 cells
brenda
the expression of GGTIalpha in cultured hippocampal neurons gradually increases and peaks at approximately 8 days in vitro
brenda
the expression of GGTIbeta in cultured hippocampal neurons gradually increases and peaks at approximately 8 days in vitro
brenda
-
uterine smooth muscle cells
brenda
-
3109, 81609, 134923, 135380, 135422, 246966, 394027, 647146, 647288, 659578, 662492, 666112, 666114, 666122, 668117, 669637, 670363, 670668, 671275, 676162, 682106, 683344, 688009, 689224, 690097, 709612, 733958, 734529, 735602, 738895, 750212, 758983, 772981, 777560
brenda
adult, PCC together with methylmalonyl-CoA mutase and in whole rat embryonic central nervous system, both at E15.5 and E18.5
brenda
-
all regions
brenda
-
DAO is restricted to the lower brainstem, cerebellum and spinal cord, decreasing levels in the midbrain, the cortex and hippocampus
brenda
-
distribution, overview
brenda
expressed during central nervous system neurogenesis
brenda
-
expression pattern of Cyp27a1 and other related genes in primary cultures of glia and neurons
brenda
high expression level
brenda
-
immunohistochemical localization analysis, high enzyme content in oligodendrocytes along with CC1, and in white matter, including the corpus callosum and the cerebellar white matter, less abundant enzyme content in grey matter, including cerebral cortex, descending neuronal fibers, and microglial cells, no enzyme in astroyctes and forebrain, overview
brenda
PCCalpha is present in all regions of the central nervous system. PCCalpha is present in the whole embryonic central nervous system, both at E15.5 and E18.5, predominantely in the periventricular zones of telencephalon, midbrain and rhombencephalon
brenda
-
regiospecific distribution of DHODH, immunohistochemic analysis, overview
brenda
-
brenda
-
highest levels of expression in nucleus accumbens, taenia tecta, cerebellar cortex, cerebral cortical layer I, hippocampus, hypothalamus, mesencephalic raphe nuclei, central and lateral amygdala, and the circumventricular organs
brenda
-
in hippocampus the enzyme activity is significantly higher than in striatum and cortex. Significant increase in cortical membrane-associated N-Sase activity with age
brenda
-
in rat brain, the P-protein is confined to astrocytes. The intensity of astrocyte staining varies with regions, with the strongest staining in the hippocampus, the cerebellar cortex, the Bergmann glia in the cerebellum and the Muller cells in the retina
brenda
in the cerebellar cortex, SIRT5 can be found in Purkinje cells, and is mainly distributed in the cytoplasm, but is not markedly expressed in the molecular layer or granular layer cells
brenda
-
ischemic cortex after transient focal cerebral ischemia. Both the mRNA and protein levels of PC1 in ischemic cortices decrease gradually at 4, 8, and 16 hours of reperfusion after 100 min of middle cerebral artery occlusion. After 24 hours of reperfusion, enhanced intensities of signals for PC1 protein are observed, while signals for PC1 mRNA remain low
brenda
-
mRNA expression in ipsilateral and contralateral cortices. At day 3 post-ischemia, dipeptidyl peptidase IV, 8 and aminopeptidase N are identified in activated microglia and macrophages in the ipsilateral cortex. Seven days post artery occlusion, dipeptidyl peptidase IV immunoreactivity is found in the perikarya of surviving cortical neurons of the ipsilateral hemisphere. At the same time point, dipeptidyl peptidase IV, 8 and aminopeptidase N are targeted in astroglial cells. Total dipeptidyl peptidase IV, 8 and 9 activities remain constant in both hemispheres until day 3 post experimental ischemia, but are increased to 165% in the ipsilateral cortex at day 7
brenda
-
mRNA expression in ipsilateral and contralateral cortices. Dipeptidyl peptidase II and aminopeptidase N are up-regulated ipsilaterally from 6 h to 7 days post ischemia
brenda
-
no significant changes in the enzyme activity between morphine-treated and control samples
brenda
-
brenda
-
and dendrites
brenda
-
cerebellar, both isoforms CNP1 and CNP2
brenda
-
DGK-Igamma
brenda
-
DGK-III
brenda
-
isozyme alpha
brenda
-
the specific activities of Gal-Tr is nearly normal or slightly elevated in all the three Purkinje cell abnormality mutants
brenda
B5DEJ6, F1M4T7, O08560, O35078, O70196, P22071, P27791, P29476, P53610, P97675, Q04631, Q5M819, Q63604, Q6AYK3, Q8R431, Q924C3, Q99NB2, Q9ES71, Q9QZC4, Q9WTZ3
-
993, 5119, 28967, 94468, 95240, 134945, 137183, 394027, 440196, 440197, 440198, 440202, 440203, 440220, 440232, 440236, 490643, 638235, 639661, 645561, 645562, 645805, 645807, 646167, 647155, 650180, 650849, 651265, 651779, 653243, 653349, 653621, 653676, 654196, 655140, 658362, 659578, 660009, 660815, 662959, 663839, 664468, 664469, 664475, 664576, 665836, 669619, 672851, 673929, 675509, 675783, 677509, 679180, 679431, 679665, 680122, 681285, 681315, 681523, 681643, 682110, 682114, 682285, 683389, 683923, 683926, 685334, 685455, 686293, 686294, 686868, 688220, 688608, 689159, 691556, 691561, 692560, 693368, 693768, 694379, 696139, 698035, 698337, 699606, 700411, 700456, 702967, 704640, 705262, 705502, 707107, 707363, 707929, 708263, 708319, 708464, 709257, 711639, 711794, 712050, 712817, 713119, 714639, 715984, 716351, 720554, 721741, 725082, 727633, 731972, 739114, 741580, 758981, 759850, 761598, 762271, 762503, 762740, 765779
brenda
-
33% of activity membrane associated
brenda
abundantly expressed in neurons of
brenda
-
ACC is inhibited in Cu-deficient cerebella
brenda
-
activity in neuroglia cells, no activity in small granule cells, Purkinje cells, remified dendrites and myelinated fibers
brenda
adult, highest level, Purkinje and granular layers
brenda
-
alpha and beta isozymes, cerebellar nuclei
brenda
-
alpha2 and beta1 abundant in Purkinje cells, small cells close to Purkinje cells express high levels of alpha1 mRNA, alpha2 and beta1 expression very high and homogeneous in the granule cell layer
brenda
-
and pons
brenda
Bermann glia
brenda
-
cerebellar cultures
brenda
-
cerebellar granule cells
brenda
-
cerebellar granule layer
brenda
-
cerebellar postsynaptic density fraction, both isoforms CNP1 and CNP2 are expressed in cerian populations of cerebellar cells, in oligodendrocytes, Purkinje cells and unidentified PSD95-positive cells, not in granule cells
brenda
-
cerebrum, cerebellum and brain stem of 14 and 21 days old rats
brenda
-
creatine kinase activity is not altered if rats are submitted to renal ischemia
brenda
-
development of phospholipase D activity during ageing. Enzyme activity is identical in adult and aged nuclear fraction, increases by 25% from adult to aged cerebellum in mitochondrial-synaptosomal fraction, decreases by 18% from adult to aged cerebellum in the microsomal fraction and increases by 14% from adult to aged cerebellum in cytosolic fraction
brenda
-
distinct cellular layers: Purkinje cell layer, molecular cell layer, granule cell layer + white matter
brenda
-
enzyme is abundantly expressed in the developing rat cerebellum, in particular molecular layer, the region enriched with Purkinje cell dendrites
brenda
expression of AACS mRNA in the cerebellum is restricted primarily to glial cells
brenda
expression of CK1epsilon-2, CK1epsilon-1
brenda
GGTIbeta protein level and/or GGTI activity increase gradually from P0 to adult in rat cerebellum
brenda
-
granule cells
brenda
-
high level of expression
brenda
-
highest enzyme activities in synaptic membranes from cerebellum, hypothalamus, hippocampus
brenda
-
in Purkinje cells
brenda
-
isozyme PAP1 in all subcellular fractions, isozyme PAP2 in cytosol
brenda
-
isozymes alpha, betaI, betaII, gamma, delta, epsilon, lambda, eta, theta, and zeta
brenda
-
low ACE mRNA expression
brenda
-
low enzyme activity
brenda
-
low enzyme level
brenda
low expression level
brenda
-
low level both of expression and activity
brenda
-
myelin sheet
brenda
-
neonatal
brenda
-
neurons
brenda
-
neurons of adult animal
brenda
-
of the fetus
brenda
-
ontogenetic isozyme profiling
brenda
pons, medulla and the Purkinje and granular layers
brenda
-
present at weaker levels
brenda
Purkinje cells, highest levels
brenda
-
significant decrease in activity following aluminium exposure. Post-treatment with centrophenoxine restores the altered enzyme activity
brenda
-
specific activities of Gal-Tr in the granule cell layer and white matter is approximately 66% of that in the molecular layer. Gal-Tr in the homogenate of cerebellum declines by approximately 35-45% from postnatal day 3 to 14. Gal-Tr activity in the granule cells does not change with age. The relative Gal-Tr activity in granule cells to homogenate is between 0.13 and 0.23
brenda
-
specific activity is reduced by 50% soon after birth and then remains practically the same with development
brenda
strongest PDE9A expression in Purkinje cells
brenda
SULT1A1
brenda
-
the contribution of glucokinase to total glucose-phosphorylating activity is of 13.3% in the cerebellum
brenda
-
within the myelin sheets
brenda
B5DEJ6, F1M4T7, P06685, P06686, P06687, P23457, P29476, P32738, P36970, P97519, P97675, Q64428, Q8R431, Q924C3, Q9EPZ8, Q9EQV6, Q9Z330
-
28967, 134945, 246958, 246966, 392796, 639661, 642132, 643998, 646125, 646167, 646382, 647025, 650849, 653348, 653676, 655140, 661404, 661406, 665981, 666467, 667459, 669637, 669904, 675537, 677433, 679085, 679180, 680913, 682110, 682113, 682114, 682117, 682284, 682902, 683344, 686054, 686293, 686868, 687078, 688009, 688220, 689209, 690750, 691558, 691561, 692128, 692192, 692231, 693782, 695204, 695973, 697749, 697804, 698337, 699679, 699690, 700430, 700433, 702966, 703574, 705501, 705502, 706540, 708319, 711695, 713122, 716346, 716351, 723652, 725082, 725768, 727633, 728179, 730237, 731627, 731972, 736678, 740102, 752408, 758981, 759850, 761014, 762503, 762740, 763094, 765297, 766395, 777716
brenda
-
about 10% of the ACE2 gene expression in kidney cortex
brenda
-
activity below detection limit of 0.1 fmol/mg protein/min
brenda
-
activity increases gradually during development
brenda
-
agmatinase is localised pre- and postsynaptically, to dendritic spines, spine and non-spine terminals, and dendritic profiles. In dendritic spines, labelling displayed a tendency towards the postsynaptic density
brenda
-
beta1 subunit mRNA widely distributed through all cortical areas and cell layers with higher intensity in layer V, alpha2 mRNA homogeneously distributed through all cortical layers and alpha1 expression higher in layers IIIII and V
brenda
-
colocalization with somatostatin, carboxypeptidase-E and PC1 in pyramidal and non-pyramidal neurons. PC2 exhibits 30% colocalization with somatostatin and 44% with carboxypeptidase-E
brenda
-
colocalization with somatostatin, carboxypeptidase-E and PC2 in pyramidal and non-pyramidal neurons. Colocalization with carboxypeptidase-E confined to pyramidal neurons of deeper layer. PC1 exhibits 26% colocalization with somatostatin and 34% with carboxypeptidase-E
brenda
-
cortical cells dissociated in cell culture
brenda
-
developing, intereurons, the majority of cortical tyrosine hydroxylase cells at all ages contains phosphorylated tyrosine hydroxylase
brenda
-
distribution of sPLa2-IIe, sPLA2-V, and sPLA2-X is mainly neuronal with highest abundance in cerebral cortex and hippocampus. Enzymes are differentially induced by kainic acid
brenda
expression of CK1epsilon-3
brenda
fetal
brenda
-
frontal cortex and posterior cortex
brenda
-
glial culture from
brenda
-
high enzyme level
brenda
-
high expression
brenda
-
high PC2 protein content at early ischeic reperfusion hour, which decreases with reperfusion time
brenda
-
highest levels of expression in nucleus accumbens, taenia tecta, cerebellar cortex, cerebral cortical layer I, hippocampus, hypothalamus, mesencephalic raphe nuclei, central and lateral amygdala, and the circumventricular organs. Distinct presence in mossy fiber terminals of cerebellar cortex
brenda
immunoreactive cells are found in 3 days old but not in 1-month-old male rats
brenda
-
in cerebral cortex creatine kinase activity is inhibited 6 and 12 h after renal ischemia. Only N-acetylcysteine or N-acetylcysteine plus deferoxamine are able to prevent the inhibition on the enzyme
brenda
in cerebral cortex expression of AACS mRNA is restricetd to neuronal cells
brenda
-
increase in enzymic activity from birth to day 30, decrease afterwards, highest enzymic activity at day 30, highest affinity for enzyme at day 365, relative abundance of enzyme is highest at day 15 of ontogeny
brenda
-
isozyme type III
brenda
-
isozymes CaMKIdelta and CaMKIalpha
brenda
-
membrane-bound COMT activities in the cerebral cortex are significantly reduced in high-salt loaded Dahl salt-sensitive rats compared with normal-salt loaded Dahl salt-sensitive rats
brenda
-
mild expression of PC1 and moderate expression of PC2. PC1 and PC2 in cerebral cortex colocalizes in pyramidal and non-pyramidal neurons with carboxypeptidase-E and somatostatin
brenda
-
neuron
brenda
-
no significant changes in enzyme level upon feeding ethanol-containing Lieber-DeCarli liquid diet
brenda
not adult
brenda
-
PLD2 expression is observed in the marginal zone from the earliest stage and then declines and completely disappears by embryonic day 20
brenda
-
prefrontal, expression of isozymes 5alpha-R1 and 5alpha-R2
brenda
-
presence of both arginine decarboxylase and arginase in principal neurons and putative interneurons
brenda
-
specific expression of POP in glutamatergic pyramidal neurons of the cerebral cortex, particularly in the primary motir and somatosensory cortices
brenda
-
strong activity
brenda
-
synaptosome
brenda
-
synaptosomes
brenda
-
the contribution of glucokinase to total glucose-phosphorylating activity is of 15.3% in the cerebral cortex
brenda
-
-
brenda
-
low activity
brenda
-
-
brenda
-
moderate expression of alpha1 and alpha2 mRNAs in many white matter tracts, beta1 mRNA expression is very low
brenda
-
-
brenda
-
UCH-L1 is significantly elevated in cerebrospinal fluid following controlled cortical impact and middle cerebral artery occlusion, as a model of ischemic stroke, in rats, overview
brenda
-
440203, 440228, 491258, 645561, 645562, 647183, 651779, 653243, 653360, 669619, 673929, 680122, 712050, 726048, 741580, 749270
brenda
-
cerebrum, cerebellum and brain stem of 14 and 21 days old rats
brenda
-
embryonal, isozyme expression analysis, PAD2 expression occurs also in 19- to 21-day-old embryos at a developmental stage well before myelination begins, overview
brenda
-
relatively high enzyme expression just after birth, the content gradually decreases thereafter
brenda
-
significant decrease in activity following aluminium exposure. Post-treatment with centrophenoxine restores the altered enzyme activity
brenda
-
-
brenda
-
enzyme secretion
brenda
-
brenda
articular
brenda
-
malignant, swarm chondrosarcoma
brenda
-
MIPP expression pattern in developing chondrocytes
brenda
-
mRNA is ubiquitously expressed in all cell layers of proliferating to hypertrophic chondrocytes
brenda
-
no activity in resting chondrocytes and the matrix of reserve zone
brenda
-
-
brenda
-
extracellular, secretion to the medium
brenda
-
-
brenda
-
high levels of P3H2 mRNA are expressed
brenda
-
brenda
adult and embryo
brenda
-
adult brain
brenda
-
epithelial cells
brenda
-
high level both of expression and activity
brenda
-
highest activity in brain
brenda
-
role of FAAH in epithelial cells of the choroid plexus may be to control the concentration of oleamide in the cerebrospinal fluid. FAAH may exert an important regulatory role in shaping the duration and magnitude of the sleep-inducing effect of endogenously or exogenously derived oleamide
brenda
-
brenda
-
forebrain and cerebral cortex
brenda
-
-
brenda
-
secretion, not immunologically related to tissue-type enzyme or blood factor XIIIa
brenda
-
-
brenda
-
glutathione-independent enzyme
brenda
-
marked enzyme immunoreactivity in primary afferent neurones of the spiral ganglion and synaptic regions of the inner and outer hair cells
brenda
-
-
brenda
-
aldosterone-sensitive, NAD+ specificity
brenda
O88422, P04041, P06762, P08430, P38483, P83645, Q4KLZ0, Q5BQE6, Q62833, Q63707, Q91XT9, Q925R7, Q9R0C5
-
1327, 1664, 2271, 2420, 2423, 28971, 30798, 37069, 37080, 80992, 95240, 135460, 135465, 137183, 208880, 208881, 246966, 286343, 390925, 394033, 485173, 486070, 487246, 487250, 488192, 488193, 488370, 489362, 491200, 638139, 638140, 638281, 649525, 659135, 664560, 664566, 671212, 675723, 675803, 682957, 685921, 686565, 688598, 689353, 692039, 692565, 693127, 697266, 702810, 708300, 710627, 711688, 712050, 713952, 721049, 725056, 734537, 734744, 742246, 742557, 745890, 749371, 752416, 778606
brenda
-
colonic HKalpha2
brenda
distal
brenda
-
distal end
brenda
-
enzyme activity is significantly elevated at 8 h after intradermal injection of carageenan or urate crystals, falling to normal levels by day 3
brenda
-
enzyme present in small amounts, distribution of BB-type MB-type and MM-type iszozymes
brenda
-
high activity
brenda
-
in the distal part of the colon but not in proximal colon
brenda
-
increased PSR activity in case of colitis
brenda
-
low expression level of ADH5
brenda
low level
brenda
-
malignant and non-malignant areas, mucosal cells
brenda
mRNA expressions of vanin-1 significantly increases in the kidney, but not in the colon, during colitis
brenda
-
potential for Gpx1 and Gpx2 redundancy in lymphatic tissue, but not in epithelial cells of the colon crypt or in the lamina propria, sub-mucosa, muscularis or serosa
brenda
ppGaNTase-T6
brenda
ppGaNTase-T9
brenda
-
proximal and distal colon
brenda
-
smMLCK expresses in almost every tissue, including colon
brenda
-
strongest expression of isoform SPCA2
brenda
-
surface epithelium and crypt epithelium
brenda
-
-
brenda
-
RPMI
brenda
-
RPMI colon tumor
brenda
-
-
2423, 135413, 135465, 393670, 488370, 637988, 638138, 638139, 638322, 639316, 697058, 702810
brenda
-
high activity
brenda
-
high levels of activity of both forms of the enzyme, nonglycosylated and glycosylated
brenda
-
normal mucosa, non-malignant mucosa, tumour
brenda
-
-
489334, 637291, 637294, 637297, 699091, 699416, 707558, 709639, 717275, 742448, 744301, 766721
brenda
-
actilyse
brenda
-
liver enzyme
brenda
-
pure enzyme
brenda
-
purified PKC from brain
brenda
-
recombinant enzyme
brenda
-
recombinant enzyme expressed in Spodoptera frugiperda cells
brenda
recombinant His-tagged enzyme expressed from Spodoptera frugiperda cells
brenda
-
-
brenda
-
NTPDase3
brenda
-
brenda
-
in corneal epithelial layer, stromal layer, and endothelial layer
brenda
-
-
brenda
-
vascular walls and endothelium
brenda
-
brenda
-
presence of enzyme immunoreactive material at birth, progressive reduction with age with complete loss at postnatal day 18
brenda
-
-
brenda
-
of the penis
brenda
at estrus, activity is 7.6fold greater in the old corpus luteum compared to new corpus luteum
brenda
-
caspase-9 activity increases in the old corpus luteum at estrus, during the functional luteolysis
brenda
-
enzyme activity during stages of pseudo-pregnancy, 20alpha-hydroxysteroid dehydrogenase activity increases from day 1 to day 12, overview
brenda
immunostaining for caspase-2 increases as the luteal phase progresses
brenda
-
significant increase in mRNA for PGHS-2 after treatment with prostaglandin F2alpha. PGHS-1 mRNA content remains unchanged
brenda
-
weak expression of 3beta-hydroxysteroid dehydrogenase in newly formed corpora lutea, which gradually increases followed by decrease on day 20. In vascularised apical region of young corpora lutea, luteal cells with more intensive immunostaining predominate. Distribution of 3beta-hydroxysteroid dehydrogenase and androgen receptor differ within various generations of corpora lutea
brenda
-
4222, 28967, 81293, 646167, 661442, 662331, 662492, 664474, 665836, 669925, 676753, 685344, 685885, 686054, 686293, 688545, 688608, 689215, 689232, 690099, 691888, 693989, 694363, 694373, 694399, 697761, 698337, 700426, 700470, 705454, 707107, 707801, 710589, 713122, 716346, 720443, 720554, 730237, 759850, 762017, 774724, 774967
brenda
-
15-20% inhibition of complex II activity in striatum and hippocampus by methylmalonic acid at low concentrations of sucinate in the medium, but not in the peripheral tissue. the inhibitory property only occurs after exposing brain homogenates for at least 10 min with the acid, suggesting that this inhibition is mediated by indirect mechanisms
brenda
-
age-related increases in isoform PDE8A3 protein expression are confirmed in hippocampus of old versus young rodents
brenda
-
BACE1 is significantly and time-dependently increased in the ipsilateral striatum
brenda
-
changes in caspase-3, amyloid beta and BACE1 levels are detected in rat striatum on different days after middle cerebral artery occlusion using immunostaining. The positive labeled cells of activated caspase-3, amyloid beta, and BACE1 are significantly and time-dependently increased in the ipsilateral striatum
brenda
-
creatine kinase activity is not altered if rats are submitted to renal ischemia
brenda
-
dorsal
brenda
-
dorsal striatum
brenda
-
high levels of HDC protein are also found in the striatum
brenda
-
in a rat ischemia model the striatum is examined at 24, 72 and 144 h after reperfusion and compared with rats in normal conditions. At 24 h after reperfusion, the number of the nitric oxide synthase-positive neurons and the percentage of those co-expressing argininosuccinate synthetase and argininsuccinate lyase and nitric oxide synthase are significantly increased in the animals with a longer survival
brenda
-
in hippocampus the enzyme activity is significantly higher than in striatum and cortex. Age-related decreases in the hippocampal and striatal cytosolic N-Sase activities are accompanied by increases in the membrane N-Sase activities
brenda
-
myelin sheet
brenda
-
PDE10A is highly expressed in the medium spiny neurons of the striatum
brenda
-
the catalase activity in striatum is significantly decreased in the lesioned group as compared to sham group and pretreatment with Withania somnifera reverses its activity significantly and dose dependently in the lesioned goup pretretaed with 100 mg/kg 200 mg/ml or 300 mg/kg body weight extracts of Withania somnifera orally as compared to lesioned group
brenda
unilateral injection of 6-hydroxydopamine produces no change in striatal MAO-A or MAO-B activity, but following the double lesion, MAO-B activity increases by 37.5% with no change in MAO-A activity
brenda
-
a subpopulation of
brenda
-
GRK2
brenda
-
-
brenda
-
of H35 hepatoma cells
brenda
-
of mesangial cells, active renin is significantly higher in the cell lysate than in culture medium. Inactive prorenin is similar for the intracellular and extracellular compartments. Free active renin is the predominant form found in both cell compartments. Mesangial cells in culture are able to synthesize and translate renin mRNA probably as inactive prorenin which is mostly processed to active renin inside the cells. The cells secrete both forms of the enzyme but at lower level compared with intracellular content
brenda
-
secreted into medium by infected insect cells
brenda
-
synovial fibroblasts
brenda
-
-
brenda
-
pregnant and pseudopregnant
brenda
-
-
brenda
-
in the inner molecular layer
brenda
-
brenda
-
L4 and L5
brenda
-
5129, 36028, 37080, 95240, 137183, 208687, 441531, 441560, 487932, 488736, 658687, 665149, 665705, 673552, 675803, 678455, 678547, 683802, 692039, 692281, 694562, 702810, 708300, 712050, 718751, 752495
brenda
-
enzyme activity level is highest in duodenum
brenda
exclusive expression in
brenda
-
low expression level of ADH5
brenda
-
myenteric ganglion
brenda
-
villous surface. HCO3- secretion increases alkaline phosphatase activity by increasing local pH at its catalytic site. Alkaline phosphatase hydrolyzes luminal phosphates, presumably ATP, which increases HCO3- secretion via activation of P2 receptors
brenda
-
cartilage
brenda
-
ECE-1 promotes re-sensitization of SP-induced inflammation
brenda
at embryonic day 12.5, RALDH1 mRNA is present in the posterior region of oral ectoderm
brenda
at embryonic day 12.5, RALDH2 mRNA is present in part of the anterior oral ectoderm
brenda
-
289020, 485020, 485024, 486818, 486841, 640826, 640828, 640829, 640830, 640835, 653360, 655198, 660679, 664240, 664861, 672991, 673910, 678070, 682537, 682806, 683493, 686015, 691037, 693451, 697749, 705286, 705612, 705936, 705939, 709738, 710453, 754463, 764825, 773618
brenda
-
basal expression of glutamate-cysteine ligase catalytic subunit and regulatory subunit is 59fold and 25fold higher in visceral yolk sac, respectively, compared to the embryo
brenda
by embryonic day 15, the transcript is localized to cells that will eventually become exocrine in nature, high levels of expression in the choroid plexus, the developing myocardium, kidney, CNS, dorsal root ganglia, and testes
brenda
-
day 18-20
brenda
E15 Sprague-Dawley rat embryos
brenda
early
brenda
-
embryo bone
brenda
embryo kidney 293 cells
brenda
-
embryonic brain
brenda
-
glutamic acid decarboxylase in E18 embryonic hippocampal neurons
brenda
-
heart
brenda
hippocampal neurons obtained from 17.5-day-old embryos
brenda
in embryos (E15.5 and E18.5), PCCalpha shows a much higher expression level in the entire central nervous system than in the liver
brenda
p38-delta is expressed predominantly in the developing gut and the septum transversum in the mouse embryo at 9.5 days, its expression begins to be expanded to many specific tissues in the 12.5-day embryo. At 15.5 days, p38-delta is expressed virtually in most developing epithelia in embryos
brenda
primary embryonic metanephric mesenchymal cells
brenda
vitamin K-dependent carboxylase mRNA expression in early rat embryonic development
brenda
-
Rat-2
brenda
-
SV-3T3
brenda
-
brenda
-
AMP-deaminase plays a role in formation of NH3 by endometrium stroma cells and its release into extracellular space during acetylcholine stimulation
brenda
-
491712, 673910, 673918, 686904, 689994, 697044, 697266, 703348, 709149, 710120, 716346, 733408, 744161, 744875, 749869, 754999, 772258
brenda
-
cell line RV-ECT
brenda
cerebral
brenda
down regulation in endothelial cells in cirrhotic rats
brenda
-
expresses PDE4, 7, and 8
brenda
-
from striatum
brenda
-
glomerular endothelial cell
brenda
-
high expression level
brenda
immunostaining for caspase-2 increases as the luteal phase progresses
brenda
-
LPL is synthesized by parenchymal cells, from which it is secreted and then transported to the lumen surface of endothelial cells
brenda
-
marrow stromal cell-brain microvascular endothelial cell contact coculture and indirect co-culture of marrow stromal cell and brain microvascular endothelial cell
brenda
-
microcapillary endothelial cell, adult brain
brenda
of brain
brenda
the expression of the carboxylesterases ES4 and ES10 endothelial cells is 5-10fold lower than that in hepatocytes
brenda
-
-
brenda
-
and vascular walls of coronary arteries
brenda
-
aortic, higher activity in aged compared to young rats
brenda
-
arterial endothelium
brenda
-
capillary and artery endothelia of the brain, liver and kidney
brenda
-
endothelial enzyme
brenda
-
in healthy hearts, DDAHI is absent, and DDAHII is localized to endothelium and endocardium with a similar distribution to that of eNOS
brenda
-
isoform III
brenda
-
isozyme endothelial lipase
brenda
-
isozyme PGF synthase I in endothelial cells of the whole area of the spinal cord, and isozyme PGF synthase II in endothelial cells of the blood vessels only
brenda
-
liver, lung, adrenal glandcolon, isoform II
brenda
-
lung, uterus, stomach
brenda
-
normal aortic endothelium. Co-distribution of prostaglandin cyclase and cyclooxygenase COX-1, with only minor expression of cyclooxygenase COX-2 in endothelium
brenda
-
prostate endothelial cells
brenda
pulmonary artery endothelial cell
brenda
-
vascular
brenda
-
-
brenda
-
expressed in nerve cell bodies and nerve fibres of the enteric nervous system
brenda
-
isoform BB (brain) is the predominant isozyme expressed in enteric glial cells and rare neurons of the myenteric and submucosal plexuses. Isoform MM (muscle) appears in cells which are, according to their location and morphology, probably interstitial cells of Cajal. Both glycogen phosphorylase isoforms are expressed in longitudinal and circular intestinal smooth muscle layers
brenda
-
-
brenda
dynamin-1, endocrine cell of the gastric mucosa
brenda
dynamin-2, endocrine cell of the gastric mucosa
brenda
low abundance of dynamin-3, endocrine cell of the gastric mucosa
brenda
-
brenda
-
intestinal, brush border
brenda
-
jejenum
brenda
-
localization at the apical membrane of the enterocyte
brenda
-
occurs exclusively on the basolateral membrane of enterocytes
brenda
-
-
brenda
-
one h after the onset of pilocarpineinduced status, staining of active glycogen phosphorylase is reduced in most regions of the hippocampus and entorhinal cortex relative to saline-injected controls. One week after status, there is increased active glycogen phosphorylase and total glycogen phosphorylase, especially in the inner molecular layer, where synaptic reorganization of granule cell mossy fibre axons occurs
brenda
-
presubiculum, but not subiculum, is strongly reactive for glycogen phosphorylase. Glycogenolytic demand in Layers I and II is organized in a modular fashion and demand can be modified by brief exposure of animals to a novel holeboard
brenda
-
-
brenda
-
significantly increased agmatine levels in the prefrontal, entorhinal, and perirhinal cortices in a T-maze training group relative to the control group
brenda
-
-
brenda
-
isolated from peritoneal lavage and gastric wall
brenda
-
-
brenda
presence of mRNA as well as protein of both subunits of 3-methylcrotonyl-CoA carboxylase in ependymocyte, microglial cell and oligodendrocyte cultures derived from the brains of newborn rats
brenda
-
brenda
-
epidermal keratinocyte
brenda
-
from newborn rats
brenda
-
of mouse hind-paw
brenda
-
of newborn rats
brenda
-
stratum corneum, skin
brenda
-
stratum granulosum
brenda
-
733, 35874, 36043, 80870, 80874, 80891, 94883, 94885, 94892, 94898, 94899, 94906, 94907, 95240, 134901, 134923, 171343, 208687, 285604, 347987, 389528, 396193, 396196, 396210, 396220, 486489, 487931, 489380, 637909, 640772, 640775, 647183, 651779, 653094, 658248, 664560, 665109, 666799, 668207, 670266, 670742, 671678, 685333, 690339, 697743, 702514
brenda
-
caput and cauda
brenda
-
caput, corpus and cauda region
brenda
-
caput, corpus, cauda
brenda
-
clear cells in all epdididymal regions, not in principal cells
brenda
-
concentrated in caput corpus of epididymis
brenda
epididymal fat, increased activity upon cessation of wheel running. Increase in mtGPAT protein might contribute to the overshoot in triacylglycerol synthesis
brenda
-
epididymal fat, presence of a functional glucose-6-phosphate-transporter hexose-6-phosphate dehydrogenase 11beta-hydroxysteroid dehydrogenase type 1 system
brenda
-
epididymal luminal fluid
brenda
-
epididymis capa, epididymis cauda
brenda
-
epithelium
brenda
-
epithelium, NTPDase1
brenda
-
from caput, corpus and caudal region of epididymis
brenda
-
glutathione-independent enzyme
brenda
-
GPX5
brenda
high activity
brenda
high content
brenda
-
initial segment
brenda
low expression level
brenda
-
no activity in the stromal cells or endothelial cells, but weak immunoreactivity in the epididymal epithelial cells
brenda
specific expression of isoform RNase9, especially in caput and corpus. Expression is andorgen-dependent
brenda
-
very high enzyme concentration in Golgi apparatus of epididymal duct epithelium from initial segment to intermediate caput, although much lower amounts of enzyme are in efferent ducts, distal caput, corpus and cauda. Even in the initial segment and caput epididymis, only low levels of soluble enzyme form are detected in the fluid
brenda
-
642921, 642928, 650814, 668500, 671253, 673210, 688137, 693323, 696852, 698665, 707573, 707951, 729810, 744161, 745597, 768934
brenda
-
alveolar epithelial type II cell, ATII cell
brenda
-
basolateral sides
brenda
-
columnar epithelial cell
brenda
-
of prostate
brenda
-
of renal convoluted tubules, of uterine glands
brenda
-
of several tissues including stomach, intestine, colon, prostate glands, and endometrium
brenda
-
parietal epithelial cells of Bowman's capsules and some tubular epithelia in the kidney
brenda
-
primary, PLD1
brenda
-
renal
brenda
-
small intestine
brenda
-
vascular epithelial cell
brenda
-
81609, 209933, 392084, 645792, 660670, 666926, 673479, 689353, 690351, 710899, 733064, 734537
brenda
-
airway
brenda
-
airway epithelia
brenda
Q9QX71
alveolar
brenda
-
alveolar and bronchial, type I and type II cells
brenda
-
alveolar, higher content compared to the lung parenchyma
brenda
-
analysis of GRK2 localization in alveolar epithelium
brenda
-
basal lamina of epithelium of intestine, nasal cavity, choroids plexus, skin and intracellular storage vesicles
brenda
-
biliary
brenda
-
ciliary
brenda
-
enzyme is found in luminal and glandular epithelial cells and in stroma during late pregnancy
brenda
-
ependymal epithelium, adult brain, developing embryonic brain
brenda
-
epithelial cells of the basal layer, co-localization of isoform mPGES-1 and COX-2 after induction of oesophagitis
brenda
epithelial cells, both intercalated cells and principal cells
brenda
esophageal and duodenal
brenda
glomerular
brenda
-
intestinal
brenda
-
isozyme IP33K-C
brenda
-
lung
brenda
-
lung epithelial cell
brenda
-
NTPDase1 in epididymal, NTPDase3 in secretory
brenda
-
of the intestine
brenda
-
of the proximal and distal tubule
brenda
-
of the vas defernes
brenda
-
of vile ducts and blood vessel walls in portal tracts
brenda
-
proximal tubular
brenda
-
renal
brenda
-
retinal pigment epithelium
brenda
transporting epithelial cells of brain
brenda
-
vestibular sensory epithelium, in transitional cells therein, which are parasensory cells located between the sensory epithelium and the dark cells, and in dark cells
brenda
-
-
brenda
the enzyme is increased in contracting versus resting muscles
brenda
-
1121, 1124, 2269, 30778, 30780, 30798, 35981, 35982, 35991, 37413, 37427, 37435, 81039, 95254, 134162, 134165, 134170, 134180, 134807, 134808, 134809, 135127, 171169, 210687, 210705, 210708, 210716, 286013, 286014, 286015, 286019, 286020, 286021, 286023, 286024, 287002, 287073, 287910, 391879, 485555, 485560, 485592, 485595, 485596, 485600, 485605, 485610, 485615, 486535, 487569, 487983, 489738, 489933, 637814, 642661, 643983, 645547, 645550, 646121, 649263, 650445, 654021, 655210, 656386, 657143, 659111, 659592, 664486, 666969, 667841, 667861, 673458, 687064, 690828, 694894, 695426, 699227, 700654, 701160, 706843, 707559, 708111, 708981, 713186, 713204, 716429, 721833, 730995, 733517, 740635, 749869, 750070, 761410, 771625
brenda
-
2 isoenzymes
brenda
-
activities of catalase activity shows similar behavior after the exhaustive exercise bout, with a maximum activity at 3 h after the exercise. Activity tends to fall at 4 h after the exercise in comparison with 3 h
brenda
-
contains 2 major forms of enzyme: high-activity type and low-activity type
brenda
-
enzyme present in small amounts, distribution of BB-type MB-type and MM-type iszozymes
brenda
extracts, bleomycin hydrolase detection by Western blot
brenda
-
hexokinase type I
brenda
-
only one enzyme form
brenda
-
pentylenetetrazol-induced epileptic seizure is accompanied by significantly reduced catalase activity
brenda
-
plasma membrane
brenda
-
R-type isozyme
brenda
-
soluble form
brenda
-
transcript of R mRNA is detected
brenda
-
brenda
-
gene for cathepsin C is upregulated compared to Barrett's esophagus
brenda
-
37080, 80992, 208880, 208881, 487253, 489149, 647183, 651779, 669619, 675803, 692281, 718751
brenda
basal cells
brenda
-
epithelium from normal control Barrett's esophagus
brenda
-
in the mucosa
brenda
-
brenda
-
pancreas exocrine acini
brenda
-
-
brenda
-
fast limb muscle, high activity of isoenzyme CA3, message levels of isoenzyme CA2 and CA4 are higher in extraocular muscle than in extensor digitorum longus, expression of isoenzyme CA5 is equivalent in extraocular muscle and extensor digitorum longus
brenda
-
488023, 653243, 653360, 664240, 679690, 683383, 701187, 711688, 723021, 723270, 725072, 731960, 758876
brenda
-
anterior uveal and scleral complex
brenda
-
endothelial cell in choroid and ciliary body
brenda
retina
brenda
-
-
brenda
-
epididymal
brenda
-
-
brenda
-
order of hydrogen sulfide production rates for different tissues are: liver (777 nM/min/g), followed by uterus (168 nM/min/g), fetal membranes (22.3 nM/min/g), placenta (11.1 nM/min/g), compared to human placenta (200 nM/min/g)
brenda
-
4142, 94961, 392077, 438418, 439148, 439198, 485374, 485404, 640828, 640829, 687639, 710108
brenda
-
M2-type isozyme
brenda
prenatal nicotine exposure leads to decreased expression and increased DNA methylation in the proximal promoter of acetoacetyl-CoA synthetase
brenda
B5DFD5, D4A4P4, O35776, O35795, P07861, P19468, P38062, P85973, P97687, Q5DRK1, Q8CH92, Q8CH93
-
5181, 81609, 95818, 393080, 485020, 485024, 488440, 639928, 646729, 647611, 659334, 662512, 664560, 664876, 666182, 666513, 672441, 672957, 673210, 674900, 676029, 676808, 677503, 687597, 692214, 695615, 697266, 699654, 699690, 700089, 707551, 707555, 707951, 709420, 709572, 713591, 717454, 718543, 727094, 735083, 738594, 755250, 760109, 774376
brenda
-
1HIRc B cells (overexpressing the human insulin receptor), embryonic cell line 3Y1, both with elevated kinase activity after treatment with mitogens, e.g. insulin or epidermal growth factor
brenda
-
3T3-L1 cells, low activity
brenda
-
3Y1 cell
brenda
-
CaM-KI
brenda
-
cardiac
brenda
-
cardiac, ventricular
brenda
-
colocalized with cyclooxygenase-2
brenda
-
cultured cells
brenda
-
fibroblasts
brenda
-
IR fibroblasts
brenda
-
L-carnitine inhibits angiotensin II increased NADPH oxidase activity and intracellular ROS levels in cardiac fibroblasts
brenda
-
neonatal cardiac myofibroblasts
brenda
perivascular, epineurial and perineurial
brenda
portal fibroblasts
brenda
-
primary from fetal lung
brenda
primary lung fibroblast
brenda
-
ras-transformed
brenda
-
RFL-6 cell
brenda
-
RFL6
brenda
-
secretion of free soluble enzyme
brenda
-
the enzyme activity is higher in normal Rat-2 fibroblast compared to transformed NM-16 cells
brenda
-
-
brenda
-
transformed embryo cell line, can be induced by a tumor promoter
brenda
-
-
brenda
-
enzyme activity is 18% of the activity found in normal livers
brenda
-
665662, 665836, 669636, 671799, 675523, 676319, 697223, 699667, 699831, 702963, 702967, 705283, 737427, 762271
brenda
-
alpha and beta isozymes
brenda
-
developing embryonic brain
brenda
-
embryonic spinal cord
brenda
-
HO-1 mRNA levels are 66% of those in liver
brenda
-
impaired spatial working memory and altered choline acetyltransferase immunoreactivity and nicotinic receptor binding in rats exposed to intermittent hypoxia during sleep
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isoform cPLA2-alpha
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synaptosomal fraction
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-
-
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ATCC CRL 8305, thyroid cells, CNP is firmly associated with FRTL-5 cells
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ATCC CRL8305
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IL-1alpha/IFNgamma-induced down-regulation of thyroperoxidase is not affected by Th3 cytokines
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thyroid cell
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thyroid cells
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thyroid follicular cell line
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-
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coeliac ganglia
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cultured trigeminal ganglia, similar expression profile of enzyme and type 2 bradykinin receptor
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dorsal root
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dorsal root ganglia
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dorsal root ganglion
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dorsal root ganglion and sympathetic celiac ganglion. mRNA for the NAD(P)H oxidase subunits NOX1, NOX2, NOX4, p47phox, and p22phox is present in both celiac ganglion and dorsal root ganglion, mRNA for NOX4 is significantly higher in celiac ganglion than in dorsal root ganglion. Catalytic subunit p22phox mRNA and protein expression is greater in celiac ganglion of hypertensive rats but not in dorsal root ganglion. Subunit p47phox mRNA and protein, as well as Rac-1protein, are significantly decreased in hypertensive dorsal root ganglion but not in celiac ganglion. Subunit p47phox is translocated from cytoplasm to membrane in hypertensive celiac ganglion but not in hypertensive dorsal root ganglion
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i.e. Auerbach's plexus
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intramuscular plexus
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retinal
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satellite cells of dorsal root ganglia
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superior cervical
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superior cervical ganglia
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sympathetic autonomic ganglia, no activity in paravertebral superior cervical ganglia or in perikarya of any sympathetic ganglion. The superior mesenteric ganglia of aged and diabetic rats, in which dysplasia is prominent, fail to show involvement of diaphorase containing nerve terminals
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2421, 4142, 4144, 4145, 4147, 30779, 30780, 30785, 30798, 36855, 36867, 208394, 486323, 638980, 639086, 643819, 645819, 645825, 650814, 671240, 698948, 708405
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analysis of expression of the cancer-related protein ornithine decarboxylase (ODC) in nontransformed gastric mucosa, relationship between expression level of the enzyme and mucosal proliferation, overview
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chief cells, coordinated decrease of pepsinogen, furin, and transforming growth factor beta
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in the gastric epithelium
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during experimental gastric ulcer healing induced by acetic acid injection MMP-3 and MMP-3 expression is increased in stromal cells of the gastric mucosa bordering the ulcer. MMP-13 RNAs are confined to the upper layers of the granulation tissue
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induced by acetic acid injection
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-
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after 10 days of cold exposure an increase of 2.8fold in Dio2 activity is detected in white glycolytic gastrocnemius but not in red oxidative gastrocnemius fibers
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ischemic and contralateral non-ischemic legs
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overexpression of isozyme PDK4 during starvation or diabetes, reversible by insulin
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red portion of the muscle
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135558, 135559, 647915, 679649, 691934, 692281, 692565, 708300, 711688, 718751, 719901, 754898
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atrial- and C-type natriuretic peptide stimulated membrane-bound GC
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intraluminal, intestinal microvillar membrane, and mucosa, in the intestinal tract, the activity of alkaline SMase is much higher than the activity of neutral and acid SMase, overview
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-
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both ADAM10 and ADAM17, EC 3.4.24.86, are present during all stages of spermatogenesis
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both ADAM10, EC 3.4.24.81, and ADAM17 are present during all stages of spermatogenesis
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differentiating rat germinal cell, presence of both enzyme isoforms of 60 kDa and 110 kDa
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highly expressed at and after meiosis
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-
much lower activity than in Sertoli cells
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primary culture
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testicular, specifically expressed in
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testicular, TESK1 mRNA in the testis is detectable only after the 18th day of postnatal development of mice and is mainly expressed in the round spermatids
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-
-
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a pituitary carcinoma celll line
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a pituitary tumor cell line
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pituitary tumor-derived cell line
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-
-
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-
AC4 and AC6
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pituitary cell line
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-
somato-lactotrope cell
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-
-
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-
from maxillary and mandibular jaws, semi-quantitative RT-PCR analysis, overview
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quantitative determination of content of membrane type-I MMP, TIMP-2 and MMP-2 mRNA and proteins
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renin is present in the vascular endothelium and intensely expressed in the epithelial basal layer of periodontally affected gingival tissue
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-
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pars glandularis
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-
-
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cerebellar glia cell
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olfactory bulb ensheathing glia in explant cultures
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primary culture of mixed glia. Incubation of cultures in the presence of fibrillar amyloid beta1-42 induces the assembly and the activation of NADPH oxidase, and triggers the production of superoxide anion-derived reactive oxygen species. Pretreatment of microglia with melatonin dose-dependently prevents the activation of NADPH oxidase and decreases the production of reactive oxygen species. Melatonin inhibits the phosphorylation of the p47phox subunit of NADPH oxidase via a PI3K/Akt-dependent signalling pathway, blocks the translocation of p47phox and p67phox subunit to the membrane, down-regulates the binding of p47phox to gp91phox, and impairs the assembly of NADPH oxidase
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645561, 645562, 661658, 664925, 683874, 686537, 689224, 690635, 695162, 710106, 710112, 712120, 739070, 763094
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a substantial proportion of astrocytic and microglial profiles are immunolabeled for both diacylglycerol lipase alpha and NAPE-PLD. NAPE-PLD immunoreactivity on glial profiles at the vicinity of synapses is only occasionally observed. Results suggest that both neurons and glial cells can synthesize and release anandamide in the superficial spinal dorsal horn. Anandamide can predominantly be released from nonsynaptic dendritic and glial compartments
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C6 glial cell
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cortical glial cell, in both neurons and glia, Nrf2 expression and treatment with chemopreventive Nrf2 activators, including 3H-1,2-dithiole-3-thione and sulforaphane, upregulate sulfiredoxin, an enzyme responsible for reducing hyperoxidized peroxiredoxins
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expression of AACS mRNA in the cerebellum is restricted primarily to glial cells
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from newborn rat brain
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high enzyme content
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isoform BB (brain) is the predominant isozyme expressed in enteric glial cells
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mesencephalic neuron-glial culture and reconstituted culture
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microglial cells become KAT-I immunoreactive only after treatment with 6-hydroxydopamine
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neuron-glial cell culture
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oligodendrocyte-enriched cultures of neonatal rat brain glial cells, CNP2
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primary culture
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primary culture. Proliferation induced by fibrillar beta-amyloid peptide Abeta1-40 is mediated both by microglial release of TNF-alpha and by production of hydrogen peroxide by enzyme
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quantitative analysis of enzyme content at different epileptic stages compared to control rats, overview
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satellite glial cells in dorsal root ganglia. HMGCS1 but not HMGCS2 immunoreactivity in satellite glial cells is reduced in the fifth lumbar (L5) dorsal root ganglion that contain axotomized neurons following L5 spinal nerve ligation in rats. HMGCS1 protein level in axotomized L5 dorsal root ganglia is reduced after spinal nerve ligation to 66% at 3 days and 58% at 28 days of its level in control samples, whereas HMGCS2 protein is comparable between injured and control dorsal root ganglia
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throughout the rostrocaudal extent of the brain
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-
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Rugli cells
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135401, 650371, 662380, 671608, 687604, 688759, 690140, 694138, 697101, 705283, 709276
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astrocytic
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C6-glioma cells
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-
C6Bu-1 rat glioma cell, isoenzyme PI-PLC-beta1
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hexokinase I, predominant in normal brain
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hexokinase II, increased in brain tumors, ethylnitrosourea-induced 36B-10 astrocytic F-344 rat brain tumor cell line
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-
high expression level of MMP-2 increasing during growth
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high expression level of MMP-9 increasing during growth
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-
-
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C-6 cell, half-life of the enzyme is 6 h
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-
-
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lateral
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-
-
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isoform 11beta-HSD1 is clearly expressed while isoform 11beta-HSD2 is much less prominent, 11beta-HSD1 protein expression predominates in endothelial cells and varies during periods of growth
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-
-
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mesangial cell culture
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-
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expression in granules cells and seminiferous tubules of pubertal gonads
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gonadal adipose tissue
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-
-
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diabetic animals treated with BioGHK incorporated collagen (Peptide Incorporated Collagen) show significant higher levels of catalase due to the ability of GHK to attract macrophages and cytokines towards the wound environment
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-
-
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cerebellar granule cells are treated with GCS inhibitor D-threo-2-palmitoylamino-3-pyrrolidino-1-propanol which induces an increase in log-chain ceramides, loss of viability and dramatic changes in neuron/neurite morphology
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dentate granule cell. Pyridoxal kinase immunoreactivity is not increased after induction of long-term potentiation and not involved in increase in the efficiency of high frequency stimulus-induced potentiation of populations spike amplitude when compared with saline-, or Tat-protein-treated animals
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of the input layer of cerebellar cortex
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primary
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primary cerebellar, cultured
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-
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cultured cell
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-
periovulatory granulosa cell
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-
primary
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primary cultures of granulosa cells matured in vitro with follicle-stimulating hormone and testosterone
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the luteinizing granulosa cells of the corpus luteum express the highest levels of Htra3
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-
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CPE expression occurs in gastrin synthesizing cells and in gastrin-somatostatin progenitor cells
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low activity
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lowest level in oesophagus and stomach and a shallow diminishing gradient from proximal small intestine to distal colon and rectum
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lumen
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mitochondrial isoform, secretory epithelia throughout digestive tract, cytosolic isoform, autonomic innervation of digestive tract
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-
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rat hepatoma cell line
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-
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hepatoma cell line, determination of PDK4 expression level in presence or absence of farnesoid X receptor agonists
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liver cell
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B0BMT9, D3ZKT0, P00787, P22791, P32038, P56574, P70531, Q62833, Q68FX9, Q68FY0, Q80Z29
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673668, 681031, 691037, 700147, 703088, 703143, 707088, 729556, 731364, 733123, 738284, 739053, 740117, 740279, 742055, 742457, 743622, 760043, 760364, 760639, 764408, 766124, 770227, 776083, 777838, 779401
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a cell line with myogenic potential derived from embryonic rat heart
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components of Porphyromonas gingivalis spent culture medium not only result in increased total MEK-1 and ERK-1 protein products, but also cause increased cellular size, DNA fragmentation, and nuclear condensation
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embryonic heart myoblastic cells, cells grown in cell culture and treated with ethyl-p-chlorophenoxyisobutyrate (clofibrate), no effect of clofibrate on enzyme activity
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myoblastic cell line
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neonatal rat cardiomyoblasts
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quantitative real-time-PCR expression analysis of ATE1
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undifferentiated neonatal cardiomyocyte. In heat-shocked cells aconitase activity is reduced
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-
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extracellular matrix, dermal papilla, and follicular epithelium
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B0BMT9, D3ZKT0, O08557, O08680, O35920, O55171, O88267, O88422, O88483, O88484, P04177, P04694, P04764, P04797, P05708, P10860, P11960 and P35738, P13233, P15684, P15791, P16636, P21708, P26819, P27791, P27881, P30099, P32038, P37136, P42893, P47820, P49185, P54645, P56558, P56574, P63329, P70531, P85973, P97629, P97711, Q00972, Q14U74, Q4KLP0, Q5BQE6, Q5GF25, Q5M819, Q5XI78, Q62761, Q62762, Q62763, Q62967, Q63065, Q63415, Q63704, Q63707, Q64428, Q64559, Q64591, Q6AYB2, Q6IUU3, Q6MG60, Q6P4Z6, Q769K2, Q7TQ90, Q811A3, Q8VHT6, Q91V26, Q91XT9, Q920F5, Q925R7, Q99NA5, Q99NI4, Q99P39, Q99PR0, Q9ER34, Q9ES66, Q9JHX4, Q9R0C5
-
563, 572, 675, 702, 733, 756, 787, 988, 989, 995, 1354, 1384, 1537, 1627, 1664, 1743, 3002, 3009, 3014, 3134, 3413, 3415, 3416, 3962, 4009, 4423, 4542, 4555, 4844, 4849, 4860, 5112, 5119, 28967, 28971, 31365, 35908, 36043, 36321, 37064, 37069, 37599, 80849, 80892, 80903, 80906, 80916, 80917, 80941, 80992, 81223, 81283, 81307, 94261, 94308, 94389, 94468, 94558, 94808, 94883, 94892, 94898, 94904, 94906, 94908, 94912, 94925, 94935, 94942, 94948, 95042, 95053, 95069, 95070, 95240, 95254, 114223, 114233, 134703, 134888, 134933, 134945, 135126, 135236, 135422, 135474, 137040, 137041, 137045, 137183, 171965, 207968, 208367, 208432, 208687, 208880, 208881, 208998, 209002, 209015, 209028, 209031, 209292, 209701, 210006, 210007, 210232, 210233, 210237, 210239, 246962, 246969, 285604, 285684, 285720, 285918, 286013, 286024, 286182, 286183, 286184, 286204, 286269, 286343, 286516, 286520, 286521, 286536, 286540, 286749, 286767, 287301, 287308, 288148, 288174, 288893, 289134, 289158, 289278, 326411, 348941, 349041, 349056, 349060, 349070, 349074, 389464, 390346, 390629, 390714, 390826, 390925, 391044, 391071, 391199, 391541, 391879, 392038, 392350, 392616, 392624, 392734, 393016, 393223, 393796, 394033, 394352, 394366, 394432, 394699, 394810, 394811, 394817, 394867, 394871, 395105, 395924, 396035, 396043, 396065, 396117, 396118, 396418, 438244, 439944, 439946, 439989, 441356, 441507, 441508, 441514, 441556, 486103, 486293, 486294, 486295, 486323, 486403, 486537, 486542, 486556, 486558, 486559, 486567, 486584, 486618, 486631, 487344, 487348, 487403, 487404, 487407, 487416, 487417, 487418, 487421, 487422, 487423, 487424, 487429, 487430, 488281, 489611, 489616, 489741, 490038, 490757, 491019, 491168, 491258, 491403, 491630, 491732, 491769, 636998, 637126, 637616, 637619, 637754, 638109, 638784, 639430, 639636, 640009, 640014, 640017, 640019, 640023, 640031, 640037, 640039, 640103, 640173, 640174, 640298, 640302, 640303, 640306, 640324, 640330, 640578, 640583, 640585, 640587, 640594, 640598, 640599, 640774, 640814, 640920, 641091, 641346, 641392, 641572, 641769, 642152, 642159, 642164, 642165, 642371, 642385, 642400, 642403, 642420, 642440, 642558, 642641, 642661, 643312, 643693, 643812, 644005, 645269, 645561, 645562, 645807, 645974, 645975, 645978, 645987, 645994, 646121, 646161, 646163, 646164, 646182, 646415, 646435, 647141, 647183, 647495, 648105, 648785, 648786, 648790, 648792, 649426, 649789, 650198, 650338, 651443, 651779, 652365, 653127, 653857, 654021, 654149, 654401, 654699, 655525, 655957, 656431, 657678, 657738, 657744, 657761, 658458, 658792, 658837, 658885, 659111, 659168, 659354, 659673, 661046, 661455, 661458, 661495, 661498, 661636, 662256, 662693, 662837, 662841, 663275, 664215, 664240, 664555, 664561, 664566, 664711, 665064, 665109, 665243, 665633, 666150, 666213, 666322, 666534, 666799, 667361, 667821, 667841, 668262, 668528, 668540, 668828, 668892, 669164, 669619, 671244, 671249, 671278, 671302, 671950, 672227, 672280, 672348, 672941, 673007, 673313, 673460, 673668, 673882, 673909, 674063, 674380, 674503, 675105, 675240, 675537, 675740, 675943, 676101, 676131, 676337, 677475, 677574, 677832, 677930, 679659, 680069, 680099, 680103, 680212, 681000, 681284, 682957, 683045, 683354, 683926, 683958, 684668, 684819, 685238, 685433, 685980, 685983, 686054, 686124, 686125, 686560, 687078, 687479, 688042, 688220, 688447, 689094, 690344, 690359, 690363, 690880, 690886, 691037, 691398, 691566, 691656, 691657, 692058, 692060, 692187, 692267, 692365, 693075, 693127, 693180, 693787, 693847, 694175, 694346, 694874, 695076, 695196, 695410, 695446, 695493, 695601, 697152, 697220, 697266, 697521, 697523, 697580, 697831, 698056, 698332, 699005, 699625, 699690, 699744, 700110, 700360, 700512, 700652, 701008, 701155, 701313, 701443, 702387, 702536, 702619, 702742, 702967, 703084, 703589, 703811, 703993, 705266, 705523, 705679, 706844, 707036, 708109, 708150, 708398, 708501, 708649, 708684, 708981, 708982, 709562, 709566, 709653, 709921, 710682, 711289, 711328, 711688, 711965, 712050, 712851, 712943, 714033, 715435, 715787, 718751, 720117, 720858, 720974, 721929, 722774, 722780, 723006, 725456, 727633, 730008, 732583, 732697, 732777, 733056, 735626, 735627, 736429, 736550, 739745, 740117, 740438, 740641, 741458, 742031, 742055, 742246, 742457, 742814, 742889, 745267, 745402, 745890, 748220, 749749, 750212, 750281, 751698, 751816, 752416, 752912, 753121, 753779, 753895, 759114, 759138, 760109, 760364, 760466, 760639, 760901, 761409, 762101, 762271, 762496, 762615, 763049, 763067, 763515, 764408, 766792, 768943, 770227, 771943, 773803, 773845, 775302, 778606, 779444
brenda
-
0.0013 mg Prx I per mg of soluble protein Prx I, 0.002 mg Prx II per mg of soluble protein, 0.0033 mg Prx III per mg of soluble protein, 0.0005 mg Prx V per mg of soluble protein and 0.0003 mg Prx VI per mg of soluble protein
brenda
110 kDa subunit
brenda
-
12-day administration of agents that either inhibit the synthesis of circulating angiotensin II or block the activity of angiotensin II at the AT1 receptor induce an increase in cardiac ACE2 mRNA, accompanied by increases in cardiac membrane ACE2 activity in rats medicated with either losartan or both losartan and lisinopril
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-
2 isoforms of CPT I
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-
2fold activity under cold stress. Injection of the angiotensin converting enzyme inhibitor enalapril malate prevented the increase of tyrosine hydroxylase under cold stress
brenda
3.3fold increase in mRNA after 6 h of hypoxia
brenda
-
85% of liver activity
brenda
A-type enzyme expression
brenda
-
about 35% of the ACE2 gene expression in kidney cortex
brenda
abundantly expressed
brenda
-
aconitase-specific activity increases by 12% at 2% O2 compared to 21% O2
brenda
-
activation of the prosurvival phosphatidylinositol 3-kinase-Akt pathway is involved in the protective action of poly(ADP-ribose) polymerase 1 inhibition in a model of donor heart procurement and hypothermic storage
brenda
-
activities in adult tissues are only 10-40% of those found in newborn
brenda
-
activity declines 34% during 30 min of ischemia
brenda
-
activity increased significantly in the diazinon treated group compared with the control group
brenda
-
adult
brenda
-
almost exclusively the nonglycosylated form of the enzyme
brenda
-
at the protein level, but not at the mRNA level, the content of brain isoform of glycogen phosphorylase is similar in heart and brain. MM is more abundant in the heart than in the brain. Muscle isoform of glycogen phosphorylase is more abundant in the heart than in the brain. The brai