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(-)-maackiain biosynthesis
-
-
PWY-2464
(-)-medicarpin biosynthesis
-
-
PWY-2463
(1'S,5'S)-averufin biosynthesis
-
-
PWY-5954
(1,4)-beta-D-xylan degradation
-
-
PWY-6717
(3R)-linalool biosynthesis
-
-
PWY-7709
(3R)-N-[(2S)-1-hydroxy-6-[(3R)-3-isocyanobutanamido]hexan-2-yl]-3-isocyanobutanamide biosynthesis
-
-
PWY-8320
(3S)-linalool biosynthesis
-
-
PWY-7141
(4R)-carvone biosynthesis
-
-
PWY-5928
(4S)-carvone biosynthesis
-
-
PWY-7443
(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
(5R)-carbapenem carboxylate biosynthesis
(5Z)-dodecenoate biosynthesis I
-
-
PWY0-862
(5Z)-dodecenoate biosynthesis II
-
-
PWY-7858
(5Z)-icosenoate biosynthesis
-
-
PWY-5361
(7Z,10Z,13Z)-hexadecatrienoate biosynthesis
-
-
PWY-7590
(8E,10E)-dodeca-8,10-dienol biosynthesis
-
-
PWY-7654
(9Z)-tricosene biosynthesis
-
-
PWY-7035
(aminomethyl)phosphonate degradation
-
-
PWY-7805
(Kdo)2-lipid A biosynthesis (E. coli)
-
-
KDO-LIPASYN-PWY
(Kdo)2-lipid A biosynthesis (generic)
-
-
PWY-8285
(Kdo)2-lipid A biosynthesis (H. pylori)
-
-
PWY2DNV-2
(Kdo)2-lipid A biosynthesis (P. gingivalis)
-
-
PWY-8247
(Kdo)2-lipid A biosynthesis (P. putida)
-
-
PWY-8075
(Kdo)2-lipid A biosynthesis I (Brucella)
-
-
PWY2B4Q-7
(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
(Z)-butanethial-S-oxide biosynthesis
-
-
PWY-6900
(Z)-phenylmethanethial S-oxide biosynthesis
-
-
PWY-6539
1,2-dichloroethane degradation
-
-
12DICHLORETHDEG-PWY
1,3-beta-D-glucan biosynthesis
-
-
PWY-6773
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-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-cis-3-hydroxyretinal biosynthesis
-
-
PWY-7043
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
2,2'-dihydroxybiphenyl degradation
-
-
PWY-7009
2,3-dihydroxybenzoate biosynthesis
-
-
PWY-5901
2,3-dihydroxybenzoate degradation
-
-
PWY-7480
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-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-hydroxybiphenyl degradation
-
-
PWY-7008
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-(imidazol-5-yl)lactate salvage
-
-
PWY-5029
3-chlorocatechol degradation
-
-
3-chlorocatechol degradation I (ortho)
-
-
PWY-6089
3-chlorocatechol degradation II (ortho)
-
-
PWY-6193
3-chlorocatechol degradation III (meta pathway)
-
-
PWY-6214
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-methylarginine biosynthesis
-
-
PWY-6511
3-methylbutanol biosynthesis (engineered)
-
-
PWY-6871
3-methylthiopropanoate biosynthesis
-
-
PWY-5389
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-amino-3-hydroxybenzoate degradation
-
-
PWY-7006
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-chlorobenzoate degradation
-
-
PWY-6215
4-chlorocatechol degradation
-
-
PWY-6087
4-chloronitrobenzene degradation
-
-
PWY-5645
4-coumarate degradation (aerobic)
-
-
PWY-8002
4-coumarate degradation (anaerobic)
-
-
PWY-7046
4-deoxy-L-threo-hex-4-enopyranuronate degradation
-
-
PWY-6507
4-ethylphenol degradation (anaerobic)
-
-
PWY-6080
4-hydroxy-2(1H)-quinolone biosynthesis
-
-
PWY-6661
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-hydroxyphenylacetate degradation
4-methylphenol degradation to protocatechuate
-
-
PWY-7700
4-nitrophenol degradation I
-
-
PWY-5487
4-nitrophenol degradation II
-
-
PWY-5488
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-nitroanthranilate degradation
-
-
PWY-7044
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 III (Chlamydia)
-
-
PWY-7539
6-hydroxymethyl-dihydropterin diphosphate biosynthesis IV (Plasmodium)
-
-
PWY-7852
7-(3-amino-3-carboxypropyl)-wyosine biosynthesis
-
-
PWY-7286
7-dehydroporiferasterol biosynthesis
-
-
PWY-7155
8-amino-7-oxononanoate biosynthesis I
-
-
PWY-6519
8-amino-7-oxononanoate biosynthesis IV
-
-
PWY-8203
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
9-lipoxygenase and 9-hydroperoxide lyase pathway
-
-
PWY-5408
ABH and Lewis epitopes biosynthesis from type 1 precursor disaccharide
-
-
PWY-7832
ABH and Lewis epitopes biosynthesis from type 2 precursor disaccharide
-
-
PWY-7831
abscisic acid biosynthesis
-
-
PWY-695
Ac/N-end rule pathway
-
-
PWY-7800
Acarbose and validamycin biosynthesis
-
-
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 II
-
-
PWY-5535
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
acridone alkaloid biosynthesis
-
-
PWY-5958
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
acyl-[acyl-carrier protein] thioesterase pathway
-
-
PWY-5142
acylceramide biosynthesis and processing
-
-
PWY-8042
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
-
-
agarose degradation
-
-
PWY-6816
ajmaline and sarpagine biosynthesis
-
-
PWY-5301
alanine racemization
-
-
PWY-8072
Alanine, aspartate and glutamate metabolism
-
-
aldoxime degradation
-
-
P345-PWY
alginate degradation
-
-
PWY-6986
alkane biosynthesis I
-
-
PWY-7032
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
allantoin degradation to ureidoglycolate I (urea producing)
-
-
PWY-5697
allantoin degradation to ureidoglycolate II (ammonia producing)
-
-
PWY-5698
alliin metabolism
-
-
PWY-5706
allopregnanolone biosynthesis
-
-
PWY-7455
alpha-amyrin biosynthesis
-
-
PWY-5377
alpha-dystroglycan glycosylation
-
-
PWY-7981
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 II
-
-
PWY-7378
aminopropylcadaverine biosynthesis
-
-
PWY0-1303
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 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
ansatrienin biosynthesis
-
-
PWY-8040
anteiso-branched-chain fatty acid biosynthesis
-
-
PWY-8173
anthocyanin biosynthesis
-
-
PWY-5125
anthocyanin biosynthesis (pelargonidin 3-O-glucoside)
-
-
PWY-7267
apratoxin A biosynthesis
-
-
PWY-8361
Arabinogalactan biosynthesis - Mycobacterium
-
-
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 II
-
-
PWY-8101
arsenate detoxification III
-
-
PWY-8263
arsenate detoxification IV (mycothiol)
-
-
PWY-6421
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 I
-
-
SO4ASSIM-PWY
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
autoinducer AI-1 biosynthesis
-
-
PWY-6157
autoinducer AI-2 biosynthesis I
-
-
PWY-6153
autoinducer AI-2 biosynthesis II (Vibrio)
-
-
PWY-6154
avenanthramide biosynthesis
-
-
PWY-8157
bacilysin biosynthesis
-
-
PWY-7626
backdoor pathway of androgen biosynthesis
-
-
PWY-8200
bacterial bioluminescence
-
-
PWY-7723
baicalein degradation (hydrogen peroxide detoxification)
-
-
PWY-7214
baicalein metabolism
-
-
PWY-7212
baumannoferrin biosynthesis
-
-
PWY-7988
benzene degradation I (aerobic)
-
-
PWY-5450
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
Benzoxazinoid biosynthesis
-
-
benzoxazinoid glucosides biosynthesis
-
-
benzoyl-CoA biosynthesis
-
-
PWY-6458
benzoyl-CoA degradation
-
-
benzoyl-CoA degradation I (aerobic)
-
-
PWY-1361
berberine biosynthesis
-
-
PWY-3901
bergamotene biosynthesis I
-
-
PWY-6243
beta-(1,4)-mannan degradation
-
-
PWY-7456
beta-1,4-D-mannosyl-N-acetyl-D-glucosamine degradation
-
-
PWY-7586
beta-alanine biosynthesis I
-
-
PWY-3981
beta-alanine biosynthesis II
-
-
PWY-3941
beta-alanine biosynthesis III
-
-
PWY-5155
beta-alanine biosynthesis IV
-
-
PWY-5760
beta-alanine degradation I
-
-
BETA-ALA-DEGRADATION-I-PWY
beta-alanine degradation II
-
-
PWY-1781
beta-Alanine metabolism
-
-
beta-carboline biosynthesis
-
-
PWY-5877
beta-D-glucuronide and D-glucuronate degradation
-
-
PWY-7247
beta-D-mannosyl phosphomycoketide biosynthesis
-
-
PWY-7740
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 biosynthesis, neutral pathway
bile acids deconjugation
-
-
PWY-8135
Biosynthesis of 12-, 14- and 16-membered macrolides
-
-
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
-
-
Biosynthesis of vancomycin group antibiotics
-
-
Biosynthesis of various secondary metabolites - part 1
-
-
Biosynthesis of various secondary metabolites - part 3
-
-
biotin biosynthesis from 8-amino-7-oxononanoate I
-
-
PWY0-1507
biotin-carboxyl carrier protein assembly
-
-
PWY0-1264
biphenyl degradation
-
-
PWY5F9-12
bis(guanylyl molybdopterin) cofactor sulfurylation
-
-
PWY-8164
bisabolene biosynthesis (engineered)
-
-
PWY-7102
bisphenol A degradation
-
-
PWY-7757
Bisphenol degradation
-
-
bisucaberin biosynthesis
-
-
PWY-6381
bombykol biosynthesis
-
-
PWY-7423
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
C20,20 CDP-archaeol biosynthesis
-
-
PWY-6349
C25,25 CDP-archaeol biosynthesis
-
-
PWY-8365
C30 carotenoid biosynthesis
-
-
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
-
-
cadaverine biosynthesis
-
-
PWY0-1601
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
capsiconiate biosynthesis
-
-
PWY-6027
Carbapenem biosynthesis
-
-
carbaryl degradation
-
-
PWY-8111
carbazole degradation
-
-
PWY-6550
carbofuran degradation I
-
-
PWY-8286
carbofuran degradation II
-
-
PWY-8287
carbofuran degradation III
-
-
PWY-8288
Carbon fixation in photosynthetic organisms
-
-
Carbon fixation pathways in prokaryotes
-
-
cardenolide glucosides biosynthesis
-
-
PWY-6036
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
catechol degradation to beta-ketoadipate
-
-
CATECHOL-ORTHO-CLEAVAGE-PWY
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 and hemicellulose degradation (cellulolosome)
-
-
PWY-6784
cellulose biosynthesis
-
-
PWY-1001
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
chanoclavine I aldehyde biosynthesis
-
-
PWY-6493
chelerythrine biosynthesis
-
-
PWY-7507
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
chlorinated phenols degradation
-
-
PWY-6197
Chloroalkane and chloroalkene degradation
-
-
Chlorocyclohexane and chlorobenzene degradation
-
-
chlorogenic acid biosynthesis I
-
-
PWY-6039
chlorogenic acid degradation
-
-
PWY-6781
chlorophyll metabolism
-
-
chlorosalicylate degradation
-
-
PWY-6107
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 III
-
-
PWY-7167
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
-
-
cinnamoyl-CoA biosynthesis
-
-
PWY-6457
cis-abienol biosynthesis
-
-
PWY18C3-13
cis-geranyl-CoA degradation
-
-
PWY-6672
cis-vaccenate biosynthesis
cis-zeatin biosynthesis
-
-
PWY-2781
Citrate cycle (TCA cycle)
-
-
CMP phosphorylation
-
-
PWY-7205
CMP-2-keto-3-deoxy-D-glycero-D-galacto-nononate biosynthesis
-
-
PWY-6140
CMP-3-deoxy-D-manno-octulosonate biosynthesis
-
-
PWY-1269
CMP-8-amino-3,8-dideoxy-D-manno-octulosonate biosynthesis
-
-
PWY-7674
CMP-diacetamido-8-epilegionaminic acid biosynthesis
-
-
PWY-7719
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
CMP-pseudaminate biosynthesis
-
-
PWY-6143
CO2 fixation in Crenarchaeota
-
-
CO2 fixation into oxaloacetate (anaplerotic)
-
-
PWYQT-4429
cobalamin salvage (eukaryotic)
-
-
PWY-7974
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 I
-
-
P261-PWY
coenzyme M biosynthesis II
-
-
PWY-6643
colanic acid building blocks biosynthesis
-
-
COLANSYN-PWY
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
coptisine biosynthesis
-
-
PWY-8030
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
crepenynate biosynthesis
-
-
PWY-6013
crotonate fermentation (to acetate and cyclohexane carboxylate)
-
-
PWY-7401
crotonyl-CoA/ethylmalonyl-CoA/hydroxybutyryl-CoA cycle (engineered)
-
-
PWY-7854
curacin A biosynthesis
-
-
PWY-8358
cuticular wax biosynthesis
-
-
PWY-282
cutin biosynthesis
-
-
PWY-321
Cutin, suberine and wax biosynthesis
-
-
cyanide detoxification II
-
-
PWY-7142
Cyanoamino acid metabolism
-
-
cyanophycin metabolism
-
-
PWY-7052
cyclic electron flow
-
-
PWY-8270
cyclopropane fatty acid (CFA) biosynthesis
-
-
PWY0-541
cylindrospermopsin biosynthesis
-
-
PWY-8045
Cysteine and methionine metabolism
-
-
cytidylyl molybdenum cofactor sulfurylation
-
-
PWY-8165
cytochrome c biogenesis (system I type)
-
-
PWY-8147
cytochrome c biogenesis (system II type)
-
-
PWY-8146
cytochrome c biogenesis (system III type)
-
-
PWY-8145
cytokinin-O-glucosides biosynthesis
-
-
PWY-2902
cytosolic NADPH production (yeast)
-
-
PWY-7268
D-Amino acid metabolism
-
-
D-arabinitol degradation I
-
-
DARABITOLUTIL-PWY
D-arabinose degradation III
-
-
PWY-5519
D-arabinose degradation IV
-
-
PWY-8331
D-arabinose degradation V
-
-
PWY-8334
D-cycloserine biosynthesis
-
-
PWY-7274
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-galacturonate degradation II
-
-
PWY-6486
D-galacturonate degradation III
-
-
PWY-8391
D-gluconate degradation
-
-
GLUCONSUPER-PWY
D-glucuronate degradation I
-
-
PWY-5525
D-glucuronate degradation II
-
-
PWY-6501
D-glucuronate degradation III
-
-
PWY-8390
D-lactate to cytochrome bo oxidase electron transfer
-
-
PWY0-1565
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-tagatose degradation
-
-
PWY-8324
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
-
-
dehydro-D-arabinono-1,4-lactone biosynthesis
-
-
PWY3O-6
dermatan sulfate biosynthesis
-
-
PWY-6568
dermatan sulfate degradation I (bacterial)
-
-
PWY-7646
desferrioxamine B biosynthesis
-
-
PWY-6376
desferrioxamine E biosynthesis
-
-
PWY-6375
detoxification of reactive carbonyls in chloroplasts
-
-
PWY-6786
di-homo-gamma-linolenate metabolites biosynthesis
-
-
PWY-8396
di-myo-inositol phosphate biosynthesis
-
-
PWY-6664
di-trans,poly-cis-undecaprenyl phosphate biosynthesis
-
-
PWY-5785
diacylglycerol and triacylglycerol biosynthesis
-
-
TRIGLSYN-PWY
diacylglycerol biosynthesis (PUFA enrichment in oilseed)
-
-
PWY-6804
diethylphosphate degradation
-
-
PWY-5491
digitoxigenin biosynthesis
-
-
PWY-6032
DIMBOA-glucoside biosynthesis
-
-
PWY-6950
dimethyl sulfide biosynthesis from methionine
-
-
PWY-7793
dimethyl sulfide degradation I
-
-
PWY-6047
dimethylsulfoniopropanoate biosynthesis I (Wollastonia)
-
-
PWY-6054
dimethylsulfoniopropanoate biosynthesis II (Spartina)
-
-
PWY-6055
dimethylsulfoniopropanoate biosynthesis III (algae and phytoplankton)
-
-
PWY-6053
dimethylsulfoniopropanoate degradation I (cleavage)
-
-
PWY-6046
dimorphecolate biosynthesis
-
-
PWY-5368
dimycocerosyl phthiocerol biosynthesis
-
-
PWY-7744
dimycocerosyl triglycosyl phenolphthiocerol biosynthesis
-
-
PWY-7743
diphenyl ethers degradation
-
-
PWY-7747
diphthamide biosynthesis I (archaea)
-
-
PWY-6482
diphthamide biosynthesis II (eukaryotes)
-
-
PWY-7546
dipicolinate biosynthesis
-
-
PWY-8088
dissimilatory sulfate reduction I (to hydrogen sufide))
-
-
DISSULFRED-PWY
Diterpenoid biosynthesis
-
-
divinyl ether biosynthesis I
-
-
PWY-5406
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-3-acetamido-3,6-dideoxy-alpha-D-glucose biosynthesis
-
-
PWY-7318
dTDP-3-acetamido-alpha-D-fucose biosynthesis
-
-
PWY-6953
dTDP-4-O-demethyl-beta-L-noviose biosynthesis
-
-
PWY-7301
dTDP-6-deoxy-alpha-D-allose biosynthesis
-
-
PWY-7413
dTDP-alpha-D-forosamine biosynthesis
-
-
PWY-6808
dTDP-alpha-D-mycaminose biosynthesis
-
-
PWY-7414
dTDP-alpha-D-olivose, dTDP-alpha-D-oliose and dTDP-alpha-D-mycarose biosynthesis
-
-
PWY-6973
dTDP-alpha-D-ravidosamine and dTDP-4-acetyl-alpha-D-ravidosamine biosynthesis
-
-
PWY-7688
dTDP-beta-D-fucofuranose biosynthesis
-
-
PWY-7312
dTDP-beta-L-4-epi-vancosamine biosynthesis
-
-
PWY-7440
dTDP-beta-L-digitoxose biosynthesis
-
-
PWY-7657
dTDP-beta-L-megosamine biosynthesis
-
-
PWY-7104
dTDP-beta-L-mycarose biosynthesis
-
-
PWY-6976
dTDP-beta-L-olivose biosynthesis
-
-
PWY-6974
dTDP-beta-L-rhamnose biosynthesis
-
-
DTDPRHAMSYN-PWY
dTDP-D-desosamine biosynthesis
-
-
PWY-6942
dTDP-L-daunosamine biosynthesis
-
-
PWY-7814
dTDP-N-acetylthomosamine biosynthesis
-
-
PWY-7315
dTDP-N-acetylviosamine biosynthesis
-
-
PWY-7316
dTDP-sibirosamine biosynthesis
-
-
PWY-8380
dTDPLrhamnose biosynthesis
-
-
dTMP de novo biosynthesis (mitochondrial)
-
-
PWY66-385
dZTP biosynthesis
-
-
PWY-8289
ecdysone and 20-hydroxyecdysone biosynthesis
-
-
PWY-7300
echinatin biosynthesis
-
-
PWY-6325
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
ephedrine biosynthesis
-
-
PWY-5883
epiberberine biosynthesis
-
-
PWY-8031
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
erythromycin D biosynthesis
-
-
PWY-7106
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
Escherichia coli serotype O:9 O antigen biosynthesis
-
-
PWY-8250
Escherichia coli serotype O:9a O antigen biosynthesis
-
-
PWY-7905
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
-
-
ethiin metabolism
-
-
PWY-5708
Ethylbenzene degradation
-
-
ethylbenzene degradation (anaerobic)
-
-
PWY-481
eumelanin biosynthesis
-
-
PWY-6498
even iso-branched-chain fatty acid biosynthesis
-
-
PWY-8175
extended VTC2 cycle
-
-
PWY4FS-13
factor 420 biosynthesis II (mycobacteria)
-
-
PWY-5198
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
fenchol biosynthesis II
-
-
PWY-6445
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 IV (thiol-independent)
-
-
FORMASS-PWY
formaldehyde oxidation VII (THF pathway)
-
-
PWY-7909
formate assimilation into 5,10-methylenetetrahydrofolate
-
-
PWY-1722
formate oxidation to CO2
-
-
PWY-1881
formate to dimethyl sulfoxide electron transfer
-
-
PWY0-1356
formate to nitrite electron transfer
-
-
PWY0-1585
formononetin conjugates interconversion
-
-
PWY-2904
fructan biosynthesis
-
-
PWY-822
fructan degradation
-
-
PWY-862
fructose 2,6-bisphosphate biosynthesis
-
-
PWY66-423
Fructose and mannose metabolism
-
-
fructose degradation
-
-
PWY0-1314
fusicoccin A biosynthesis
-
-
PWY-6659
GABA shunt I
-
-
GLUDEG-I-PWY
GABA shunt II
-
-
PWY-8346
gala-series glycosphingolipids biosynthesis
-
-
PWY-7840
galactitol degradation
-
-
GALACTITOLCAT-PWY
gallate biosynthesis
-
-
PWY-6707
gallate degradation III (anaerobic)
-
-
P3-PWY
gamma-butyrobetaine degradation II
-
-
PWY-3621
gamma-glutamyl cycle
-
-
PWY-4041
gamma-hexachlorocyclohexane degradation
-
-
GAMMAHEXCHLORDEG-PWY
gamma-linolenate biosynthesis II (animals)
-
-
PWY-6000
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-L-galactose biosynthesis
-
-
PWY-5115
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
gellan degradation
-
-
PWY-6827
genistein conjugates interconversion
-
-
PWY-2345
gentisate degradation I
-
-
PWY-6223
geranyl diphosphate biosynthesis
-
-
PWY-5122
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 amide metabolism
-
-
PWY-4181
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
glutathionylspermidine biosynthesis
-
-
PWY-4121
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 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
glycogen degradation III (via anhydrofructose)
-
-
PWY-7662
glycolate and glyoxylate degradation
-
-
glycolate and glyoxylate degradation II
-
-
GLYOXDEG-PWY
glycolipid desaturation
-
-
PWY-782
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
gossypol biosynthesis
-
-
PWY-5773
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
guanine and guanosine salvage III
-
-
PWY-6618
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 a biosynthesis
-
-
PWY-7856
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
hemoglobin degradation
-
-
PWY-6423
heparan sulfate biosynthesis
-
-
PWY-6558
heparan sulfate degradation
-
-
PWY-7651
heparin degradation
-
-
PWY-7644
heptadecane biosynthesis
-
-
PWY-6622
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
hordatine biosynthesis
-
-
PWY-6448
hyaluronan degradation
-
-
PWY-7645
hydrogen oxidation I (aerobic)
-
-
P283-PWY
hydrogen oxidation II (aerobic, NAD)
-
-
PWY-5382
hydrogen production II
-
-
PWY-6758
hydrogen production III
-
-
PWY-6759
hydrogen production VI
-
-
PWY-6780
hydrogen production VIII
-
-
PWY-6785
hydrogen sulfide biosynthesis II (mammalian)
-
-
PWY66-426
hydrogen to dimethyl sulfoxide electron transfer
-
-
PWY0-1577
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
hydroxymethylpyrimidine salvage
-
-
PWY-6910
hyperxanthone E biosynthesis
-
-
PWY-7169
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 alkaloid biosynthesis
-
-
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 V (bacteria and fungi)
-
-
PWY-5026
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
ipsdienol biosynthesis
-
-
PWY-7410
iron reduction and absorption
-
-
PWY-5934
Isoflavonoid biosynthesis
-
-
isoflavonoid biosynthesis I
-
-
PWY-2002
isoflavonoid biosynthesis II
-
-
PWY-2083
isoleucine metabolism
-
-
isoprene biosynthesis II (engineered)
-
-
PWY-7391
isoprenoid biosynthesis
-
-
isopropanol biosynthesis (engineered)
-
-
PWY-6876
Isoquinoline alkaloid biosynthesis
-
-
itaconate biosynthesis I
-
-
PWY-5750
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 I
-
-
PWY-6575
juvenile hormone III biosynthesis II
-
-
PWY-6650
kappa-carrageenan degradation
-
-
PWY-6821
Kdo transfer to lipid IVA (Brucella)
-
-
PWY2B4Q-6
Kdo transfer to lipid IVA (E. coli)
-
-
KDOSYN-PWY
Kdo transfer to lipid IVA (generic)
-
-
PWY-8284
Kdo transfer to lipid IVA (H. pylori)
-
-
PWY2DNV-1
Kdo transfer to lipid IVA (Haemophilus)
-
-
PWY-7675
Kdo transfer to lipid IVA (P. gingivalis)
-
-
PWY-8246
Kdo transfer to lipid IVA (P. putida)
-
-
PWY-8074
Kdo transfer to lipid IVA (Vibrio cholerae serogroup O1 El Tor)
-
-
PWY-8284-1
Kdo-lipid A biosynthesis (Vibrio cholerae serogroup O1 El Tor)
-
-
PWY-8378
Kdo8N transfer to lipid IVA
-
-
PWY-7676
ketogenesis
-
-
PWY66-367
L-alanine biosynthesis I
-
-
ALANINE-VALINESYN-PWY
L-alanine biosynthesis II
-
-
ALANINE-SYN2-PWY
L-alanine biosynthesis III
-
-
PWY0-1021
L-alanine degradation I
-
-
ALADEG-PWY
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 III
-
-
PWY-5517
L-arabinose degradation IV
-
-
PWY-7295
L-arabinose degradation V
-
-
PWY-8329
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 II (AST pathway)
-
-
AST-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 IX (arginine:pyruvate transaminase pathway)
-
-
PWY-5742
L-arginine degradation V (arginine deiminase pathway)
-
-
ARGDEGRAD-PWY
L-arginine degradation VI (arginase 2 pathway)
-
-
ARG-PRO-PWY
L-arginine degradation VII (arginase 3 pathway)
-
-
ARG-GLU-PWY
L-arginine degradation VIII (arginine oxidase pathway)
-
-
ARGDEG-IV-PWY
L-arginine degradation X (arginine monooxygenase pathway)
-
-
ARGDEG-V-PWY
L-arginine degradation XI
-
-
PWY-5024
L-arginine degradation XII
-
-
PWY-7523
L-arginine degradation XIII (reductive Stickland reaction)
-
-
PWY-8187
L-arginine degradation XIV (oxidative Stickland reaction)
-
-
PWY-6344
L-ascorbate biosynthesis I (plants, L-galactose pathway)
-
-
PWY-882
L-ascorbate biosynthesis II (plants, L-gulose pathway)
-
-
PWY4FS-11
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 I (bacterial, anaerobic)
-
-
PWY0-301
L-ascorbate degradation II (bacterial, aerobic)
-
-
PWY-6961
L-ascorbate degradation III
-
-
PWY-6960
L-asparagine biosynthesis I
-
-
ASPARAGINE-BIOSYNTHESIS
L-asparagine biosynthesis II
-
-
ASPARAGINESYN-PWY
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 biosynthesis VII (from S-sulfo-L-cysteine)
-
-
PWY-7870
L-cysteine biosynthesis VIII (Thermococcus kodakarensis)
-
-
PWY-8009
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-fucose degradation I
-
-
FUCCAT-PWY
L-fucose degradation II
-
-
PWY-8318
L-glutamate biosynthesis I
-
-
GLUTSYN-PWY
L-glutamate biosynthesis II
-
-
GLUTAMATE-SYN2-PWY
L-glutamate biosynthesis III
-
-
GLUTSYNIII-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-glutamine degradation II
-
-
GLUTAMINEFUM-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 IV
-
-
HISTDEG-PWY
L-histidine degradation V
-
-
PWY-5031
L-histidine degradation VI
-
-
HISHP-PWY
L-homocysteine biosynthesis
-
-
PWY-5344
L-homomethionine biosynthesis
-
-
PWY-1186
L-homophenylalanine biosynthesis
-
-
PWY-7275
L-homoserine biosynthesis
-
-
HOMOSERSYN-PWY
L-idonate degradation
-
-
IDNCAT-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-leucine biosynthesis
-
-
LEUSYN-PWY
L-leucine degradation I
-
-
LEU-DEG2-PWY
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 VII
-
-
PWY-5311
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 cycle II (plants)
-
-
PWY-7270
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 II
-
-
PWY-3462
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-proline degradation II (reductive Stickland reaction)
-
-
PWY-8186
L-pyrrolysine biosynthesis
-
-
PWY-6994
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 biosynthesis
-
-
TRPSYN-PWY
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 II
-
-
PWY-3461
L-tyrosine biosynthesis III
-
-
PWY-6120
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
lacinilene C biosynthesis
-
-
PWY-5828
lactate fermentation to acetate, CO2 and hydrogen (Desulfovibrionales)
-
-
PWY-8377
lacto-series glycosphingolipids biosynthesis
-
-
PWY-7839
lactose and galactose degradation I
-
-
LACTOSECAT-PWY
lactose degradation III
-
-
BGALACT-PWY
laminaribiose degradation
-
-
PWY-6778
lanosterol biosynthesis
-
-
PWY-6132
leucodelphinidin biosynthesis
-
-
PWY-5152
leucopelargonidin and leucocyanidin biosynthesis
-
-
PWY1F-823
leukotriene biosynthesis
-
-
PWY66-375
Limonene and pinene degradation
-
-
limonene degradation IV (anaerobic)
-
-
PWY-8029
linalool biosynthesis I
-
-
PWY-7182
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 A-core biosynthesis (Salmonella)
-
-
PWY1R65-1
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
Lipoarabinomannan (LAM) biosynthesis
-
-
lipoate biosynthesis and incorporation I
-
-
PWY0-501
lipoate biosynthesis and incorporation II
-
-
PWY0-1275
lipoate biosynthesis and incorporation III (Bacillus)
-
-
PWY-6987
lipoate biosynthesis and incorporation IV (yeast)
-
-
PWY-7382
lipoate biosynthesis and incorporation V (mammals)
-
-
PWY0-501-1
Lipoic acid metabolism
-
-
Lipopolysaccharide biosynthesis
-
-
lipoprotein posttranslational modification
-
-
PWY-7884
lipoxin biosynthesis
-
-
PWY66-392
long chain fatty acid ester synthesis (engineered)
-
-
PWY-6873
long-chain fatty acid activation
-
-
PWY-5143
lotaustralin degradation
-
-
PWY-6002
lupanine biosynthesis
-
-
PWY-5468
lupulone and humulone biosynthesis
-
-
PWY-5132
luteolin biosynthesis
-
-
PWY-5060
luteolin triglucuronide degradation
-
-
PWY-7445
macrolide antibiotic biosynthesis
-
-
malate/L-aspartate shuttle pathway
-
-
MALATE-ASPARTATE-SHUTTLE-PWY
maltose degradation
-
-
MALTOSECAT-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 I
-
-
MANNIDEG-PWY
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
menaquinol-4 biosynthesis II
-
-
PWY-7998
menthol biosynthesis
-
-
PWY-3061
metabolism of amino sugars and derivatives
-
-
metabolism of disaccharids
-
-
Metabolism of xenobiotics by cytochrome P450
-
-
methane oxidation to methanol I
-
-
PWY-1641
Methanobacterium thermoautotrophicum biosynthetic metabolism
-
-
PWY-6146
methanofuran biosynthesis
-
-
PWY-5254
methanogenesis from acetate
-
-
METH-ACETATE-PWY
methanogenesis from CO2
-
-
methanogenesis from H2 and CO2
-
-
METHANOGENESIS-PWY
methanogenesis from methanol
-
-
CO2FORM-PWY
methanol oxidation to carbon dioxide
-
-
PWY-7616
methanol oxidation to formaldehyde IV
-
-
PWY-5506
methiin metabolism
-
-
PWY-7614
methionine metabolism
-
-
methoxylated aromatic compound degradation II
-
-
PWY-8305
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
methyl-coenzyme M oxidation to CO2
-
-
PWY-5209
methyl-coenzyme M reduction to methane
-
-
METHFORM-PWY
methylamine degradation II
-
-
PWY-6965
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 III
-
-
PWY-5453
methylglyoxal degradation V
-
-
PWY-5458
methylglyoxal degradation VI
-
-
MGLDLCTANA-PWY
methylglyoxal degradation VIII
-
-
PWY-5386-1
methylsalicylate biosynthesis
-
-
PWY18C3-22
methylsalicylate degradation
-
-
PWY-6184, PWY18C3-24
methylwyosine biosynthesis
-
-
PWY-7285
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
molybdenum cofactor biosynthesis
-
-
molybdenum cofactor sulfulylation (eukaryotes)
-
-
PWY-5963
molybdopterin biosynthesis
-
-
PWY-6823
momilactone A biosynthesis
-
-
PWY-7477
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
mRNA capping II
-
-
PWY-7379
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
mycobacterial sulfolipid biosynthesis
-
-
PWY-7746
mycobactin biosynthesis
-
-
PWY185E-1
mycolate biosynthesis
-
-
PWYG-321
mycolyl-arabinogalactan-peptidoglycan complex biosynthesis
-
-
PWY-6397
mycothiol biosynthesis
-
-
PWY1G-0
mycothiol oxidation
-
-
PWY1G-126
myo-inositol biosynthesis
myo-inositol degradation I
-
-
P562-PWY
N-3-oxalyl-L-2,3-diaminopropanoate biosynthesis
-
-
PWY-8071
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-end rule pathway I (prokaryotic)
-
-
PWY-7801
N-Glycan biosynthesis
-
-
N-hydroxy-L-pipecolate biosynthesis
-
-
PWY-7861
N-methylpyrrolidone degradation
-
-
PWY-7978
N1-methyl-N3-aminocarboxypropyl-pseudouridine-modified rRNA biosynthesis
-
-
PWY-8341
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 bd oxidase electron transfer II
-
-
PWY0-1568
NADH to cytochrome bo oxidase electron transfer I
-
-
PWY0-1335
NADH to cytochrome bo oxidase electron transfer II
-
-
PWY0-1567
NADH to dimethyl sulfoxide electron transfer
-
-
PWY0-1348
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
-
-
naphthalene degradation (aerobic)
-
-
PWY-5427
naringenin biosynthesis (engineered)
-
-
PWY-7397
neolacto-series glycosphingolipids biosynthesis
-
-
PWY-7841
neolinustatin bioactivation
-
-
PWY-7092
Neomycin, kanamycin and gentamicin biosynthesis
-
-
neurosporaxanthin biosynthesis
-
-
PWY-6681
Nicotinate and nicotinamide metabolism
-
-
nicotine biosynthesis
-
-
PWY-5316
nicotine degradation I (pyridine pathway)
-
-
P181-PWY
nicotine degradation IV
-
-
PWY66-201
nicotine degradation V
-
-
PWY66-221
nitrate reduction I (denitrification)
-
-
DENITRIFICATION-PWY
nitrate reduction II (assimilatory)
-
-
PWY-381
nitrate reduction III (dissimilatory)
-
-
PWY0-1321
nitrate reduction IV (dissimilatory)
-
-
PWY-5674
nitrate reduction IX (dissimilatory)
-
-
PWY0-1581
nitrate reduction VII (denitrification)
-
-
PWY-6748
nitrate reduction VIII (dissimilatory)
-
-
PWY0-1352
nitrate reduction VIIIb (dissimilatory)
-
-
PWY0-1573
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 fixation I (ferredoxin)
-
-
N2FIX-PWY
nitrogen remobilization from senescing leaves
-
-
PWY-6549
Nitrotoluene degradation
-
-
nocardicin A biosynthesis
-
-
PWY-7797
noradrenaline and adrenaline degradation
-
-
PWY-6342
norspermidine biosynthesis
-
-
PWY-6562
noscapine biosynthesis
-
-
PWY-7138
Novobiocin biosynthesis
-
-
nucleoside and nucleotide degradation (archaea)
-
-
PWY-5532
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
oleoresin monoterpene volatiles biosynthesis
-
-
PWY-5423
omega-sulfo-II-dihydromenaquinone-9 biosynthesis
-
-
PWY-7781
One carbon pool by folate
-
-
ophiobolin F biosynthesis
-
-
PWY-7720
ophthalmate biosynthesis
-
-
PWY-8043
orthanilate degradation
-
-
2ASDEG-PWY
Other glycan degradation
-
-
Other types of O-glycan biosynthesis
-
-
oxalate degradation II
-
-
PWY-6695
oxalate degradation III
-
-
PWY-6696
oxalate degradation IV
-
-
PWY-6697
oxalate degradation V
-
-
PWY-6698
oxalate degradation VI
-
-
PWY-7985
oxidative decarboxylation of pyruvate
-
-
Oxidative phosphorylation
-
-
oxidative phosphorylation
-
-
palmatine biosynthesis
-
-
PWY-5470
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 II (plants and bacteria)
-
-
PWY-5366
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
pectin degradation I
-
-
PWY-7246
pectin degradation II
-
-
PWY-7248
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
perillyl aldehyde biosynthesis
-
-
PWY-6436
periplasmic disulfide bond formation
-
-
PWY0-1599
periplasmic disulfide bond reduction
-
-
PWY0-1600
petrobactin biosynthesis
-
-
PWY-6289
petroselinate biosynthesis
-
-
PWY-5367
Phenazine biosynthesis
-
-
phenol degradation I (aerobic)
-
-
PWY-5418
phenolic malonylglucosides biosynthesis
-
-
PWY-6930
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
phenylmercury acetate degradation
phenylpropanoid biosynthesis
-
-
PWY-361
Phenylpropanoid biosynthesis
-
-
phenylpropanoid biosynthesis
-
-
phenylpropanoid biosynthesis, initial reactions
-
-
PWY1F-467
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 VI
-
-
PWY-6826
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
phosphatidylinositol mannoside biosynthesis
-
-
PWY-7885
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
-
-
phosphonoacetate degradation
-
-
P483-PWY
phosphopantothenate biosynthesis I
-
-
PANTO-PWY
phosphopantothenate biosynthesis II
-
-
PWY-3961
phosphopantothenate biosynthesis III (archaea)
-
-
PWY-6654
photorespiration I
-
-
PWY-181
photorespiration II
-
-
PWY-8362
photorespiration III
-
-
PWY-8363
photosynthesis light reactions
-
-
PWY-101
photosynthetic 3-hydroxybutanoate biosynthesis (engineered)
-
-
PWY-7218
phylloquinol biosynthesis
-
-
PWY-5027
phytate degradation I
-
-
PWY-4702
phytate degradation II
-
-
PWY-4781
phytochelatins biosynthesis
-
-
PWY-6745
phytochromobilin biosynthesis
-
-
PWY-7170
phytol degradation
-
-
PWY66-389
phytosterol biosynthesis (plants)
-
-
PWY-2541
pinitol biosynthesis I
-
-
PWY-6738
pinobanksin biosynthesis
-
-
PWY-5059
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
polybrominated dihydroxylated diphenyl ethers biosynthesis
-
-
PWY-7934
Polycyclic aromatic hydrocarbon degradation
-
-
polyhydroxybutanoate biosynthesis
-
-
PWY1-3
polyhydroxydecanoate biosynthesis
-
-
PWY-6657
Polyketide sugar unit biosynthesis
-
-
polyphosphate metabolism
-
-
PWY-8138
porphyran degradation
-
-
PWY-6815
Porphyrin and chlorophyll metabolism
-
-
ppGpp metabolism
-
-
PPGPPMET-PWY
preQ0 biosynthesis
-
-
PWY-6703
Primary bile acid biosynthesis
-
-
proanthocyanidins biosynthesis from flavanols
-
-
PWY-641
procollagen hydroxylation and glycosylation
-
-
PWY-7894
progesterone biosynthesis
-
-
PWY-7299
proline to cytochrome bo oxidase electron transfer
-
-
PWY0-1544
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
protective electron sinks in the thylakoid membrane (PSII to PTOX)
-
-
PWY1YI0-7
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 of mannoproteins (cis-Golgi, yeast)
-
-
PWY-8323
protein N-glycosylation processing of proteins targeted for retention in cellular organelles (cis-Golgi, yeast)
-
-
PWY-8322
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 Pupylation and dePupylation
-
-
PWY-7893
protein S-nitrosylation and denitrosylation
-
-
PWY-7798
protein SAMPylation and SAMP-mediated thiolation
-
-
PWY-7887
protein ubiquitination
-
-
PWY-7511
protocatechuate degradation I (meta-cleavage pathway)
-
-
P184-PWY
protocatechuate degradation III (para-cleavage pathway)
-
-
PWY-6336
PRPP biosynthesis
-
-
PWY0-662
pseudouridine degradation
-
-
PWY-6019
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 biosynthesis II
-
-
PWY-6466
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 nucleobases salvage I
-
-
PWY-7183
pyrimidine nucleobases salvage II
-
-
PWY-7194
pyrimidine ribonucleosides degradation
-
-
PWY0-1295
pyrimidine ribonucleosides salvage I
-
-
PWY-7193
pyrimidine ribonucleosides salvage II
-
-
PWY-6556
pyrimidine ribonucleosides salvage III
-
-
PWY-7195
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)-acetoin I
-
-
PWY-5938
pyruvate fermentation to (R)-acetoin II
-
-
PWY-5939
pyruvate fermentation to (R)-lactate
-
-
PWY-8274
pyruvate fermentation to (S)-acetoin
-
-
PWY-6389
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
pyruvate to cytochrome bd oxidase electron transfer
-
-
PWY-7545
pyruvate to cytochrome bo oxidase electron transfer
-
-
PWY-7544
quercetin glucoside degradation (Allium)
-
-
PWY-7133
quercetin sulfate biosynthesis
-
-
PWY-6199
queuosine biosynthesis I (de novo)
-
-
PWY-6700
queuosine biosynthesis II (queuine salvage)
-
-
PWY-8105
queuosine biosynthesis III (queuosine salvage)
-
-
PWY-8106
quinate degradation I
-
-
QUINATEDEG-PWY
quinate degradation II
-
-
PWY-6416
quinoxaline-2-carboxylate biosynthesis
-
-
PWY-7734
Rapoport-Luebering glycolytic shunt
-
-
PWY-6405
raspberry ketone biosynthesis
-
-
PWY-5393
reactive oxygen species degradation
-
-
DETOX1-PWY-1
reductive acetyl coenzyme A pathway
-
-
reductive acetyl coenzyme A pathway I (homoacetogenic bacteria)
-
-
CODH-PWY
reductive acetyl coenzyme A pathway II (autotrophic methanogens)
-
-
PWY-7784
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
rhizobactin 1021 biosynthesis
-
-
PWY-761
Riboflavin metabolism
-
-
ribose phosphorylation
-
-
RIBOKIN-PWY
ricinoleate biosynthesis
-
-
PWY-7618
roseoflavin biosynthesis
-
-
PWY-7863
rosmarinic acid biosynthesis I
-
-
PWY-5048
rosmarinic acid biosynthesis II
-
-
PWY-5049
roxarsone degradation I
-
-
PWY-8260
rubber biosynthesis
-
-
PWY-5815
Rubisco shunt
-
-
PWY-5723
rutin degradation
-
-
PWY-6848
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 I
-
-
PWY-6754
S-methyl-5'-thioadenosine degradation II
-
-
PWY-6756
S-methyl-5'-thioadenosine degradation III
-
-
PWY-6753
S-methyl-5'-thioadenosine degradation IV
-
-
PWY0-1391
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
saframycin A biosynthesis
-
-
PWY-7671
salicin biosynthesis
-
-
PWY-6766
salicortin biosynthesis
-
-
PWY-6763
salicylate biosynthesis I
-
-
PWY-6406
salicylate biosynthesis II
-
-
PWY-8321
salicylate degradation I
-
-
PWY-6183
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
salvigenin biosynthesis
-
-
PWY-7325
santalene biosynthesis II
-
-
PWY-6836
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 II
-
-
PWY-6935
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
-
-
shikimate degradation I
-
-
SHIKIMATEDEG-PWY
sitosterol degradation to androstenedione
-
-
PWY-6948
solasodine glycosylation
-
-
PWY18C3-4
sophorolipid biosynthesis
-
-
SOPHOROSYLOXYDOCOSANOATE-SYN-PWY
sophorosyloxydocosanoate deacetylation
-
-
SOPHOROSYLOXYDOCOSANOATE-DEG-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 II
-
-
PWY-6440
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
spongiadioxin C biosynthesis
-
-
PWY-7935
sporopollenin precursors biosynthesis
-
-
PWY-6733
stachyose degradation
-
-
PWY-6527
staphyloferrin A biosynthesis
-
-
PWY-7990
staphylopine biosynthesis
-
-
PWY-8007
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 IV
-
-
PWY-6735
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
sterculate biosynthesis
-
-
PWY-4942
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
sulfoacetaldehyde degradation I
-
-
PWY-1281
sulfolactate degradation II
-
-
PWY-6637
sulfolactate degradation III
-
-
PWY-6638
sulfopterin metabolism
-
-
sulfur volatiles biosynthesis
-
-
PWY-6736
superoxide radicals degradation
-
-
DETOX1-PWY
superpathway of (Kdo)2-lipid A biosynthesis
-
-
KDO-NAGLIPASYN-PWY
superpathway of 5-aminoimidazole ribonucleotide biosynthesis
-
-
PWY-6277
superpathway of coenzyme A biosynthesis III (mammals)
-
-
COA-PWY-1
superpathway of dimethylsulfoniopropanoate degradation
-
-
PWY-6049
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 mycolate biosynthesis
-
-
PWY-6113
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
superpathway of UDP-N-acetylglucosamine-derived O-antigen building blocks biosynthesis
-
-
PWY-7332
syringate degradation
-
-
PWY-6339
Taurine and hypotaurine metabolism
-
-
taurine biosynthesis I
-
-
PWY-5331
taurine biosynthesis II
-
-
PWY-7850
taurine biosynthesis III
-
-
PWY-8359
taurine degradation IV
-
-
PWY0-981
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
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
tetrachloroethene degradation
-
-
PCEDEG-PWY
tetradecanoate biosynthesis (mitochondria)
-
-
PWY66-430
tetrahydrofolate biosynthesis I
-
-
PWY-6614
tetrahydrofolate biosynthesis II
-
-
PWY2DNV-11
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 I (E. coli)
-
-
PWY-6894
thiamine diphosphate biosynthesis II (Bacillus)
-
-
PWY-6893
thiamine diphosphate biosynthesis III (Staphylococcus)
-
-
PWY-6907
thiamine diphosphate biosynthesis IV (eukaryotes)
-
-
PWY-6908
thiamine diphosphate salvage I
-
-
PWY-6896
thiamine diphosphate salvage II
-
-
PWY-6897
thiamine diphosphate salvage III
-
-
PWY-6898
thiamine diphosphate salvage IV (yeast)
-
-
PWY-7356
thiamine phosphate formation from pyrithiamine and oxythiamine (yeast)
-
-
PWY-7357
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
toxoflavin biosynthesis
-
-
PWY-7991
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
trans-lycopene biosynthesis II (oxygenic phototrophs and green sulfur bacteria)
-
-
PWY-6475
traumatin and (Z)-3-hexen-1-yl acetate biosynthesis
-
-
PWY-5410
trehalose biosynthesis I
-
-
TRESYN-PWY
trehalose biosynthesis II
-
-
PWY-881
trehalose biosynthesis III
-
-
TREHALOSESYN-PWY
trehalose biosynthesis IV
-
-
PWY-2622
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
tricin biosynthesis
-
-
PWY-7995
trimethylamine degradation
-
-
PWY-6968
trimethylamine N-oxide biosynthesis
-
-
PWY-8292
tRNA charging
-
-
TRNA-CHARGING-PWY
tRNA methylation (yeast)
-
-
PWY-6829
tRNA processing
-
-
PWY0-1479
tRNA splicing I
-
-
PWY-6689
tRNA splicing II
-
-
PWY-7803
tRNA-uridine 2-thiolation (cytoplasmic)
-
-
PWY-7888
tRNA-uridine 2-thiolation and selenation (bacteria)
-
-
PWY-7892
tropane alkaloid biosynthesis
-
-
tropane alkaloids biosynthesis
-
-
PWY-5317
Tropane, piperidine and pyridine alkaloid biosynthesis
-
-
trypanothione biosynthesis
-
-
TRYPANOSYN-PWY
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-galactose biosynthesis
-
-
PWY-7344
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-beta-L-rhamnose biosynthesis
-
-
PWY-3261
UDP-GlcNAc biosynthesis
-
-
UDP-N-acetyl-alpha-D-mannosaminouronate biosynthesis
-
-
PWY-7335
UDP-N-acetyl-beta-L-fucosamine biosynthesis
-
-
PWY-7330
UDP-N-acetyl-beta-L-quinovosamine biosynthesis
-
-
PWY-7331
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 I
-
-
PWY-5703
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
vindoline, vindorosine and vinblastine biosynthesis
-
-
PWY-5292
viridicatumtoxin biosynthesis
-
-
PWY-7659
vitamin B1 metabolism
-
-
vitamin B12 metabolism
-
-
Vitamin B6 metabolism
-
-
vitamin B6 metabolism
-
-
vitamin D3 biosynthesis
-
-
PWY-6076
vitamin D3 metabolism
-
-
vitamin E biosynthesis (tocopherols)
-
-
PWY-1422
vitamin E biosynthesis (tocotrienols)
-
-
PWY-7436
volatile benzenoid biosynthesis I (ester formation)
-
-
PWY-4203
wax esters biosynthesis I
-
-
PWY-5884
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
(5R)-carbapenem carboxylate biosynthesis

-
-
PWY-5737
(5R)-carbapenem carboxylate biosynthesis
-
-
4-hydroxymandelate degradation

-
-
4-HYDROXYMANDELATE-DEGRADATION-PWY
4-hydroxymandelate degradation
-
-
4-hydroxyphenylacetate degradation

-
-
3-HYDROXYPHENYLACETATE-DEGRADATION-PWY
4-hydroxyphenylacetate degradation
-
-
adipate degradation

-
-
PWY-8354
bile acid biosynthesis, neutral pathway

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

-
-
PWY66-301
catecholamine biosynthesis
-
-
cis-vaccenate biosynthesis

-
-
PWY-5973
cis-vaccenate 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
-
-
ketogluconate metabolism

-
-
KETOGLUCONMET-PWY
ketogluconate metabolism
-
-
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
phenylmercury acetate degradation

-
-
P641-PWY
phenylmercury acetate degradation
-
-
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.
-
32, 126, 133, 262, 288, 395, 634, 641, 783, 858, 992, 1004, 1068, 1074, 1081, 1145, 1214, 1320, 1359, 1361, 1363, 1377, 1387, 1469, 1504, 1593, 1667, 1668, 1669, 1680, 1681, 1682, 1687, 1712, 1713, 1739, 1917, 2267, 2289, 2292, 2323, 2367, 2544, 2652, 2654, 2655, 2833, 2846, 3023, 3028, 3032, 3053, 3076, 3098, 3102, 3131, 3494, 3597, 3797, 3811, 3812, 3813, 3820, 3844, 3860, 3872, 3904, 3962, 3983, 3984, 3992, 3995, 3998, 4002, 4005, 4006, 4008, 4015, 4020, 4036, 4043, 4050, 4051, 4052, 4142, 4151, 4155, 4156, 4158, 4163, 4176, 4180, 4183, 4207, 4358, 4429, 4436, 4446, 4665, 4667, 4668, 4675, 4689, 4690, 4696, 4699, 4765, 4777, 4783, 5111, 5128, 5859, 5881, 7410, 16278, 23590, 26860, 26865, 26867, 28973, 29366, 29417, 29578, 29597, 29699, 29700, 29734, 29736, 29737, 29739, 29743, 29749, 29871, 29874, 30157, 30159, 30362, 30369, 31018, 31019, 31022, 31026, 31028, 31030, 31034, 31035, 31042, 31043, 31379, 31409, 31410, 31411, 33494, 33625, 33865, 33867, 33868, 33869, 34308, 34457, 34502, 34541, 34795, 34820, 34845, 34951, 34955, 34957, 34960, 34961, 34968, 34969, 35013, 35214, 35969, 36009, 36029, 36030, 36034, 36037, 36151, 36152, 36209, 36248, 36323, 36484, 36630, 36662, 36714, 36717, 36941, 37076, 37413, 37418, 37426, 37428, 37432, 37440, 37446, 80886, 80911, 80912, 80945, 80963, 80965, 80969, 80975, 81017, 81045, 81047, 81083, 81088, 81113, 81241, 81275, 81307, 81328, 81354, 81639, 81644, 81646, 94261, 94274, 94310, 94340, 94392, 94445, 94472, 94576, 94610, 94914, 95052, 95074, 95156, 95158, 95240, 95250, 95311, 95370, 95494, 95576, 95756, 95760, 95763, 95765, 95768, 95770, 95771, 95775, 95776, 95792, 95795, 95798, 95811, 95815, 114175, 114183, 114189, 133832, 133870, 133894, 134068, 134090, 134091, 134171, 134180, 134185, 134200, 134280, 134316, 134324, 134343, 134344, 134347, 134398, 134399, 134523, 134574, 134575, 134750, 134923, 134933, 134935, 134939, 134941, 134945, 134971, 134990, 134991, 135123, 135130, 135154, 135162, 135188, 135217, 135278, 135285, 135363, 135392, 135404, 135446, 135494, 135595, 135618, 135627, 135959, 135966, 136046, 136445, 136449, 136451, 136471, 136480, 136481, 137041, 137042, 137044, 137045, 137046, 137047, 137048, 137075, 137084, 137125, 137128, 137130, 137140, 137150, 137167, 137174, 137178, 137179, 137264, 137363, 170718, 170737, 170749, 170753, 170777, 170969, 170992, 170995, 170998, 171003, 171240, 171397, 171572, 171989, 172002, 172061, 172064, 172065, 172116, 172129, 172131, 172136, 172157, 208356, 208377, 208675, 208703, 208709, 208710, 208715, 208758, 208875, 208877, 208880, 208881, 208889, 208896, 208901, 208902, 208903, 208907, 208911, 208913, 208914, 208922, 208928, 208929, 208931, 208933, 208989, 209027, 209035, 209036, 209057, 209374, 209381, 209382, 209384, 209385, 209386, 209417, 209419, 209422, 209428, 209431, 209527, 209528, 209529, 209559, 209637, 209729, 209742, 209897, 209932, 209935, 209962, 210049, 210226, 210248, 210262, 210381, 210383, 210385, 210387, 210397, 210398, 210410, 210422, 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brenda
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SwissProt
brenda
-
TrEMBL
brenda
-
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760840, 760847, 760851, 760882, 760903, 760948, 760967, 760988, 760989, 761038, 761063, 761135, 761140, 761203, 761207, 761215, 761232, 761241, 761323, 761325, 761421, 761460, 761505, 761586, 761592, 761639, 761661, 761662, 761670, 761702, 761717, 761721, 761749, 761750, 761759, 761773, 761805, 761817, 761824, 761970, 761984, 761989, 761995, 762015, 762199, 762226, 762237, 762284, 762323, 762364, 762381, 762399, 762410, 762416, 762424, 762431, 762461, 762493, 762673, 762748, 762756, 762857, 762900, 762934, 763094, 763156, 763218, 763251, 763263, 763340, 763475, 763509, 763613, 763702, 763721, 763831, 763853, 763900, 764034, 764039, 764052, 764206, 764262, 764296, 764298, 764386, 764408, 764438, 764439, 764524, 764531, 764557, 764558, 764569, 764575, 764641, 764652, 764663, 764699, 764921, 764930, 764939, 765022, 765042, 765163, 765189, 765255, 765394, 765402, 765436, 765456, 765459, 765484, 765669, 765751, 765794, 765804, 765902, 766084, 766105, 766239, 766425, 766441, 766463, 766499, 766574, 766594, 766598, 766659, 766745, 766757, 766795, 766865, 766868, 766875, 766886, 766887, 766914, 766972, 766987, 767075, 767084, 767088, 767093, 767104, 767132, 767156, 767185, 767193, 767226, 767231, 767248, 767249, 767270, 767271, 767284, 767318, 767320, 767353, 767373, 767380, 767381, 767383, 767485, 767498, 767521, 767599, 767615, 767649, 767839, 767840, 767859, 767872, 767898, 767904, 767966, 767982, 767994, 768005, 768037, 768040, 768048, 768056, 768060, 768095, 768354, 768414, 768427, 768443, 768453, 768454, 768459, 768526, 768593, 768636, 768650, 768944, 769030, 769037, 769295, 769326, 769428, 769499, 769545, 769939, 769951, 769995, 770004, 770038, 770039, 770135, 770147, 770148, 770164, 770179, 770182, 770194, 770223, 770230, 770231, 770248, 770263, 770264, 770283, 770467, 770518, 770652, 770768, 770770, 770787, 770792, 771024, 771025, 771027, 771085, 771309, 771312, 771315, 771355, 771385, 771399, 771417, 771420, 771432, 771570, 771612, 771625, 771764, 771790, 771831, 771832, 771842, 772120, 772162, 772188, 772205, 772244, 772308, 772374, 772378, 772423, 772643, 772718, 772727, 772728, 772772, 772805, 772836, 772846, 772848, 772879, 772885, 772911, 772964, 772968, 772977, 773118, 773141, 773152, 773199, 773200, 773301, 773302, 773358, 773411, 773436, 773437, 773503, 773556, 773569, 773570, 773611, 773613, 773617, 773621, 773622, 773624, 773630, 773638, 773769, 773801, 773912, 773916, 773974, 774178, 774244, 774277, 774319, 774332, 774364, 774533, 774570, 774585, 774600, 774601, 774606, 774614, 774615, 774618, 774635, 774661, 774714, 774716, 774828, 774843, 774851, 774891, 774969, 775360, 775394, 775407, 775481, 775502, 775508, 775518, 775538, 775903, 775940, 775951, 775999, 776025, 776075, 776277, 776371, 776392, 776401, 776426, 776437, 776529, 776532, 776533, 776537, 776560, 776575, 776642, 776664, 776665, 776666, 776671, 776672, 776681, 776687, 776699, 776709, 776726, 776733, 776791, 776796, 776819, 776860, 776889, 776922, 776924, 776925, 776933, 776939, 776963, 776966, 776969, 776981, 777152, 777173, 777187, 777197, 777219, 777226, 777253, 777277, 777285, 777294, 777366, 777386, 777387, 777391, 777461, 777472, 777523, 777552, 777562, 777586, 777589, 777593, 777696, 777727, 777736, 777809, 777820, 777826, 777831, 777833, 777914, 777929, 777961, 778004, 778023, 778029, 778156, 778159, 778193, 778234, 778254, 778256, 778307, 778308, 778388, 778418, 778456, 778531, 778535, 778567, 778571, 778580, 778594, 778605, 778606, 778650, 778726, 778767, 778819, 778820, 778826, 778852, 779191, 779221, 779273, 779323, 779331, 779375, 779399, 779436
A0A0B6VJJ9, A0A0R4J0B4, A0A0U1RNF2, A0A1Y7VM56, A0A286YDB8, A0A286YDC5, A1L361, A2A5Z6, A2A6C4, A2A935, A2AJQ3, A2AMS3, A2AWA9, A2RTH5, A6X919, A7MCT6, A7RDN6, B1AVY7, B1AXV0, B1PSD9, B2RWS6, B2RXZ1, B2RY43, B5THE3, C4B4E7, C4MLH8, D0VLQ4, D0VLQ5, D3KU66, D3YZG8, D3Z6W3, D6MZJ6, E9PYH3, E9Q3E1, E9Q5F9, E9QAN8, E9QAS3, F2WWK6, G3X982, H2BL43, J3QMK6, L0N7N1, O08643, O08663, O08736, O08832, O08912, O09005, O09008, O09010, O09046, O09106, O09159, O09160, O09174, O35074, O35083, O35205, O35298, O35403, O35453, O35469, O35490, O35632, O35657, O35674, O35678, O35728, O35855, O35945, O35969, O54754, O54804, O54827, O54864, O54909, O54983, O55028, O55060, O55123, O55143, O55239, O70133, O70138, O70250, O70281, O70370, O70475, O70546, O70571, O70582, O88533, O88561, O88622, O88673, O88693, O88736, O88829, O88839, O88876, O88895, O88962, O88967, O88974, O89023, P00375, P04095, P04247, P05202, P06745, P06797, P06801, P06802, P06803, P07310, P07564, P07607, P07858, P08680, P09041, P09242, P09411, P09470, P09838, P0DMN7, P11928, P13707, P14404, P14901, P15105, P15327, P16015, P16330, P16460, P16675, P16858, P17439, P17532, P18242, P18293, P18894, P19096, P19157, P21447, P21661, P21812, P21836, P21958, P21981, P23188, P23738, P23953, P24472, P24527, P24529, P24822, P26443, P26638, P28271, P28352, P28474, P28649, P28650, P28825, P28843, P28862, P29121, P29477, P29758, P30987, P32020, P32921, P33173, P33434, P33587, P34884, P34960, P35505, P35576, P35821, P38585, P38649, P39054, P39098, P39654, P39655, P40935, P41216, P41245, P45700, P46467, P47713, P47739, P47740, P47934, P48410, P48758, P48760, P48999, P49586, P49891, P49935, P50096, P50247, P50285, P50428, P50429, P50544, P51658, P51830, P51908, P52430, P52480, P53690, P54310, P54763, P54818, P54823, P54987, P55249, P56389, P56528, P57791, P58242, P58281, P59384, P59997, P60330, P60334, P61922, P62331, P62746, P63239, P70245, P70269, P70288, P70313, P70352, P70424, P70665, P70704, P97321, P97353, P97363, P97377, P97464, P97467, P97478, P97501, P97821, P97872, P98063, P98197, P98199, P98200, Q00493, Q01065, Q01320, Q02053, Q03059, Q04447, Q04519, Q04750, Q05117, Q05769, Q05A13, Q09324, Q09M02, Q0E9Q7, Q148T8, Q148W0, Q14AZ4, Q14DK4, Q16654, Q1HFZ0, Q2HXL6, Q2M4J5, Q2NL51, Q35066, Q3TD49, Q3TH56, Q3TIF7, Q3TME3, Q3TMX7, Q3TPJ9, Q3TSG4, Q3TUA9, Q3TWN3, Q3TXU5, Q3TYD4, Q3U214, Q3U2J5, Q3U2K5, Q3U3S6, Q3U4G3, Q3U4H6, Q3UEG6, Q3UEP4, Q3UGX3, Q3UIZ8, Q3UJD6, Q3UN02, Q3UNX5, Q3UP47, Q3URK3, Q3USF0, Q3UWM4, Q3UX61, Q3UXZ9, Q3UYH7, Q3V1F8, Q3V1T4, Q3V3R1, Q4FZD7, Q4JK59, Q501J6, Q540F5, Q5BL07, Q5EG47, Q5MPP0, Q5NCY0, Q5NGY0, Q5RJG7, Q5SGK3, Q5SSF7, Q5SVQ0, Q60592, Q60597, Q60700, Q60710, Q60715, Q60759, Q60928, Q60935, Q61006, Q61153, Q61176, Q61188, Q61193, Q61263, Q61285, Q61391, Q61419, Q61481, Q61503, Q61526, Q61576, Q61609, Q61656, Q61753, Q61768, Q61771, Q61846, Q61907, Q61941, Q62073, Q62086, Q62087, Q62167, Q63880, Q63886, Q64105, Q64176, Q64237, Q64285, Q64311, Q64323, Q64374, Q64455, Q64459, Q64467, Q64520, Q64521, Q64669, Q64687, Q68ED3, Q69ZF3, Q6DFW5, Q6IQX7, Q6NXL6, Q6P1C1, Q6P1G2, Q6P1Y8, Q6P549, Q6P5C5, Q6P5E8, Q6P7W0, Q6P9P6, Q6PCM1, Q6PCN3, Q6PDK2, Q6PDN3, Q6PDX6, Q6PF93, Q6PGB8, Q6Q477, Q6SKR2, Q6T707, Q6UQ17, Q6VVW9, Q6WQJ1, Q6YGZ1, Q6ZPJ3, Q6ZPS2, Q6ZPY7, Q6ZQ11, Q6ZQ88, Q6ZQB6, Q71B07, Q71KT5, Q75NR7, Q769J6, Q78JN3, Q7TMR0, Q7TMS5, Q7TNZ4, Q7TPH6, Q7TQA3, Q7TQC5, Q7TSV6, Q7TT16, Q80TQ2, Q80UN9, Q80UP3, Q80V26, Q80V42, Q80V72, Q80VQ0, Q80W94, Q80WB5, Q80Y84, Q80ZJ1, Q811L6, Q811Q9, Q88531, Q8BFP9, Q8BG87, Q8BGL3, Q8BH00, Q8BH61, Q8BH69, Q8BHC7, Q8BHN3, Q8BI55, Q8BJ37, Q8BJ64, Q8BJQ9, Q8BLF1, Q8BLR9, Q8BM11, Q8BML1, Q8BNJ2, Q8BNZ5, Q8BP74, Q8BSF4, Q8BTY1, Q8BU30, Q8BUG2, Q8BUH8, Q8BVE8, Q8BW72, Q8BWD2, Q8BWF0, Q8BWT1, Q8BZ21, Q8BZA9, Q8BZH1, Q8C0N2, Q8C0T9, Q8C129, Q8C196, Q8C1A5, Q8C1F4, Q8C2B3, Q8C2W3, Q8C3P7, Q8C725, Q8C863, Q8C9W3, Q8CAE2, Q8CC86, Q8CE08, Q8CE90, Q8CF93, Q8CFY4, Q8CG03, Q8CG71, Q8CGC7, Q8CGY8, Q8CHK3, Q8CHT0, Q8CIG3, Q8CIH5, Q8CIW5, Q8I719, Q8JZL3, Q8JZR0, Q8JZV9, Q8K023, Q8K0L2, Q8K154, Q8K1E6, Q8K1M6, Q8K1R3, Q8K1R7, Q8K297, Q8K2C8, Q8K2I3, Q8K2X1, Q8K341, Q8K354, Q8K3K7, Q8K3V4, Q8K409, Q8K469, Q8K4Q7, Q8K4T1, Q8K4X7, Q8QZR5, Q8R071, Q8R084, Q8R0F8, Q8R0I0, Q8R0X7, Q8R173, Q8R1G2, Q8R1K1, Q8R2H9, Q8R2W9, Q8R387, Q8R3I2, Q8R3J5, Q8R418, Q8R4K8, Q8VCC2, Q8VCD7, Q8VCF1, Q8VCH6, Q8VCN3, Q8VCT4, Q8VCX1, Q8VCZ9, Q8VD53, Q8VDC0, Q8VDG3, Q8VDK1, Q8VDL4, Q8VDP3, Q8VDQ1, Q8VDW4, Q8VDZ4, Q8VE10, Q8VEB1, Q8VEI3, Q8VEK0, Q8VEM8, Q8VHK9, Q8VHL1, Q8VHQ9, Q8VI15, Q8VI47, Q8VI95, Q8VI97, Q8VID5, Q8VIJ7, Q91UZ4, Q91V01, Q91VE0, Q91VE3, Q91VF2, Q91VL8, Q91VY5, Q91WC3, Q91WC9, Q91WG8, Q91WN4, Q91WP0, Q91WT7, Q91WT9, Q91WU5, Q91XE0, Q91XQ5, Q91XU3, Q91Y82, Q91YE2, Q91YE3, Q91YI6, Q91YP2, Q91ZI8, Q91ZP3, Q91ZQ5, Q91ZV4, Q91ZW2, Q920A5, Q922B1, Q922B2, Q922E4, Q922H2, Q922Q1, Q922S4, Q923E4, Q924S2, Q924X2, Q924X7, Q96KQ7, Q99J39, Q99J72, Q99JW2, Q99KE1, Q99KI0, Q99KK2, Q99KS6, Q99L44, Q99LD8, Q99LF4, Q99LH2, Q99LJ8, Q99LQ7, Q99LY2, Q99MK8, Q99MN1, Q99MY8, Q99MZ7, Q99N23, Q99N42, Q99NF1, Q99PU5, Q9CPU0, Q9CQ62, Q9CQ65, Q9CQG1, Q9CRB3, Q9CRY7, Q9CVD2, Q9CW42, Q9CWH6, Q9CWS0, Q9CWY8, Q9CXI0, Q9CXT6, Q9CY64, Q9CYK2, Q9CYT6, Q9CZ42, Q9CZN8, Q9CZS1, Q9CZU6, Q9CZW4, Q9CZX0, Q9D020, Q9D099, Q9D0K2, Q9D0R2, Q9D110, Q9D142, Q9D1P2, Q9D2G2, Q9D2R0, Q9D379, Q9D3G9, Q9D411, Q9D5U2, Q9D6R2, Q9D819, Q9D964, Q9D975, Q9D9V3, Q9DA37, Q9DB60, Q9DBB8, Q9DBE0, Q9DBF1, Q9DBG1, Q9DBI0, Q9DBJ1, Q9DBL9, Q9DBT9, Q9DC23, Q9DC28, Q9DC50, Q9DCX8, Q9EP75, Q9EPS3, Q9EPW0, Q9EQ20, Q9EQC0, Q9EQH2, Q9EQQ9, Q9EQW7, Q9ESU6, Q9ESW4, Q9JHD1, Q9JHD2, Q9JHE3, Q9JHE4, Q9JHF7, Q9JHI5, Q9JHK6, Q9JHR7, Q9JI60, Q9JI78, Q9JIF0, Q9JIP7, Q9JIQ8, Q9JIX9, Q9JJE7, Q9JJF9, Q9JJJ7, Q9JJZ4, Q9JK38, Q9JK42, Q9JL18, Q9JLC3, Q9JLF6, Q9JLJ2, Q9JLT2, Q9JLV6, Q9JM14, Q9JM51, Q9JMK0, Q9NYQ2, Q9QUI0, Q9QUP4, Q9QWR8, Q9QXG4, Q9QY15, Q9QY36, Q9QY93, Q9QYC7, Q9QYR9, Q9QZ05, Q9QZS6, Q9QZW0, Q9R008, Q9R014, Q9R062, Q9R0B9, Q9R0E2, Q9R112, Q9R118, Q9R1E6, Q9R1L5, Q9R1S3, Q9WTK2, Q9WTN0, Q9WTR2, Q9WTS2, Q9WTU0, Q9WU19, Q9WU79, Q9WUB3, Q9WUE3, Q9WUP4, Q9WV07, Q9WV54, Q9WV60, Q9WV68, Q9WV86, Q9WVE0, Q9WVK5, Q9WVM8, Q9WVP6, Q9Z0F8, Q9Z0K8, Q9Z0R9, Q9Z0S1, Q9Z110, Q9Z148, Q9Z186, Q9Z1M7, Q9Z1T6, Q9Z1X2, Q9Z2A5, Q9Z2A9, Q9Z2D1, Q9Z2V5, Q9Z2W0
UniProt
brenda
isozyme AC1
-
-
brenda
isozyme AC8
UniProt
brenda
(C57/B6), wild type and Vanin 1-/- and +/+ mice
-
-
brenda
(MMU)Minpp1
SwissProt
brenda
10-weeks-old male C75BL/6 mice
-
-
brenda
11beta-hydroxysteroid dehydrogenase type 1
-
-
brenda
129 SvEv wild-type and Sc1-/- mice
-
-
brenda
129/Sv and C57BL/6 strain hybrids, isozyme GC-A
UniProt
brenda
129/Sv and C57BL/6J mice
-
-
brenda
129/Sv mice
-
-
brenda
129/SvJ mice
-
-
brenda
129/SvJ wild-type mice
-
-
brenda
129/SvJae and C57BL/6J, treatment starts at an age of 9 weeks
-
-
brenda
129:BL6 background
-
-
brenda
129S6 genetic background or mixed 129S6/C57Bl6 mice
-
-
brenda
129Sv background
-
-
brenda
14-week-old male C57BL/6J wild-type and legumain-deficient mice analyzed
SwissProt
brenda
15-19 days old
-
-
brenda
2 forms have the same primary sequence
-
-
brenda
2 isoforms ALAS-1 and ALAS-2, a houskeeping form and an erythroid-specific form
-
-
brenda
2 isoforms L-CPT I and M-CPT I
-
-
brenda
2 isoforms: CNP1 and CNP2
-
-
brenda
2 isozymes A and B
-
-
brenda
2 isozymes encoded by a single gene and translated from 2 different splicing variants
-
-
brenda
2 isozymes I and II
-
-
brenda
2 isozymes PGKA and PGKB
-
-
brenda
2 isozymes SEP and splicing variant SEPDELTA which lacks 69 base pair nucleotide segment following the transmembrane helix
SwissProt
brenda
2 isozymes SPHK1 and SPHK2
-
-
brenda
2 isozymes: X-chromosome encoded PGK1 and chromosome 17 encoded PGK2, 3 genetic variants of PGK2: PGK2A, PGK2B, PGK2C
-
-
brenda
2 subunits encoded by 2 genes
-
-
brenda
2 types of PKA
-
-
brenda
26-weeks-old male mice
-
-
brenda
3 days old
-
-
brenda
3 enzyme forms
-
-
brenda
3 forms, products of different genes: MI, MII, MIII
-
-
brenda
3 isoforms exist in mouse macrophages differentiated by substrate specificity and Ca2+-dependence
-
-
brenda
3 isoforms TR1, TR2, TR3
-
-
brenda
3 isozymes
-
-
brenda
3 isozymes alpha, beta, and gamma
-
-
brenda
3 isozymes HAS1, HAS2, and HAS3 encoded by genes HAS1, HAS2, and HAS3
-
-
brenda
3 isozymes LH1-3, isozyme LH2 occurs in 2 splicing variant, 2a and 2b, the first without insert
-
-
brenda
3 isozymes Neu-1, Neu-2, and Neu-3
-
-
brenda
3 isozymes of enzyme Dhcr7 through alternative splicing of gene Dhcr7
SwissProt
brenda
3 strains: C57BL/6J, SWR/J and A/J
-
-
brenda
3-ketoacyl-CoA thiolase A
SwissProt
brenda
3-ketoacyl-CoA thiolase B
SwissProt
brenda
3-week-old Swiss CD1 female mice
-
-
brenda
4 isoforms mGRK6-A, mGRK6-B, mGRK-C, and mGRK-D by alternative splicing
-
-
brenda
4 isozymes, termed LOX-like proteins 1-4, i.e. LOXL1-4
-
-
brenda
4 peroxisome proliferator-induced genes, isozymes CTE-I, MTE-I, PTE-Ia, and PTE-Ib
-
-
brenda
4-week-old C57BL/6 mice
SwissProt
brenda
4-week-old male Balb/cA mice
-
-
brenda
5 enzyme forms: MMCP-1A to MMCP-1E
-
-
brenda
6-8 week-old male BALB/c mice
-
-
brenda
6-week-old Balb/C male mice
-
-
brenda
6-week-old female CD1 mice
SwissProt
brenda
60-80 day old CD-1 mice
-
-
brenda
67 R6/2 mice and 31 wild-type B6CBAFI/J mice, gene Ckb
UniProt
brenda
7 weeks old male diabetic (db/db) and control (db/m) mice, 7 days adjusted
-
-
brenda
8- to 10-week-old C57/BL6 mice
-
-
brenda
8-10 weeks old male ICR mice
-
-
brenda
8-12-weeks-old hairless SKH-1 mice
-
-
brenda
8-weeks-old female C57BL/6N mice
-
-
brenda
81.5% identities to human ortholog
SwissProt
brenda
93.4% identities to human ortholog
SwissProt
brenda
96.5% identities to human ortholog
SwissProt
brenda
a catalytically active monoclonal antibody fragment
-
-
brenda
a Leydig tumor strain
-
-
brenda
a recombinant vaccinia virus vector is used to coexpress mouse prohormone convertase PC1 and PC2 in the constitutively secreting cell line BSC-40 and in the endocrine tissue-derived cell lines PC12 and AtT-20
-
-
brenda
a transgenic mouse model, with the NADPH-P450 reductase (Cpr) gene deleted in a lung-specific and doxycycline-inducible fashion (lung-Cpr-null)
-
-
brenda
AC1
UniProt
brenda
AC2
UniProt
brenda
AC3
UniProt
brenda
AC5
UniProt
brenda
AC6
UniProt
brenda
AC7
UniProt
brenda
AC8
UniProt
brenda
activity requires TAB1 (TAK1 binding protein), binding of TAB1 promotes autophosphorylation of TAK1
-
-
brenda
acts as acyl-protein thioesterase/lysophospholipase, cf. EC 3.1.1.5
SwissProt
brenda
acts as acyl-protein thioesterase/lysophospholipase, cf. EC 3.1.2.22
SwissProt
brenda
Ada-/- mice
-
-
brenda
adult 6-week-old C57BL/6 mice
-
-
brenda
adult B6SJLF1 mice, structurally and functionally diverse enzyme forms: lysyl oxidase and 4 LOX-like proteins LOXL, LOXL2, LOXL3, and LOXL4, probably existing splicing variants of LOXL3
-
-
brenda
adult balb/c mice
SwissProt
brenda
adult C57/BL6 mice
-
-
brenda
adult C57BL6 mice
-
-
brenda
adult F1 mice and postnatal day-14, -22, -30, and -60 mice
-
-
brenda
adult male Albino Swiss mice
-
-
brenda
adult male C57 BL/6 mice, peroxisomal isozyme PTE-2
SwissProt
brenda
adult male C57BL/6 mice
-
-
brenda
adult male C57BL/6 mice, isozyme AC1
UniProt
brenda
adult male C57BL/6 mice, isozyme AC8
UniProt
brenda
adult male C57BL/6J mice
-
-
brenda
adult male C57BL6 mice and B1 vacuolar proton pumping ATPase deficient mice
-
-
brenda
adult male DBA2 mice
SwissProt
brenda
adult, male C57BL/6 mice
-
-
brenda
age 3 and 30 months, no change in enzyme activtiy with age or diet
-
-
brenda
aging does not influence the response to the hormonal and xenobiotic signaling for enzyme Sult2A1 induction
-
-
brenda
aiiA
-
-
brenda
Albino male CF1
-
-
brenda
albino mice
-
-
brenda
albino Swiss mice
-
-
brenda
ALDRP
-
-
brenda
all of the detectable lysine decarboxylase activity is due to the action of ornithine decarboxylase
-
-
brenda
alpha and beta subunits of complex component E1 (BCKD), a tetramer (alpha2beta2), cf. EC 1.2.4.4
UniProt
brenda
alpha isoform
UniProt
brenda
alpha isoform, liver, inducible by CCl4
-
-
brenda
alpha,alpha-enolase
SwissProt
brenda
alpha-L-iduronidase (IDUA) knockout mutant variant, gene B4GALNT1
SwissProt
brenda
alpha-L-iduronidase (IDUA) knockout mutant variant, gene St3gal5
Uniprot
brenda
alpha-L-iduronidase (IDUA) knockout mutant variant, gene ST8SIA1
UniProt
brenda
alpha-synuclein knock-out mutant
-
-
brenda
alpha/beta-, and gamma-subunit encoding genes
UniProt
brenda
alphaPax6cre mice
-
-
brenda
alpha-chain
SwissProt
brenda
altered enzyme encoded by amplified genes in cultured fibroblasts
-
-
brenda
alternative splicing variants, overview
SwissProt
brenda
and blast crisis CML mice and MLL-AF9 mice
UniProt
brenda
and R6/2 mutant mice
SwissProt
brenda
and rd10 mutants
-
-
brenda
and strain DBA/2JJcl
-
-
brenda
and strains LP/J, CBAxC57, C57L/J, Nude
-
-
brenda
anemic Mask mouse
-
-
brenda
animals with experimental autoimmune encephalomyelitis
-
-
brenda
ApcMin/+ mice bearing a defect in the adenomatous polyposis coli gene which leads to development of many adenomas
-
-
brenda
Apoe-/- mice
-
-
brenda
Apoe-/- mice, Tie2-Cre mice, and SIRT6-floxed (SIRT6flox/flox) mice
SwissProt
brenda
apolipoprotein E-deficient mice, which display vascular oxidative stress
-
-
brenda
apolipoprotein E-null mice
-
-
brenda
apolipoprotein E4 transgenic mice
-
-
brenda
APP23 mouse
-
-
brenda
at least 3 different isozymes PKNalpha/PKN-1/PAK-1, PKNbeta, and PRK2/PKNgamma/PAK-2
-
-
brenda
at least two splicing variants
SwissProt
brenda
atherosclerosis-prone apolipoprotein E-deficient C57BL/6J mice
-
-
brenda
athymic female MF-1 nude mice
-
-
brenda
ATP7A
SwissProt
brenda
ATP7B
SwissProt
brenda
ATP7B; 2 weeks old and 20 weeks old, wild-type and deficient in copper-transporting ATPase ATP7B (-/-)
SwissProt
brenda
B-type creatine kinase; gene Ckb
UniProt
brenda
B16 melanoma cells
-
-
brenda
B6 and 129 strain, adults and embryos
-
-
brenda
B6 background
-
-
brenda
B6 CBA wild type mice
-
-
brenda
B6 mice
-
-
brenda
B6.129S4-Prkce/tm1/Msg/J mice and Prcke/tm1/Msg-2-3
-
-
brenda
B6C3F1/J mice, mating C57BL/6J female mice to C3H/HeJ male mice
-
-
brenda
B6D2F1 (C57BL/6 × DBA2) mice or ICR mice, and B6D2-Tg(CAG/ Su9-DsRed2, Acr3-EGFP)RBGS002Osb (RBGS, Red Body Green Sperm) mice
UniProt
brenda
BAC-1.2F5 immortalized by transfection with replication-deficient SV40 DNA
-
-
brenda
BACE1-null and wild-type mice at the ages of 2 and 5 months
SwissProt
brenda
BALB mice, gene GARS
-
-
brenda
Balb-C line, vitamin A sufficient and deficient diet fed
Uniprot
brenda
Balb-c mice
UniProt
brenda
BALB/c
208382, 209492, 209639, 209641, 209644, 209648, 209649, 209651, 209653, 209656, 209659, 209661, 209662, 209668, 487420, 488018, 670056, 680014
-
-
brenda
BALB/c
SwissProt
brenda
BALB/c
UniProt
brenda
Balb/c and C57BL/6 mice
-
-
brenda
BALB/c and C57BL/6 mice, isozyme ART2
-
-
brenda
Balb/c and F1 (C57BL×Balb/c) specific pathogen-free female
-
-
brenda
Balb/c female mice
SwissProt
brenda
Balb/c lung carbonic anhydrase IV
-
-
brenda
Balb/c mice
645680, 665903, 668428, 674075, 675206, 676036, 676170, 676292, 682129, 683450, 683523, 683816, 683885, 690355, 691617, 691875, 697807, 698328, 698375, 699408, 707085, 708156, 708766, 709979, 711675, 713551
-
-
brenda
Balb/c mice, C57BL6/J female mice
-
-
brenda
BALB/c mice, isozyme PKGIalpha
-
-
brenda
BALB/c mice, STAT-6-/- mice, and IL-4Ralpha-/- mice
-
-
brenda
BALB/c mouse
-
-
brenda
BALB/c mouse, ppGaNTase-T6, -T1 and -T4
-
-
brenda
BALB/c strain
-
-
brenda
BALB/cA Jcl-ny mice, BALB/cnu/nu mice, and NIKaly/aly mice
-
-
brenda
BALB/cJ mice
-
-
brenda
BalbC mice
SwissProt
brenda
BDF1 mice
-
-
brenda
BDF1, gad (CBA/RFM) and Uchl3 knockout (C57BL/6J) female and male mice
-
-
brenda
bearing colon 26 adenocarcinoma
-
-
brenda
bearing Ehrlich ascites tumor
-
-
brenda
beta,beta-enolase
SwissProt
brenda
beta-ARK 1
-
-
brenda
beta3GnT7
SwissProt
brenda
beta4-GalT-I
-
-
brenda
beta4-GalT-II
-
-
brenda
beta4-GalT-III
-
-
brenda
beta4-GalT-IV
-
-
brenda
beta4-GalT-V
-
-
brenda
bifunctional 17beta-hydroxysteroid dehydrogenase type 10/2-methyl-3-hydroxybutyryl-CoA dehydrogenase
-
-
brenda
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase
-
-
brenda
bifunctional ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1
UniProt
brenda
bifunctional apurinic/apyrimidinic sites lyase and m6A demethylase, cf. EC 4.2.99.18
SwissProt
brenda
bifunctional ATP sulfurylase/adenosine 5'-phosphosulfate kinase
-
-
brenda
bifunctional enzyme
-
-
brenda
bifunctional enzyme possessing glucosaminyl N-deacetylase and N-sulfotransferase activity
-
-
brenda
bifunctional enzyme possessing heparan sulfate N-deacetylase and N-sulfotransferase activity
SwissProt
brenda
bifunctional enzyme, gene folh1
-
-
brenda
bifunctional enzyme, racemization of serine and alpha,beta-elimination of L-serine
-
-
brenda
bifunctional enzyme, racemization of serine and elimination of L-serine and L-serine-O-sulfate to form pyruvate
-
-
brenda
bifunctional enzyme, racemization of serine and elimination of L-serine and L-serine-O-sulfate to form pyruvate
Swissprot
brenda
bifunctional enzymes, racemization of serine and alpha,beta-elimination of L-serine
-
-
brenda
bifunctional enzymes, racemization of serine and elimination of L-serine to form pyruvate
-
-
brenda
bifunctional glutamate/proline-tRNA ligase
UniProt
brenda
bifunctional inositol phosphate kinase and lipid kinase
-
-
brenda
bifunctional L-fucose mutarotase, EC 5.1.3.29, and L-rhamnose mutarotase
SwissProt
brenda
bifunctional NAD-dependent methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase
-
-
brenda
bifunctional peptidase and (3S)-lysyl hydroxylase
UniProt
brenda
bifunctional peptidase and (3S)-lysyl hydroxylase JMJD7
UniProt
brenda
bifunctional peptidase and arginyl hydroxylase
UniProt
brenda
bifunctional polynucleotide phosphatase/kinase, cf. 3.1.3.32
UniProt
brenda
bifunctional polynucleotide phosphatase/kinase, cf. EC 2.7.1.78
UniProt
brenda
bifunctional protein with glutathione peroxidase activity and phospholipase A2 activity
SwissProt
brenda
bifunctional sphingolipid delta(4)-desaturase/C4-monooxygenase
UniProt
brenda
bifunctional triokinase/FMN cyclase
UniProt
brenda
bifunctional U8 snoRNA-decapping enzyme and IDP phosphatase
SwissProt
brenda
bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase, splice variant hGNE2
-
-
brenda
bifunctional UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase
-
-
brenda
bifunctional UMP synthase contains activities of EC 2.4.2.10 and EC 4.1.1.23
-
-
brenda
bioinformatic approaches are used to exploit bacterial operons to identify a putative omega-amidase by confirming this identification through characterization of the candidate protein
-
-
brenda
Black Swiss mice
-
-
brenda
bleomycin hydrolase-deficient cells from mice
SwissProt
brenda
both mitochondrial and cytosolic isoform, expression in human fibroblast. Inverse relationship between the amount of enzyme expressed in target cells and their susceptibility to senescence as shown by changes in replicative potential, cell cycle, expression of p21 and p53. Lipid peroxidation, oxidative DNA damage, and intracellular peroxide generation is higher and cellular redox status shifts to a prooxidant condition in cells expressing low levels of enzyme
-
-
brenda
brain-specific isozyme, 3 isozymes with differences in the 5'-end sequences, overview
SwissProt
brenda
Btk
SwissProt
brenda
C-57/B6 mice
-
-
brenda
C-type PFK
SwissProt
brenda
C2GlcNAcT-I deficient mice
-
-
brenda
C3H mice
-
-
brenda
C3H mice implanted with MH134 cells
-
-
brenda
C3H/An
SwissProt
brenda
C3H/He female mice
-
-
brenda
C3H/HeN mice
-
-
brenda
C3H/HeN mice
UniProt
brenda
C3KO or wild-type mice
-
-
brenda
C56BL/6-CBA hybrid mice
-
-
brenda
C57 and Balb/C mice
-
-
brenda
C57 and nitric oxide synthase-1 knockout mice
-
-
brenda
C57 black mice, murine ascites tumor lines, T-cell lymphoma EL4, Moloney virus-induced lymphoma YAC, mouse melanoma M4(original designation RPMI 7272), 3T3-SV40
-
-
brenda
C57-albino male mice
-
-
brenda
C57/B16
-
-
brenda
C57/B6 and BALB/c mice, gene atp8a2
UniProt
brenda
C57/B6 mice
-
-
brenda
C57/B6-J mice
-
-
brenda
C57/BL 6J mice
-
-
brenda
C57/Bl mice
-
-
brenda
C57/Bl mice
SwissProt
brenda
C57/Bl-6 mice
-
-
brenda
C57/BL6
-
-
brenda
C57/BL6 mice
-
-
brenda
C57/BL6 mice or APP/PS1 mice
-
-
brenda
C57/BL6 mice, isozyme ERAP1
-
-
brenda
C57/Bl6 strain
-
-
brenda
C57/BL6, C57/10Scn, and C57/10J mice
-
-
brenda
C57B/Ka-Thy1.1 mice at 6-10 weeks of age
-
-
brenda
C57B1/6
-
-
brenda
C57B1/6J male mouse
-
-
brenda
C57B6 mice
-
-
brenda
C57B6/J mice
-
-
brenda
C57B6/S129 mice
SwissProt
brenda
C57BI/6 mice
-
-
brenda
C57BI/6J mice
-
-
brenda
C57BL strain
-
-
brenda
C57BL, wild type and p53KO mice
-
-
brenda
C57BL/10J
-
-
brenda
C57BL/6
-
-
brenda
C57BL/6
SwissProt
brenda
C57BL/6
UniProt
brenda
C57BL/6 and 129/J mice
-
-
brenda
C57BL/6 and BALB/c mice
-
-
brenda
C57BL/6 and F1 (C57BL/6 x 129/Sv) wild-type mice
-
-
brenda
C57BL/6 genetic background
-
-
brenda
C57Bl/6 male mice
-
-
brenda
C57BL/6 mice
669716, 669717, 671959, 673481, 675204, 680845, 680875, 681543, 681911, 682112, 682136, 683046, 683054, 683480, 683525, 683738, 683741, 683863, 684007, 684350, 684803, 686304, 687032, 688149, 688223, 689353, 690342, 690367, 690860, 691542, 693098, 693776, 695619, 697358, 698165, 698235, 698935, 699321, 699336, 699337, 699349, 700198, 700471, 700916, 701687, 702101, 702855, 703809, 704003, 704426, 704943, 704949, 704951, 705402, 707042, 707048, 707370, 707851, 707992, 708146, 708250, 708448, 708597, 708599, 708641, 709116, 709821, 710118, 711666, 711942, 711959, 712637, 712901
-
-
brenda
C57BL/6 mice
SwissProt
brenda
C57BL/6 mice
UniProt
brenda
C57BL/6 mice and SOD1-G93A transgenic mice (model of amyotrophic lateral sclerosis)
-
-
brenda
C57BL/6 mice either wild-type for cathepsin K, CK+/+, heterozygous for cathepsin K, CK+/-, or deficient in cathepsin K, CK-/-, all transgenically expressing human tumor necrosis factor
-
-
brenda
C57BL/6 mice, BALB/c mice, and CB-17/lcr-Prkdcscid/Crl, i.e. BALB/c SCID, mice
-
-
brenda
C57BL/6 mice, enzyme forms: lysyl oxidase LOX and lysyl oxidase-like protein LOXL
-
-
brenda
C57BL/6 mice, four isoforms alpha, beta2, gamma, and delta, of CaMKI
-
-
brenda
C57BL/6 mice, gene Ndst1
-
-
brenda
C57Bl/6 mice, isozyme AC1
UniProt
brenda
C57Bl/6 mice, isozyme AC8
UniProt
brenda
C57BL/6 mice, isozyme sGCalpha1
-
-
brenda
C57BL/6 mice, isozymes NDST-1-4
-
-
brenda
C57BL/6 mice, no TMT activity in but not BALB/c or 129/Sv mice
-
-
brenda
C57BL/6 mice, seven SULT2A genes including SULT2A1
-
-
brenda
C57BL/6 mice, several enzyme forms
-
-
brenda
C57BL/6 mice, two isozymes Atp8a1 and flippase
-
-
brenda
C57BL/6 mice, wild-type and MMP13-/- mice
-
-
brenda
C57BL/6 wild-type mice
-
-
brenda
C57BL/6 wild-type mice or murine strains deficient in either subunits IKKalpha, IKKbeta, or IKKgamma, overview
-
-
brenda
C57BL/6 wild-type or homozygous Siae deficient knockout mice, and B6.129S7-Rag1-deficient mice
-
-
brenda
C57BL/6 wild-type, isozyme ppGalNAcT-1, encoded by gene Galnt1, and isozymes ppGalNAcT-2, and ppGalNAcT-3
-
-
brenda
C57Bl/6 WT mice
-
-
brenda
C57BL/6, 129Sv mice
-
-
brenda
C57Bl/6, 129X1/SvJ, DBA/2, and BALB/cJ mice, genes Tph1 and Tph2 encoding isozymes TPH1 and TPH2, respectively
-
-
brenda
C57BL/6, C57BL/6-129S5, Vav1-iCre, and NKp46-iCre mice
UniProt
brenda
C57BL/6, female, healthy or with experimental autoimmune uveoretinitis (EAU)
-
-
brenda
C57BL/6, FVB/NJ, or MMP-9-/-, with FVB/NJ background, mice
-
-
brenda
C57BL/6-129S mice
-
-
brenda
C57BL/6-N mice
-
-
brenda
C57BL/6J
-
-
brenda
C57BL/6J
SwissProt
brenda
C57BL/6J and 129 SVJ mice
-
-
brenda
C57BL/6J and 129S6/SvEv mice
-
-
brenda
C57BL/6J and CASA/Rk mice, and a hybrid of both
-
-
brenda
C57BL/6J and CAST/Ei
UniProt
brenda
C57BL/6J and CD2F1 mice
-
-
brenda
C57BL/6J and grt mice, two isozymes encoded by genes Tpst1 and Tpst2
-
-
brenda
C57BL/6J and ob/ob mice
-
-
brenda
C57BL/6J background
-
-
brenda
C57BL/6J mic, BALB/c, C3H/HeJ, DBA/2, ddY, and ICR mice
-
-
brenda
C57BL/6J mice
666125, 668096, 670691, 673003, 673451, 674449, 675063, 679103, 679653, 681530, 683454, 687713, 689178, 693736, 700611, 701011, 703241, 703618, 704431, 705505, 706094, 707070, 708021, 709009, 709065, 709745, 710082, 711567, 712913
-
-
brenda
C57BL/6J mice
SwissProt
brenda
C57BL/6J mice
UniProt
brenda
C57BL/6J mice and class II MHC-deficient mice
-
-
brenda
C57BL/6J mice and male ob/ob mice
-
-
brenda
C57BL/6J mice, gene EPHX2
SwissProt
brenda
C57BL/6J mice, gene PHGDH
-
-
brenda
C57BL/6J mice, genes Mdr1a, Mdr1b, and Mdr2
-
-
brenda
C57BL/6J mice, isozymes ACC1 and ACC2
-
-
brenda
C57BL/6J mice, SCID mice, and BALB/c mice
-
-
brenda
C57BL/6J strain
-
-
brenda
C57BL/6J, after tretmend with an NOS inhibitor used as a model of chronic nitric oxide expression
-
-
brenda
C57BL/6J, PCSK4 gene is transcribed into a major mRNA and several shorter isoforms resulting from alternate splicing
UniProt
brenda
C57BL/6mice
-
-
brenda
C57BL/6Njcl mice
-
-
brenda
C57Bl/B6 and 129S6/SvEvTac mice
-
-
brenda
C57BL/six mice
-
-
brenda
C57BL6
-
-
brenda
C57BL6 male mice
-
-
brenda
C57Bl6 mice
-
-
brenda
C57Bl6 mice
SwissProt
brenda
C57BL6 mice, gene ephx2
SwissProt
brenda
C57BL6/129SVJ and FVBN wild-type mice
-
-
brenda
C57BL6/J
SwissProt
brenda
C57Bl6/J mice
-
-
brenda
C57BL6J and murine cell lines P815B murine mastocytoma cells
-
-
brenda
C57BL76J mice, gene msrA
-
-
brenda
C57BLKsJ lepr-/-db/db mice, diabetc mice
-
-
brenda
C75BL/6 mice
-
-
brenda
calcpain-2, catalytic subunit
SwissProt
brenda
caloric restricted young (3 months) and old (30 months) male C57BL/6J mice
-
-
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
CaMKIgamma
SwissProt
brenda
cAMP-dependent protein kinase catalytic subunit alpha
SwissProt
brenda
cAMP-dependent protein kinase catalytic subunit beta
SwissProt
brenda
carbonic anhydrase V
-
-
brenda
carbonic anhydrase VII
-
-
brenda
carbonic anhydrase XIV
Uniprot
brenda
carboxypeptidase N, small subunit
Swissprot
brenda
catalytic subunit
SwissProt
brenda
catalytic subunit p110alpha; isozyme PI3Kalpha
SwissProt
brenda
catalytic subunit p110delta; isozyme PI3Kdelta
SWissProt
brenda
cathepsin B or E deficient mice strains backcrossed into C57BL/6 mice
-
-
brenda
cathepsin G-deficient mice and wild-type mice
-
-
brenda
CBA and RFM mice
-
-
brenda
CD-1 genetic background
-
-
brenda
CD-1 mice and C57B/6 mice
-
-
brenda
CD-1 mice, BALB/cJ mice and C57BL/6 mice
SwissProt
brenda
CD-1 mouse
-
-
brenda
CD-1 strain
-
-
brenda
CD1 and C3H/An
-
-
brenda
CD1 mice
-
-
brenda
CD38-deficient strain, bifunctional enzyme, distinct from CD157 and CD38
-
-
brenda
CD43 knockout and CD43 wild type mice, on the C57BL/6 background
-
-
brenda
Cdc42flox mice
-
-
brenda
Cdkn1a-null mice
UniProt
brenda
cDNA of the beta subunit; studies on beta subunit
SwissProt
brenda
Cds1; Cds1
SwissProt
brenda
Cds2; Cds2
SwissProt
brenda
cell lines BML1-ME, NIH3T3, PA317 and PE 501
-
-
brenda
cell lines YAC, P815
-
-
brenda
cf. 1.14.16.1
SwissProt
brenda
cf. 3.1.3.48
SwissProt
brenda
cf. caspase-4, EC 3.4.22.57
768451, 770002, 770138, 770172, 770188, 770759, 770782, 771415, 771444, 771849, 772221, 772912, 773810, 773812, 774702, 774708
SwissProt
brenda
cf. caspase-4, EC 3.4.22.57; C57BL/6 and and BALB/c mice
SwissProt
brenda
cf. EC 1.13.11.31, EC 1.13.11.12
UniProt
brenda
cf. EC 1.13.11.33
UniProt
brenda
cf. EC 1.13.11.33, EC 1.13.11.12
UniProt
brenda
cf. EC 1.14.11.27, EC 1.14.11.65, EC 1.14.11.66
UniProt
brenda
cf. EC 1.14.11.27, EC 1.14.11.65, EC 1.14.11.69
UniProt
brenda
cf. EC 1.14.11.27, EC 1.14.11.66, EC 1.14.11.69
UniProt
brenda
cf. EC 1.14.11.65, EC 1.14.11.66, EC 1.14.11.69
UniProt
brenda
cf. EC 1.14.11.66
UniProt
brenda
cf. EC 2.1.1.367
SwissProt
brenda
cf. EC 2.1.1.368
SwissProt
brenda
cf. EC 2.3.1.15
SwissProt
brenda
cf. EC 2.3.1.15
UniProt
brenda
cf. EC 2.3.1.51
UniProt
brenda
cf. EC 2.3.2.23
SwissProt
brenda
cf. EC 2.3.2.24
SwissProt
brenda
cf. EC 2.4.1.37, EC 2.4.1.40
UniProt
brenda
cf. EC 2.7.1.60
Uniprot
brenda
cf. EC 2.7.7.1
UniProt
brenda
cf. EC 2.7.7.18
UniProt
brenda
cf. EC 2.7.7.43
UniProt
brenda
cf. EC 2.7.8.1
UniProt
brenda
cf. EC 2.7.8.2
UniProt
brenda
cf. EC 3.1.3.16
SwissProt
brenda
cf. EC 3.1.3.18, EC 3.1.3.21, EC 3.1.3.48
SwissProt
brenda
cf. EC 3.1.3.48
SwissProt
brenda
cf. EC 3.1.4.1
UniProt
brenda
cf. EC 3.1.4.17
SwissProt
brenda
cf. EC 3.1.4.17
UniProt
brenda
cf. EC 3.1.4.17 and Ec 3.1.4.35
SwissProt
brenda
cf. EC 3.1.4.35 and EC 3.1.4.53
Uniprot
brenda
cf. EC 3.1.6.1
SwissProt
brenda
cf. EC 3.1.6.18
SwissProt
brenda
cf. EC 3.2.1.113
UniProt
brenda
cf. EC 3.2.1.183
Uniprot
brenda
cf. EC 3.2.2.31
SwissProt
brenda
cf. EC 3.4.1.35
SwissProt
brenda
cf. EC 3.4.1.53
SwissProt
brenda
cf. EC 3.6.1.1
SwissProt
brenda
cf. EC 3.6.1.9
UniProt
brenda
cf. EC 4.1.1.11
UniProt
brenda
cf. EC 4.1.1.29
UniProt
brenda
cf. EC 4.2.99.18
-
-
brenda
cf. EC 4.2.99.18
SwissProt
brenda
cf. EC 4.2.99.18
UniProt
brenda
cf. EC. 4.2.99.18
SwissProt
brenda
cf. ECs 2.3.1.121, 2.3.1.67
SwissProt
brenda
cf. ECs 2.3.1.23, 2.3.1.67
SwissProt
brenda
Charles River male mice
-
-
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 II isoform PI3K-C2beta
-
-
brenda
class III alcohol dehydrogenase
-
-
brenda
class III enzyme
-
-
brenda
cohort of 63 PyMT transgenic mice, either deficient for MMP-3 or wild-type controls
-
-
brenda
commentary
-
-
brenda
commercial product
-
-
brenda
comparison of the mouse, rat, and human ogt genes
UniProt
brenda
constitutive isozyme HO-2
UniProt
brenda
construction of -/- and +/- knockout mutants
-
-
brenda
construction of GNMT knockout mice, loss of enzyme results in highly elevated levels of free methionine and S-adenosyl-L-methionine
SwissProt
brenda
conventional, novel, and atypical isozyme types, overview
-
-
brenda
CPA6 precursor
SwissProt
brenda
creation of mice with angiotensin converting enzyme expression limited to selected tissue types
-
-
brenda
cross between 129/Sv and C57BL/6 mouse strains
-
-
brenda
CTP synthetase type I
SwissProt
brenda
CTP synthetase type II
SwissProt
brenda
CX3CR1GFP mice carrying aldose reductase mutant alleles
SwissProt
brenda
cyclooxygenase-2 knock-out mice
-
-
brenda
cyclosporin-treated mice
-
-
brenda
CYP27B1 knockout mice, normal development when fed a 1alpha,25-dihydroxyvitamin D replacement or a high-calcium diet
-
-
brenda
CYP8B1 enzyme activity is absent in HNF4alphaDELTAL mice
-
-
brenda
cytochrome b5/cytochrome b5 reductase fusion protein, exists also as a variant where the whole exon 12 is deleted
SwissProt
brenda
cytokine-inducible in macrophage
-
-
brenda
cytokine-inducible in macrophage
UniProt
brenda
cytosolic deoxyguanosine kinase 2, amino-terminally truncated isoform
SwissProt
brenda
db/db mice lacking the hypothalamic leptin receptor, representing a model of type 2 diabetes mellitus
-
-
brenda
DBA mice, mastocyma P815 (ATCC TIB 64)
-
-
brenda
DBA/1J mice
-
-
brenda
DBA/2 mice
-
-
brenda
DBA/2 mouse
-
-
brenda
DBA/2, CBA/2 C57Bl/6J and CD1 mice
-
-
brenda
DBA/2, CBA/2 C57Bl/6J and CD1 mice
UniProt
brenda
DBA/2: liver, spleen, thymus
-
-
brenda
DBA/2J
-
-
brenda
DBA/2J mice
-
-
brenda
DBA/2J, DBA/2N and BALB/c mice carrying the 1473G allele, and C57BL/6J and C57BL/6N mice carrying the 1473C allele
-
-
brenda
DcoH2 (dimerization cofactor of HNF1alpha)
Uniprot
brenda
DCS, complete gene and exon 27; gene mthfd1 encodes the cytosolic isozyme which is a trifunctional methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetase enzyme DCS, a mitochondrial monofunctional 10-formyltetrahydrofolate synthetase isozyme is encoded by a different gene
SwissProt
brenda
DD1, DD2, DD3, DD4
-
-
brenda
deer mice
-
-
brenda
deficient in enzyme activity of isoform I or of isoform II
-
-
brenda
definite classification as EC 1.13.11.11 based on protein sequence
SwissProt
brenda
definite classification as EC 1.13.11.52 based on protein sequence
SwissProt
brenda
deletion mutant
-
-
brenda
Dexter-ras-myc cell line
-
-
brenda
DGAT1
SwissProt
brenda
DGAT2
SwissProt
brenda
DGKalpha isoform
UniProt
brenda
DGKepsilon isoform
SwissProt
brenda
DGKzeta isoform
UniProt
brenda
DGS654A transgenic line
-
-
brenda
diabetes-susceptible DBA/2 mice
-
-
brenda
diabetic C57BL6 mice
-
-
brenda
diabetic ob/ob mice
-
-
brenda
diacylglycerol kinase alpha
UniProt
brenda
diacylglycerol kinase zeta
UniProt
brenda
different splice isoforms of nNOS, e.g. splicing variant nNOSalpha
-
-
brenda
dihydrodiol dehydrogenase EC 1.3.1.20 and 3(17)alpha-hydroxysteroid dehydrogenase EC 1.1.1.59 activities reside on a single protein
-
-
brenda
distribution of short and long forms of tRNase Z reviewed
-
-
brenda
DLPP1 gene
SwissProt
brenda
DNA ligase I and II
-
-
brenda
DNMT1
-
-
brenda
Dnmt3a
SwissProt
brenda
Dnmt3b
SwissProt
brenda
Down syndrome model Ts65Dn mice
-
-
brenda
Dyrk1A+/- and tgYAC152f7 genotypes
SwissProt
brenda
dystrophic
-
-
brenda
E1 component subunit alpha
UniProt
brenda
EC-2, clonal Ras/Myc-immortalized fibroblast cell line
-
-
brenda
Egr1 genetically modified mice, several isozymes through allelic difference of HisRS between 129/Sv and C57Bl/6J strains
-
-
brenda
Ehrlich ascites carcinoma cells
485359, 485360, 485361, 485363, 485365, 485368, 485369, 485375, 485382, 485384, 485390, 485393, 485398, 485402, 485404
-
-
brenda
Ehrlich ascites cells
-
-
brenda
Ehrlich ascites line Swiss mice
-
-
brenda
Ehrlich ascites tumor cells
-
-
brenda
Ehrlich's ascites tumor cells and various gastrointestinal tumors
-
-
brenda
eight-week-old female mice
-
-
brenda
embryo
-
-
brenda
ENU4
-
-
brenda
enzyme belongs to the subfamily of adamalysins which is part of the superfamily of zinc-dependent proteases
-
-
brenda
enzyme complex
SwissProt
brenda
enzyme Dnmt3b
SwissProt
brenda
enzyme form type I, 3 isozymes alpha, beta, gamma in several splicing variants
-
-
brenda
enzyme forms A and B
-
-
brenda
enzyme forms cGKI, in 2 isoforms cGKIalpha and cGKIbeta, and cGKII
-
-
brenda
enzyme forms: DD1, DD3
-
-
brenda
enzyme inhibition by specific antisense oligonucleotide inhibitors, reduction of enzyme expression, reduction of fatty acid synthesis and secretion, increase in fatty acid oxidation
-
-
brenda
enzyme is a bifunctional selenoprotein
-
-
brenda
enzyme is essential for embryonic development
-
-
brenda
enzyme isoform AOX1 gene and its homologue AOH1 are inducible by 2,3,7,8-tetrachlorodibenzo-p-dioxin. Transcriptional induction through aryl hydrocarbon receptor pathway
-
-
brenda
enzyme-deficient CELKO and wild-type mice
-
-
brenda
enzyme-deficient mutant and normal littermate mice
-
-
brenda
enzyme-deficient strain
-
-
brenda
erythrocyte-specific pyruvate kinase gene PKLR
-
-
brenda
erythroid specific isoform
-
-
brenda
erythroid-specific isoform
-
-
brenda
expressed as haemagglutinin-tagged fusion protein in COS-1 cells or HeLa cells
UniProt
brenda
expressed in baculoviral system
-
-
brenda
expressed in baculoviral system
SwissProt
brenda
expressed in Pichia pastoris
Uniprot
brenda
expression in baculovirus system, membrane-bound complete enzyme and soluble domain
-
-
brenda
expression in Chinese hamster ovary cells
-
-
brenda
expression in CHO-K1 cells
-
-
brenda
expression in Escherichia coli
-
-
brenda
expression in F9-2 cell
-
-
brenda
expression in HEK cells
Swissprot
brenda
expression in HEK-293 cell
-
-
brenda
expression in human embryonic kidney HEK 293-F cells
SwissProt
brenda
expression of GMD is higher in macrophages than in endothelial cells
-
-
brenda
expression of the enzyme in HeLa cells
-
-
brenda
EXT1 protein
-
-
brenda
extensive overview of literature data concerning inhibitors and substrates
-
-
brenda
F2 hybrids of strains C57BL/6 and CC57BR
SwissProt
brenda
F508del mouse, mouse model with well-characterized intestinal pathology
-
-
brenda
fast acetylator strain C57BL6, slow acetylator strain A/J
-
-
brenda
fasted
-
-
brenda
fed a diet containing 20% or 12% protein. Acid RNase and DNASE II activity increase according to the dietary protein content. In mice fed a 20% protein diet, growth hormone treatment decreases both activites
-
-
brenda
fed lipid-lowering drug diet containing clofibrate, nafenopin or Wy-14,643
-
-
brenda
fed with normal or cholesterol-enriched diet
-
-
brenda
feeding of phytol results in induction of carnitine O-octanoyltransferase as well as catalase, phytanoyl-CoA hydroxylase, peroxisomal 3-ketoacyl-CoA thiolase, and straight-chain acyl-CoA oxidase
-
-
brenda
female (C3H/HeJ × 129/J)F1 (C31) hybrid mice
-
-
brenda
female albino mouse
-
-
brenda
female and castrated male animals
Uniprot
brenda
female and male 129SVJ mice
-
-
brenda
female and male C57BL/6 mice
-
-
brenda
female and male C57BL/6 mice
UniProt
brenda
female and male C57BL/6 mice, gene AOC3
-
-
brenda
female and male C57BL/6J mice
-
-
brenda
female and male ICR mice, Balb/c mice
-
-
brenda
female and male mice
-
-
brenda
female and male Swiss albino mice
-
-
brenda
female and male Swiss/129 mice
-
-
brenda
female BALb/c
-
-
brenda
female BALB/c and C57Bl/6 mice
UniProt
brenda
female BALB/c mice
-
-
brenda
female BALB/c mice and A/J mice
-
-
brenda
female BALB/c nude mice
-
-
brenda
female C3H/HeOuJ and C57BL/6 mice
-
-
brenda
female C57/BL/6J mice
-
-
brenda
female C57BL/6
-
-
brenda
female C57BL/6 mice
-
-
brenda
female C57BL/6/129S mice, wild-type and ob/ob mice
-
-
brenda
female C57BL/6J mice
-
-
brenda
female C57BL/8 mice
-
-
brenda
female C57BL?6J
-
-
brenda
female CB17-SCID mice
-
-
brenda
female Harlan Sprague-Dawley mice
-
-
brenda
female ICR
-
-
brenda
female ICR mice
-
-
brenda
female ICR mice, ovariectomized or sham-operated, treated with or without daily restraint stress conditions for 6 h per day over 3 weeks
SwissProt
brenda
female mice
-
-
brenda
female SJL/J mice and mice with adoptively transferred myelin basic protein-specific experimental autoimmune encephalomyelitis
-
-
brenda
female wild-type and NAD(P)H oxidase deficient gp91phox knock-out mice
-
-
brenda
female wild-type C57BL/6 mice
-
-
brenda
female, 4 weeks old
-
-
brenda
females from strain C57B1/6 and males from strain CBA
-
-
brenda
fetal B6129 mice
-
-
brenda
fetuses (embryonic day 17) Pemt -/- and wild type mice and 12-week-old Pemt -/- and wild type mice. For E17 fetal brain microarrays, 11 separate oligoarrays (comparing wild type and Pemt -/-) including 4 dye-flip experiments are perfomed and indentified differntially expressed genes: 107 significant genes with increased expression and 379 significant genes with decreased expression. For adult brain microarrays, 8 separate oligoarrays (comparing wild type and Pemt -/-) including 4 dye-flip experiments are perfomed and identified differentially expressed genes: 381 significant genes with increased expression and 1037 significant genes with decreased expression.
-
-
brenda
floxed Pofut1 (Pofut1F/F) mice and Pofut1 heterozygous mice (Pofut1+/-)
-
-
brenda
FMO1; gene FMO1
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
for binding studies the X-ray structure of murine p38alpha is used
SwissProt
brenda
for docking studies the X-ray structure of murine p38alpha is used
-
-
brenda
formamidase II
-
-
brenda
four 12-lipoxygenase: 1.platelet-type 12-lipoxygenase, 2. leukocyte-type lipoxygenase, 3. epidermal-type lipoxygenase, 4. 12(R)-lipoxygenase
-
-
brenda
four described H3K4me3 demethylases, named KDM5A-D
-
-
brenda
four different isoforms generated by alternative splicing
-
-
brenda
four-days-old ICR mice
-
-
brenda
fragment
SwissProt
brenda
fragment
UniProt
brenda
fragment; male BALB/c mice
SwissProt
brenda
Furth mouse
-
-
brenda
FVB/N mice
-
-
brenda
FVB/N, C3H/HeN, and C57BL/6N mice
-
-
brenda
FVB/NJ mice
-
-
brenda
G93A-SOD1 transgenic mice
SwissProt
brenda
G9a histone methyltransferase
-
-
brenda
galT gene
SwissProt
brenda
gamma isoform
UniProt
brenda
gamma-chain
SwissProt
brenda
Gardner lymphosarcoma
-
-
brenda
GCC; Balb/c mice
UniProt
brenda
GenBank accession numbers are PTP36-A: AF170902, PTP36-B: AF170903, PTP36-C: AF170904
-
-
brenda
GenBank accession numbers are PTP36-A: AF170902, PTP36-B: AF170903, PTP36-C: AF170904
Uniprot
brenda
GenBank AF125043
Uniprot
brenda
GenBank D64141
-
-
brenda
gene 15-Pgdh
-
-
brenda
gene Adamts13
-
-
brenda
gene ADAMTS2; gene ADAMTS2
UniProt
brenda
gene Afmid
-
-
brenda
gene AGPAT8
-
-
brenda
gene Agps
UniProt
brenda
gene Aibp
UniProt
brenda
gene Aicda
-
-
brenda
gene ALAS-2
-
-
brenda
gene ALAS-E
-
-
brenda
gene alas2
UniProt
brenda
gene ALG2
UniProt
brenda
gene AOF1
-
-
brenda
gene arsM
-
-
brenda
gene Asah2
-
-
brenda
gene Ash2l encoding the Set1/Ash2 histone methyltransferase complex subunit ASH2
SwissProt
brenda
gene asl
-
-
brenda
gene ASPA
Uniprot
brenda
gene ATE-1 specifies at least six isoforms which are produced through alternative splicing and are expressed at varying levels in mouse tissues
-
-
brenda
gene ATP7A
-
-
brenda
gene B3gnt5
-
-
brenda
gene B3gnt6
UniProt
brenda
gene Bcmo1
SwissProt
brenda
gene Capn5
SwissProt
brenda
gene CASP-7
-
-
brenda
gene Casp11
-
-
brenda
gene cbp
-
-
brenda
gene cdo
-
-
brenda
gene CERK
UniProt
brenda
gene cers2
SwissProt
brenda
gene Ch25h
-
-
brenda
gene Ch25h
Swissprot
brenda
gene Chst3, C6st, or Gst0; isozyme C6ST-1
SwissProt
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 COQ2
-
-
brenda
gene cpt1c, brain-specific isozyme CPT1c
-
-
brenda
gene csgalnact1
UniProt
brenda
gene csgalnact2
UniProt
brenda
gene Ctsk
-
-
brenda
gene CYP27A1
-
-
brenda
gene CYP27A1
UniProt
brenda
gene Cyp4f18
-
-
brenda
gene CYP7A1
SwissProt
brenda
gene DGAT1; gene DGAT1
SwissProt
brenda
gene DGAT2; gene DGAT2
SwissProt
brenda
gene dgkdelta with two variants delta1 and delta2
-
-
brenda
gene Dhps
-
-
brenda
gene Dyn1
UniProt
brenda
gene eEF-2K
SwissProt
brenda
gene EPHX2
SwissProt
brenda
gene EXT1
UniProt
brenda
gene ext2
UniProt
brenda
gene fgl2
-
-
brenda
gene Fmo3; gene FMO3
UniProt
brenda
gene GAD67
-
-
brenda
gene gclC and gclM, encoding the catalytic and the modifier subunit
-
-
brenda
gene Gcn5
-
-
brenda
gene GGPS1
UniProt
brenda
gene GNTPAB
UniProt
brenda
gene GRHPR
-
-
brenda
gene Gucy2g encoding isozyme GC-G
UniProt
brenda
gene gzmA
SwissProt
brenda
gene gzmB
SwissProt
brenda
gene hadh
-
-
brenda
gene hemA
-
-
brenda
gene HPRT
-
-
brenda
gene Hsepi
-
-
brenda
gene IDUA
-
-
brenda
gene Ihpk1
-
-
brenda
gene Ikbke
-
-
brenda
gene IP6K1
SwissProt
brenda
gene IP6K3
UniProt
brenda
gene Itpka
UniProt
brenda
gene Itpkb
UniProt
brenda
gene Itpkc
UniProt
brenda
gene KLK1, glandular kallikrein 1 precursor
SwissProt
brenda
gene KLK11, glandular kallkrein K11 precursor
SwissProt
brenda
gene KLK13 or EGFB2, glandular kallikrein K13 precursor
SwissProt
brenda
gene KLK3 or NGFG
SwissProt
brenda
gene KLK6, glandular kallikrein K6 precursor
SwissProt
brenda
gene KLK8
SwissProt
brenda
gene KLK8 or PRSS19 or NRPN or BSP1
SwissProt
brenda
gene KLK9, glandula kallikrein K9 precursor
SwissProt
brenda
gene KLKB1 or KLK3 or PK, plasma kallikrein precursor
SwissProt
brenda
gene lcat
-
-
brenda
gene lfng
-
-
brenda
gene lfng
Uniprot
brenda
gene Lipe
-
-
brenda
gene LIPIN1
-
-
brenda
gene Lonp1
SwissProt
brenda
gene Lpcat2
SwissProt
brenda
gene Lpcat2; gene Lpcat2
SwissProt
brenda
gene lpla2
-
-
brenda
gene Lrat
-
-
brenda
gene mGPI1 clone
Uniprot
brenda
gene mif
-
-
brenda
gene mLCB2
-
-
brenda
gene mmp-3
UniProt
brenda
gene Mmp13
-
-
brenda
gene Mmp2
UniProt
brenda
gene MMP9
UniProt
brenda
gene Mogat2
UniProt
brenda
gene mthfr
SwissProt
brenda
gene mylk1, encoding two isozymes: the endothelial, long or nonmuscle 220-kDa MLCK and a short, smooth muscle 130-kDa MLCK
-
-
brenda
gene Naalad2
SwissProt
brenda
gene Ndst1
-
-
brenda
gene nmdmc
SwissProt
brenda
gene Nmnat1
SwissProt
brenda
gene Nnt
-
-
brenda
gene oas1b encoding isozyme Oas1b
-
-
brenda
gene Ovch2
UniProt
brenda
gene p450scc
-
-
brenda
gene parp-1
-
-
brenda
gene Pfkfb2
SwissProt
brenda
gene PFKFB3, isozyme iPFK2 is inducible
SwissProt
brenda
gene PHEX
-
-
brenda
gene PIG-P
Swissprot
brenda
gene Pik3c2alpha
SwissProt
brenda
gene PIKfyve
UniProt
brenda
gene Plod3
SwissProt
brenda
gene png1
-
-
brenda
gene Pnpla2
-
-
brenda
gene PNPO
-
-
brenda
gene POFUT1
Uniprot
brenda
gene porc
-
-
brenda
gene prep
-
-
brenda
gene prkg1, encoding isozyme PKG I in two splice variants, PKG Ialpha and Ibeta, and gene prkg2 encoding isozyme PKG II
-
-
brenda
gene PRSS17
Q9JIS2
SwissProt
brenda
gene PRSS8
SwissProt
brenda
gene PRSS8
UniProt
brenda
gene pte-2, isozyme PTE-II
SwissProt
brenda
gene Rap1b
UniProt
brenda
gene rnaseh1
-
-
brenda
gene selD
SwissProt
brenda
gene sext1 and ext2
-
-
brenda
gene SMOX, splice variant isozymes SMOalpha and SMOmu
SwissProt
brenda
gene SMPD1
-
-
brenda
gene SMPD3
SwissProt
brenda
gene SMPDL3A
UniProt
brenda
gene Soat1
UniProt
brenda
gene spdS
-
-
brenda
gene SPS1
UniProt
brenda
gene sps2
SwissProt
brenda
gene ST14
-
-
brenda
gene ST3GAL5
Uniprot
brenda
gene t1
UniProt
brenda
gene t2
UniProt
brenda
gene trmU
SwissProt
brenda
gene uch l1
-
-
brenda
gene uch-L1
-
-
brenda
gene uchl3
-
-
brenda
gene VKORC1
-
-
brenda
generation of CerK-null mice
-
-
brenda
genes ATP7A and ATP7B
-
-
brenda
genes CCT1-8 encoding subunits TCP-1-alpha, TCP-1-beta, TCP-1-gamma, TCP-1-delta, TCP-1-epsilon, TCP-1-zeta, TCP-1-eta, and TCP-1-theta
P11983, P80314, P80318, P80315, P80316, P80317, P80313, P42932
UniProt
brenda
genes CTE-I, MTE-I, PTE-Ia and PTE-Ib with different subcellular localization and corresponding targeting sequence, phylogenetic study
SwissProt
brenda
genes encoding subunits TAP1 and TAP2; C57BL/6 (H-Zb), and BALB/c (H-2d) mice
UniProt
brenda
genes Entpd1, 2, 3, 5, 6, and Entpd8
-
-
brenda
genes gclC and gclM
-
-
brenda
genes GCLC and GCLM encoding catalytic heavy chain subunit and modifier light chain subunits
UniProt
brenda
genes gclC and gclM encoding the two subunits of the enzyme
-
-
brenda
genes lfng and mfng
-
-
brenda
genes Lox or LoxL1
-
-
brenda
genes Lpin1 and Lpin2
-
-
brenda
genes Lpin1, Lpin2, and Lpin3
-
-
brenda
genes METTL11A and METTL11B
-
-
brenda
genes sps2 and sps1
SwissProt
brenda
genes uchl1 and uchl3, C57BL/6J and gad, i.e. gracile axonal dystrophy, mice
-
-
brenda
Girk2(Wv) (Weaver) mutant mice
-
-
brenda
glandular kallikrein K3 precursor
SwissProt
brenda
glandular kallikrein K5 precursor
SwissProt
brenda
glandular kallikrein K8 precursor
SwissProt
brenda
glucose-6-phosphatase catalytic subunit 1
UniProt
brenda
glucose-6-phosphatase catalytic subunit 1; db/db mice and db/+ m mice
UniProt
brenda
glutamate decarboxylase 67-green fluorescent protein, GAD67-GFP, knock-in mice
-
-
brenda
Golgi alpha1,2-mannosidase IA
UniProt
brenda
Golgi alpha1,2-mannosidase IB
UniProt
brenda
granzyme A precursor; interleukin 4-deficient BALB/c mice and wild-type BALB/c controls
SwissProt
brenda
GRK2; C56BL/6-CBA hybrid mice
-
-
brenda
GRK5; C57BL/six mice
UniProt
brenda
GRK6; C57BL/six mice
UniProt
brenda
hairless mice strain Cr1:SKH1-hr
-
-
brenda
healthy and diabetic db/db mice with type 2 diabetes
-
-
brenda
healthy and heart-failure rats
-
-
brenda
healthy and Schistosoma-infected animals
-
-
brenda
heart isozyme PFKFB2; genes PFKFB1-4, four isozymes
SwissProt
brenda
heavy, catalytic subunit
SwissProt
brenda
HEK-293 cells stably expressing 17beta-HSD12
UniProt
brenda
hematopoietic prostaglandin D2 synthase
-
-
brenda
heterozygous APP23 transgenic mice overexpressing human-type amyloid precursor protein (APP) carrying a double mutation (K670N/M671L) and age-matched C57BL/6J wild-type littermates
UniProt
brenda
heterozygous BALB/cByJ-fld/+ mice
Uniprot
brenda
heterozygous for cystathionine beta-synthase and wild-type
-
-
brenda
heterozygous sv129 x BL/6 background mice
-
-
brenda
high expression
-
-
brenda
high fat-fed mice
-
-
brenda
high IgA mouse used as model of human IgA nephropathy
-
-
brenda
high-affinity form and low-affinity form
-
-
brenda
high-mobility- and low-mobility tyrosinase
-
-
brenda
higher enzymic activity in females than in males. Circadian rhythm of enzyme activity in the second week of post-natal development is associated with ultradian components, and around 8 weeks of post-natal development the circadian rhythm is stabilized
-
-
brenda
HL-1 mice
-
-
brenda
HL-60 cell lines with stable transfections with the cDNA for mouse IDPc
-
-
brenda
homozygous deficiency in enzyme
-
-
brenda
homozygous disruption of the Capn2 gene (encoding the catalytic subunit of m-calpain) results in preimplantation embryonic lethality between the morula and blastocyst stage
SwissProt
brenda
homozygous LDL-receptor-knockout mice, heterozygous ob/+, and wild-type C57BL6 mice
-
-
brenda
homozygous PTP1B-deficient animal, hyperresponsive to insulin and leptin and resistant to diet-induced obesity
-
-
brenda
HS3ST-2 gene
-
-
brenda
Hsd:ICR (CD-1) outbred albino mice, postnatal day 27 male mice and day 28 male mice
-
-
brenda
human tau transgenic mice Thr231
UniProt
brenda
human tumor necrosis factor-alpha transgenic mice, 4 and 8 weeks old, and age-matched CBA x C57B1/6 wild-type controls
-
-
brenda
hybrid B6/129
-
-
brenda
hybrid C57BL6J/129Sv
-
-
brenda
hydrophilic and hydrophobic isoform
-
-
brenda
hydrophobic form appears to be identical to steroid sulfatase, hydrophilic form: no steroid sulfatase activity
-
-
brenda
hypertensive mice with spontaneous intracranial hemorrhage
-
-
brenda
hyperuricemic mice induced by potassium oxonate
-
-
brenda
hypomorphic mouse model in which exons 2 and 3 of PARG gene have been deleted
-
-
brenda
hypoxia-inducible
-
-
brenda
hypoxic mice
-
-
brenda
i.e. glycine dehydrogenase component P-protein, cf. EC 1.4.4.2
UniProt
brenda
I/LnJ and KK/HlJ inbred strains and cross breeds between KK/HlJ and I/LnJ
UniProt
brenda
ICGN strain as a model for renal fibrosis
-
-
brenda
ICR mice
-
-
brenda
ICR, CD-1, mice
UniProt
brenda
identified as pre-B-cell colony-enhancing factor
-
-
brenda
IGnT A, 2 isoenzymes: IGnT A and B
UniProt
brenda
IGnT B, 2 isoenzymes: IGnT A and B
UniProt
brenda
IkappaBalpha and IkappaBbeta
-
-
brenda
IKK-alpha and IKK-beta
-
-
brenda
immature and adult Swiss CD1 mice
-
-
brenda
immature female mice, isoform Pin1
SwissProt
brenda
IMPA1
SwissProt
brenda
IMPA2
SwissProt
brenda
IMPDH type II
-
-
brenda
IMPDH2
UniProt
brenda
in addition to 17alphahydroxylase/17,20-lyase activity, enzyme can also act as squalene epoxidase
-
-
brenda
inactivation of the enzyme is done in knockout mice
-
-
brenda
inbred strain C3H/He
-
-
brenda
inbred strain C57BL/6J
-
-
brenda
inducible by cytokines IL-4, and IL-12/STAT4
-
-
brenda
inducible enzyme
UniProt
brenda
inducible HO-1 isozyme and constitutive HO-2 isozyme
-
-
brenda
inducible in erythroleukemia cells
-
-
brenda
inducible isozyme PFKFB3; genes PFKFB1-4, four isozymes
SwissProt
brenda
inducible oxygenase domain
UniProt
brenda
infected with Salmonella typhimurium and Pseudomonas aeruginosa
-
-
brenda
infected with Sendai virus
-
-
brenda
infected with Theiler's murine encephalomyelitis virus, gene Klk6
-
-
brenda
injection of glucagon elevates activity
-
-
brenda
InsP6 kinase 1
SwissProt
brenda
intact, athymic, female MF-1 nude mice (in vivo tumor growth model), ovariectomized, athymic, female MF-1 nude mice (hormone-dependent in vivo tumor growth model)
-
-
brenda
IRAP knockout mice
-
-
brenda
isoenzyme A2, B2 and C2
-
-
brenda
isoenzyme alpha
-
-
brenda
isoenzyme CTRA-1
-
-
brenda
isoenzyme mu
-
-
brenda
isoenzyme pi
-
-
brenda
isoenzymes AC2 and AC4
-
-
brenda
isoenzymes PAPS 1 and 2
-
-
brenda
isoenzymes ppGaNTase-T4 and -T1
-
-
brenda
isoenzymes T1, T2, T3 and T4
-
-
brenda
isoenzymes type 1 and type 2
-
-
brenda
isoform 1
UniProt
brenda
isoform 1, 17beta-HSD1
-
-
brenda
isoform 12/15 lipoxygenase, cf. EC 1.13.11.31
UniProt
brenda
isoform 12/15 lipoxygenase, cf. EC 1.13.11.33
UniProt
brenda
isoform 2
-
-
brenda
isoform 3OST1
SwissProt
brenda
isoform ACAT1
UniProt
brenda
isoform ACAT2
SwissProt
brenda
isoform Acot12
SwissProt
brenda
isoform Acot5
SwissProt
brenda
isoform Adcy1
UniProt
brenda
isoform Adcy2
UniProt
brenda
isoform Adcy3
UniProt
brenda
isoform Adcy4
UniProt
brenda
isoform Adcy5
UniProt
brenda
isoform Adcy6
UniProt
brenda
isoform Adcy7
UniProt
brenda
isoform Adcy8
UniProt
brenda
isoform Adcy9
Uniprot
brenda
isoform AK1
SwissProt
brenda
isoform AK2
SwissProt
brenda
isoform ALDH1B1
UniProt
brenda
isoform ALDH2
SwissProt
brenda
isoform ALDH3A1
UniProt
brenda
isoform ALDH7A1
UniProt
brenda
isoform AOX1
UniProt
brenda
isoform AOX2
UniProt
brenda
isoform Aox3
UniProt
brenda
isoform AOX4
UniProt
brenda
isoform arylsulfatase B, in liver of Schistosoma-infected mouse
-
-
brenda
isoform CD13
-
-
brenda
isoform CD38
-
-
brenda
isoform CerS2
SwissProt
brenda
isoform CerS5
SwissProt
brenda
isoform CerS6
SwissProt
brenda
isoform CFTR
-
-
brenda
isoform CHIP
Uniprot
brenda
isoform CPT1C
UniProt
brenda
isoform Ddah1
UniProt
brenda
isoform Ddah2
UniProt
brenda
isoform Decr1
UniProt
brenda
isoform deoxyribonuclease-2-alpha
SwissProt
brenda
isoform DGAT2
-
-
brenda
isoform DGAT2
SwissProt
brenda
isoform diacylglycerol lipase-alpha
UniProt
brenda
isoform diacylglycerol lipase-beta
UniProt
brenda
isoform DNase IIbeta
-
-
brenda
isoform DS-epi1 (Dse)
UniProt
brenda
isoform DS-epi2 (Dse-like)
UniProt
brenda
isoform dual oxidase 2
-
-
brenda
isoform ecto-5'-nucleotidase, control and dystrophic Lama2dy animals
-
-
brenda
isoform ENPP2
UniProt
brenda
isoform EphX2, cf. EC 3.1.3.76
SwissProt
brenda
isoform EphX2, cf. EC 3.3.2.10
SwissProt
brenda
isoform FMO5
UniProt
brenda
isoform GALNT1
Uniprot
brenda
isoform Galnt3
SwissProt
brenda
isoform GALNT4
UniProt
brenda
isoform GDE4
UniProt
brenda
isoform GLD-2
-
-
brenda
isoform glucose-6-phosphatase 2
UniProt
brenda
isoform Gpx1
UniProt
brenda
isoform HDAC2
-
-
brenda
isoform HDAC2
UniProt
brenda
isoform HDAC3
-
-
brenda
isoform HDAC3
UniProt
brenda
isoform HemK1
UniProt
brenda
isoform HemK2
Q6PRU9
UniProt
brenda
isoform IIalpha
-
-
brenda
isoform inositol 1,4,5-trisphosphate 3-kinase B
UniProt
brenda
isoform INPP5E
SwissProt
brenda
isoform INPP5f
UniProt
brenda
isoform iodotyrosine dehalogenase 1
UniProt
brenda
isoform IP6K1
SwissProt
brenda
isoform IRAP
-
-
brenda
isoform JMJD2d
UniProt
brenda
isoform Jmjd3
UniProt
brenda
isoform KDM3A
UniProt
brenda
isoform KDM4A
UniProt
brenda
isoform KDM4A, cf. EC 1.14.11.66
UniProt
brenda
isoform KDM4A, cf. EC 1.14.11.69
UniProt
brenda
isoform KDM4B, cf. EC 1.14.11.66
UniProt
brenda
isoform KDM4B, cf. EC 1.14.11.69
UniProt
brenda
isoform KDM4D
UniProt
brenda
isoform KDM5A
UniProt
brenda
isoform KIFC5A
-
-
brenda
isoform LARGE1
UniProt
brenda
isoform LARGE2
UniProt
brenda
isoform lipocalin-type prostaglandin-D synthase
-
-
brenda
isoform LPCAT1
SwissProt
brenda
isoform lunatic fringe
Uniprot
brenda
isoform lysyl hydroxylase 1
UniProt
brenda
isoform Man1a1
UniProt
brenda
isoform Man1a2
UniProt
brenda
isoform Mdr1a
-
-
brenda
isoform Mdr3
-
-
brenda
isoform Mdr3, i.e. ABCB1A
-
-
brenda
isoform MGAT2
-
-
brenda
isoform MICAL2
UniProt
brenda
isoform MMP13
SwissProt
brenda
isoform mPGES-1
-
-
brenda
isoform MTMR2
UniProt
brenda
isoform N-acyl phosphatidylethanolamine phospholipase D
-
-
brenda
isoform NAT1
-
-
brenda
isoform Neu1
UniProt
brenda
isoform Nit1
-
-
brenda
isoform Nit2
-
-
brenda
isoform NMNAT1
SwissProt
brenda
isoform NMNAT1, cf. EC 2.7.7.1
SwissProt
brenda
isoform NMNAT1, cf. EC 2.7.7.18
SwissProt
brenda
isoform NMNAT2
UniProt
brenda
isoform NMNAT3
SwissProt
brenda
isoform NMNAT3, cf. EC 2.7.7.1
SwissProt
brenda
isoform NMNAT3, cf. EC 2.7.7.18
SwissProt
brenda
isoform NMT-1
SwissProt
brenda
isoform NMT-2
SwissProt
brenda
isoform Nox1
-
-
brenda
isoform NoxII
-
-
brenda
isoform Nqo1
-
-
brenda
isoform PAD2
SwissProt
brenda
isoform PDE1
-
-
brenda
isoform PDE4
-
-
brenda
isoform PDE6
-
-
brenda
isoform PDE7A1
-
-
brenda
isoform phosphatidylinositol 4-phosphate 5-kinase alpha
-
-
brenda
isoform phosphatidylinositol 4-phosphate 5-kinase type Igamma
-
-
brenda
isoform PIP5Kalpha
UniProt
brenda
isoform PIP5Kbeta
UniProt
brenda
isoform PIP5Kgamma
UniProt
brenda
isoform PLD1
SwissProt
brenda
isoform PLD2
SwissProt
brenda
isoform PMCA2
UniProt
brenda
isoform ppGalNAcT-1
-
-
brenda
isoform Prdm16
UniProt
brenda
isoform Prdm3
UniProt
brenda
isoform PRMT7
SwissProt
brenda
isoform prostaglandin G/H synthase 1
UniProt
brenda
isoform prostaglandin G/H synthase 2
UniProt
brenda
isoform protein tyrosine phosphatase alpha, enzyme-deficinet animal
-
-
brenda
isoform Rdh10
-
-
brenda
isoform RDH12
-
-
brenda
isoform RNF180
UniProt
brenda
isoform SGMS1
SwissProt
brenda
isoform SGMS2
SwissProt
brenda
isoform SMS1
SwissProt
brenda
isoform SMS2
SwissProt
brenda
isoform SphK1a
-
-
brenda
isoform SPP2c
UniProt
brenda
isoform SPPL2a
UniProt
brenda
isoform SPPL2b
UniProt
brenda
isoform ST8SiaII
SwissProt
brenda
isoform ST8SiaIV
SwissProt
brenda
isoform Sulf1, cf. EC 3.1.6.1
SwissProt
brenda
isoform Sulf1, cf. EC 3.1.6.14
SwissProt
brenda
isoform SULT1A1
UniProt
brenda
isoform TAP2
UniProt
brenda
isoform TARS
UniProt
brenda
isoform TARSL2
UniProt
brenda
isoform topoisomerase IIbeta
-
-
brenda
isoform UbcH7
UniProt
brenda
isoform UbcM3
UniProt
brenda
isoform UBR5
UniProt
brenda
isoform UCHL1
SwissProt
brenda
isoform UFD2a
UniProt
brenda
isoform UFD2b
AI390103
Genbank
brenda
isoform Utx
UniProt
brenda
isoforms A and B
Uniprot
brenda
isoforms A and B, bifunctional enzymes, racemization of serine and elimination of L-serine and L-serine-O-sulfate to form pyruvate
-
-
brenda
isoforms alpha, beta
UniProt
brenda
isoforms alpha1, alpha2, beta
-
-
brenda
isoforms G1 and G4
-
-
brenda
isoforms mPanK1alpha, mPanK1beta
SwissProt
brenda
isoforms Rdh11, Rdh12
-
-
brenda
isoforms type 2, type 3 and type 5 adenylyl cyclase
-
-
brenda
isozyme 11beta-HSD1
-
-
brenda
isozyme 11beta-HSD1; isozyme 11beta-HSD1
SwissProt
brenda
isozyme 11beta-HSD2; isozyme 11beta-HSD2
SwissProt
brenda
isozyme AC5
-
-
brenda
isozyme ACC1; gene ACACA, encoding isozyme ACC1 or ACC-alpha
SwissProt
brenda
isozyme ACC2; gene ACACB, encoding isozyme ACC2 or ACC-beta
Q6JIZ0
SwissProt
brenda
isozyme ACVI
-
-
brenda
isozyme AKR1C21
-
-
brenda
isozyme alpha of p38 MAP kinase
-
-
brenda
isozyme alpha, exon 1
UniProt
brenda
isozyme alpha, exon 2
UniProt
brenda
isozyme alpha, exon 2'
Uniprot
brenda
isozyme alpha, exon 3
UniProt
brenda
isozyme alpha, exons 4-8
UniProt
brenda
isozyme alpha, exons 9-11
UniProt
brenda
isozyme ART2
-
-
brenda
isozyme AWAT1
UniProt
brenda
isozyme AWAT2
Swissprot
brenda
isozyme beta
SwissProt
brenda
isozyme CaMKIIalpha
-
-
brenda
isozyme CaMKIIdelta exists in two splicing variants deltaB and deltaC in the heart
-
-
brenda
isozyme Cyp4a12
-
-
brenda
isozyme EPXH2B
SwissProt
brenda
isozyme Fmo1, gene FMO1
UniProt
brenda
isozyme Fmo2, gene FMO2
UniProt
brenda
isozyme Fmo3, gene FMO3
UniProt
brenda
isozyme Fmo4, gene FMO4
UniProt
brenda
isozyme Fmo5, gene FMO5
UniProt
brenda
isozyme Gad65; gene gad65 encoding isozyme Gad65
UniProt
brenda
isozyme Gad67; gene gad67 encoding isozyme Gad67
UniProt
brenda
isozyme gamma
-
-
brenda
isozyme GST T1-1
-
-
brenda
isozyme HAS2
SwissProt
brenda
isozyme HAS2, gene has2
SwissProt
brenda
isozyme HDAC2
UniProt
brenda
isozyme HO-1, an inducible heat-shock protein
UniProt
brenda
isozyme IIbeta
-
-
brenda
isozyme iNOS
-
-
brenda
isozyme IP6K1
SwissProt
brenda
isozyme IP6K2
UniProt
brenda
isozyme IP6K3
UniProt
brenda
isozyme LPP-1
-
-
brenda
isozyme mGne1
Uniprot
brenda
isozyme mGne2
TrEMBL
brenda
isozyme MsrB3
SwissProt
brenda
isozyme NAT1; male mice, isozyme NAT1
SwissProt
brenda
isozyme NAT2; male mice, isozyme NAT2
SwissProt
brenda
isozyme NDST1
SwissProt
brenda
isozyme NDST2
SwissProt
brenda
isozyme NDST3
SwissProt
brenda
isozyme NDST4
SwissProt
brenda
isozyme NOS1
-
-
brenda
isozyme P3H1; isozyme P3H1
UniProt
brenda
isozyme P3H2; isozyme P3H2
UniProt
brenda
isozyme P3H3; isozyme P3H3
UniProt
brenda
isozyme PanK1alpha
-
-
brenda
isozyme PDK4
-
-
brenda
isozyme PI 3-kinase gamma
-
-
brenda
isozyme PI3K-C2alpha
SwissProt
brenda
isozyme PI3Kgamma
-
-
brenda
isozyme PKCdelta
-
-
brenda
isozyme PKCepsilon
-
-
brenda
isozyme PLD2
-
-
brenda
isozyme retGC
-
-
brenda
isozyme SK1 splicing variant a
SwissProt
brenda
isozyme SMS1
-
-
brenda
isozyme SMS2
-
-
brenda
isozyme SPHK1; 2 isozymes SPHK1 and SPHK2, several splicing variants
SwissProt
brenda
isozyme SPHK2; 2 isozymes SPHK1 and SPHK2, several splicing variants
SwissProt
brenda
isozyme TC45
-
-
brenda
isozyme TPST1
-
-
brenda
isozyme TPST2
-
-
brenda
isozyme Tssk4; isozyme Tssk4, is also named Tssk5
A3QQQ9
UniProt
brenda
isozyme type-1
-
-
brenda
isozyme type-2
-
-
brenda
isozyme type-3
-
-
brenda
isozymes 11beta-HSD1 and 11beta-HSD2
-
-
brenda
isozymes 11beta-HSD1 and 11beta-HSD2
SwissProt
brenda
isozymes AC-I-AC-IX
-
-
brenda
isozymes AC4 and AC9
-
-
brenda
isozymes ACI-ACIX
-
-
brenda
isozymes ADH1 and ADH4
-
-
brenda
isozymes AGPAT1,2,3, and 5
-
-
brenda
isozymes AK-L and AK-S; a long and a short isozyme, i.e. AK-L and AK-S
SwissProt
brenda
isozymes alpha, beta, gamma, and delta of p38
SwissProt
brenda
isozymes ART1, ART2.2, and ART5
-
-
brenda
isozymes ATXalpa-ATXdelta
-
-
brenda
isozymes CaMKII alpha, beta, gamma, and delta
-
-
brenda
isozymes colonic HKalpha2 and gastric HKalpha1
-
-
brenda
isozymes GC-A to GC-G
-
-
brenda
isozymes HAS2 and HAS3
-
-
brenda
isozymes IP6K1; Fluc+-eGFP+ transgenic mice, isozymes IP6K1
SwissProt
brenda
isozymes IP6K2; Fluc+-eGFP+ transgenic mice, isozymes IP6K2
UniProt
brenda
isozymes IP6K3; Fluc+-eGFP+ transgenic mice, isozymes IP6K3
UniProt
brenda
isozymes L1 and L3
-
-
brenda
isozymes LPP1, LPP-2, and LPP-3
-
-
brenda
isozymes LPP1-3, several splicing variants of LPP1
-
-
brenda
isozymes MAT I-MAT III
-
-
brenda
isozymes mPGES-2, mPGES-1, and cPGES
-
-
brenda
isozymes MsrB1, MsrB2, and MsrB3
-
-
brenda
isozymes MsrB1-3
-
-
brenda
isozymes NDST1-4
-
-
brenda
isozymes NMT1 and NMT2
-
-
brenda
isozymes NO-GC1 and NO-GC2
-
-
brenda
isozymes nSMase1 and nSMase2
-
-
brenda
isozymes of sPLA2 groups IIE, III, V, and X
Uniprot
brenda
isozymes PARP-1 and PARP-2
-
-
brenda
isozymes PDE1A, PDE1B, PDE1C
-
-
brenda
isozymes peroxisomal PTE-Ia and PTE-Ib
-
-
brenda
isozymes PIP5K1A, PIP5K1B, and PIP5K1C
-
-
brenda
isozymes PIP5Kalpha, PIP5Kbeta, and PIP5Kgamma
UniProt
brenda
isozymes PKCepsilon and PKCzeta
-
-
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 PON1 and PON2
-
-
brenda
isozymes SENP2, SENP2-M, and SENP2-S
-
-
brenda
isozymes SMS1 and SMS2
-
-
brenda
isozymes SRD5alpha1, SRD5alpha2, and SRD5alpha3
-
-
brenda
isozymes SULT2B1a and SULT2B1b
SwissProt
brenda
isozymes TPH1 and TPH2
-
-
brenda
isozymes TPST-1 and TPST-2
-
-
brenda
isozymes: cytosolic CTE-I, mitochondrial MTE-I
-
-
brenda
isozymne AC1
-
-
brenda
Jak2
SwissProt
brenda
JNK1
SwissProt
brenda
JNK1; male C3H/HeN mice
SwissProt
brenda
JNK2
SwissProt
brenda
JNK2; male C3H/HeN mice
SwissProt
brenda
JNK3; male C3H/HeN mice
SwissProt
brenda
K/BxN serum transfer model of arthritis, isoforms PI3Kdelta and PI3Kgamma
-
-
brenda
K5-IkBa mice
-
-
brenda
K6/ODC mice
-
-
brenda
Ker/Norm wild-type mice and K6/ODC transgenic mice
-
-
brenda
keratin 6 (K6)-spermidine/spermine N1-acetyltransferase (SSAT) transgenic mice, B6D2F2 background
SwissProt
brenda
knock-out mice, heterozygous, +/-choline kinase alpha deficient
-
-
brenda
knockout and heterozygous mice
-
-
brenda
Kunming mice
SwissProt
brenda
Kunming strain mice
-
-
brenda
Kunming White, outbred
-
-
brenda
L1210
-
-
brenda
L1210 cells
-
-
brenda
L1210 lymphoma cells
-
-
brenda
L1210 lymphoma cells, amethopterin-resistant
-
-
brenda
L5178 murine leukemia cell line
-
-
brenda
L929-cells
-
-
brenda
LCytb
UniProt
brenda
lean and obese animals
-
-
brenda
leukocyte-type isoform C2GnT-1, gene Gcnt1
UniProt
brenda
LH3 gene Plod3 with LH and GGT activity
SwissProt
brenda
light, regulatory subunit
UniProt
brenda
littermate embryo
-
-
brenda
littermate mice
-
-
brenda
liver enzyme
UniProt
brenda
LMTK-cells
-
-
brenda
Lon protease homolog 2, peroxisomal
UniProt
brenda
London APP mice and C57BL/6 mice
-
-
brenda
London APP transgenic mouse model of Alzheimer's disease that expresses human amyloid precursor protein containing the wild-type beta-secretase site
-
-
brenda
long and short isoform
-
-
brenda
long and short isoform
Uniprot
brenda
long splicing variant
SwissProt
brenda
low-activity isozyme ADH2
Uniprot
brenda
LSL-KrasG12D/+ and p48Cre/+ mice
SwissProt
brenda
lysophospholipase and subunit beta and subunit gamma
UniProt
brenda
lysophospholipase I and II
-
-
brenda
M2 subunit; BALB/3T3 cells, ATCC CCL 163
SwissProt
brenda
macrophage migration inhibitory factor MIF
-
-
brenda
male
-
-
brenda
male 129J mice
-
-
brenda
male adult C57/Bl6 mice
-
-
brenda
male adults
-
-
brenda
male albino
-
-
brenda
male albino Swiss-Webster mice
-
-
brenda
Male albino SwissWebster
-
-
brenda
male and female C57BL/6J mice
-
-
brenda
male and female mice
-
-
brenda
male animal
-
-
brenda
male apoE knockout mice
SwissProt
brenda
male apolipoprotein knockout (apoE KO) mice
UniProt
brenda
male ASKO mice, strain B6:129X1-Snca
-
-
brenda
male B57CL/6 mice
-
-
brenda
male B6/129 mice
-
-
brenda
male B6C3F1 mouse
-
-
brenda
male Balb-c mice
-
-
brenda
male BALB/c mice
-
-
brenda
male BALB/c mice
UniProt
brenda
male BALB/c mice, C57BL/6 mice with a7nAChR deficiency and wild-type littermates
-
-
brenda
male Balb/c or CD1 mice
-
-
brenda
male Balb/cA, 3-4 week old
-
-
brenda
male C3H/He, C57BL/6, and BALB/c mice
-
-
brenda
male C3H/HeN mice
-
-
brenda
male C57/B16 N mice
-
-
brenda
male C57/BL6 mice
-
-
brenda
male C57B/6 mice
-
-
brenda
male C57B1/129SV
-
-
brenda
male C57BI/6 mice, genes GAD65 and GAD67 encoding the 65-kDa and the 67-kDa isozymes of glutamic acid decarboxylase
-
-
brenda
male C57BJ/6J mice
-
-
brenda
male C57BL mice, 2 isozymes SPHK1 and SPHK2, isozyme SPHK1 exists in 2 splicing variants a and b
-
-
brenda
male C57BL/6
SwissProt
brenda
male C57BL/6 and BALB/c mice
-
-
brenda
male C57BL/6 mice
666130, 677984, 681270, 683316, 687789, 690388, 701629, 702079, 702962, 708289, 709098, 709779
-
-
brenda
male C57BL/6 mice
SwissProt
brenda
male C57BL/6 mice and type II diabetic mice
-
-
brenda
male C57BL/6J and BALB/cByJ mice, mice infected with influenza virus for experiments, enzyme mRNA levels in influenza infected mice are different from healthy mice
-
-
brenda
male C57BL/6J mice
-
-
brenda
male C57BL/6J mice
SwissProt
brenda
male C57BL/6J mice
UniProt
brenda
male C57BL/6J mice, tissue-specific isozymes L-CPT1 and M-CPT1
-
-
brenda
male C57BL/6N mice and STR/ort mice
-
-
brenda
male C57BL/6N x Sv/129 mice and peroxisome proliferator-activated receptor alpha (PPARalpha) null mice, mice fed ethyl-p-chlorophenoxyisobutyrate (clofibrate) for 14 days, activity is increased by 3-fold in normal mice fed clofibrate but not in PPARalpha null mice
-
-
brenda
male C57BL/6NCrj mice
-
-
brenda
male C57BL/6Njcl mice
-
-
brenda
male C57Bl6 mice
-
-
brenda
male C57BL6 mice, isozymes FMO1, FMO3, and FMO5
-
-
brenda
male C57BL6 mouse
-
-
brenda
male C57BL6/J mice
-
-
brenda
male C57BL6/J mice and C57BLKS/J db/db mice
SwissProt
brenda
male C57BL6/J mice, isozyme PanK3 and PanK1beta
-
-
brenda
male C57Bl6/J mice, isozymes ACC1 and ACC2
-
-
brenda
male C57BL6J mice
-
-
brenda
male C57BL7& mice, isozyme PFKFB3
-
-
brenda
male C75B1/6 mice
-
-
brenda
male C75Bl mice
-
-
brenda
male C75BL/6 mice
-
-
brenda
male C75BL/6 mice, 11beta-HSD1
-
-
brenda
male C75BL/6J mice
-
-
brenda
male C75BL/6J mice
Uniprot
brenda
male corticotropin-releasing hormone knockout mice (C57B1/129SV, 20-25 g, approximately 12 weeks old) and wild type mice
-
-
brenda
male DBA/1 mice, naive or with collagen-induced arthritis (CIA) after immunization with type II collagen, and male and female C57BL/6 mice
SwissProt
brenda
male DBA/1J mice
-
-
brenda
male ddY mice
-
-
brenda
male FVB-N
-
-
brenda
male FVB/N mice
SwissProt
brenda
male FVB/NJ mice
UniProt
brenda
male gracile axonal dystrophy, gad, mice lacking UCH-L1, and male uchl3 knockout mice, two isozymes UCH-L1 and UCH-L3 encoded by genes uchl1 and uchl3
-
-
brenda
male ICR
-
-
brenda
male ICR mice
-
-
brenda
male ICR mice and Swiss mice
-
-
brenda
male Kunming mice
-
-
brenda
male mice
-
-
brenda
male mice
SwissProt
brenda
male mice, isozymes TPST-1 and TPST-2
-
-
brenda
male mice, maintained on Teklad rodent diet no. 8604
-
-
brenda
male NMRI mice
-
-
brenda
male nude mice, BALB/c nu/nu 5-6 weeks old
-
-
brenda
male ob/ob, B6.V-Lepob/J mice and male ob/+ C57BL/6J mice
-
-
brenda
Male Slc:ddy mice
-
-
brenda
male specific-pathogen-free ICR mice
-
-
brenda
male strain C57-black6/SV mice, isozyme MLCK-210
-
-
brenda
male Sv/129 mice
-
-
brenda
male Swiss mice
-
-
brenda
male Swiss mice
SwissProt
brenda
male Swiss strain mice
-
-
brenda
male Swiss Webster mice
-
-
brenda
male Swiss Webster mice infected by malaria pathogen Plasmodium berghei ANKA
-
-
brenda
male Swiss-Webster
-
-
brenda
male withdrawal seizure-prone, WSP, and -resistant, WSR, mice
-
-
brenda
male, construction of GNMT knockout mice
-
-
brenda
male, homo- or heterozygously lacking transaldolase
-
-
brenda
MAO A and MAO B are encoded by separate genes
-
-
brenda
mast cell tumor, grown in LAF mice
-
-
brenda
mast cell-deficient WBB6F1/Kit-KitÂxa0W/KitÂxa0W-v mice
SwissProt
brenda
mastocytoma cell line P-815
-
-
brenda
Mdr2 (+/-), Mdr2 (+/+) and wild type FVB/NJ female mice, 8-10 weeks old
-
-
brenda
MEK mutant K14-MEK mice
-
-
brenda
MEK1
SwissProt
brenda
MEK2
SwissProt
brenda
melanocyte cell lines
-
-
brenda
membrane-associated precursor
SwissProt
brenda
membrane-bound dipeptidase-1, membrane-bound dipeptidase-2, membrane-bound dipeptidase-3
-
-
brenda
meprin A, from male BALB/c
-
-
brenda
methods of enzyme determination
-
-
brenda
MFUT-I
P97327
SwissProt
brenda
MFUT-II
SwissProt
brenda
Mgat2 enzymatic activity, but not mRNA transcript levels, differ significantly among the three strains (PL/J C57BL/6 129/Sv)
-
-
brenda
MGAT3 gene is a pseudogene in mice
-
-
brenda
mice deficient in apolipopotein E (apoE -/-) in a C57BL/6J background
-
-
brenda
mice deficient in methionine adenosyltransferase 1a have chronic hepatic deficiency of S-adenosylmethionine and increased oxidative stress, and develop hepatocellular carcinoma
-
-
brenda
mice heterozygous for a mutation in LCAD, strain B6.129S6-Acadltm1Uab Hsd
-
-
brenda
mice heterozygous for PTEN (+/-) on the C57BL6 genetic background
-
-
brenda
mice injected i.p. with 106 Plasmodium berghei ANKA infected red blood cells
UniProt
brenda
mice lacking peroxisome proliferator-activated receptor alpha and age-matched wild-type Sv/129 mice
-
-
brenda
mice model for kidney ischemia reperfusion injury and for acute kidney allograft rejection
-
-
brenda
mice with a gene-trap of prolyl endopeptidase
-
-
brenda
mice with mixed genetic backgrounds 129/SvJ/Sv and C57BL/6, genes NDST1 and NDST2
-
-
brenda
microsomal and cytosolic isoforms
UniProt
brenda
milk
Uniprot
brenda
mitochondrial deoxyguanosine kinase 1
SwissProt
brenda
mitochondrial p48 enzyme MT-ACT48-1, isozyme 1
SwissProt
brenda
mitochondrial p48 enzyme MT-ACT48-2, isozyme 2
SwissProt
brenda
mitochondrial UNG1 and nuclear UNG2 are both encoded by the UNG gene
-
-
brenda
mixed C57Bl/6 x SVJ/129 background mice
-
-
brenda
MKK4
SwissProt
brenda
MKK7
UniProt
brenda
MMP-7-/- mice and age-matched C57BL/6 mice
-
-
brenda
MNof, Tip60, Qkf, Moz, and Morf
-
-
brenda
moderate to intermediate murine model of hyperhomocysteinaemia. Using wild type and heterozygous cystathionine beta-synthase deficient mice fed a methionine enriched diet or a control diet
-
-
brenda
more than 20 inbred, recombinant and congenic strains
-
-
brenda
mouse
1413, 134056, 172057, 172058, 209001, 209287, 209492, 209588, 209590, 209593, 209596, 209598, 209602, 209639, 209641, 209644, 209648, 209649, 209651, 209653, 209656, 209659, 209661, 209662, 209668, 210501, 210512, 210547, 210549, 210601, 210604, 210647, 246982, 285272, 285329, 286172, 286175, 286177, 286181, 286182, 286196, 286669, 286672, 286827, 288890, 289225, 390107, 390108, 439023, 440005, 485515, 485519, 485520, 485557, 485561, 485715, 485717, 485718, 485719, 485721, 485724, 485725, 485731, 485737, 485739, 485972, 486290, 486295, 486296, 486298, 487413, 487420, 487421, 487422, 487423, 487424, 487428, 487433, 488109, 488112, 488115, 488122, 638979, 638980, 638981, 638983, 638984, 638987, 638988, 638991, 638992, 638994, 638995, 639003, 639010, 639012, 639013, 639915, 640058, 640059, 640067, 640136, 640203, 640834, 640835, 641701, 642684, 642710, 644210, 645295, 645321, 645385, 645735, 645785, 645899, 645900, 645901, 645906, 646858, 646859, 646881, 646882, 646885, 646887, 646889, 649082, 649264, 649273, 649460, 649536, 649753, 650078, 650131, 650203, 650461, 650764, 650972, 651181, 651411, 651486, 651536, 651862, 651892, 651902, 651913, 651914, 651921, 651976, 652026, 652031, 652060, 652132, 652135, 652145, 652159, 652193, 652245, 652469, 652500, 652608, 653125, 653220, 653300, 653715, 653856, 674881
-
-
brenda
mouse
SwissProt
brenda
mouse
Uniprot
brenda
mouse cell line
-
-
brenda
mouse embryo cell lines: 3T3, 3T6, B-3T3, 3T12
-
-
brenda
mouse model for spontaneous steatohepatitis in which the gene for the MAT1A isoenzyme encoding AdoMet synthetase has been disrupted
-
-
brenda
mouse model of globoid cell leukodystrophy or Krabbes disease, of Tay-Sachs disease, Sandhoff disease, GM1 gangliosidosis and Niemann-Pick type C1 disease
-
-
brenda
mouse model of infantile neuronal ceroid lipofuscinosis
-
-
brenda
mouse model of mild Mthfr deficiency
-
-
brenda
mouse models of Charcot-Marie-Tooth disease type 2D, CMT2D, are established
-
-
brenda
mouse monoclonal anti-GRK1 (G-proteinassociated rhodopsin kinase-1)
SwissProt
brenda
mouse neuroblastoma * rat glioma hybrid cell line
-
-
brenda
mouse pheochromocytoma cell lines 862L and 10/9CRC1 from tumors arising in separate mice with a heterozygous knockout of the neurofibromatosis gene Nf1
-
-
brenda
mouse skin carcinogenesis model, isoforms 2alpha, 2beta
-
-
brenda
mouse strain, ICR and C3H/He
-
-
brenda
mouse strains defective in specialized DNA polymerases are used for studying their function
-
-
brenda
mouse treated with clofibrate, a peroxisome proliferator
-
-
brenda
mouse, 2 isoenzymes: I and II
-
-
brenda
mouse, AtT-20 cells
-
-
brenda
mouse, bifunctional mitochondrial enzyme
-
-
brenda
mouse, brain TTK cDNA nucleotide sequence, same accession number in EMBL/DDBJ
SwissProt
brenda
mouse, C57B/6J
-
-
brenda
mouse, C57BL/6J
-
-
brenda
mouse, cDNA clone MMRNACAR, EMBL data bank accession number
UniProt
brenda
mouse, corticotrophic AtT-20 cell line
-
-
brenda
mouse, Ehrlich ascites tumor cells
-
-
brenda
mouse, H-2K cells
-
-
brenda
mouse, ICR strain
SwissProt
brenda
mouse, inbred strains C57BL, DBA, Peru, SM and SWR
-
-
brenda
mouse, inbred strains CBA/J, CBA/Ca, CBA/CaH, CBA/CaHN, C57B1/6
-
-
brenda
mouse, mitochondrial isoform
SwissProt
brenda
mouse, NCS strain
-
-
brenda
mouse, neuB gene product accession. no.
Q9JJH0
SwissProt
brenda
mouse, neuroblastoma
-
-
brenda
mouse, normal and Jimpy mutant, maximum enzyme activity at 17-19 days after birth
-
-
brenda
mouse, Omnibank B6.129
SwissProt
brenda
mouse, overview
-
-
brenda
mouse, Protein Data Bank accession number
UniProt
brenda
mouse, sarcoma 180
-
-
brenda
mouse, strain BAGG-Swiss
-
-
brenda
mouse, strain C57/BL6, GenBank accession number
Uniprot
brenda
mouse, strain C57BL/6
-
-
brenda
mouse, strain C57BL76J
-
-
brenda
mouse, strain CD-1
-
-
brenda
mouse, strain D57Bl/6J
-
-
brenda
mouse, strain ICR and C3H/He
-
-
brenda
mouse, strain J774
-
-
brenda
mouse, strain MRL/lpr
-
-
brenda
mouse, strain NMR1
-
-
brenda
mouse, Swiss mice
-
-
brenda
mouse, wild type and knockout mutants
Uniprot
brenda
mouse; female mice, 8 weeks old, induced with experimental allergic encephalomyelitis (EAE), induction phase, acute phase, and chronic phase, C57BL/6 genetic background
SwissProt
brenda
mPus1p, 3 isoforms generated by alternative splicing
SwissProt
brenda
mPus3p
SwissProt
brenda
mRNA capping enzyme
SwissProt
brenda
MsrB is a selenoprotein
-
-
brenda
multifunctional enzyme with activity of Ec 5.3.3.8, EC 4.2.1.17 and EC 1.1.1.35
-
-
brenda
multifunctional enzyme, cf. EC 4.3.1.17 and EC 4.3.1.18 and EC 5.1.1.18
Swissprot
brenda
multiple forms
-
-
brenda
multiple isozymes: classical isozymes alpha, betaI, betaII, and gamma, novel isozymes delta, epsilon, eta, and theta, and atypical isozymes zeta and lambda
-
-
brenda
murine cell lines NIH 3T3, Balb/C 3T3, Balb/C 3T3-SV-T2(SV40-transformed), C3H 10T1/2, YAC(Moloney virus transformed), PSI-2(a murine ecotropic packaging cell line)
-
-
brenda
murine model for cell therapy-induced type I diabetes
SwissProt
brenda
murine model of hyper-IgD syndrome
-
-
brenda
Mus musculus
-
-
brenda
Mus musculus
UniProt
brenda
muscle creatine kinase mice
SwissProt
brenda
mutant line of T-lymphoma S49 cells
-
-
brenda
mutant Lrat-/- and Rpe65-/- mice, models of human Leber congenital amaurosis
-
-
brenda
mutant mouse bearing amino acid differences in Naip5, one of the NOD-like receptors (NLRs), one of the adaptor proteins for caspase-1 activation
-
-
brenda
N(6)-adenosine-methyltransferase non-catalytic subunit (SwissProt)
SwissProt
brenda
native and mutant mice, mutant embryos are growth retarded and die in utero
-
-
brenda
ND4 Swiss Webster mice, suckling copper-deficient mice via copper-deficient diet
-
-
brenda
neonatal FVB/n cell line and alphaAE7 transgenic mice line 75a (as a source of apoptotic lens cells)
-
-
brenda
neuron-specific isozyme UCH-L1, mice with gracile axonal dystrophy
-
-
brenda
neuropsin precursor
SwissProt
brenda
newborn C57/Bl6J mice
-
-
brenda
newborn C57bl/6 mice
-
-
brenda
newborn congenic C57BL/6J non-agouti black mice
-
-
brenda
newborn mice
-
-
brenda
newborn Swiss mice
-
-
brenda
newborn, CF57 strain
-
-
brenda
NIH 3T3
-
-
brenda
NIH Swiss mice
-
-
brenda
NIH Swiss nude mice
-
-
brenda
NIH-3T3 cells
-
-
brenda
NIH3T3 (ATCC CRL-1658)
-
-
brenda
NIH3T3 fibroblasts
-
-
brenda
NMNAT1
SwissProt
brenda
NMNAT3
SwissProt
brenda
NMRI
Uniprot
brenda
NMRI, female, average weight 20 g
-
-
brenda
NMRI/Bom strain
-
-
brenda
NMRI/Kisslegg strain
-
-
brenda
NMT1; isozyme NMT1
SwissProt
brenda
NMT2; isozyme NMT2
SwissProt
brenda
no enzyme activity in TS-4 deficient mice
-
-
brenda
no enzyme activity in TS-5 deficient mice
SwissProt
brenda
NOD/Lt, NOD/lpr, NOD.TNFR-/- and C57BL/mice, or strain 129(H-2b) backcrossed onto BL/6 for a minimum of 10 generations
-
-
brenda
nondiabetic C57BL6 and CD-1 mice, and diabetic NOD mice and Pd-NOD mice, gene lipin1
-
-
brenda
nonobese diabetic female BALB/c mice
-
-
brenda
normal and alkaptonuric mice, which completely lack HTO
-
-
brenda
normal and ApoE-/- mice
-
-
brenda
normal and mutant cell line defective in arachidonate-CoA ligase
-
-
brenda
normal and mutant mice, mutant mice appear normal at birth but die 7-21 days postpartum due to neurological and intestinal problems
-
-
brenda
normal and mutant mice, mutant mice die in utero due to severe vascular abnormalities
-
-
brenda
normal and nitric oxide synthase 2-knockout mice
-
-
brenda
normal and transforming PCPH proteins: PCPH, PCPH proto-oncogene and mt-PCPH, PCPH oncogene having guanosine diphosphatase activity
-
-
brenda
normal and twitcher mice
-
-
brenda
normal mouse and NADPH-cytochrome P450 deletion mutant
-
-
brenda
normal or with genetically induced muscular dystrophy
-
-
brenda
novascularization is significantly impaired in cathepsin L-deficient mice
-
-
brenda
NPP6
Swissprot
brenda
nude mice
-
-
brenda
nude mice
UniProt
brenda
nude mice, 2 enzyme forms with one or five isoforms, respectively
-
-
brenda
NUDT7alpha
UniProt
brenda
NZB/W F1 mice
-
-
brenda
OAS1b is derived from feral mouse strain, MSM
UniProt
brenda
ob/ob mice
-
-
brenda
ob/ob mice and age-matched C57/BL littermates as non-obese controls, phenotype comparison, overview
SwissProt
brenda
ob/ob mice and age-matched C57/BL littermates as non-obese controls, phenotype comparison, overview
UniProt
brenda
ob/ob mice, isoform SCD4, tissue-specific regulation by leptin and dietary factors
SwissProt
brenda
ob/ob mouse, animal model for diabetes
-
-
brenda
ODC1; Swiss CD1 mice
SwissProt
brenda
OF-1 Swiss mouse
-
-
brenda
OT1 and OT2 mice
SwissProt
brenda
ovalbumin-sensitized Balb/c mice
-
-
brenda
overexpressed in Escherichia coli BL21
SwissProt
brenda
overview
-
-
brenda
P15920 i.e. Atp6v0a2, Q9Z1G4 i.e. Atp6v0a1
P15920, Q9Z1G4
UniProt
brenda
P288 leukemia cells
-
-
brenda
P29416 i.e. subunit alpha, P20060 i.e. subunit beta
SwissProt
brenda
P35486 i.e. E1 component subunit alpha, Q9D051 i.e. E1 component subunit beta
UniProt
brenda
p38 MAPK isozyme alpha
-
-
brenda
p70 ribosomal S6 kinase 1 S6K1 and its homologue ribosomal S6 kinase 2 S6K2
-
-
brenda
P9, BN/2, P8115, EL4,YAC, 3T3
-
-
brenda
PAD2; CD-1 mice
SwissProt
brenda
PAD4; CD-1 mice
UniProt
brenda
PAD6
UniProt
brenda
PAP activity is attributed to the protein GLD2
-
-
brenda
parental allele identity is inferred via a G3A single-nucleotide polymorphism between the Mus musculus C57BL6 (B6) and Mus musculus castaneus CAST/Ei (CAST) strains in exon 6 at nucleotide 645
UniProt
brenda
PC-1
-
-
brenda
PCAF and CBP
-
-
brenda
PDIA3; C57BL/6 mice
UniProt
brenda
peptidyl arginine deiminase I, II and III
-
-
brenda
peptidylarginine deiminase type II
-
-
brenda
PEX1
UniProt
brenda
PEX6
UniProt
brenda
phagocyte NADPH oxidase-deficient mice
-
-
brenda
PI3-C2gamma
SwissProt
brenda
PI3KC2alpha
-
-
brenda
pilocarpine-induced epileptic mouse model
UniProt
brenda
PKC isoforms can be split into three groups: conventional, novel and atypical, overview
-
-
brenda
PLC-beta
-
-
brenda
PLCbeta1
-
-
brenda
PLCbeta1a and PLCbeta1b
SwissProt
brenda
PLCdelta
-
-
brenda
PLCdelta1
SwissProt
brenda
PLCgamma2-deficient mice
UniProt
brenda
PLCzeta
SwissProt
brenda
PLD1 and PLD2
-
-
brenda
PLSCR1
UniProt
brenda
PLSCR4
UniProt
brenda
post-weaning mice
-
-
brenda
PP2Aflox/flox wild-type
-
-
brenda
ppGalNAc-T13, subsequently termed ppGalNAc-T8
-
-
brenda
PPT1
-
-
brenda
precursor
O35310, O54732, P11152, P33435, P57748, P97857, Q02853, Q04592, Q05915, Q60813, Q61586, Q8R534, Q9R001
SwissProt
brenda
precursor
UniProt
brenda
precursor; C3H/HeN and C3H/HeJ mice
SwissProt
brenda
precursor; comparative and phylogenetic analysis of alpha-L-fucosidase genes
SwissProt
brenda
pregnant
-
-
brenda
pregnant female and male NMRI mice
-
-
brenda
pregnant mice
-
-
brenda
pregnant mice, 3 isozymes HAS1, HAS2, and HAS3
-
-
brenda
prolyl 4-hydroxylase subunit alpha-1
UniProt
brenda
prolyl 4-hydroxylase subunit alpha-2
SwissProt
brenda
Protein data bank: 1NPM, for crystal structure
SwissProt
brenda
PTP36-D: Af170905, tissue-dependent expressions of isoforms
Uniprot
brenda
Q61239 i.e. subunit alpha, Q8K2I1 i.e. subunit beta
UniProt
brenda
Q6P6J0 i.e. subunit ADAT2, Q6PAT0 i.e. subunit ADAT3
SwissProt
brenda
Q8C3P7: METTL3, N6-adenosine-methyltransferase 70 kDa subunit. Q3UIK4: METTL14, N6-adenosine-methyltransferase non-catalytic subunit
SwissProt
brenda
Q91W43 i.e. glycine dehydrogenase component P-protein, cf. EC 1.4.4.2, O08749 i.e. dihydrolipoyl dehydrogenase component L-protein, cf. EC 1.8.1.4
UniProt
brenda
Q920A7 i.e. subunit Afg3l1, Q8JZQ2 i.e. subunit Afg3l2
UniProt
brenda
Q9EP82 i.e. noncatalytic subunit WDR4, Q9Z120 i.e. methyltransferase METTL1
SwissProt
brenda
Q9JMA2: catalytic subunit 1 (QTRT1), B8ZXI1: accessory subunit 2 (QTRT2)
SwissProt
brenda
Q9WV86: p60 ATPase-containing subunit, Q8BG40: p80 subunit
SwissProt
brenda
radiation-sensitive strain BALB/c and the radiation-resistant strain C57BL
-
-
brenda
random bred ICR and at least 35 inbred, recombinant and congenic strains
-
-
brenda
random-bred mice, infected with Schistosoma mansoni
UniProt
brenda
rat somatomammotroph cell line, GH4C1 infected with vaccinia virus recombinants of murine PC1
-
-
brenda
rd1, rd10, P23H/P23H mutant strains
UniProt
brenda
Rdh11
SwissProt
brenda
Rdh12
SwissProt
brenda
recombinant
-
-
brenda
recombinant
SwissProt
brenda
recombinant
UniProt
brenda
recombinant and native enzyme
-
-
brenda
recombinant bone morphogenetic protein-1 produced by a baculovirus system
-
-
brenda
recombinant cytoplasmic isoforms M, B and mitochondrial isoform
-
-
brenda
recombinant enzyme
-
-
brenda
recombinant enzyme
SwissProt
brenda
recombinant enzyme
UniProt
brenda
recombinant enzyme Dct-lacZ fusion protein
-
-
brenda
recombinant enzyme expressed in Escherichia coli
-
-
brenda
recombinant enzyme with N-terminal HA-tag
-
-
brenda
recombinant enzyme, expressed in MCF-7 human breast carcinoma cells
-
-
brenda
recombinant enzyme, expression in A-549 and EBC-1 cell. Enzyme overexpression results in increased invasive capacity in response to nerve growth factor, increased adhesion to brain tissue, and increased expression of integrin alpha3 and beta1 subunits. Administration of enzyme overexpressing A-549 cells to mice results in micrometastatic foci in brain and multiple metastatic colonies in the lungs
-
-
brenda
recombinant enzyme, expression in human colon cancer cell line HT29 cells. Overexpression of enzyme enhances growth factor-mediated induction of endocytosis and dynamic recycling of E-cadherin. Enzyme constitutively interacts with E-cadherin, the two proteins co-localize at the plasma membrane
-
-
brenda
recombinant enzyme, forms Ate1-3 and Ate1-4 of enzyme resulting from alternative splicing are specific for N-terminal Cys residues
-
-
brenda
recombinant protein
SwissProt
brenda
recombinant protein expressed in Escherichia coli
-
-
brenda
recombinant, enzyme Dnmt3A
SwissProt
brenda
recombinant, enzyme Dnmt3B
SwissProt
brenda
recombinantly expressed in Hela cells
-
-
brenda
recombinantly expressed in yeast
-
-
brenda
renal cell carcinoma tumor-bearing mice
-
-
brenda
retinoid X receptor gamma-deficient mice, increase in activity of skeletal enzyme isoform
-
-
brenda
retinol dehydrogenase isoform RDH12
-
-
brenda
retired Swiss-Webster breeder mice
UniProt
brenda
Rj:NMRI mice
SwissProt
brenda
Rj:NMRI mice
TrEMBL
brenda
Rpt1 or 26S protease regulatory subunit 7
UniProt
brenda
Rpt2 or 26S protease regulatory subunit 4
UniProt
brenda
Rpt3 or 26S protease regulatory subunit 6B
UniProt
brenda
Rpt4 or 26S protease regulatory subunit 10B
UniProt
brenda
Rpt5 or 26S protease regulatory subunit 6A
UniProt
brenda
Rpt6 or 26S protease regulatory subunit 8
UniProt
brenda
S3T3(ATCC CCL-92)
-
-
brenda
Sc5d deletion leads to intrauterine growth tardation, craniofacial abnormalities, including cleft palate and micrognathia, and limb patterning defects
-
-
brenda
selenomethionine-containing enzyme MsrB
-
-
brenda
senescence-accelerated prone 8 mouse model of age-related dementia
-
-
brenda
senescence-accelerated prone mouse 6, i.e. SAMP6
-
-
brenda
sepiapterin reductase-null mice
-
-
brenda
sequence with additional 92 bp sequence found in lung, EMBL: AF242911
SwissProt
brenda
several different isozymes
-
-
brenda
several isoenzymes
-
-
brenda
several isozymes
-
-
brenda
several isozymes, classification, overview
-
-
brenda
several isozymes, e.g. isozyme PAP2A, i.e. LPP-1
-
-
brenda
several strains, overview, genes fmo1, fmo2, fmo3, and fmo5
-
-
brenda
short, inactive splicing variant
SwissProt
brenda
single gene
-
-
brenda
single gene
SwissProt
brenda
single gene and alternative splicing resulting in several variants
UniProt
brenda
six week old, male, LDL receptor-deficient
Uniprot
brenda
SMS2
SwissProt
brenda
SOAT1 or ACAT1
UniProt
brenda
SOAT2 or ACAT2
SwissProt
brenda
species differences regarding rodent and human ACE2 in terms of substrate specificity and inhibitors
-
-
brenda
sphingosine kinase isoform 1
SwissProt
brenda
sphingosine kinase isoform 2
SwissProt
brenda
SPHK2
SwissProt
brenda
splice variant 1
SwissProt
brenda
splice variant 2
SwissProt
brenda
splice variant 3
A7UAK6
SwissProt
brenda
splice variant isozymes SMOalpha and SMOmu
-
-
brenda
ST1a4
-
-
brenda
ST1c4
SwissProt
brenda
ST6Gal I
-
-
brenda
ST6Gal II
-
-
brenda
ST6GAL1
SwissProt
brenda
strain 129, strain C57Bl/6 chimaera/ly9.l-
-
-
brenda
strain C57BL/6 resistant to infection by Leishmania major, and strain BALB/c susceptible to infection with Leishmania major
-
-
brenda
strain C57BL/6J and DBA/2J
-
-
brenda
strain C57BL/6J, strain BALB/c, strain Black Swiss
-
-
brenda
strain C57BL10.RIIIH2r-Mmp3tm1Mol/Ztm is abbreviated as BL10
UniProt
brenda
strain Col2CreERT
-
-
brenda
strain lacking methionine sulfoxide reductase MsrA
-
-
brenda
strain senescence-accelerated mouse prone/8
SwissProt
brenda
strains C3H/HeJ and C57BL/6
-
-
brenda
strains C57BL and 129S2
SwissProt
brenda
strains R6/2, C57BL/6J, and B6/CBA
UniProt
brenda
strains SM/J and LG/J
-
-
brenda
streptozotocin-induced diabetic apoE-deficient mouse
-
-
brenda
streptozotocin-induced diabetic mice
SwissProt
brenda
studies on BLMH knockout mice, B6.129Blmhtm1Geh/J null animals
SwissProt
brenda
subtype alpha
SwissProt
brenda
subtype beta
SwissProt
brenda
subunit A
UniProt
brenda
subunit alpha
UniProt
brenda
subunit alpha-1 and subunit alpha-2
UniProt
brenda
subunit beta
UniProt
brenda
subunit gamma
SwissProt
brenda
subunit IV isoform 2; subunit IV isoform 2
SwissProt
brenda
subunit UQCRC1
UniProt
brenda
subunits A, B1 (brain isoform), C1, D1, E1, G1, and S1
P50516, P62814, Q9Z1G3, P51863, P50518, Q9CR51, Q9R1Q9
SwissProt
brenda
subunits A, B1 (kidney isoform), C1, D1, E1, G1, and S1; C57BL/6J, BALB/c, and nude mice
P50516, Q91YH6, Q9Z1G3, P51863, P50518, Q9CR51, Q9R1Q9
SwissProt
brenda
subunits alpha1 and beta1
UniProt
brenda
subunits CCT1, CCT2, CCT3, CCT4, CCT5, CCT6, CCT7, and CCT8
P11983, P80314, P80318, P80315, P80316, P80317, P80313, P42932
UniProt
brenda
subunits METTL14 and METTL3
SwissProt
brenda
subunits Naa20 and Naa25 of enzyme complex NatB
UniProt
brenda
subunits paraplegin and Afg3L2
-
-
brenda
subunits Pmpca and Pmpcb
SwissProt
brenda
subunits SRalpha and SRbeta
Q9DBG7, P47758
UniProt
brenda
subunits TAP1 and TAP2
UniProt
brenda
SULT-N or St1d1
SwissProt
brenda
SULT1B1
SwissProt
brenda
super-ovulating C57BL6/SJL hybrid mice, gene GlUD1
UniProt
brenda
SV/129 male and female mice
-
-
brenda
Sv/129 mice
-
-
brenda
Sv129 mice
-
-
brenda
SV129/C57BL/6J mouse line, female mice
UniProt
brenda
SW strain and C57B1/6J strain
-
-
brenda
Swiss adult male mice
-
-
brenda
Swiss albino
-
-
brenda
Swiss albino and RIII strain, both infected with mammary tumour virus, uninfected: C57BL strain
-
-
brenda
Swiss albino male mice
-
-
brenda
Swiss albino mice
-
-
brenda
Swiss albino mice, 2 months old
-
-
brenda
swiss mice
-
-
brenda
Swiss mice and FVB/N mice
-
-
brenda
Swiss mouse
-
-
brenda
Swiss strain
-
-
brenda
Swiss strain, male
SwissProt
brenda
Swiss Webster mice
-
-
brenda
Swiss-Webster
-
-
brenda
Swiss-Webster albino
-
-
brenda
Swiss-Webster strain DBA/2
-
-
brenda
Swiss/129 mice, isozymes soluble guanylate cyclase alpha1beta and alpha2beta1
-
-
brenda
Swiss/Webster mice
-
-
brenda
TAP1 and TAP2 subunits
UniProt
brenda
testis-specific isoform KIF17b
-
-
brenda
testis-specific serine/threonine protein kinase 5 variant alpha; alternatively spliced variant alpha of the testis-specific isozyme
A3QQQ9
UniProt
brenda
testis-specific serine/threonine protein kinase 5 variant beta; alternatively spliced variant beta of the testis-specific isozyme
A9P6P7
SwissProt
brenda
testis-specific serine/threonine protein kinase 5 variant delta; alternatively spliced variant delta of the testis-specific isozyme
A9P6P9
SwissProt
brenda
testis-specific serine/threonine protein kinase 5 variant gamma; alternatively spliced variant gamma of the testis-specific isozyme
A3QQR1
SwissProt
brenda
Tg8 is a transgenic mouse strain lacking a functional MAO A gene
SwissProt
brenda
the mouse SMS1 gene is subject to alternative splicing and gives rise to full-length SMS1 as well as two truncated proteins that contain the N-terminal SAM domain and the first two of the six transmembrane domains
-
-
brenda
three deiodinase isozymes Dio1, Dio2, and Dio3
-
-
brenda
three different size transcripts 2.8, 4.5 and 6.6 kb, the bigger ones lead to active proteins after expression
-
-
brenda
three dynamin isoforms, dynamin1-dynamin3, and multiple splice variants for each of the three dynamins
-
-
brenda
three lipins, C57BL/6J and BALB/cByJ-Lpin1+/fld mice
-
-
brenda
three-week-old virgin female mice
-
-
brenda
tight-skin 1 mouse strain
UniProt
brenda
tissue-nonspecific isozyme
Uniprot
brenda
TLR4-/- mice
SwissProt
brenda
TPH1; isozyme TPH1
UniProt
brenda
TPH2; isozyme TPH2
SwissProt
brenda
transgenes PPL-1 and PPL-2
-
-
brenda
transgenic
-
-
brenda
transgenic animals with beta-cell-specific overexpression or inactivation of enzyme
-
-
brenda
transgenic APP TG2576 mice
-
-
brenda
transgenic expression in rat
-
-
brenda
transgenic expression in Ren2 rat
-
-
brenda
transgenic male CD2F1 mice overexpressing SSAT
-
-
brenda
transgenic mice are developed using a construct consisting of the human SP-C promotor and full-length rat prostacyclin synthase cDNA
-
-
brenda
transgenic mice containing exon 1 of the human huntigton gene
-
-
brenda
transgenic mice in which PHGPx is overexpressed solely in the mitochondrion
SwissProt
brenda
transgenic mice strain Tg2576
SwissProt
brenda
transgenic mice with Alzheimer's disease-like neuropathology
-
-
brenda
transgenic mice with cardiac-specific expression of a dominant-negative 14-3-3h protein mutant (DN 14-3-3h) after induction of experimental diabetes. Marked downregulation of thioredoxin reductase in DN 14-3-3h mice compared to wild-type mice after induction of diabetes
-
-
brenda
transgenic mouse
-
-
brenda
transgenic mouse line overexpressing SSAT
-
-
brenda
transgenic mouse lines SVT125, 127 and 248, expressing the SV40 large T-antigen gene
-
-
brenda
transgenic mouse model of Menkes disease
SwissProt
brenda
transgenic mouse with a replacement of the Pts allele, encoding the 6-pyruvoyl-tetrahydropterin synthase, by an in-frame insertion in exon 2 with the beta-galactosidase gene generating a fusion protein containing the N-terminal 35 amino acids for 6-pyruvoyl-tetrahydropterin synthase followed by the beta-galactosidase
-
-
brenda
transgenic, kinase-active liver PKF-2, FVB background
SwissProt
brenda
treated with scopolamine
-
-
brenda
trifunctional enzyme with phosphoribosylamine-glycine ligase activity, glycinamide ribonucleotide transformylase activity, and aminoimidazole ribonucleotide synthetase activity
-
-
brenda
trifunctional enzyme, cf. EC 4.3.1.17 and EC 4.3.1.18
Swissprot
brenda
trifunctional enzyme, cf. EC 4.3.1.17 and EC 5.1.1.18
Swissprot
brenda
trifunctional enzyme, cf. EC 4.3.1.18 and EC 5.1.1.18
Swissprot
brenda
trifunctional enzyme, cf. EC 5.1.1.18 and EC 4.3.1.17
Swissprot
brenda
trifunctional enzyme, cf. EC 5.1.1.18 and EC 4.3.1.18
Swissprot
brenda
truncated form
-
-
brenda
tumor cells implanted on the dorsal skin flap over the calvaria of female mice
-
-
brenda
tumor cells were implanted onto the calvaria of female mice
-
-
brenda
twi +/i C57BL6 mice
-
-
brenda
twi +/i C57BL6 mice and wild-type mice
-
-
brenda
twitcher mouse
-
-
brenda
two closely related isoforms, Rap1A and Rap1B
-
-
brenda
two CSS2 splice variants, CSS2A and CSS2B
-
-
brenda
two enzyme forms with different acid sensitivity and tissue location
-
-
brenda
two evolutionary conserved splicing isoforms of Pcyt2, Pcyt2alpha and Pcyt2beta, and a third splicing isozyme Pcyt2gamma are encoded by a single Pcyt2 gene
-
-
brenda
two isoforms derived by alternative spicing, isofoms 2 contains a 22 amino acid insert
-
-
brenda
two isoforms of topoisomerase II, termed alpha and beta
-
-
brenda
two isoforms X1 and isoform X2
UniProt
brenda
two isozymes Acc1 and Acc2
-
-
brenda
two isozymes CTalpha and CTbeta2
-
-
brenda
two isozymes of the catalytic subunit, p110alpha and p110beta
-
-
brenda
two isozymes, mitochondrial GABA-T and synaptosomal GABA-T
-
-
brenda
two LMW-PTP isozymes
-
-
brenda
two mouse Gne mRNA transcripts, encoding mGne1 and mGne2, gene Gne
Uniprot
brenda
type 2 diabetic Agouti-K mice
-
-
brenda
type 2 diabetic C57BL/6J mice
-
-
brenda
type 2 diabetic KK/Ta mouse
-
-
brenda
type I and type II enzyme isoforms
-
-
brenda
type I enzymes, isozyme gamma
-
-
brenda
type I isoform
-
-
brenda
type II membrane-bound zinc metalloprotease
-
-
brenda
type-2 isozyme
-
-
brenda
U-type creatine kinase; gene Ckmt1
UniProt
brenda
UGT1A6; C57BL/6 crossed with DBA/2, gene UGT1A6
UniProt
brenda
untreated and clofibrate-treated animals
-
-
brenda
untreated and clofibrate-treated male C57B1/6 animals
-
-
brenda
untreated, fasted or Wy-14643-treated wild type and peroxisome proliferator activated receptor alpha-/- mice
-
-
brenda
V-type proton ATPase 16 kDa proteolipid subunit c
UniProt
brenda
vanin-1
-
-
brenda
vanin-3
-
-
brenda
VavP-Bcl2 model mice
SwissProt
brenda
viral FLIP transgenic mice
SwissProt
brenda
virgin female
UniProt
brenda
W10 mice, mouse model for prostate carcinoma
-
-
brenda
warfarin-susceptible strain
-
-
brenda
white, mongrel, 3-months-old, female mice
-
-
brenda
wild type and and isoform Pin1-/- mice
-
-
brenda
wild type and Aqp7 knock out mice (Aqp7-/-), 14- to 18-week-old animals
-
-
brenda
wild type and Aqp7 knockout male mice and mouse 3T3-L1 cell line
-
-
brenda
wild type and mutant enzymes C360A, K69A and C70S
-
-
brenda
wild type embryonic fibroblast and cells with a MAP3K deletion used for experiments
-
-
brenda
wild type mouse fibroblasts and deficiency mutant cell line gro2C
-
-
brenda
wild type mouse fibroblasts and deficiency mutant cell line Sog9, EXT1 protein
-
-
brenda
wild type, lethally irradiated acute intermittent porphyria mice, porphyria mice injected with bone marrow cells from wild type C57BL/6-CD45.1 mice or from acute intermittent porphyria mice
UniProt
brenda
wild-type
-
-
brenda
wild-type 129/P3J mice and 129/SvJ SR-A-/- mice
SwissProt
brenda
wild-type 129SvEv mice and mutant mice
-
-
brenda
wild-type and artherosclerotic mice
-
-
brenda
wild-type and ceruloplasmin knockout mice
Uniprot
brenda
wild-type and ceruloplasmin knockout mice based on strain C57BL/6 J
-
-
brenda
wild-type and CTSB-deficient female and male mice
-
-
brenda
wild-type and deoxycorticosterone acetate plus high salt, i.e. DOCA-salt, hypertensive mice, gene EPHX2
SwissProt
brenda
wild-type and endoglin +/- mice
-
-
brenda
wild-type and enzyme component C3 deletion mutant
-
-
brenda
wild-type and enzyme deficient mice (DLS+/-, C57BL/6, and 129SV/EV hybrid)
-
-
brenda
wild-type and enzyme-null mutant animal
-
-
brenda
wild-type and farnesoid X receptor-null mice
-
-
brenda
wild-type and gad, i.e. gracile axonal dystrophy, mice, isozymes UCH-L1, UCH-L3, UCH-L4, and UCH-L5
-
-
brenda
wild-type and HDAC4-deficient mice
-
-
brenda
wild-type and homozygous Clock mutant mice
SwissProt
brenda
wild-type and IKKalpha- mice
-
-
brenda
wild-type and knock-out mutant
-
-
brenda
wild-type and mutant lacking arachidonate-specific acyl-CoA synthetase
-
-
brenda
wild-type and neurological er mouse mutant
-
-
brenda
wild-type and pi null mutant
-
-
brenda
wild-type and PIMT knock-out mice
SwissProt
brenda
wild-type and reductase inhibitor resistant L1210 cell line
-
-
brenda
wild-type and transgenic mice, C57BL/6J strain, EpoR-HM mice
SwissProt
brenda
wild-type and transgenic mice, mice heterozygous for a Dyrk1A targeted mutation (Dyrk1A+/2), maintained in a C57BL/6J-129Ola (C57-129) mixed genetic background
SwissProt
brenda
wild-type and type 3 deiodinase knockdown mice
SwissProt
brenda
wild-type and type 3 deiodinase knockdown mice
UniProt
brenda
wild-type and type 3 deiodinase knockout mice, infected with Streptococcus pneumoniae
-
-
brenda
wild-type and type 3 deiodinase knockout mice, infected with Streptococcus pneumoniae
UniProt
brenda
wild-type BALB/c mice, mast cell-deficient W/W v mice, and IL-1-KO BALB/c mice, deficient in both Iinterleukin-1alpha and interleukin-1beta
-
-
brenda
wild-type BPN and hypertensive BPH mice
-
-
brenda
wild-type C57Bl/6 and male Cyp8b1 knockout mice on a mixed 129Sv/Ev-C57Bl/6 background
-
-
brenda
wild-type C57BL/6 and mutant Cola1(I)r/r mice
-
-
brenda
wild-type C57BL/6 and mutant gad, i.e. gracile axonal dystrophy, mice
-
-
brenda
wild-type C57BL/6 mice
-
-
brenda
wild-type C57BL/6 mice and B6 RAG12/2 gene-targeted mice
-
-
brenda
wild-type C57BL/6 mice, Alzheimer's double disease mice, and amyotrophic lateral sclerosis SOD1-G93A mice
-
-
brenda
wild-type C57BL/6 mice, and mutant B6 Rag2-/- and SP6 Rag2-/- Tg mice
-
-
brenda
wild-type C57BL/6J mice
-
-
brenda
wild-type C57BL/6N mice and farnesoid X receptor FXR-null mice
-
-
brenda
wild-type DW/J mice and mutant grt mice
-
-
brenda
wild-type EC-4
-
-
brenda
wild-type FVB/N and Tg-CYP2D6 mice
-
-
brenda
wild-type male C57BL/6J mice and leptin receptor-deficient obese Leprdb/db (db/db) male mice
UniProt
brenda
wild-type mice and enzyme-deficient mutant strain C57BI/6 mice
-
-
brenda
wild-type mice and mdx-mice with adult mdx-muscles malformed with distorted neuromuscular junctions and impaired regulation of acetylcholine receptors
-
-
brenda
wild-type mice, and knock-out mice deficient in dihydrolipoyl dehydrogenase
-
-
brenda
wild-type mice, Cftr-null mice, homozygous F508del mice, and Cftr-/- littermates
-
-
brenda
wild-type or homozygous knockout mice
-
-
brenda
wild-type strain 129/SvJ
-
-
brenda
wild-type strain C57BL/6 and enzyme-deficient strain, 3 isozymes IP3-3KA, IP3-3KB, and IP3-3KC
-
-
brenda
wild-type strain C57BL/6J mice, the isogenic von Willebrand factor-deficient strain 129x1/SvJ, and the ADAMTS13-deficient gene knock-out strain CAST/EiJ
-
-
brenda
wild-type Wistar and LBK1-KO mice
-
-
brenda
wild-type, CFTR-DELTAF508 mutant, and CFTR-KO mice
-
-
brenda
wild-type, Cu,Zn-superoxide dismutase transgenic, and NAD(P)H oxidase-knockout mice placed on a normal or high cholesterol diet
-
-
brenda
wild-type, NO synthase-deficient C57BL/6 mice, and cGKI-deficient 129/Sv mice
-
-
brenda
with acute pneumococcal otitis media
-
-
brenda
with factor D deficiency
-
-
brenda
with selective genetic inactivation of the dicarboxypeptidase activity of testis angiotensin-converting enzyme
-
-
brenda
with ventilator-induced lung injury
-
-
brenda
wobbler mouse
-
-
brenda
YAC128 mice
-
-
brenda
young and old mice with and without caloric restriction
-
-
brenda
young male and female BALB/c mice
-
-
brenda
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
-
pheochromocytoma cell line
brenda
-
brenda
-
lymphoma cell, expression of enzyme is induced upon contact of cell with endothelial cells
brenda
-
lymphoma cell, expression of enzyme is induced upon contact of cell with endothelial cells. Enzyme expression is also induced following exposure to interleukins IL-4, IL-6, and IL-13, but not IL-1
brenda
-
-
brenda
-
tumor-induced dysregulation of endocytic activity of dendritic cells is mediated by reduced activity of several members of the small Rho GTPase family
brenda
-
fibroblast cell line
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
a4 is the dominant subunit a isoform expressed in these cells
brenda
-
mouse mammary tumor cell line
brenda
-
brenda
-
-
brenda
-
brenda
-
pheochromocytoma cell line
brenda
-
melanotic hybrid cell
brenda
-
melanotic hybrid cell
brenda
-
brenda
-
brenda
-
brenda
-
-
brenda
abdominal aortic aneurysm, PDE1C is not expressed in normal aorta
brenda
-
-
brenda
-
-
brenda
-
stellate cells
brenda
-
-
brenda
pre-adipocytes, predominantly
brenda
-
Y-1 cell, increased activity of catalase in tumor cells recombinantly overexpressing IGFBP-2 probably mediated through IGF-independent mechanisms
brenda
-
brenda
-
cell line R 1.1: wild-type, Sahn 12: mutant clone
brenda
-
NTPDase1 and NTPDase2
brenda
-
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
Tmprss2 and Tmprss4 are coexpressed in alveolar and bronchial regions
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
specialized cell that deposits tooth enamel
brenda
-
brenda
-
LOX is highly expressed in early gestational amnion tissue (12-14 weeks)
brenda
-
-
brenda
-
-
brenda
-
GRK2, no expression of GRK3
brenda
-
-
brenda
-
ovary
brenda
-
-
brenda
-
-
brenda
-
embryonic
brenda
-
-
brenda
-
high expression rate
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
low-grade astrocytoma
brenda
-
-
brenda
KIF5B is concentrated in the central spindle during cytokinesis in both primary chondrocytes and chondrogenic ATDC5 cells
brenda
-
-
brenda
-
brenda
-
brenda
-
primary cell line, murine B-cells are isolated from spleen by a negative depletion
brenda
-
-
brenda
-
tumor-induced dysregulation of endocytic activity of dendritic cells is mediated by reduced activity of several members of the small Rho GTPase family
brenda
-
brenda
-
-
brenda
-
wild type, G2N2C and Tb3A transgenic BCC cell lines expressing Gli2 under the control of the keratin 5 promoter
brenda
-
-
brenda
receptor activator of nuclear factor kappa B ligand-differentiated, expression of CaMKI and CaMKIIgamma
brenda
-
brenda
-
brenda
-
-
brenda
Q920A7 and Q8JZQ2
radial astrocytes of the cerebellum
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
isoform CaMKII-beta is abundant in OFF bipolar cells, which form electrical synapses in the outer and the inner retina
brenda
-
Burkitt's lymphoma cell line
brenda
-
-
brenda
-
-
brenda
-
12, 16 and 20 weeks after initiation of BBN treatment: higher PyNpase level in invasive carcinoma and hyperplasia compared to controls
brenda
-
-
brenda
-
-
brenda
-
skeletal and nonskeletal tumor cell
brenda
-
brenda
-
brenda
-
brenda
-
-
brenda
ENPP2 is strongly down-regulated with age in stromal stem cells that produce osteoblasts and make bone. ENPP2 plays an important role in early osteoblast differentiation
brenda
-
-
brenda
-
-
brenda
-
mineral-associated fraction
brenda
-
-
brenda
-
-
brenda
-
brenda
first mandibular arch
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
epithelial cells of the bronchiole, PON1
brenda
-
-
brenda
-
brenda
-
CSD is expressed in the glandular epithelium of the bulbourethral gland
brenda
-
CD45-negative variant of BW5147
brenda
-
-
brenda
-
thymoma cell line served as host for vesicular stomatitis virus
brenda
-
-
brenda
-
brenda
-
C1300 neuroblastoma M1 clonal cell line
brenda
-
colon cancer cell
brenda
mammary gland epithelial cell line
brenda
-
-
brenda
-
mouse embryonic fibroblast cell oncogenically transformed with both E1A and ras, and containing wild-type p53
brenda
-
mouse embryonic fibroblast cell oncogenically transformed with both E1A and ras, and containing p53-/-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
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-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
specific expression of SULT1E1
brenda
-
-
brenda
-
-
brenda
lysophosphatidylcholine acyltransferase 4 (LPCAT4) mRNA expression and LPCAT enzymatic activity towards oleoyl-, linoleoyl-, (5Z,8Z,11Z,14Z)-eicosatetraenoyl-, and docosahexaenoyl-CoA increases in the late stage of chondrogenic differentiation, when mineralization occurs
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
gamma-carboxylase gene targeting
brenda
-
brenda
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
-
brenda
-
brenda
-
brenda
-
colon 26 tumor cells transplanted in BALB/c mice
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
the enzyme is secreted into the apical medium of polarized cultures of rabbit connecting tubule and cortical collecting duct cells
brenda
-
-
brenda
-
brenda
-
area 1
brenda
-
-
brenda
-
GRK2
brenda
-
brenda
-
brenda
-
brenda
-
brenda
-
714671, 736266, 736275, 736914, 737293, 754951, 759354, 759782, 770038, 777140, 778418
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
from days 6 to 8 of pregnancy, the signals for Lox mRNA and protein are strongly detected in the decidual cells
brenda
-
the GD3 synthase gene may be involved in early tooth development, particularly in the proliferation of dental epithelium
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
thrombin induces a phosphoinositide 3-kinase-Akt pathway-dependent acquisition of dermal-sheath-like properties by dermal papilla cells in vitro, involving increased proliferation rate, acquisition of myofibroblastic contractile properties and a decreased capacity to sustain growth and survival of keratinocytes. The thrombin inhibitor protease nexin 1 regulates all those effects in vitro. Control of thrombin signaling interferes with hair follicle dermal cells plasticity to regulate their function
brenda
-
brenda
-
brenda
-
-
brenda
-
renal distal tubular epithelial cell line. CYP27B1 gene expression is unchanged after treatement with parathyroid hormone or after high Ca2+ exposure
brenda
-
brenda
-
-
brenda
-
level of enzyme mRNA and protein increases from testis to epididymis to ductus deferens, main cell types containing enzyme are Leydig cells of testis, epithelial cells and some stromal cells
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
fibre tracts of the encephalon, PON1
brenda
-
-
brenda
-
isozyme GC-B
brenda
-
-
brenda
-
-
brenda
-
brenda
moderate expression
brenda
-
-
brenda
-
-
brenda
-
specifically expressed in enteroendocrine cell of the murine colon and ileum
brenda
microglial cell
brenda
-
mouse endothelial cell line EOMA
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
eWAT
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
high expression
brenda
-
-
brenda
-
brenda
-
cell line derived from FM3A
brenda
an asynchronously proliferating population of carcinoma cells
brenda
-
-
brenda
-
embryonal carcinoma cell
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
keratinized surface epithelium
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
of the stomach, mainly LOXL, mucous-secreting cells
brenda
-
-
brenda
-
-
brenda
-
-
brenda
a spermatocyte cell line
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
in the embryonic cortex, nestin-positive precursors and betaII-tubulin positive neurons from E12-E13 primary cortical precursor cell culture
brenda
-
-
brenda
-
U-1242 MG, N-Cadherin cleavage occurs at a higher level in glioblastoma cells than in non-neoplastic astrocytes
brenda
-
-
brenda
-
brenda
predominantly expressed on glomerular endothelial cells
brenda
-
-
brenda
-
-
brenda
in the kidney, constitutive Adamts5 expression in adult tissue
brenda
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
lowering cyclic adenosine-3',5'-monophosphate levels by expression of a cAMP-specific phosphodiesterase decreases intrinsic pulsatile gonadotropin-releasing hormone secretion from GT1 cells
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
COMT2 is highly expressed in sensory hair cells of the inner ear
brenda
-
brenda
-
skin
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
brenda
-
brenda
-
brenda
-
brenda
-
brenda
-
CD4+
brenda
-
-
brenda
activity is restricted to progenitor and precursor B cells. Enhanced BP-1 expression on virus-transformed pre-B cells and on normal pro-B cells stimulated by the interleukin 7 growth factor
brenda
-
brenda
-
-
brenda
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
Hepa-1
brenda
-
-
brenda
-
brenda
from neonatal mice
brenda
-
brenda
-
PI4KIIalpha is strongly reduced in the nerve terminals of mocha hippocampal mossy fibers
brenda
-
brenda
-
-
brenda
-
immortalized hippocampal neuron
brenda
-
-
brenda
-
brenda
-
the mRNA expression of EXT2, one of the crucial enzymes for heparan sulfate-glycosaminoglycan synthesis, is markedly up-regulated in injured hypoglossal motor neurons after axotomy
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
isoform COMT2
brenda
-
-
brenda
-
-
brenda
diffuse labelling of
brenda
-
brenda
-
brenda
-
brenda
-
novel taste learning elicited biphasic (acute and long-tasting) activation of two distinct lysine acetyltransferase activities along with the EPK/MAPK cascade in insular cortex
brenda
-
brenda
-
simple, stratified, and pseudo-stratified epithelium of the integumentary system
brenda
-
isoform AC5
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
isoform Sulf1 level in the nucleus pulposus is higher compared with Sulf2 at the age of 1 and 6 months and significantly declines with aging
brenda
-
high relative expression of catE in adenomas and carcinomas relative to normal epithelium
brenda
-
brenda
-
brenda
-
proximal
brenda
-
brenda
-
-
brenda
-
P-LAP is located in the periphery in early gestation, located in both the periphery and inner cells during mid-gestation, located only in inner cells in late gestation
brenda
-
-
brenda
-
-
brenda
-
macrophage cell, infection with Mycobacterium bovis strain AS-1 lacking an arginine permease. AS-1 infection enhances enzyme activity in resting J774.1 cells. Intracellular growth of AS-1 is enhanced by inhibition of enzyme and of ornithine decarboxylase using L-norvaline and difluoromethylornithine treatment
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
STI571-resistant cells
brenda
-
brenda
MCA3D (non-tumorigenic keratinocytes) highest IKK alpha expression, PDVC57 (moderately carcinogenic keratinocytes) show an important reduction in IKK alpha expression, HACa4 cells (highly tumorigenic) expression of IKK alpha is almost absent
brenda
-
brenda
-
-
brenda
represents as much as 1% of total cytosolic protein in the kidney
brenda
-
-
brenda
KLN205-MUC1, lung cancer cell line, higher expression of beta3GnT7 in cancer cell lines with low degrees of invasiveness
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
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brenda
-
-
brenda
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brenda
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brenda
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-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
oral cavity
brenda
-
brenda
-
cells express higher levels of cytosolic acetyl-CoA synthetase ACSS2 under hypoxia than normoxia. Knockdown of ACSS2 by RNA interference in tumor cells enhances tumor cell death under long-term hypoxia in vitro. The ACSS2 suppression slows tumor growth in vivo. Tumor cells excrete acetate and the quantity increases under hypoxia, the pattern of acetate excretion follows the expression pattern of ACSS2. The ACSS2 knockdown leads to a corresponding reduction in the acetate excretion in tumor cells
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
4 lung adenocarcinoma cell lines (KC1KC4) from lung tumors in KC mice and 2 lung adenocarcinoma cell lines (K1 and K2) from Cdkn1aWT K-rasLA1 mice. Expression levels of the third gene of interest, LH2, are 10-30 times higher in the highly metastatic KC cells and include both LH2 isoforms, full-length (LH2b) and spliced at exon 13 (LH2a)
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
FUT7 mRNA remarkably highly expressed in mouse lymphoid tumor cell line TIB-63
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
intense immunofluorescent staining for 15-hydroxyprostaglandin dehydrogenase in macula densa and glomerulus of cyclooxygenase-2 knock-out mice
brenda
-
-
brenda
-
brenda
-
diploid FSK3 mouse mammary epithelial cells
brenda
Q9JIS2
-
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
brenda
-
a C57BL/6-derived methylcholantrene-induced fibrosarcoma cell line
brenda
-
brenda
-
brenda
-
isozymes SMS1 and SMS2
brenda
-
brenda
-
brenda
brain, low expression level
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
mRNA level of isoform Rdh10 declines during development, with strong and lasting expression in the meninges and choroid plexuses. Expression is also present in the striatum
brenda
-
-
brenda
-
brenda
-
brenda
monoamine oxidase A promoter is regulated by the circadian-clock components BMAL1, NPAS2, and PER2. A mutation in the clock gene Per2 in mice leads to reduced expression and activity of MAOA in the mesolimbic dopaminergic system
brenda
-
-
brenda
-
embryoid bodies made of MG1.19 cells. PILSAP is highly expressed at the beginning of the observed period (day 3), decreased thereafter, and increases again through day 10
brenda
-
-
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
inner medullary collecting duct 3 cell
brenda
-
-
brenda
-
type II lung epithelial cell
brenda
-
-
brenda
-
a mammary adenocarcinoma cell line
brenda
-
mouse mammary tumour cell
brenda
-
brenda
-
brenda
-
-
brenda
-
MOPC 315
brenda
-
-
brenda
-
brenda
-
renal proximal tubular epithelial cell line. CYP27B1 gene expression is elevated in response to parathyroid hormone. High Ca2+ exposure represses CYP27B1 gene expression in both dose and time-dependent fashion
brenda
-
a vasopressin-responsive cell culture model of cortical collecting duct, proteomic analysis of cytoplasmic fractions from mpkCCD cells, overview
brenda
-
immortal mpkCCDc14 cell line, derived from transgenic mice
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
wild-type mouse embryonic fibroblasts
brenda
-
immortalized mouse fibroblasts lacking topoisomerase IIbeta
brenda
-
primary
brenda
-
-
brenda
-
-
brenda
-
high expression
brenda
skeletal muscle stem cell
brenda
-
-
brenda
-
-
brenda
-
brenda
-
prostate tumor cell line
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
isozymes SMS1 and SMS2
brenda
-
high level of expression
brenda
-
of somites
brenda
-
glial cell line
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
N2a cells stably expressing the vector pEGFP
brenda
-
N2a cells stably expressing human amyloid prepcursor protein Swedish mutation
brenda
-
TCAP-1-responsive hypothalamic cell line
brenda
-
microglial cell
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
NAA10 expression decreases with the induction of differentiation in NB4 cells, but the level of NAA11 remains unchanged
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
brenda
AOH2 and AOH3
brenda
-
-
brenda
-
brenda
-
all 9 membrane-associated adenylate cyclases
brenda
-
-
brenda
-
under resting conditions, Neu 7 astrocytes exhibit a high basal level of stellation, protease activated receptors PAR1 and PAR2 cause a significant reversal of astrocyte stellation
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
from A/J mice
brenda
-
-
brenda
N1E-115
brenda
-
-
brenda
of the neural tube of 10-day-old embryos
brenda
-
-
brenda
-
-
brenda
-
brenda
-
pituicytes
brenda
-
-
brenda
-
-
brenda
-
non-neuronal cholinergic cell
brenda
-
-
brenda
-
brenda
-
-
brenda
-
no significant differences of ChAT activity are measured at both 19 and 24 months of age between Ts65Dn mice and normogenic animals
brenda
-
selectively expressed in Bowman's glands
brenda
-
-
brenda
-
brenda
-
-
brenda
-
isozyme GC-D is exclusively expressed in the olfactory neuroepithelium in rodents
brenda
-
-
brenda
-
and vibrissae follicles, expression of isoform Rdh10 from early stages in regions where sensory receptors appear and mesenchymal/epithelial interactions take place
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
keratinocytes in tongue, hard palate, bucca, gingiva, and lip
brenda
-
-
brenda
-
in the oral cavity, strong reactivity for KLK7 in orthotopic murine tumors, immunohistochemical analysis, overview
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
light-dependent localizations of the transducin-alpha subunit Gtalpha
brenda
-
brenda
-
NTPDase1
brenda
-
-
brenda
-
brenda
PON1
brenda
-
-
brenda
-
glandular stomach
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
a pancreatic cancer cell line
brenda
-
brenda
-
brenda
-
-
brenda
-
brenda
-
acinar cell during embryogenesis, endocrinic cell and exocrinic cell in adult
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
highest expression
brenda
-
-
brenda
-
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
brenda
-
brenda
-
-
brenda
-
pepsin-secreting, in the basal part of the stomach, only LOX, no LOXL
brenda
-
-
brenda
-
-
brenda
Q3UIK4 AND Q8C3P7
-
brenda
enzyme expression during bone development
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
(PEC) isolated from naive C57BL/6 mice of from lipopolysaccharide-treated mice
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
pheochromocytomas are tumors of adrenal chromaffin cells. Phenylethanolamine N-methyltransferase mRNA levels are markedly increased by glucocorticoid administration. Dexamethasone elicites approximately 800fold increases in phenylethanolamine N-methyltransferase mRNA levels in mouse pheochromocytoma 862L cells and approximately 75fold increases for mouse pheochromocytoma 10/9CR1 cells. Glial cell line-derived neurotrophic factor and cpt-cAMP alone each produce little or no change in baseline phenylethanolamine N-methyltransferase mRNA levels. In both cell lines, dexamethasone-stimulated increases in phenylethanolamine N-methyltranferase mRNA levels are reduced approximately 90% by prior tratment with cAMP. Glial cell line-derived neurotrophic factor reduces dexamethasone effects on phenylethanolamine N-methyltransferase mRNA levels by 40% in mouse pheochromocytoma 862L cells, while not supressing the dexamethasone response in mouse pheochromocytoma 10/9CRC1 cells. Pretreatment with cAMP and afterwards treatment with glial cell line-derived neurotrophic factor before additon of dexamethasone reduced phenylethanolamine N-methyltransferase expression in mouse pheochromocytoma 862L and 10/9CRC1 cells to 0.1% and 5.5% of their corresponding DEX induced maxima.
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
brenda
-
AC9
brenda
-
-
brenda
-
brenda
an immortalized epididymal cell line, quantitative enzyme expression analysis, overview
brenda
-
-
brenda
MICAL2 expression increases during myogenic differentiation of adult and pluripotent stem cells
brenda
-
cathepsin H is highly expressed in the secretory organelles of alveolar type II pneumocytes
brenda
-
-
brenda
-
-
brenda
-
brenda
high expression
brenda
-
FL5.12
brenda
-
brenda
-
lipin-2
brenda
-
-
brenda
Q0E9Q7
-
brenda
-
-
brenda
-
brenda
CYLD is drastically upregulated during RANKL-induced differentiation of preosteoclasts
brenda
-
-
brenda
-
ESR-586, grown subcutaneously
brenda
-
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
higher enzyme activity than in F9 EC cells
brenda
-
-
brenda
-
FL5.12
brenda
-
brenda
-
brenda
-
-
brenda
-
transgenic animals
brenda
-
-
brenda
TMPRSS2 protease is highly expressed in metastatic prostate cancers
brenda
-
brenda
-
brenda
-
-
brenda
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brenda
-
-
brenda
-
-
brenda
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brenda
-
-
brenda
-
brenda
-
-
brenda
-
brenda
-
endothelial cell line
brenda
-
brenda
-
-
brenda
-
-
brenda
-
microglial cell line
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
derived from monocyte/macrophage cell line RAW 264.7
brenda
P21958 AND P36371
-
brenda
-
-
brenda
-
brenda
-
of human and rat but not in guinea pig, cattle, goat or pig
brenda
-
brenda
-
-
brenda
-
RAG
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
the enzyme is mainly found in proximal tubules, localized inside the tubular epithelial cells
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
tumor-induced dysregulation of endocytic activity of dendritic cells is mediated by reduced activity of several members of the small Rho GTPase family
brenda
P21958 AND P36371
-
brenda
-
-
brenda
-
strong expression in adult
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
cultured T-lymphoma cells
brenda
-
-
brenda
-
expression in in both the epithelial and stromal elements, low enzyme activity
brenda
3LL carcinoma and T10 sarcoma, overexpression of PDGF-alpha receptor in high-metastatic clones
brenda
-
isolated from skeletal muscle
brenda
-
a hypothalamic neuronal cell line
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
of embryo
brenda
-
strong expression in adult
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
METTL21C is exclusively expressed in slow MYH7-positive skeletal muscle fibers
brenda
-
-
brenda
-
brenda
PON1
brenda
low amounts of NOX3
brenda
-
adenylosuccinate synthetase expression is downregulated in SM-5 cells
brenda
-
adenylosuccinate synthetase expression is downregulated in SM-7 cells
brenda
-
-
brenda
-
brenda
dopaminergic cells
brenda
-
-
brenda
-
-
brenda
-
-
brenda
spermatogonial, somatic ACE (sACE), but not testicular ACE (tACE), is expressed in mouse cultured spermatogonial stem cells (SSCs)
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
skin
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
consistent with having a role in the growth of MAP2-positive neurites, TTLL7 accumulates within a MAP2-enriched somatodendritic portion of superior cervical ganglion, as does polyglutamylated beta-tubulin
brenda
-
-
brenda
-
expressed in sustentacular cells of the olfactory epithelium but not, or much less, in most olfactory receptor neurons
brenda
-
brenda
-
colon, uterus
brenda
-
-
brenda
-
endothelial cell line
brenda
-
-
brenda
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
T-ALL cell
brenda
-
Beko cell, spontaneous T-cell lymphoma cell line derived from T-cell receptor beta knockout mice, only KDM5A and KDM5C are expressed
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
TGFalpha-transfected mouse hepatocyte cell line
brenda
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
submedial thalamic nucleus
brenda
-
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
-
adenylosuccinate synthetase expression is downregulated in thymic lymphoma cells
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
-
brenda
only in jaw containing the developing tooth buds appreciable levels of the enzyme
brenda
-
localized predominantly to the extracellulat matrix of chondrocytes and to primary trabeculae of the skeleton
brenda
-
-
brenda
-
prostate tumor cell line
brenda
motor trigeminal nucleus
brenda
-
-
brenda
-
brenda
paravertebral trunk of the sympathetic nervous system
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
brenda
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
uterus
brenda
low mRNA expression
brenda
-
-
brenda
-
proliferating cell, LOXL expression, adult tissues
brenda
-
induced thrombus
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
ventral palladium, approximately 60% of cannabinoid-1 receptor-labeled axonal profiles oppose or converge with axon terminals containing N-acylphosphatidylethanolamine-hydrolyzing phospholipase D immunoreactivity
brenda
-
brenda
-
-
brenda
high expression level
brenda
-
-
brenda
-
restricted mesenchymal and epithelial regions. Its localization and strength changes during the hair cycle. Activity in the dermal papilla is moderate in very early anagen, reaches a maximal level in early anagen, decreases at the proximal region of dermal papilla after mid anagen, and is kept at a low level during catagen. The bulbar dermal sheath shows intense alkaline phosphatase activity only in early anagen. Most bulbar epithelium does not show alkaline phosphatase activity, germinative epidermal cells that are adjacent to the alkaline phosphatase-negative dermal papilla cells become alkaline phosphatase-positive in mid anagen and rearrange in a single layer so as to encapsulate the dermal papilla in mid catagen. During catagen, the outermost layer of bulbar epithelium becomes alkaline phosphatase-positive, which could be follicular epithelial precursors migrating from the bulge. Before the initiation of hair formation, alkaline phosphatase activity in the bulbar epithelium rapidly decreases and that in dermal papilla increases. These dynamic changes of alkaline phosphatase expression might be related to functions of the dermal papilla in hair induction and also to reconstruction of the bulbar structure during the hair cycle
brenda
-
brenda
-
-
brenda
-
high activity
brenda
-
brenda
-
-
brenda
-
intense immunoreactivity
brenda
-
-
brenda
-
-
brenda
-
-
brenda
-
murine thymic lymphoma cells
brenda
-
brenda
sEH is highly expressed throughout the body
brenda
wild-type bone-marrow-derived macrophage cells
brenda
-
mouse lymphoma cell
brenda
-
the level of the enzyme in theses cells decreases as the cells differentiate
brenda
-
YT 5 cell
brenda
-
brenda
-
brenda
-
brenda
O55239, P06801, P11983 AND P80314 AND P80318 AND P80315 AND P80316 AND P80317 AND P80313 AND P42932, P13516, P13707, P49891, P54310, P98191, Q01320, Q14DK4, Q3UP47, Q5MPP0, Q60823, Q61586, Q61907, Q64685, Q64FW2, Q6PD10, Q8BZA9, Q8C0N2, Q8C129, Q8C3P7 and Q3UIK4, Q8K2C8, Q8K341, Q8VDQ1, Q91ZP3, Q99KQ4, Q99L43, Q9D1P2, Q9D4M9, Q9DAK9, Q9DCV3, Q9R0B9, Q9R0E1, Q9R0E2, Q9Z1B3
-
660895, 662593, 665636, 669191, 671758, 675967, 676001, 679436, 679509, 680814, 681269, 683133, 685345, 685541, 686411, 687562, 687766, 688978, 690828, 691065, 693100, 693213, 693792, 694155, 694496, 695943, 697625, 699948, 699992, 700121, 700180, 700994, 701352, 702061, 702510, 703277, 705517, 707547, 708289, 708998, 709417, 709666, 709772, 709945, 712594, 714316, 714794, 715603, 715609, 716113, 719858, 721490, 722732, 723139, 725979, 727116, 727427, 729290, 734433, 735631, 736797, 738392, 738826, 739138, 740424, 740711, 745769, 746212, 747492, 751121, 754109, 755129, 755404, 756106, 757661, 757868, 758179, 759485, 759503, 760740, 760988, 761503, 763507, 766262, 766965, 773571, 775940, 776664, 776666, 776707, 777384, 778279, 778388, 779345
brenda
3T3-L1 adipocyte
brenda
3T3-L1 adipocytes express Acod1 and have attenuated inflammatory signaling with itaconate treatment
brenda
-
3T3-L1 fibroblasts differentiated into adipocytes
brenda
-
activity increases during adipogenesis
brenda
-
adipocyte
brenda
adipocyte cell line
brenda
adipocytes, enzyme expression during differentiation of adipocytes, maximal at day 8, overview
brenda
-
AKR1B3 mRNA 9 is expressed in preadipocytes, and its level increases about 4fold at day 1 after initiation of adipocyte differentiation, and then quickly decreases the following day to a level lower than that in the preadipocytes
brenda
-
ATCC CL-173
brenda
-
CL 173 (ATCC)
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-
conjugated linoleic acid decreases SCD1 gene expression
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-
CPT I and CPT II
brenda
-
differentiation of cells causes a strong increase in 11beta-hydroxysteroid dehydrogenase protein levels, occuring late in the differentiation protocol. Reduction of 11beta-hydroxysteroid dehydrogenase activity in 3T3-L1 fibroblasts, achieved by pharmacological inhibition or adenovirally mediated delivery of short hairpin RNA constructs, specifically blocks the ability of inactive glucocorticoids to drive 3T3-L1 differentiation. Even modest increases in exogenous 11beta-hydroxysteroid dehydrogenase expression in 3T3-L1 fibroblasts, to levels comparable with endogenous 1 11beta-hydroxysteroid dehydrogenase in differentiated 3T3-L1 adipocytes, are sufficient to block adipogenesis
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-
elevated enzyme activity during cell differentiation in adipose tissue
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Gpat3 mRNA increases 60fold during differentiation of 3T3-L1 preadipocytes to mature adipocytes, suggesting a critical role in adipocytes
brenda
HER2 is absent in undifferentiated cultures of adipocytes, not subjected to hormonal treatment but processed at the same time as the differentiating cultures from day 0 to day 14. Expression of HER2 significantly augments during the differentiation of preadipocytes. HER2 acculmulation reaches a maximum at day 9
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-
isozyme PKNalpha
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isozyme SCD1 is dramatically induced during 3T3L1 differentiation
brenda
-
lipin-1 and lipin-2
brenda
marked induction of AceCS1 mRNA and protein during differentiation of 3T3-L1 cells, neither AceCS2 mRNA nor protein is detected in undifferentiated or differentiated 3T3-L1 cells
brenda
-
mRNA expression increases 8-fold during the first 12 hr postinduction and subsequently declines to preinduction levels by day 3. Xanthine dehydrogenase activity is maximally induced at 24 hr postinduction, while xanthine oxidase activity remains relatively unchanged
brenda
pre- and post-adipocytes
brenda
-
preadipocyte cell line
brenda
-
preadipocytes have a very low expression of AOX1, in 2 days differentiated cells AOX1 is induced and is not further upregulated in 3, 7 and 9 days differentiated cells. AOX1 mRNA is nearly four-fold higher in 2 days differentiated cells when compared to preadipocytes and doubles from days 2 to 6
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scopoletin significantly increases lipoprotein lipase activity in 3T3-L1 adipocytes
brenda
-
synthetic peroxisome proliferator-activated receptor beta/delta, and gamma agonists markedly up-regulate Gys-2 mRNA and protein expression in mouse 3T3-L1 adipocytes
brenda
O08529, O08643, O70475, P50516 AND Q91YH6 AND Q9Z1G3 AND P51863 AND P50518 AND Q9CR51 AND Q9R1Q9, Q61239 and Q8K2I1
-
brenda
enzyme activity is highly increased in the cancer cell line
brenda
-
expression of GM3S mRNA is greater in the highly metastatic 4T1 tumor cells than in the nonmetastatic 67NR cells
brenda
-
murine breast adenocarcinoma cell line
brenda
-
-
brenda
-
B cell line
brenda
-
B-cell line
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a Balb/c mice-derived mouse cell line
brenda
-
mouse embryo fibroblast cell, thermosensitive for ubiquitin-activating enzyme E1
brenda
-
abdominal skin
brenda
-
fat pad, detection of enzyme protein despite of absence of the mRNA sinal after reverse transcription-polymerase chain reaction
brenda
-
brenda
highest expression
brenda
-
-
brenda
-
alveolar
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p21-deficient (KC) and -replete (K) murine lung adenocarcinoma cells, increased LH2 enzyme activity
brenda
O35083, O35490, O54732, O55055, O55239, P13516, P39654, P48026, P53690, P54071, Q14DK4, Q3UP47, Q5NCY0, Q60823, Q61586, Q61907, Q64685, Q64FW2, Q6PD10, Q6ZQ88, Q8BHG1, Q8C0N2, Q8C129, Q8C3P7 and Q3UIK4, Q8CHP8, Q8K2C8, Q8K3K7, Q8R2H9, Q8VDQ1, Q91ZP3, Q91ZV4, Q91ZX6, Q922E4, Q9D1P2, Q9D2R0, Q9DCV3, Q9JJS6, Q9QZT4, Q9R0B9, Q9R0E1, Q9R0E2, Q9R1E6
-
94261, 486505, 486513, 486577, 638598, 640924, 656247, 656794, 660790, 662593, 666733, 667411, 671758, 671816, 676001, 676029, 677869, 680191, 680814, 683048, 685541, 687562, 687766, 690827, 691065, 692365, 693792, 694155, 694494, 694939, 697625, 699948, 699992, 700121, 700180, 700994, 701352, 701612, 702061, 707547, 708339, 708593, 709009, 709226, 709417, 709666, 709772, 709945, 710639, 714316, 714678, 714794, 724817, 725979, 728342, 728552, 729291, 729337, 729338, 736018, 736797, 737600, 738392, 739155, 742239, 744226, 745769, 746212, 751474, 753372, 753384, 754109, 754442, 754828, 755129, 755404, 756106, 756599, 757377, 757571, 757661, 759485, 760172, 760351, 761047, 761503, 761916, 763507, 766262, 766965, 771400, 771625, 773437, 773571, 775882, 776664, 776666, 776707, 777158, 778388, 778820
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-
3T3-L1
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72-5ptase is expressed in differentiated 3T3-L1 adipocytes
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acetylation of alpha-tubulin is up-regulated during adipogenesis, and adipocyte development is dependent on alpha-tubulin acetylation
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-
adipocytes retrovirally engineered from murine embryonic fibroblasts
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brown adipocyte
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-
CTSK is active mainly in the early stages of adipogenesis
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EST is predominantly expressed in stromal vascular cells (pre-adipocytes). Consistent with the pre-adipocyte pattern of expression, the expression of EST is dramatically reduced in differentiated 3T3-L1 cells or mature primary adipocytes
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-
GPAT3 mRNA is dramatically upregulated during adipocyte differentiation
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high expression
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high Pcyt2 mRNA content. Negligible amount of Pcyt2beta mRNA, high amount of Pcyt2alpha mRNA
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highly expressed in differentiating adipocytes. When adipocyte differentiation is complete there is two fold increase in nocturnin protein compared to undifferentiated controls
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-
hormone-sensitive lipase is negatively regulated by perilipin, lipolysis of storage triacylglycerides
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-
Immunocyto-fluorescence microscopy reveals that ATX is detected in 3T3F442A adipocytes and is almost undetectable in 3T3F442A preadipocytes. 3T3F442A mouse preadipose cell line
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-
inducible expression of isozyme PFKFB3
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-
insulin-sensitive mouse 3T3-L1 adipocytes
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-
isoform Nox4 is expressed at high levels in white and brown preadipocytes. Differentiation into adipocytes results in a decrease in their NOX4 mRNA content. In intact adipose tissue, the majority of NOX4 expressing cells are localized within the preadipocyte containing stromal/vascular fracftion. Alterations in NOX4 expression reflects changes in the ratio of adipocyte/interstitial fractions
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-
isozyme type II
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-
major SSAO form expressed in mouse adipocytes is encoded by the AOC3 gene
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-
mitochondrial acyltransferase
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-
NNMT expression profile, overview
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of mammary gland
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PON1
brenda
-
primary
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Prmt1 is highly expressed in major metabolic organs and cell types, including thermogenic fat tissue and adipocytes
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-
sEH is synthesized in adipocytes and expression levels increase upon differentiation of 3T3-L1 preadipocytes. Although normalized sEH mRNA and protein levels do not differ in the fat pads from mice receiving a regular or a high-fat diet, total adipose sEH activity is higher in the obese mice. Peroxisome proliferator-activated receptor gamma agonists increase the expression of sEH in mature 3T3-L1 adipocytes in vitro and in adipose tissue in vivo
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the expression of GPAT2 is downregulated when 3T3-L1 cells differentiate into adipocytes, while GPAT1, 3, and 4 are upregulated (10fold, over 60, and 5fold, respectively)
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the expression of GPAT2 is downregulated when 3T3-L1 cells differentiate into adipocytes, while GPAT1, 3, and 4 are upregulated 10fold, over 60fold, and 5fold, respectively
brenda
-
the major SSAO form expressed in mouse adipocytes is encoded by the AOC3 gene
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-
There is no difference in glycerol mRNA level between control 3T3-L1 adipocytes and 3T3-L1 Aqp7-RNAi transfected adipocytes, whereas a 4fold enzymatic activation of glycerol kinase is observable in Aqp7 knockout adipocytes (activity assay: 50 mM TrisHCl, pH 7.2, 5 mM ATP, 10 mM MgCl2, 100 mM KCl, 2.5 mM DTT, 4 mM glycerol, 500 microM 3H-glycerol, for 90 min at 37°C).
brenda
-
tight regulation of enzyme expression with differentiation
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-
-
brenda
-
contains high amounts
brenda
-
There is no difference in the mRNA levels and activities of adipose glycerol kinase between Aqp7-/- and Aqp7+/+ mice at 10 weeks of age. Adipose glycerol kinase activity of Aqp7-/- mice is significantly higher than that of wild type mice under the 12 h fasting state. The fat pads of the Aqp7-/- knockout mice are significantily larger than those of wild type mice at 20 weeks of age.
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A0A1Y7VM56, D3YZG8, O55239, P06801, P13011, P13516, P17532, P33434, P34884, P39654, P48758, P50136 AND Q6P3A8, P54310, Q05A13, Q14DK4, Q3UWM4, Q61586, Q61907, Q64FW2, Q6PCM1, Q7TQA3, Q8BNZ5, Q8C0N2, Q8C129, Q8CFY4, Q8CGV2, Q8K2C8, Q8K4X7, Q91ZX6, Q922E4, Q99JY8, Q99NF1, Q9D142, Q9D4M9, Q9JJS6, Q9JM51
-
80886, 80911, 391072, 486597, 487574, 646087, 655309, 655415, 656247, 659340, 666733, 668419, 671825, 674449, 674487, 676029, 679083, 680845, 686052, 687766, 688978, 690342, 690828, 692007, 693213, 693508, 694827, 695943, 696445, 698813, 700178, 706094, 706844, 708339, 709226, 710071, 711078, 711387, 711800, 713952, 715609, 716101, 723909, 728552, 730704, 733414, 734262, 735599, 739138, 742239, 744160, 744436, 746542, 751977, 754109, 754442, 754880, 756563, 757868, 761505, 762424, 762713, 763507, 766965, 766972, 767185, 769995, 771399, 772888, 778594, 779331, 779345
brenda
ACAT1 expression is significantly increased in the adipose tissue of ob/ob mice
brenda
-
ATGL is the predominant TG lipase in adipose tissue
brenda
-
axillae
brenda
-
brown adipose tissue
brenda
brown and white, high expression level
brenda
-
brown and white, weak expression of Acot7 in male mice
brenda
despite a lower expression, murine autotaxin alpha is detected in brain and adipose tissue
brenda
enzyme Acod1 is expressed in adipose tissue during inflammation and obesity. Quantitative reverse transcription PCR enzyme expression analysis in wild-type and mutant Acod1-/- mice adipose tissue
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-
expression analysis, overview
brenda
expression detected by RT-PCR
brenda
-
expression of Gys-2 is significantly reduced in adipose tissue of peroxisome proliferator-activated receptor alpha-/-, peroxisome proliferator-activated receptor beta/delta-/- and peroxisome proliferator-activated receptor gamma+/- mice
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gonadal white adipose tissue (gWAT), inguinal white adipose tissue (iWAT), and brown adipose tissue (BAT)
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high expression
brenda
high expression level
brenda
-
high expression level of ATGL
brenda
highest expression in white adipose tissue, moderate in brown adipose tissue
brenda
-
HSL and ATGL
brenda
-
increase of enzyme expression in diabetic animals
brenda
-
injection of Scd1 sequence-specific antisense oligodeoxynucleotides decreases Scd1 gene expression in brown and white adipose tissue as well as in liver
brenda
-
isoform 11beta-HSD1 is highly expressed in freshly isolated omental adipose stromal vascular cells, predominantly in preadipocytes. The enzxyme acts as an 11beta-reduxtase, reactivating glucocorticoids. Glucocorticoid reactivation is higher in intact mesenteric cells than in thigh and axillary depots
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-
isozyme Acc1
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-
lipin-1
brenda
-
lipin-1 accounts for all of the PAP1 activity in adipose tissue and skeletal muscle
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low content
brenda
low expression
brenda
low expression level
brenda
-
low expression, 3.38fold higher than in liver
brenda
-
male white epididymal fat pad, no expression in brown fat
brenda
-
mesenteric and gonadal white adipose tissue and brown adipose tissue
brenda
-
PAP1 activity increases during adipogenesis
brenda
-
range of enzyme activity differs up to 4fold among mink, mice, chinese hamster, rat and guinea pig
brenda
retroperitonea, high mRNA expression
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SCD1
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SCD1 isoform
brenda
-
significantly reduced LPL activity in parametrial adipose tissue from mice fed with conjugated linoleic acid
brenda
specific expression of ATGL
brenda
-
SSAO activity is present in white adipose tissues of wild type but is absent in AOC3KO mice
brenda
-
subcutaneous and gonadal adipose tissue
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-
subcutaneous and gonadal adipose tissue. Significantly reduced MMP-3 expression in MMP-10-deficient adipose tissues
brenda
TPH1 expression in white adipose tissue shows significant associations with mitochondrial fatty acid oxidation and development pathways of other tissues such as the lung and kidney
brenda
-
white and brown
brenda
-
-
brenda
-
of newborn mice
brenda
-
richest source of PC5A
brenda
-
137167, 390593, 439251, 486677, 655309, 658473, 673845, 675688, 676131, 676789, 684899, 685494, 686518, 687797, 690303, 691689, 692563, 693382, 694494, 696010, 696531, 697358, 702945, 703913, 706094, 706558, 714048, 715324, 716280, 725656, 742566, 743228, 744757, 750212, 756598, 768636
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-
3betaHSD I
brenda
-
abnormally high expression of isoform 2 enzyme in male and female
brenda
abundant expression
brenda
activity is the highest in spinal cord and brain followed by thymus, adrenal gland, heart, and genital organs
brenda
-
adrenal 5alpha-reductase expression is decreased in male withdrawal seizure-prone mice
brenda
-
adrenal cortex and adrenal medulla epinephrine cells
brenda
-
adrenergic chromaffin cells and medullary tissue
brenda
-
cleaved caspase-8 is detected in apoptotic cells in the adrenal gland
brenda
-
expressed exclusively in brain, adrenal gland and testis
brenda
expression of type 7 17beta-hydroxysteroid dehydrogenase in zona fasciculata and reticularis in the cortex
brenda
-
high expression level
brenda
-
high expression level, expression is restricted to the X-zone, adrenal 20alpha-HSD activity in male mice peaks at 3 weeks of age and disappears thereafter, whereas 20alpha-HSD enzyme activity is maintained in adrenals from nulliparous female animals
brenda
-
high expression of isoform ALAS1
brenda
highly expressed
brenda
-
HSL
brenda
-
in the three zones of the cortex, not in the medulla
brenda
isoform ACSL4
brenda
isoform Hsd3b6 immunoreactivities within the adrenal gland are essentially confined to the zona glomerulosa cells, where aldosterone is produced. No immunopositive cells are observed in the zona fasciculata
brenda
isozyme AC5
brenda
isozyme AC6
brenda
isozyme AC8
brenda
isozymes SEP and SEPDELTA
brenda
-
low activity
brenda
-
low expression
brenda
low mRNA expression
brenda
-
low transcriptional level in adrenal gland
brenda
-
mEH is particularly concentrated in the adrenal gland
brenda
-
moderate expression level
brenda
-
NAT2 expression detected in adult mice
brenda
orchidectomy increases activity of pyrrolidone carboxypeptidase type I, testosterone replacement returns it to control levels
brenda
-
orchidectomy increases activity of pyrrolidone carboxypeptidase type II, testosterone replacement returns it to control levels
brenda
-
relative high level of mRNA
brenda
sexual dimorphism of the enzyme in the adrenal
brenda
strong expression of MTE-I, expression of CTE-I, PTE-Ib, and PTE-Ia
brenda
substantial expression cortex of adrenal gland
brenda
TER mRNA
brenda
-
-
brenda
isozyme AC1
brenda
-
sustentacular cell
brenda
-
brenda
-
all 9 membrane-associated adenylate cyclases
brenda
-
-
brenda
lining of the alimentary canal
brenda
-
-
brenda
-
pancreatic alpha-cell line
brenda
-
pancreatic alpha-cell line, low expression level
brenda
-
brenda
-
high expression of enzyme
brenda
-
type II alveolar cell, presence of isoform Nat2. Exposure of cells to pathophysiologically relevant amounts of oxidants such as H2O2 or peroxyntrite, impairs the cellular biotransformation of aromatic amines
brenda
-
brenda
Tmprss2 and Tmprss4 are coexpressed in alveolar and bronchial regions
brenda
-
-
brenda
-
amelanotic tumor (F10 and B16, mouse)
brenda
-
-
brenda
detectable only in ameloblasts and odontoblasts of developing teeth
brenda
expressed exclusively in ameloblasts and odontoblasts
brenda
presence in the enamel layer, ameloblast Tomes' processes, and in the walls of ameloblast secretory vesicles
brenda
-
662962, 683926, 694391, 699924, 699969, 707932, 709603, 710118, 710797, 718064, 728178, 732081, 745971, 759804, 763094
brenda
-
basolateral
brenda
-
entire amygdala or ventroposterior quadrant of cerebral hemisphere
brenda
-
specific nuclei
brenda
-
-
brenda
-
a macrophage cell line established by immortalization of bone marrow macrophages from C57BL/6 mice with J2 recombinant retrovirus-expressing v-myc/v-raf oncogenes
brenda
-
baseline expression
brenda
-
murine macrophage cell line
brenda
O89084, P34914, P39654, P70313, Q01063, Q3UEI1, Q3UHN9, Q60680, Q61263, Q64430, Q8BHG1, Q8BNJ2, Q8VCN5, Q9DBR7, Q9ERL9 AND O54865, Q9R112
-
486698, 486703, 655134, 661521, 668543, 675622, 685864, 685975, 687732, 688603, 691656, 693930, 695134, 695485, 697149, 698205, 698209, 698211, 699756, 704431, 704619, 707303, 707582, 708018, 708238, 709124, 709564, 710821, 711762, 711763, 718009, 719196, 733703, 734180, 742845, 745938, 746708, 753291, 755457, 760461, 762448, 764408, 768455, 769091, 770262, 772258
brenda
aortic fibroblasts
brenda
-
aortic homogenate, neointima
brenda
-
aortic lesion
brenda
-
aortic ring
brenda
-
aortic rings
brenda
-
aortic sinus derived from apolipoprotein-E-knockout mouse on a high-fat diet for 6 months, enzyme expression is restricted to a subset of cells
brenda
-
atherosclerotic aorta
brenda
-
atherosclerotic lesions of apolipoprotein E-deficient mice
brenda
-
co-localization of LOX and LOXL
brenda
-
endothelial cells, PYK2
brenda
-
Exposure of mouse aortic rings to hypoxia/reoxygenation significantly increases vessel outgrowth, whereas pharmacological inhibition of NADPH oxidase or genetic deletion of the NADPH oxidase subunit, p47phox significantly suppresses these changes. Increases in myocardial serine-threonine kinase Akt and ERK1/2 activation and vascular endothelial growth factor expression are markedly blunted in the subunit p47phox-deficient mouse subjected to myocardial ischemia-reperfusion compared with the wild-type mouse
brenda
-
hemin treatment increases hemin oxidase-1 expression and activity in aorta and kidney of apolipoprotein E-deficient mice and significantly reduces both NADPH oxidase activity and superoxide generation in situ. Effects are reversed by tin protoporphyrin-IX and are not associated with changes in isoforms Nox2 or Nox4 protein levels. Inhibition of NADPH oxidase activity by hemin in the aorta is mimicked by bilirubin in vitro
brenda
-
in the macrophage-rich regions of atherosclerotic plaques
brenda
-
increased ECE-1 protein content (immunohistochemistry, immunoblot) and mRNA expression (Northern blot) in apolipoprotein E-deficient mouse
brenda
-
intact aorta
brenda
lesions at the aortic sinus and in injured carotid arteries of Apolipoprotein E deficient mice, mRNA expression increases with development of atherosclerosis in the aorta
brenda
-
of control and hyperglycemic mice
brenda
-
PC5A dominates
brenda
-
relatively high m-calpain expression levels in the inferior arch
brenda
-
significant suppression of enzyme activity in parallel with increased superoxide and enzyme nitration in the aortas of diabetic C57BL6 mice, but less effect in diabetic mice either lacking endothelial nitric oxide synthase or overexpressing human superoxide dismutase
brenda
-
smooth muscle
brenda
-
TXAS is expressed in the atherosclerotic lesion, associated with increased inflammatory cells, in particular M2 polarized macrophages
brenda
-
brenda
ASMC
brenda
-
-
brenda
constitutive Adamts5 expression in adult tissue
brenda
-
brenda
-
of muscle
brenda
-
674051, 691656, 702471, 705441, 707303, 707309, 709692, 710782, 722742, 726042, 736318, 742845, 752444, 753117, 756672
brenda
CEPT1 is elevated in diseased lower extremity arterial intima of individuals with peripheral arterial disease and diabetes
brenda
-
in artery DPIV represents 92% of the total Gly-L-Pro-4-nitroanilide-hydrolyzing activity
brenda
-
in the mesenteric arteries of streptozotocin-induced diabetic apoE-deficient mice the expression of nox4 and gp91phox, ie. nox2 subunits of NADPH oxidase are enhanced as are endothelial nitric oxide synthase mRNA and protein
brenda
-
in the vasculature, PDE5 is the predominant PDE isoform involved in degrading cGMP
brenda
-
isozymes GC-A
brenda
-
mesenteric, pulmonary and middle cerebral arteries
brenda
-
of tail
brenda
-
pulmonary
brenda
-
smooth muscle cells
brenda
-
tail
brenda
-
-
brenda
-
L1210 cell line, two isoenzymes
brenda
-
Leukemia 1210 and Sarcoma 180 cells
brenda
-
-
brenda
-
Ehrlich and Yoshida
brenda
-
Ehrlich Lettre
brenda
A0A087WPT2, E9PYH3, O08650, O08688, O08736, O35632, O54983, O70628, O88199, O89023, P05202, P28776, P29477, P29758, P30275, P34914, P45376, P56528, P70312, P70695, Q04447, Q09200, Q5XJZ8, Q61647, Q64430, Q71RI9, Q8BJQ9, Q8C1F4, Q8K4S1, Q91VF2, Q91WT7, Q91ZJ9, Q920A7 and Q8JZQ2, Q9CZR2, Q9JIF0, Q9JK42, Q9JL18, Q9QZX7
-
288890, 639002, 652975, 661837, 669923, 670415, 673870, 674360, 681092, 682552, 682561, 682867, 683448, 684002, 685439, 688183, 688514, 690828, 692073, 693776, 694406, 697771, 697808, 699680, 701258, 702065, 706532, 708506, 708599, 710118, 711642, 713109, 714348, 716344, 718266, 718403, 721714, 727869, 731628, 731882, 732139, 735715, 737427, 738897, 738901, 739113, 743355, 743358, 747183, 753120, 753753, 753898, 754574, 758876, 759251, 759849, 761135, 761984, 763094, 765401, 766436, 770264, 770274, 771312, 772879, 773613, 773621, 774714, 776681, 778767
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astrocyte-based ADK provides a critical link between astrogliosis and neuronal dysfunction in epilepsy
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cell culture
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Q9ERL9 AND O54865
cerebellar
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cerebrocortical astrocytes in primary culture, prepared from the neopallium
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contain only soluble enzyme
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cortical and hippocampal
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cortical astrocyte. Differential, cell-type specific expression of enzyme subunit IV isoform 2 in cortical astrocytes and cerebellar neurons. Presence of subunit IV isoform 2 suppresses the sensitivity of enzyme to its allosteric regulator ATP and overrules the regulation by the cellular energy level. Pivotal role of enzyme as an oxygen sensor in brain
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cortical cell culture
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cystathionine beta-synthase is associated with the generation and/or differentiation of the radial glia/astrocyte lineage cells in the developing central nervous system
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differentiated from C6 glioma cells
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double Has2/Hyal-1 immunohistochemistry reveals partial co-localization of Has2 and Hyal-2 (EC 3.2.1.36) two proteins in protoplasmic astrocytes
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expressed most strongly in astrocytes
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from forebrain, very low expression level
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in primary neurons and astrocytes lacking GD3 synthase, amyloid beta-induced cell death and amyloid beta aggregation are inhibited
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level of AGT is much reduced in mice lacking p53
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MGMT gene expression is substantially lower in knockout p53 astrocytes than in wild-type p53 astrocytes
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moderate expression levels throughout development
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omega-amidase activity is higher in astrocytes than in neurons
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only expresses PDE7
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PAD2 immunoreactivity is increased in Scrapie-infected brains, with staining detected primarily in reactive astrocytes
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plasmin evokes an increase in both phosphoinositide hydrolysis and Fura-2/AM fluorescence in cultured cortical astrocytes. Plasmin activiates extracellular signal-regulated kinase and induces a rise in intracellular Ca2+ concentration and phopho-ERK1/2 levels
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prepared from forebrain of 1-day old Swiss Webster mice
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pressure-treated astrocytes exhibit elevated PAD2 and citrullination without apparent change in PAD2 mRNA
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primary
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primary cell
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primary cell culture
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primary cortical astrocytes
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primary culture
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protoplasmic
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selectively expressed in astrocytes in adult. Expressed in a subset of Gjb6C astrocytes in the spinal cord
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stable serine racemase dimers resistant to both denaturation and reductive treatment, showing reduced racemase activity
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stable serinme racemase dimers resistant to both denaturation and reductive treatment, showing reduced racemase activity
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cultures are established from wildtype, PTEN heterozygous (+/-) mice and PTEN and Fyn kinase double heterozygous (+/-) mice
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N-Cadherin cleavage occurs at a higher level in glioblastoma cells than in non-neoplastic astrocytes
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-
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an embryonal carcinoma-derived clonal cell line
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chondrocyte progenitor cell line, developmentally specific changes in MINPP expression
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low activity in the mouse chondrogenic cell line
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-
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atrial monocyte
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-
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-
a pituitary tumour cell line
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anterior
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corticotroph tumor cell line, GRK2, no expression of GRK3
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expresses high levels of endogenous PC1/3
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-
pituitary corticotrope-derived cells
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pituitary gland cell line
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pituitary gland cell line, low expression level
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treatment with inhibitor CLIK-148 results in reduced production of adrenocorticotropic hormone and accumulation of proopiomelanocortin
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1068, 1074, 30157, 30159, 637260, 642811, 665531, 679976, 680887, 685452, 689442, 693443, 696686, 737585, 754951, 759035, 764085
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a melanoma cell line
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B16 melanoma cell
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cells express higher levels of cytosolic acetyl-CoA synthetase ACSS2 under hypoxia than normoxia. Knockdown of ACSS2 by RNA interference in tumor cells enhances tumor cell death under long-term hypoxia in vitro. The ACSS2 suppression slows tumor growth in vivo. Tumor cells excrete acetate and the quantity increases under hypoxia, the pattern of acetate excretion follows the expression pattern of ACSS2. The ACSS2 knockdown leads to a corresponding reduction in the acetate excretion in tumor cells
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melanoma cell
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melanoma cell line
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-
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only one out of seven mature B cell lines expressed ltk and the in vitro maturation of pre-B into B cells is in one case accompanied by the inactivation of ltk expression
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peripheral
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PKC isozyme expression patterns
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precursor
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primary
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TPL-2, TAK1
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-
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elevated SHMT2 expression in aggressive murine MYC-induced lymphomas
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Ly-10 DLBCL cells or WEHI-231 cells, Akt and Syk, the latter is constitutively activated in primary tumor cells
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B2RXC2, O70370, O89110, P55772, Q3TD49, Q5SSF7, Q9CUS9, Q9CXF0, Q9D8V0, Q9JJF9, Q9WVE0
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640892, 660959, 661549, 662293, 662928, 663815, 665922, 670293, 681911, 693031, 694165, 694494, 699336, 699442, 703394, 703546, 704625, 704942, 709350, 709368, 709979, 720141, 720159, 720456, 720460, 720538, 720891, 723637, 732835, 734407, 737400, 752819, 753968, 754356, 755089, 756375, 757745, 761995, 778222
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AID expression occurs first in pro-B cells and increases on further development, peak AID expression is in immature and T1 B cells from bone marrow, is lower in splenic T1 B cells, and decreases precipitously in the splenic transitional 2 and mature B-cell compartments
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B-cell line A20
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caspase-8 is dispensable for B-cell development, but its loss in B cells results in attenuated antibody production upon in vivo viral infection. Important role for caspase-8 in maintaining B-cell survival following stimulation of the Toll-like receptor (TLR)2, -3, and -4
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catalytic regulation of B cell receptor (BCR) signalling and B-cell development, knockout mice: striking decrease in number of splenic marginal zone B-cells and marginal zone B-cell precursors, reduced number in follicular B-cells, loss of recirculating B-cells in bone marrow, lymphocyte-intrinsic defects
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circulating T lymphocyte
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development and differentiation of the cells from transgenic mice lacking Txnrd2 expression is not significantly impaired
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germinal center B cell
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high expression of SENP1 in germinal center B cells
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immature B-lineage cell
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-
mechanosensitive activation of K+ channel via phospholipase C-induced depletion of phosphatidylinositol 4,5-bisphosphate
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-
peripheral
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-
primary
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Prmt1 is ubiquitously expressed in germinal center B cells (GCBC), and is upregulated in positively selected GCBCs
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-
Rap1b is more highly expressed in B cells than Rap1a
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splenic
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-
surface
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-
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-
melanoma cell line
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overexpression of functional ErbB3
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-
brenda
-
MMP-14 is weakly expressed in B16-F1 cells
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-
mouse melanoma cell
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-
680243, 681033, 685663, 685815, 693443, 700600, 703805, 708548, 715166, 718564, 732728, 736198, 748797, 764220, 776932
brenda
-
B16F10 melanoma cell
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melanoma cell
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melanoma cell line, implanted in syngenic C57BI/6J mice which then show reduced vascularization and growth
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-
murine melanoma cell line, with platelet-activating factor-induced experimental pulmonary metastasis, which is inhibited by both NF-jB and c-jun inhibitors and completelyby MMP-9 inhibitor
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-
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-
melanoma cell line
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-
-
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mouse embryo cell line: 3T12
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-
-
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conversion of mesoporphyrin is dependent on the expression of ferrochelatase, since control Balb/3T3 cells have much lower expression of ferrochelatase than the ferrochelatase transfectants
brenda
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fibroblast cell, non-dividing cells expressing enzyme subunit p53R2, but not sunit R2 protein, have reduced dNTP levels if exposed to the enzyme--specific inhibitor hydroxyurea. After DNA damage, a slow, up to 4fold increase in p53R2 expression leads to 3fold increase in dNTP pools in G0/G1 cells
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-
-
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basophils preferentially express mast cell protease 11 among the mast cell tryptase family, basophils rather than mast cells are the major source of mast cell protease-11
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-
beta-tryptase
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-
-
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-
CRL 1443 (ATCC)
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-
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-
derived from pancreatic islets
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-
insulinoma cell, treatment with islet-specific cytokine pancreatic derived factor results in elevated enzyme levels which abrogates expression of cyclin-dependent kinase inhibitor 1A
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-
PDE7A1 co-localizes with PKA II in the Golgi centrosome region
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-
-
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-
liver
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-
490500, 658473, 661575, 671262, 675601, 684333, 692501, 694494, 712435, 720288, 727891, 733064, 744436, 751394, 768455
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-
low expression of mPEGS-2 in the urothelium
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-
low level of activity
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N-butyl-N-(4-hydoxybutyl) nitrosamine (BBN) treatment for 12 weeks induces invasive cancer development in mice
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predominant expression of splice variant PMCA4a
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-
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-
Clones from two individually selected heterozygous ES cell lines are injected into blastocysts and the resultant founder chimeras bred to obtain two lines of knockout Trpt1+/- and knockout Trpt1-/-mice.
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obtained after in vitro fertilization with gametes from B6D2F1 hybrid mice and from embryo culture. The blastocysts express Ugt1a globally, in the cytoplasm and nuclei of all of the cells, presence of Ugt1a6 but not Ugt1a1, Ugt1a3, Ugt1a4, or Ugt1a9. The Ugt2b proteins are not detected, Immunofluorescence analysis and Western blot
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subluminal stroma surrounding the implanting blastocyst on day 5 of pregnancy
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UCH-L1 present in the outer layer cells of the trophectoderm. UCH-L3 present in the inner cells
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O08691, P00748, P11214, P16406, P25911, P34914, P40142, P54310, Q61176, Q64685, Q91YE2, Q9EP97, Q9EPW0
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286014, 639000, 639011, 663254, 667849, 670952, 681208, 683489, 684359, 685945, 686633, 688791, 689073, 689339, 689364, 691298, 691458, 692007, 693071, 697032, 701242, 703632, 704989, 705320, 707303, 709320, 709321, 715188, 718010, 731445, 735422, 743285, 748338, 749544, 752443, 754964, 759230, 771420, 773776
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-
ADH3 plays an important role in systemic ethanol metabolism at higher levels of blood ethanol through activation by cytoplasmic solution hydrophobicity
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-
erythrocytes show the highest activity, plasma low, and white blood cells low but highly variable levels of enzyme, circulating isomerase is derived in part from tissue sources and is in part an intrinsic blood enzyme
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-
heparin administration is associated with a significant increase in PAPP-A levels, presumably because of the detachment of PAPP-A from the vessel wall
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higher activity of isozyme SPHK1, low activity of isozyme SPHK2
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-
hyperhomocysteinaemia is a metabolic disorder associated with the development of premature atherosclerosis. Cystathionine beta-synthase activity is significantly decreased in mice with a plasma homocysteine value greater than 0.015 mg
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iNOS
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-
isozymes SPHK1 and SPHK2
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-
lipin-2, in circulating red blood cells, at ca. 10% of the levels observed in liver
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lower expression level
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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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-
peripheral blood T-cells
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-
present in circulating blood. ATX is responsible for bulk lysophosphatidic acid production in plasma. Stabilizes blood vessels and is required for embryonic vasculature by producing lysophosphatidic acid
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-
the enzyme circulates as inactive zymogen in the blood stream becoming activated upon blood clotting
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O55239, P09242, P23953, P26262, P28293, P33587, P34914, P41245, P52430, P70158, P70313, Q03059, Q61147, Q61847, Q61907, Q80W65, Q8CFA2, Q9D4B1, Q9Z2A7
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208376, 653977, 668894, 669742, 670474, 678921, 679662, 679663, 679707, 680929, 691079, 693517, 694786, 695421, 695455, 696112, 696134, 697490, 697556, 697561, 697763, 697770, 697773, 697960, 699445, 699748, 699944, 699985, 700246, 700399, 700400, 700615, 701194, 701687, 703245, 703346, 703366, 704356, 706002, 707306, 707332, 707856, 709248, 709722, 710690, 715839, 717196, 717420, 718994, 720368, 730060, 731237, 731354, 731539, 732094, 732147, 732240, 732928, 732933, 738955, 739665, 743131, 750060, 751792, 752614, 753070, 753224, 757321, 760476, 769009, 769473, 769964, 771036, 771417, 771627, 773315, 773767, 773811, 774961, 776534, 776733, 777412, 778234, 779331
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-
Aqp7-/- knockout mice have significantly lower plasma glycerol level under 12 h fasting conditions.
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-
coagulation assays
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from mice with acute kidney injury, MIOX expression is undetectable in healthy mice plasma
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-
heparin releases LPL from its in vivo binding sites allowing it to enter the blood plasma
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-
in blood plasma DPIV represents 78% of the total Gly-L-Pro-4-nitroanilide-hydrolyzing activity
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-
measurable LPL activity is present only in postheparin plasma
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PK is the 85 to 88 kDa precursor of the serine protease PKa and circulates in plasma
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-
XylT levels in plasma are approximately 200% lower than those in serum due in part to XylT released by platelets during blood clotting in vitro. In Xylt2+/+ mice, total serum XylT activity is 42% higher than in plasma. In Xylt2-/- mice, no significant difference between serum and plasma total XylT activity
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-
660860, 661393, 661509, 661575, 661660, 662277, 663994, 665810, 668260, 671951, 693350, 693894, 703078, 713689, 727242, 731536, 734581, 735971, 737419, 737595, 737929, 739146, 765022, 770262, 774211, 779399
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-
activated
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-
cell surface
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contains only HYAL2 but not HYAL1
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-
expression of cytosolic subunits of NAD(P)H oxidase p47phox and p67phox is not altered by hypercholesterolemia, however, platelets and leukocytes from high cholesterol-fed mice exhibit elevated generation of reactive oxygen species compared to normal diet mice
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-
high expression level of 12-LOX
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-
high expression of Rap1b
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-
isozyme mPA-PLA1alpha
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-
septic megakaryocytes produce platelets with acutely altered mRNA profiles, and these platelets mediate lymphotoxicity via granzyme B
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-
172002, 716432, 731821, 732263, 751366, 753360, 768503, 773817, 773974, 774570, 774618
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-
IgG1 autoantibodies detected in mice with experimental autoimmune uveoretinitis
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-
phenylbutyrate greatly decreases the adriamycin-associated elevations of serum lactate dehydrogenase and creatine kinase activities, two nonspecific widely used cardiac injury markers
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-
XylT2 is predominant. XylT levels in serum are approximately 200% higher than those in plasma due in part to XylT released by platelets during blood clotting in vitro. In Xylt2+/+ mice, total serum XylT activity is 42% higher than in plasma. In Xylt2-/- mice, no significant difference between serum and plasma total XylT activity
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-
brenda
cerebral
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-
e.g. capillaries in back skin
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endothelium of blood vessel
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-
in the walls
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-
intestinal, colonic microvessels, high endothelial venules-like vessels
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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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positive staining in blood vessels from arthritic joints as revealed by immunohistochemistry using rat monoclonal anti-murine NAMPT antibody
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-
predominantly localized to the endothelial layer of blood vessels
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time-dependent decrease in in PDI expression in thrombi following injury. Infusion of monoclonal antibodies against PDI into the circulation of mice lacking the G protein-coupled platelet receptor Par4 prior to vessel wall injury inhibits fibrin generation
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-
with a decreasing activity in tail artery, aorta and mesenteric arteries
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-
-
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bone marrow-derived mast cell, 200fold higher expression of mC4ST-1 than in bone marrow cell
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the expression GalNAc4S-6ST increases during differentiation from bone marrow cells to bone marrow-derived mast cells, the expression in bone marrow-derived mast cells is 3fold higher, than the expression in bone marrow cells
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-
brenda
-
liver cell line
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P09242, P50172, P51658, P70669, Q05144, Q3UWM4, Q3UX61, Q571E4, Q6TEK5, Q75NR7, Q8R2H9, Q8R4K8, Q9QY36, Q9R0E2
-
638810, 652666, 662547, 672947, 673845, 674990, 675017, 681953, 683711, 694494, 695956, 697011, 697012, 697066, 697150, 697775, 698935, 703618, 708647, 711675, 711688, 711853, 712131, 712433, 712462, 712933, 714633, 714682, 714836, 715704, 719437, 720086, 734347, 734358, 741242, 746171, 753513, 756675, 758107, 761361, 767185, 767650, 769422, 773630, 779307
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-
ACE is expressed in osteoblasts and hypertrophic chondrocytes in the periosteal callus during fracture healing, accompanied by expression of the angiotensin type-1 and type-2 receptors
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-
cathepsin K probe localizes adjacent to newly mineralizing bone in vivo
brenda
ENPP1 is observed throughout the cytoplasm of mature osteoblasts and osteocytes embedded in bone but not in preosteoblasts. ENPP1 is localized in close proximity of the osteoid, whereas tissue nonspecific alkaline phosphatase is found relatively distant from the osteoid
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expressed during mouse development in many tissues including bone and tooth
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-
expression during embryonic ossification. GPI-PLD is observed during both intramembraneous and endochondral ossification and localized predominantly to the extracellular matrix of chondrocytes and to primary trabecular of the skeleton
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-
expression pattern of bone-related genes by RT-PCR/quantitative real-time PCR
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-
femur and lumbar vertebra
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-
high activity
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-
isozymes ppGalNAcT-1, ppGalNAcT-2, and ppGalNAcT-3, expression patterns, overview. Expression of isozyme ppGalNAcT-1 especially in calvaria and tibia
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-
low levels of lipin-2, in bone and bone marrow, at 1020% the levels in liver
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-
MMP13 is expressed by hypertrophic chondrocytes and osteoblasts in the fracture callus
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-
ossification centers of developing bone
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-
PHOSPHO1 is restricted to mineralizing regions of bone and growth plate. 120fold higher level of PHOSPHO1 expression in bone compared with liver. Enzyme present within matrix vesicles is in an active state. Present in early hypertrophic chondrocytes of the growth plate, and in osteoblasts of trabecular surfaces and infilling primary osteons of cortical bone
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prenatal/embryonic mandibular bone, statistically significant increase in expression of caspase-12 in a decisive period of mandibular bone formation when the original mesenchymal condensation turns into vascularized bone tissue, caspase-12 expression pattern in forming mandible with a special focus on bone, overview
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-
proliferating regions of the fetal bone
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quantitative gene expression and in situ hybridization of genes associated with endochondral ossification
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-
represents about 45% of total enzyme activity
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-
the activated form of caspase-7 is detected from the beginning of ossification during embryonic development and persists postnatally in alveolar and mandibular bones as well as long bones of limbs
brenda
P0CB42, P14901, P21958 AND P36371, P21981, P33587, P41242, Q06806, Q571E4, Q5EG47, Q62137, Q8BH61, Q8BW72, Q8C1A5, Q8CIH5, Q91VY5, Q91XQ5, Q923T9, Q9JIF0, Q9JLF6, Q9JME2, Q9WV54
-
1966, 94310, 209428, 286018, 392077, 392084, 392085, 485426, 490427, 490571, 490627, 638981, 638988, 639001, 643200, 643228, 647314, 658264, 661548, 662293, 662575, 663609, 666758, 666997, 668068, 669565, 669716, 673956, 674761, 675034, 679975, 681953, 683136, 683316, 688158, 690079, 690388, 691068, 691994, 692225, 693038, 693454, 695936, 699181, 701011, 702855, 703913, 705824, 711713, 714052, 716796, 721918, 723637, 725541, 730727, 739863, 752926, 753065, 753570, 759544, 760073, 761022, 764374, 764440, 764447, 770501, 778029
brenda
-
bone marrow-derived cells are the major source of MMP-9 in the ischemic brain
brenda
-
decreased GCN5 in osteoporotic bone marrow
brenda
-
high expression level
brenda
highest levels of expression in bone marrow, brain, spleen and kidney
brenda
highest levels of expression in bone marrow, brain, spleen, kidney, and lens
brenda
-
lipin-2
brenda
low expression level
brenda
-
macrophages
brenda
maximal expression level of MsrA in kidney and liver, followed by heart, lung, brain, skeletal muscle, retina, testis, bone marrow, and blood
brenda
-
pluripotent cells of healthy and leukemic mice
brenda
proteinase 3 is considerably more expressed in bone marrow than in the peripheral blood
brenda
stromal cells
brenda
-
TRAP(+) osteoclast formation is inhibitied by exogenous addition of enzyme or of ADPribose
brenda
-
brenda
-
bone marrow cells taken from wild-type and heterozygous Nmt1-deficient mice and cultured in the presence of mouse macrophage colony-stimulating factor for differentiation into monocytes/macrophages develop in a different manner, overview
brenda
-
C4ST-2 expression occurs in the early stage bone marrow cell cultures, the process of mast cell maturation does not alter the expression, low expression at day 0, followed by an increase in expression at later stages of culture
brenda
GalNAc4S6ST expression occurs in the early stage bone marrow cell cultures, low expression at day 0, followed by an increase in expression at later stages of culture
brenda
-
NDST-2 correlates strongly with mast cell maturation, whereas the expression of the NDST-1 isoform is approximately equal at all stages of maturation. NDST-2 correlates strongly with mast cell maturation, whereas the expression of the NDST-1 isoform is approximately equal at all stages of maturation. NDST-1 expression is detected already in the early stage, day 0, bone marrow cells, but the level of expression does not increase throughout the process of mast cell maturation. NDST-2 expression follows an entirely different pattern, with low expression in day 0 and day 7 cultures, followed by a markedly increased level of expression starting from day 14 and has a continuously increased expression throughout the entire culture period. NDST-2 is downregulated after mast cell activation
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primary
brenda
-
brenda
-
LPS stimulates Sphk activity
brenda
-
727611, 731559, 731594, 731613, 731863, 732557, 732823, 732829, 756414, 757678, 766237, 766887, 769545
brenda
-
high expression
brenda
-
primary cell
brenda
A0A0U1RNF2, A0A1Y7VM56, A0A286YDB8, A2AWA9, A2RTH5, A4Q9E8, A4Q9F0, A7MCT6, A7UAK5, AI390103, B2RXC2, D6MZJ6, E9PUQ8, O08529, O08650, O08688, O08736, O08738, O08796, O08832, O08912, O08914, O09114, O09159, O35099, O35350, O35632, O35696, O35710, O35945, O35980, O54754, O54827, O54833, O54983, O55023, O55055, O70161, O70325, O70362, O70571, O70628, O88199, O88444, O88455, O88531, O88533, O88587, O88643, O88693, O88829, O88974, O89110, P00860, P05202, P05480, P05532, P06797, P06802, P08414, P08923, P10605, P11152, P11798, P14901, P15535, P16092, P16330, P16406, P17439, P17532, P18242, P18894, P23953, P24529, P25911, P28652, P28825, P28867, P29477, P29758, P34914, P38585, P41241, P41242, P41245, P45376, P47738, P47739, P47740, P48320, P49183, P50285, P50431, P50516 AND P62814 AND Q9Z1G3 AND P51863 AND P50518 AND Q9CR51 AND Q9R1Q9, P51661, P51830, P53668, P54751, P54823, P55144, P55264, P56528, P56818, P59110, P59941, P60487, P61588, P61922, P63318, P68404, P70181, P70182, P70312, P70419, P70453, P70677, P70695, P70704, P97325, P97490, P98191, P98197, P98199, P98200, Q00342, Q01063, Q01065, Q01768, Q02858, Q02956, Q04447, Q04735, Q04899, Q05117, Q08642, Q09M02, Q0E9Q7, Q0VBN2, Q11204, Q148W0, Q14DK4, Q3TCT4, Q3TDX8, Q3TFD2, Q3TPJ9, Q3TYD4, Q3U2J5, Q3U3S6, Q3ULQ2, Q3UVR3, Q3UW64, Q4KWH5, Q571E4, Q5FWI3, Q5HZI3, Q5SGK3, Q5SWU9, Q5U901, Q60629, Q60860, Q61036, Q61214, Q61391, Q61586, Q61647, Q61772, Q61831, Q61847, Q61851, Q61907, Q61941, Q61955, Q62074, Q62148, Q62413, Q63880, Q64133, Q64176, Q641K1, Q64237, Q64311, Q64430, Q64446, Q64455, Q64521, Q64689, Q64692, Q68ED3, Q69ZF3, Q6DFW5, Q6JIZ0, Q6NVG1, Q6P3D0, Q6P9S7, Q6PB93, Q6PD10, Q6PDK2, Q6PFX8, Q6TEK5, Q6UQ17, Q6V956, Q6WQJ1, Q6ZPS2, Q6ZQ88, Q71RI9, Q7TMC8, Q7TMR0, Q7TNT2, Q7TS31, Q7TS72, Q7TT16, Q80V42, Q80VA0, Q80VQ0, Q80WS1, Q80YA3, Q8BFP9, Q8BGN3, Q8BH00, Q8BH82, Q8BHC7, Q8BHG1, Q8BJQ9, Q8BK63, Q8BLI4, Q8BTY1, Q8BVQ5, Q8BW75, Q8BWD2, Q8BWF0, Q8BYI6, Q8C0N2, Q8C172, Q8C1A5, Q8C1F4, Q8CF93, Q8CFA2, Q8CGV2, Q8CGY8, Q8CHK3, Q8CI15, Q8K1B9, Q8K2C6, Q8K2C8, Q8K2X1, Q8K3F7, Q8K4Q7, Q8K4X7, Q8R071, Q8R0I0, Q8R0X7, Q8R146, Q8R3I2, Q8R3P0, Q8R4K8, Q8VCC2, Q8VCT4, Q8VHQ9, Q8VJ15, Q91UZ4, Q91UZ5, Q91V01, Q91V12, Q91VF2, Q91VY5, Q91WC9, Q91WG8, Q91WN4, Q91XE4, Q91Y74, Q91YE2, Q91YE3, Q91YI6, Q91YP2, Q91ZJ9, Q91ZP3, Q921L8, Q922E4, Q922H2, Q922J9, Q923E4, Q99J99, Q99JR6, Q99K82, Q99L43, Q99LH2, Q99LS3, Q99MU3, Q99NF1, Q99P30, Q99PU5, Q9CQF9, Q9CRY7, Q9CY64, Q9CYC6, Q9CYK2, Q9CZS1, Q9D142, Q9D379, Q9D6K9, Q9D6N1, Q9D6R2, Q9D6Y7, Q9D7V9, Q9D964, Q9DA37, Q9DAT5, Q9DBE0, Q9DBF1, Q9DBR7, Q9DC28, Q9DCV3, Q9EP97, Q9EPA7, Q9EQ20, Q9ERL9 AND O54865, Q9ES00, Q9JHE3, Q9JHE4, Q9JHR7, Q9JHW9, Q9JIF0, Q9JJ61, Q9JK42, Q9JLI6, Q9JLJ2, Q9JLT2, Q9JLT4, Q9JME2, Q9JMF7, Q9JMH6, Q9JMK2, Q9QXE0, Q9QXF8, Q9QXG4, Q9QXQ1, Q9QY36, Q9QZ08, Q9QZW0, Q9QZX7, Q9R0P9, Q9R0Y5, Q9WTP6, Q9WUD1, Q9WV54, Q9WVK8, Q9WVM8, Q9Z0F0, Q9Z0S1, Q9Z110, Q9Z183, Q9Z188, Q9Z1X2, Q9Z2A5, Q9Z2A7, Q9Z2A9, Q9Z2W0
-
995, 1712, 2655, 3983, 3984, 3992, 3995, 4006, 5119, 5122, 29871, 34807, 94340, 95156, 95158, 95250, 135162, 135188, 135380, 135392, 135404, 135595, 135961, 136046, 136451, 136480, 136481, 137041, 137042, 137047, 137048, 208703, 209001, 209006, 209381, 209384, 209588, 209593, 209596, 209598, 209602, 210536, 210547, 210549, 210552, 286172, 286175, 286177, 286181, 286182, 286475, 288884, 288890, 288893, 288926, 289268, 349267, 390377, 390654, 391072, 391421, 391716, 391752, 393074, 393220, 437671, 437708, 439251, 440192, 440198, 440226, 440236, 440239, 441556, 441577, 485592, 485600, 485613, 485614, 485617, 486012, 486026, 486296, 486505, 486620, 486703, 486975, 487306, 487744, 487749, 487753, 489182, 489214, 489220, 489315, 489318, 489408, 489823, 490106, 490109, 490180, 490266, 490425, 490426, 490427, 490484, 490500, 490512, 490538, 490619, 490621, 490624, 490636, 491033, 491043, 491044, 491045, 491048, 491080, 491171, 491197, 491228, 491230, 491237, 491238, 491577, 491805, 491833, 491839, 637032, 637034, 637035, 637037, 637038, 637051, 637114, 637200, 638223, 638234, 638552, 639002, 639004, 640348, 640590, 640591, 640834, 640835, 641701, 641740, 642558, 643277, 643818, 644508, 644806, 644999, 645693, 645699, 645705, 646881, 647288, 647321, 647323, 647325, 647328, 647436, 647460, 648105, 648242, 648681, 648747, 648750, 648768, 650498, 650742, 651451, 651538, 652079, 652546, 652665, 652975, 652979, 652983, 652984, 653212, 653990, 653992, 654196, 654851, 655125, 655987, 655991, 656001, 656097, 656184, 656242, 656339, 656596, 657550, 657678, 657722, 657796, 658159, 658202, 658213, 658473, 658832, 659082, 659216, 659263, 659765, 659946, 660505, 660686, 660688, 660892, 661410, 661575, 661642, 661649, 661660, 661820, 661837, 661844, 662284, 662341, 662412, 662592, 662688, 662848, 662950, 662962, 663275, 663382, 663539, 663916, 663924, 664179, 664193, 664358, 664556, 664865, 665074, 665457, 665488, 665541, 665570, 665810, 666117, 666130, 666461, 666465, 666467, 666718, 666719, 666735, 666749, 666968, 666973, 667443, 667504, 668092, 668122, 668183, 668226, 668357, 669344, 669517, 669606, 669913, 669928, 669945, 669946, 670241, 670742, 670857, 670952, 670956, 671173, 671302, 671825, 672182, 672276, 672484, 672502, 672524, 672852, 672863, 673005, 673247, 673325, 673332, 673352, 673509, 673693, 673829, 673844, 673846, 673910, 674360, 674370, 674598, 674602, 674650, 674746, 674804, 675029, 675031, 675514, 675552, 675556, 675688, 675978, 676029, 676088, 676170, 676172, 676174, 676186, 676192, 676265, 676319, 676338, 676849, 676852, 677856, 678560, 678978, 678984, 679076, 679509, 679653, 679707, 679781, 679864, 679875, 680097, 680678, 680705, 680814, 680880, 681093, 681524, 681526, 681531, 681545, 681927, 681929, 681949, 681953, 681962, 682107, 682118, 682129, 682136, 682137, 682561, 682957, 683342, 683344, 683369, 683389, 683447, 683448, 683453, 683509, 683628, 683795, 683796, 683911, 683920, 683926, 683929, 683961, 684050, 684899, 685854, 685881, 685890, 686020, 686028, 686040, 686293, 686295, 686638, 687034, 687352, 687931, 687987, 688281, 688506, 688541, 688556, 688604, 688741, 688763, 688791, 689183, 689219, 689222, 689717, 689776, 689817, 690084, 690096, 690142, 690346, 690606, 690687, 690694, 690828, 691071, 691173, 691219, 691306, 691548, 691701, 691726, 691926, 692058, 692473, 692501, 692517, 692584, 693022, 693047, 693184, 693213, 693254, 693369, 693382, 693508, 693730, 693731, 693750, 693760, 693766, 694156, 694172, 694372, 694387, 694406, 694494, 694880, 694942, 695144, 695188, 695235, 695485, 695933, 695988, 696037, 696295, 696531, 696990, 697041, 697178, 697587, 697749, 697807, 697808, 697809, 697810, 697898, 698099, 698162, 698177, 698870, 698879, 699007, 699650, 699663, 699682, 699694, 699830, 699924, 699968, 700082, 700126, 700128, 700315, 700411, 700429, 700449, 700465, 700471, 700472, 700475, 700481, 700609, 700611, 700956, 700999, 701258, 701626, 701654, 701958, 701998, 702028, 702065, 702144, 702387, 702433, 702948, 703132, 703133, 703504, 703701, 703852, 703913, 703961, 704085, 704418, 704461, 704668, 705248, 705272, 705284, 705289, 705313, 705327, 705402, 705495, 705699, 705702, 705903, 705911, 705927, 705928, 705932, 705939, 705940, 706094, 706444, 706492, 706517, 706532, 706536, 706558, 706836, 706844, 707099, 707118, 707471, 707553, 707620, 707931, 707932, 707935, 708043, 708300, 708311, 708415, 708540, 708598, 708599, 708683, 708809, 708981, 709151, 709152, 709248, 709270, 709271, 709425, 709589, 709602, 709603, 709607, 709611, 709627, 709632, 709644, 709745, 710051, 710066, 710071, 710075, 710086, 710102, 710115, 710359, 710451, 710797, 710839, 710899, 711078, 711369, 711573, 711611, 711642, 711688, 711720, 711800, 711918, 711942, 712067, 712462, 712648, 712677, 712685, 712824, 712831, 713022, 713025, 713338, 713362, 713420, 713952, 714048, 714338, 714339, 714348, 714664, 714682, 715134, 715324, 715979, 715983, 715985, 716218, 716277, 717285, 717393, 717760, 717836, 717870, 717922, 718064, 718096, 718328, 718403, 718539, 719813, 719872, 720100, 720176, 720288, 720289, 720293, 721502, 721528, 721714, 721881, 721926, 722000, 722332, 722348, 722689, 722771, 722788, 722906, 723022, 723024, 723102, 723558, 723586, 723599, 723653, 723787, 723918, 724210, 724231, 724397, 724953, 725110, 725404, 725423, 725446, 725595, 725753, 726042, 726664, 726851, 727869, 728034, 728178, 728379, 728931, 728949, 729306, 729337, 729350, 729568, 729845, 729989, 730056, 730475, 730704, 731222, 731296, 731563, 731564, 731702, 731755, 731882, 732061, 732081, 732086, 732139, 732360, 732366, 732504, 733064, 733093, 733629, 733737, 733906, 734393, 734695, 734781, 734803, 734999, 735062, 735078, 735714, 735877, 735972, 736193, 736427, 736550, 736820, 737260, 737267, 737402, 737403, 737741, 737961, 737998, 738198, 738349, 738551, 738593, 738904, 738910, 739050, 739069, 739172, 739405, 739439, 739531, 739661, 739828, 740246, 740991, 741023, 741103, 741302, 741420, 741458, 742002, 742426, 742553, 742853, 743036, 743133, 743140, 743354, 743355, 743581, 743836, 744272, 744291, 744436, 744500, 744832, 744851, 745044, 745347, 745523, 745596, 747019, 747183, 748047, 748126, 748296, 749361, 749865, 749873, 749951, 749965, 750453, 750614, 750657, 750705, 750882, 750995, 751019, 751053, 751572, 751697, 751912, 751919, 752186, 752416, 752700, 752926, 753126, 753187, 753349, 753513, 753726, 753927, 754028, 754045, 754143, 754262, 754384, 754629, 754712, 754779, 754898, 754907, 754910, 755153, 755995, 756102, 756106, 756392, 756522, 757163, 757321, 757567, 757868, 757869, 758103, 758126, 758401, 758477, 758876, 758964, 759020, 759108, 759416, 759502, 759758, 759804, 759838, 759849, 760145, 760219, 760319, 760334, 760595, 760629, 760638, 760851, 761038, 761135, 761587, 761594, 761717, 761805, 761824, 762011, 762237, 762284, 762381, 762614, 762971, 763218, 763304, 763340, 763475, 763478, 763743, 764034, 764296, 764298, 764392, 764558, 764701, 765255, 765436, 766972, 767088, 767381, 767487, 767650, 767662, 767859, 768414, 768455, 768493, 769108, 769284, 769810, 770004, 770262, 770274, 770282, 770300, 770466, 770968, 771000, 771309, 771312, 771384, 771572, 771587, 771588, 772188, 772196, 772421, 772774, 772848, 773308, 773611, 773613, 774037, 774211, 774364, 774365, 774687, 774713, 774715, 775270, 775350, 775484, 775518, 775826, 776275, 776371, 776681, 776687, 776936, 777082, 777088, 777412, 777914, 778254, 778606, 778726, 778761, 778767, 778829, 779444
brenda
10fold lower activity than in liver
brenda
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11beta-HSD2 in the adult brain is thought to protect mineralocorticoid receptors from inactivation by corticosterone
brenda
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12/15-LOX is selectively enhanced in the periphery, 12/15-LOX-expressing myeloid cells are enriched in the brain during chronic toxoplasmosis
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2 isoenzymes
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66 kDa and 85kDa isoforms
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93000 Da form
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a decreased expression on the protein and on the mRNA level in elderly mice and in mice overproducing amyloid-beta peptide assemblies is shown
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a knockout mouse strain of the methionine sulfoxide reductase A gene (MsrA-/-) causes an enhanced neurodegeneration in brain hippocampus relative to its wild-type control mouse brain. Deficiency in MsrA activity fosters oxidative-stress that is manifested by the accumulation of faulty proteins (via methionine oxidation), deposition of aggregated proteins, and premature brain cell death
brenda
a large degree of colocalization between transient receptor potential vanilloid type 1 and NAPE-PLD or fatty acid amide hydrolase, cycloxygenase-2, 12-lipoxygenase and catechol-O-methyltransferase is found in the hippocampal pyramidal neurons of the CA3 area of the Ammons horn and (with the exception of 12-lipoxyghenase) in some Purkinje cells
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a statistically significant induction of 8-oxo-dGTPase by 137Cs gamma radiation (given as a single whole-body dose (1 Gy/min)) is found in brains, testes and kidneys but not in lungs, hearts or livers
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abundant mRNA expression
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AC9
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ACAT1 expression
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AceCS2, low activity
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acitvity only 1% of activity in liver
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Acot7 is expressed mainly in brain and testis of male mice. In female mice, mRNA expression of Acot7 isoforms is highest in brain, lung, kidney, heart and ovary
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activity detected in almost all of the mouse organs, with higher specific activities in brain, kidney, and testis
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activity in brain is much lower than in liver
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activity is the highest in spinal cord and brain followed by thymus, adrenal gland, heart, and genital organs
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-
acyl-CoA hydrolase expression is unaffected by the lack of R-synuclein
brenda
adult
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adult and embryonic, very low Bco1 expression level
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adult and newborn
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adult/post-natal brain
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-
ALA-S activity is induced by acute administration of anaesthetics (89%), veronal (240%), and ethanol (80). ALA-S mRNA expression augmented by chronic administration of eflurane, allylisopropylacetamide and veronal
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all 9 membrane-associated adenylate cyclases
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almost all regions of mouse brain possess CerK activity, with activity especially concentrated in the cerebellum
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AMPK is widely expressed throughout the brain, including several areas controlling food intake and neuroendocrine function
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amygdala
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analysis of 3alpha-HSOR mRNA distribution in the mouse brain by in situ hybridization has shown that this enzyme is co-localized with 5alpha-R type 1 in neurons of the cerebral cortex, hippocampus, olfactory bulb, amygdala and thalamus. And 3alpha-HSOR immunoreactivity is largely distributed in both white and gray matters
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analysis of enzyme mRNA expression, transcript of approximately 2 kb length dominant
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analysis of the cellular localization of KMO in the mouse brain
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and white adipose tissue, highest expression level
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AOH2 and AOH3 mRNAs are expressed in the brain at much lower levels than AOX1 and AOH1
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astrocyte glia, activation of enzyme by glutamate neurotransmission involving alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptors
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at early postnatal stages ADK immunoreactivity is prominent in neurons, notably in cerebral cortex and hippocampus. Thereafter, adenosine kinase gradually disappears from neurons and appears in newly developed nestin- and glial fibrillary acidic protein-positive astrocytes. The region-specific downregulation of neuronal adenosine kinase coincides with the onset of myelination. After postnatal day 14, the transition from neuronal to astrocytic ADK expression is complete, except in a subset of neurons that retain ADK until adulthood in specific regions, such as the striatum
brenda
ATP7A expression is most abundant in the early postnatal period, reaching peak levels at P4 in neocortex and cerebellum. In the developing and adult brain, ATP7A levels are greatest in the choroid plexus/ependymal cells of the lateral and third ventricles. ATP7A expression decreases in most neuronal subpopulations from birth to adulthood. ATP7A expression increases in CA2 hippocampal pyramidal and cerebellar Purkinje neurons
brenda
autotaxin beta is expressed in brain and peripheral tissues. Tissue distribution of the three isoforms alpha, beta, and gamma
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autotaxin gamma is expressed in brain and peripheral tissues. Tissue distribution of the three isoforms alpha, beta, and gamma
brenda
barely detectable levels
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-
brain acyl-CoA hydrolase localizes in neurons, but not in glial cells
brenda
brain of embryo, increase of SULT4A1 expression as neurons maturate. SULT1A1 protein is only detected in adult brains
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brain-specific cytochrome P450 enzyme
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brain-specific enzyme
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-
brain-specific isozyme
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-
brain-specific PFK2 isozyme
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-
broadly distributed
brenda
Capn5 is expressed in the granule cell layers of the hippocampus and cerebellum. There is scattered expression in pons. The visual cortex shows faint signal. Most signal in the brain is in a punctate pattern
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carbonic anhydrase XIII
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carbonic anhydrase XIV
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carbonic anhydrase XV
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-
caspase-11 is upregulated in a subpopulation of cells i brain after ischemic injury
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caudate-putamen and claustrum of the basal ganglia
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CCP5 RNA levels are about 100times higher in testis than cerebellum or brain
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-
CD38-deficient strain
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central and peripheric nervous system, brain-specific isozyme
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-
cerebellar cortex Bergmann glia
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CerS5 mRNA is detected in most cells within gray and white matter of all brain regions
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cleavage products of BACE1 determined, sodium-current densities reduced in neuroblastoma cells and hippocampal cells of transgenic mice
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cleaved caspase-8 is detected in apoptotic cells in the brain
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-
coexpression with Hsp90
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comparative analysis of enzyme activities and mRNA level of Pin1 and other prolyl cis/trans isomerases
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complex I content is 19 pmol/mg of protein in the brain mitochondria
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-
contains a functional glucose-6-phosphatase complex capable of endogenous glucose production from glucose 6-phosphate, independent of blood glucose
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cortex, very low activity
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-
cortical layers
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-
corticohippocampal region
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CYP46A1 is specifically expressed in the brain received in revised form where it controls cholesterol elimination by producing 24S-hydroxylcholesterol as the accepted major metabolite
brenda
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cytochrome-c oxidase activity is abnormal in cerebellar cortex, dentate nucleus, and brainstem regions of Girk2(Wv) (Weaver) mutant mice. Metabolic alterations in cerebellar and vestibular regions are linearly correlated with poor motor coordination
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cytosolic and nuclear extracts of mouse brain tissues
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cytosolic brain-type cratine kinase
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cytosolic brain-type creatine kinase, the CK energy buffering and shuttle system seems to operate in many brain cells, in particular in the polarized large cells like neurons or hair bundle and photoreceptor cells in the sensory organs
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Dcp2 is present in embryonic brain, heart, liver, and kidney. A substantial decrease of Dcp2 is evident in heart, liver, and kidney at birth and a continual decrease to undetectable levels in the adult
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DDX17 transcripts are abundant in rat brains in early embryonic stages and becomes downregulated in late post-natal and adults, suggesting involvement during neuronal differentiation during development of the central nervous system
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developing postnatal and embryonic
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developmental regulation of autotaxin 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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-
DGKalpha
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-
distribution in brain regions, overview
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-
dorsal striatum and nucleus accumbens show a high content of isozyme AC5
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-
dorsal thalamus
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during brain development in mouse, Naa10 and Naa15 (the auxiliary subunit of NatA) are highly expressed in regions rich in proliferating and migrating cells, such as the ventricular zone, neocortex, olfactory bulb, and hippocampus. The expression of both genes is downregulated as neurons differentiate and mitotic and migratory activities subside. Then, once again, their expression increases during postnatal development in the hippocampus and during the neuronal dendritic development of Purkinje cells (PCs) in the cerebellum. This finding indicates that the regulation of expression of both genes is related to neuronal development, especially in the hippocampus and in the PCs of the cerebellum
brenda
early postnatal brain
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-
embryo
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embryo, expression pattern in the ventricular zone changes between embryonic day 14 and 16, which corresponds to the transition from neurogenesis to gliogenesis. At embryonic day 14, UCH-L1 is highly expressed in the ventricular zone, where neurogenesis actively occurs, whereas its expression is prominent in the cortical plate at embroynic day 16. UCH-L1 is very weakly detected in the ventricular zone at embryonic day 16, which corresponds to the start of gliogenesis. UCH-L1 spatially mediates and enhances neurogenesis in the embryonic brain by regulating progenitor cell morphology
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embryonic
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-
embryonic brain
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embryonic, low Bco2 expression level
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embryonic, postnatal, and adult brains
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embryonic, UCH-L1 expression in the ventricular zone changes during neurogenesis and gliogenesis, high expression level in cortical plate and ventricular zone, overview
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enzyme activity in triple transgenic Alzheimer's disease mice. Expression of TDO mRNA is significantly increased in the cerebellum of Alzheimer's disease mouse brain
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enzyme expression in the subventricular neural progenitor cells, but not in differentiated neurons. The subventricular neural progenitor cells also show a decline in Phgdh expression in type B and C cells in the aged brain
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enzyme GlcNAc-6-sulfated KS is recognized by the R-10G anti-KS antibody, of which the minimum epitope structure is Galbeta1-4GlcNAc(6S)beta1-3Galbeta1-4GlcNAc(6S), and distributes diffusely in neuropils and presents densely in close proximity to the perineuronal region of the perineuronal net (PNN)-positive neurons in the adult visual cortex
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enzyme is expressed preferentially in the white matter bundles of the entire central nervous system of adult mice with less marked expression inneuronal cell bodies. The enzyme co-localizes with myelin basic protein in myelin sheaths but not in axons
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enzyme is highly expressed in mature brain. Expression of CDK5 is already seen at embryonal 12.5 days, and it gradually increases through the embryonal stage. After birth, the expression is maintained at a high level to adulthood
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enzyme isoform I and 3alpha-hydroxysteroid dehydrogenase colocalize in hippocampal and olfactory bulb glutamatergic principal neurons and in some output neurons of amygdala and thalamus. Neither enzyme is expressed in S100beta- or glial fibrillary acidic protein-positive glial cells. Both enzymes are significantly expressed in principal GABAergic output neurons
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enzyme mRNA is up-regulated in mouse model of globoid cell leukodystrophy or Krabbes disease, of Tay-Sachs disease, Sandhoff disease, GM1 gangliosidosis and Niemann-Pick type C1 disease,. Oligodendrocytes of all these mouse models show strong immunoreactivity for enzyme, but not astrocytes or microglia
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ependymal cells
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equal expression of CCT alpha and CCT beta
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especially in frontal and temporal cortex, with the striatum having the maximal specific activity. Both the level of L-pipecolate and P2C/Pyr2C reductase-specific activity differed considerably among the different brain regions
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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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except for the olfactory bulb and cerebellum, but including the hippocampal CA1 area
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exclusive expression of isoform CTE-II
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expressed at relatively low levels in brain
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expressed exclusively in brain, adrenal gland and testis
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expressed in all regions
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expressed in all regions, high expression levl in cortex
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expressed in the forebrain limbic area of adult brain
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expressed within the brain, both during development and in adulthood
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expression and morphological analyses of PIK3C3 during mouse brain development, overview
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expression at low level
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expression at low levels
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expression detected by RT-PCR
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expression during embryonic brain development
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expression in a neuron-specific manner. The level of the major 43000 Da isoform is low until embryonic day 12.5, elevates to a peak 7 days after birth. Thereafter, it declines somewhat and reaches a steady-state level in adulthood
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expression in many parts of the developing mouse brain, in the adult brain it is expressed exclusively and abundantly in the hippocampus
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expression in white matter. Time course of expression in brain closely follows the expression of myelin-specific genes, reaching a maximum at 2-3 weeks of age
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expression levels of PAD2 protein as well as its enzyme activity are significantly increased in brain sections of Scrapie-infected mice, including hippocampus, brain stem, and striatum
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expression of alpha-I and alpha-II subunits mRNAs
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expression of ATP7A, not of ATP7B
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expression of CaMKI, CaMKII alpha, beta, gamma and delta, and CaMKIV
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expression of full-length ASPA at embryonic day 12.5, when oligodendrocyte progenitors first appear during development
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expression of GRK4 in the brain is limited to cerebellar Purkinje cells
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expression of HGO gene
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expression of isozyme CTE-I, not MTE-I
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expression of PanK2 is higher in human brain compared to mouse brain
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expression of sEH is significantly increased on day 7, 14, 21 and 28 after pilocarpine-induced status epilepticus
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expression of serine racemase and of protein interacting with C-kinase, PICK1 are developmentally regulated. In neonatal mice with knock-out of protein interacting with C-kinase, PICK1 the levels of D-serine are selectively decreased in the forebrain
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expression of the enzyme in all brain regions
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expression on brain occurs in different cells as macrophages, microglia, neurons and astrocytes
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expression pattern in frontal brain nuclei during murine embryogenesis
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expression pattern in mouse brain of TyrRS and KTP synthesis after Arg administration
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expression pattern of the enzyme in brain tissues
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extracellular matrix
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fatty liver dystrophy mice contain dramatically lower levels of Mg2+-dependent PAP activity than wild-type mice
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fetal brain
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fetal cholinergic basal forebrain
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fetal, high expression
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fifteen albino Swiss mice between the 22nd and 55th post-natal days are exercised in the following modalities: voluntary (V), acrobatic (A), acrobatic/voluntary (AV) and forced (F) and compared to inactive group (I). The A group presented higher NADPH-d activity in the cerebellar granular layer than all other groups
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forebrain cholinergic neurons
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from healthy mice and from mice infected with 139A scrapie
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from ME7-infected mice
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frontal cortex
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FRRS1L is a component of native AMPAR complexes in the brain
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GCPII
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GDE2 mRNA
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geldanamycin inhibits hemorrhage-induced increases in caspase-3 activity
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glial cells of brain, highest levels of enzyme in astrocyte-enriched cultures
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GLUD1 expression analysis
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gracile axonal dystrophy is a syndrome that emanates from dysfunctional ubiquitin carboxyl-terminal hydrolase L-1
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granule cells isolated from cerebellum
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group IIE sPLA2
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hexokinase I
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high abundance
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high 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 expression level
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high expression
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high expression in oligodendrocytes and olfactory ensheathing glia, moderate expression in astrocytes, low expression in neurons and microglia
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high expression level
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high expression level of calcineurin
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high expression level of MKK4, expression in adult and fetal brain
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high expression level, D-aspartate is abundant in the embryonic brain, but drastically decreases during postnatal development. The enzyme is located in the paraventricular and supraoptic nuclei, the cerebral cortex, the hippocampus, the dentate gyrus, the pineal gland, and the posterior pituitary gland
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high mRNA expression
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high protein expression level, neural and glial cells are positively stained
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higher aromatase expression in female compared with male cerebral vessels
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higher expression level of SULT2B1
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higher expression of isozyme IP3-3KB
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highest activity
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highest activity in the spinal cord and brain
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-
highest ALDH7A1 expression
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-
highest enzymatic activity is detected in ventral brain, followed by cortex and hippocampus
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-
highest enzyme level
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highest expression
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highest expression in testis, followed by eye, liver, skeletal muscle, heart, 7-day embryo, kidney, ovary, and brain in decreasing order
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-
highest expression level
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highest expression level. Dcp2 can be detected in the brain at all the developmental stages tested
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highest levels measured in brain and testis (4-8 times higher than in the remaining tissues)
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highest levels of expression
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highest levels of expression in bone marrow, brain, spleen and kidney
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highest levels of expression in bone marrow, brain, spleen, kidney, and lens
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highest levels of tyro3 expression in neurons
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highest POP protein densities are found in brain, kidney, testis and thymus
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highly expressed
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highly expressed during the embryonic development of the brain and decreases in the late brain development
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highly expressed in cortical and hippocampal regions and enriched in the synaptosomal membrane fraction
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highly expressed in periventricular neural progenitors in the embryonic brain
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highly expressed in the mouse brain compared to plasma and liver
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hippocamus
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hyperphosphorylation in hippocampal and cerebral regions, weak in the cerebellum
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hypotaurine is not in brain of either Vanin-1 (+/+) or Vanin-1 (-/-) mice that had been fed a non-purified rodent diet.
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hypothalamus
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IDO2
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ifMMP8 expression is upregulated in brains with cerebral ischemia
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immunohistochemic analysis of the enzyme in wild-type and mutant mouse brains, overview
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in a murine model of absent securin expression, the PTTG knock-out mouse, separase and Rad21 are over-expressed in multiple brain regions. Furthermore, Rad21 mRNA expression is highly correlated with that of securin, separase, cyclin C and sestrin 2 in fetal brains
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in adult brain Kiz-1 is expressed exclusively in neurons, not in astrocytes or oligodendrocytes. In the developing embryo, Kiz-1 is expressed in all tissues
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in adult the gene is expressed almost exclusively in the brain
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in brain DPIV represents 22% of the total Gly-L-Pro-4-nitroanilide-hydrolyzing activity
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in brain nuclear beta-galactosidase expression in neurons located in prominent catecholaminergic cell groups such as substantia nigra and locus coeruleus, in the ventral part of the hypothalamus, in the hippocampus and in the amygdala. nuclear and cytoplasmic beta-galactosidase expression in germinal periventricular layer
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in enzyme-deficient strain, accumulation of amyloid beta-protein
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in middle-aged female Mth1/Ogg1-double knockout mice 8-oxoguanine accumulation significantly increases in nuclear DNA, particularly in the dentate gyrus, subventricular zone and major island of calleja. Neurogenesis is severely impaired in subventricular zone and dentate gyrus, accompanied by major island of calleja and dentate gyrus atrophy
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in mouse brain regions, e.g. cortex, hippocampus, striatum, and midbrain, both UCH-L1M and UCH-L1S occur in varying relative amounts
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in raphe nuclei, in lateral hypothalamic nuclei and in pineal body
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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. In situ activity of isoform TG6 varies between BACHD mice in comparison to their wild-type controls. TG6 protein expression is prominent in the brains of mice
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in situ hybridisation of phosphatidylinositol 4-phosphate 5-kinase Igamma_v6 splice variant, which is not a major brain variant
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in situ hybridization experiments, developing mouse brain
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in the adult mouse brain, Rab23 is detected in betaIII tubulin positive neuronal cell bodies and are most prominent in cortex, hypothalamus and the cerebellum
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in the brain, H2S signal termination occurs partially through protein sequestration and partially through catabolism not involving sulfide:quinone reductase
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in the brain, only Oas1a, Oas1b, and Oas1g are expressed in the mice stimulated with poly I:C
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in the brain, PDE4D11 expression levels increase in the cerebellum, but decrease in the hippocampus with progressive age
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in the brain, where CSE levels are low, localizations are predominantly in white matter
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in the developing brain, Lfng is expressed in self-renewing progenitors
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in vascular smooth muscle and endothelial cell layersm in white matter. sEH in rodent brain is neither vascular nor glial, but rather neuronal. In brain parenchymal tissue, sEH is markedly expressed in neuronal cell bodies and processes, particularly within the cerebral cortex and striatum
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is largely confined to the brain, neuron-specific expression
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ischemic region, contralateral cortex
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isoform DS-epi2 is mostly expressed in the brain during postnatal development
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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 PDK2 is predominantly expressed in the arcuate nucleus at high levels but not in other areas of diabetic mouse brain
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isoform PI5P4Kalpha is expressed in adulthood, whereas isoform PI5P4Kbeta is expressed early in development
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isoform SCD-2 is predominantly expressed in brain
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isoform SMSr is the principal CPE synthase in the brain
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isoform-specific hyperactivation of calpain-2, but not calpain-1 occurs at the synapse early in the pathogenesis of Alzheimer's disease potentially contributing to the deregulation of synaptic signaling in Alzheimer's disease
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isoforms AC7 and AC9
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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 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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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 AC1
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isozyme AC1 is abundantly expressed within limbic regions of the central nervous system
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isozyme AC2
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isozyme AC3
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isozyme AC5 is abundantly expressed within limbic regions of the central nervous system
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isozyme AC6
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isozyme AC8 is abundantly expressed within limbic regions of the central nervous system
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isozyme AC8, high expression level of isozyme AC8 in numerous brain regions, including the hippocampus, thalamus, habenula, cerebellar cortex and hypothalamic supraoptic and paraventricular nuclei
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isozyme CaMKIgamma, high expression level
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isozyme CCTbeta2
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isozyme mPA-PLA1alpha
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isozyme P3H3
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isozyme type II
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isozymes dymain 1, dymanin 2, and dynamin 3
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isozymes L1, specific for neuronal cells, testis and ovary, and L3
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isozymes SEP and SEPDELTA
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isozymes SPHK1 and SPHK2
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ITPKA is mainly expressed in pyramidal cells of the hippocampal CA1 region and granule cells of the dentate gyrus
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Itpka is particularly active in neurons of the hippocampus and cerebellum
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less expression
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lesser expression of NPP6
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-
levels of SCHAD/HADII are significantly reduced in the ventral midbrain of a Parkinsons disease mouse model
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lipin-1
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lipin-1, whereas lipin-1alpha is the predominant form
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lipin-2, in the cortex, hippocampus, thalamus, and hypothalamus
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-
localization of LOX and LOXL in different tissue areas
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-
localized exclusively in neurons
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low abundance of mRNA
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low activity
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low amounts of NOX3
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low content
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low distribution in brain
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-
low enzyme content
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-
low enzyme expression
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low expression
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low expression level
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low expression level of CerS2
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low expression levels
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-
low expression of Acot12
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-
low expression, 1.96fold higher than in liver
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-
low level of isozyme T4
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-
low levels of adenosine kinase are essential to maintain adenosine-mediated endogenous neuroprotection and pathologic increases in ADK may render the brain more susceptible to injury
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low mRNA expression
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low Pcyt2 mRNA content
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-
low, but definite, levels of Gb3/CD77 are expressed in the microvascular endothelial cells of the brain cortex
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lowenzyme activity
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lower expression level
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Ltk is expressed in adult, but not in embryonic brain, in neurons of the cerebral cortex and hippocampus, but not in the cerebellum
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lymphoid ltk uses a CUG translational start codon and has a 110 amino acid putative extracellular domain. The predominant ltk mRNA in brain is alternatively spliced and predicts a protein with a substantially larger extracellular part
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m-RNA expression
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mAGPAT1, mAGPAT2, mAGPAT3, mAGPAT2 is undetectable, mAGPAT4 is expressed at high levels, mAGPAT5 expressed at high levels
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major isozyme brain acyl-CoA hydrolase, enzyme expression level during pre- and post-natal brain development
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major isozyme is CTE-I, poor expression of MTE-I, expression of PTE-Ia, no expression of PTE-Ib
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major isozyme is SPHK1
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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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measuring of the spatial and temporal pattern of enzyme expression in vivo during neocortical neurogenesis. Enzyme is expressed in all layers of the dorsal telencephalon in E10.5. At E15.5 and E17.5, expression is primarily localized to the ventricular zone. Blocking endogenous enzyme by RNAi decreases proliferation of embryoic cortical neural progenitor cells. In adult brain, strong expression is observed in rostral migratory stream and septum. Overexpression of enzyme in subventricular zone cells of adult mice significantly increases the number of cells, whereas silencing Dct enzyme by RNAi decreases the cell number
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medial habenular nucleus and lateral habenular nucleus of the habenula
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medial septum, vertical diagonal band,substantia inominata, eye field, posterior parietal and visual cortices, posterior thalamic and lateral geniculate nuclei, hippocampal formation and amygdala, midline, periventricular, reticular thalamic nuclei, and lateral prefrontal, agranular insular cortices
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median eminence and preoptic area in close proximity with LHRH cell bodies
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mEH distribution, immunohistochemical analysis, overview. mEH immunoreactivity is present in specific neuronal populations of the hippocampus, striatum, amygdala, and cerebellum, as well as in a fraction of astrocytes
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membrane preparations of frontoparietal cortex, striatum, and hippocampus isolated from the ischemic hemisphere of mouse brain 24 h after reperfusion reveal a statistically significant over 2fold increase in quantity and activity of neurolysin compared with sham-operated controls, no effect on the cerebellar enzyme activity. Functional up-regulation of neurolysin in frontoparietal cortical membranes for at least 7 days after stroke appears not to be transcriptionally or translationally regulated, but rather depends on translocation of cytosolic neurolysin to the membranes and mitochondria
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membranes isolated from mouse brain with endogenous reduced levels of cholesterol due to targeted deletion of one seladin-I allele show a reduced amount of IDE
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meprin beta co-fractionates with APP and PS1 in the same high molecular weight fraction in wild-type mouse brains, and this fraction is responsible for the majority of Abeta generation
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methyltransferase KMT2A and demethylase KDM5C co-exist in the brain, expression patterns of KMT2A and KDM5C show that the two genes are broadly expressed throughout brain regions of adult mice. Developing and aging human brains express KMT2A and KDM5C at high, steady levels
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MGL is expressed in central and peripheral axons of the fetal nervous system by embryonic day 12.5. MGL coexists with sn-1-diacylglycerol lipase alpha and CB1 cannabinoid receptors in corticofugal axons of pyramidal cells
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moderate activity
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moderate expression
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-
mouse embryonic brain tissue (E18.5) is examined
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-
mPEGS-2
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mRNA expression
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mRNA level of isoform Rdh10 declines during development, with strong and lasting expression in the meninges and choroid plexuses. Expression is also present in the striatum
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Msr activity is significantly reduced by Se deficiency
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MsrA-/- mice have compromised complex task learning capabilities relative to wild-type mice. MsrA-/- mice exhibit lower locomotor activity and altered gait that exacerbate with age. MsrA-/- mice are less responsive to amphetamine treatment. Relative to wild-type mice, MsrA-/- brains contain significantly higher levels of dopamine up to 12 months of age, while lower levels of dopamine are observed at 16 months of age. Striatal regions of MsrA-/- mice show an increase of dopamine release parallel to observed dopamine levels. It is suggested that dopamine regulation and signaling pathways are impaired in MsrA-/- mice, which may contribute to their abnormal behavior
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much of the enzyme is localized to myelin
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-
mutant brains expressing the Swedish mutant precursor of amyloid beta-peptide, enzyme level, activity and distribution, immunohistochemic analysis, overview
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NAPE-PLD is expressed by specific populations of neurons in the brain and targeted to axonal processes. In the dentate gyrus a strong mRNA signal is detected in granule cells. Immunocytochemical analysis reveales intense NAPE-PLD immunoreactivity in the axons of granule cells (mossy fibers) and in axons of the vomeronasal nerve that project to the accessory olfactory bulb. NAPE-PLD expression is detected in hippocampus, cortex, thalamus, hypothalamus, but the intensity of immunostaining is weaker than in mossy fibers
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neonatal and adult brain. Brain content of cyclic ADP-ribose is independent of the presence of enzyme
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neprilysin specific activity varies across mouse strains, with the highest activities in kidney and brain of SW mice. Aging is associated with a reduction in brain neprilysin specific activity in SW strain and C57B1/6J strain. The aging- and strain-dependent differences in neprilysin specific activity may explain, at least in part, the roles that aging and background mouse strain play in differential specification of the susceptibility towards the development of cerebral Abeta amyloidosis
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nerve fiber
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neuolastin is specifically expressed in the brain
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-
neuron-specific expression of UCH-L1
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neuronal membrane, carbonic anhydrase XIV
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-
newborn and adult mucopolysaccharidosis type IIIA brain cells have approximately 5.7% of the sulfamidase activity present in primary neural cells cultured from unaffected newborn and adult mice
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-
Nmnat2 transcript is expressed predominately in the brain
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of 11-, 15- and 17-day embryos
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of adult and developing animals, particularly in the ventricular layer of the cerebral cortex at embryonic stages
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-
of newborn mice, and adult brain cortex and stem, GLS1
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of the embryo
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of young and old mice, comparison of enzyme expression and activity in brain regions, e.g. cortex, hippocampus and cerebellum, overview
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overexpression to the forebrain, essentially the subfornical organ, inhibits both pressor and drinking responses resulting from intracerebroventricular administration of Ang-II
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-
oxidative stress in brain induces expression of MTH1 especially in microglia, thus avoiding cellular dysfunction
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-
p38 MAPK is expressed predominantly in nestin-positive cells in the cerebral cortex in embryonic day 10 brain, the expression of the protein decreases gradually during development
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-
PC2 is the most abundant PC in the brain
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PDE1B, highest expression in brain
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-
PDE4B5 is brain-specific
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PDE7A1
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-
pericyte
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-
Phgdh is constitutively expressed in the brain
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-
PKCepsilon regulates the expression of ECE-1 in the brain
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-
PLC-eta1
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PLC-eta2
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PLCeta2 is restricted to brain. PLCeta2 gradually increases during brain development. PLCeta2 is not detected in embryos. At 1 week after birth PLCeta2 is barely detected and expression is first observed at weeks after birth
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PMCA1 is ubiquitous, but is expressed most abundantly in brain, lung and intestine. The PMCA3 and PMCA4 pumps are expressed in brain, the PMCA2 pump is a brain isoform.
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-
ppGalNAc-T13 expression only in brain, exclusively in neuronal cells
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-
PPT1 is localized in the presynaptic compartment
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-
PRDM8 of 70 kDa
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predominant expression of splice variant PMCA4e
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predominantly expressed in
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predominantly expressed in testis, followed by ovary, brain, and stomach
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predominantly in neurons
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predominantly, high expression level of LPEAT2, expression pattern analysis, overview. mLPEAT2 is expressed in all regions, with a comparatively high expression in the cortex
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preferentially expressed in brain
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-
prefrontal cortex and dorsal hippocampus
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primary hippocampal neuron
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-
primary somatosensory, barrel, cortex
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-
prolonged selenium-deficient diet in MsrA knockout mice lowers thioredoxin reductase activity
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-
prosencephalic region
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-
purkinje cells and deep nuclei of the cerebellum
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-
pyramidal cells of the cerebral cortex
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-
pyramidal cells of the hippocampus
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-
pyroglutamate aminopeptidase II is predominantly localized in neuronal cells
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-
quantitative analysis of Csgalnact1 and Csgalnact2 transcripts in brain of wild-type and Csgalnact1-/- mice by real-time PCR, overview
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quite low activity of isozyme SPHK1 and isozyme SPHK2
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-
red nucleus, Darkschewitsch nucleus and medial parabrachial nucleus of the lower brainstem
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-
reduced levels of UCH-L1 mRNA (30%) and protein in a mouse model of Sandhoff disease as compared with their wild-type siblings
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-
redundancy of enzyme activity
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region- and development-dependent expression of the enzyme
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restricted distribution, strongest expression of the lysosomal enzyme
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restricted expression, Very high in subiculum and pontine nuclei, high in allocortex, granule cell layers of olfactory bulb and hippocampus, medial habenular nucleus, reticular fields, and subcommissural organ
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restricted expression: moderate in several thalamic nuclei and cerebellar Purkinje cell layer
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-
results show that docosahexaenoic acid ethyl ester enhances brain HMG-CoA reductase activity in aged mice
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SCD2 is highly expressed in the brain
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SCD2 is highly localized
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sEH distribution, immunohistochemical analysis, overview. sEH immunoreactivity is almost exclusively located in astrocytes throughout the brain, except in the central amygdala, where neurons are also positive for sEH
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-
senescence-accelerated prone mice 8 and senescence-accelerated resistant mice 1 show a drop in age-related proteolytic activity of caspase-3, overview
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Senp5 is detected in the neuropil but not in cell bodies. Strong Senp5 immunoreactivity is observed in regions with high n