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Organism related
Word Map for Organism Saccharomyces cerevisiae
- Saccharomyces cerevisiae
-
two-hybrid
- kinases
- atpase
- chromatin
- histone
- drosophila
- suppressor
- cryptococcus
- melanogaster
- lactis
- neuron
- repressor
- heme
- sensor
- disulfide
- methionine
- embryonic
- epitope
- flies
- junction
- grape
- motor
- cortical
- neck
- phagocytic
- agonist
- vaginal
- leukocyte
- mucosal
- fumigatus
- adenosine
- passage
- nadph
- pancreatic
- dendritic
- barley
- marrow
- immunogen
- transposon
- listeria
- carcinogen
- clearance
- ethylene
- monocyte
- endothelial
- porcine
- pneumocystis
- bacteriophage
- cardiac
- flour
TaxTree of Organism Saccharomyces cerevisiae
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EC NUMBER 
COMMENTARY 
-
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
transferred to EC 3.6.1.71
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
preliminary BRENDA-supplied EC number
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PATHWAY
BRENDA Link
KEGG Link
MetaCyc Link
(+)-camphor biosynthesis
-
-
PWY-6990
(-)-glycinol biosynthesis
-
-
PWY-2761
(-)-maackiain biosynthesis
-
-
PWY-2464
(-)-medicarpin biosynthesis
-
-
PWY-2463
(1'S,5'S)-averufin biosynthesis
-
-
PWY-5954
(1,3)-beta-D-xylan degradation
-
-
PWY-6789
(1,4)-beta-D-xylan degradation
-
-
PWY-6717
(3E)-4,8-dimethylnona-1,3,7-triene biosynthesis II
-
-
PWY-6007
(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
(R,R)-butanediol biosynthesis
-
-
PWY-5951
(R,R)-butanediol degradation
-
-
PWY3O-246
(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 I
-
-
PWY-3581
(S)-reticuline biosynthesis II
-
-
PWY-6133
(S,S)-butanediol biosynthesis
-
-
PWY-6390
(S,S)-butanediol degradation
-
-
PWY-6388
(Z)-butanethial-S-oxide biosynthesis
-
-
PWY-6900
(Z)-phenylmethanethial S-oxide biosynthesis
-
-
PWY-6539
1,2-dichloroethane degradation
-
-
12DICHLORETHDEG-PWY
1,2-propanediol biosynthesis from lactate (engineered)
-
-
PWY-7541
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-oxyandrogens biosynthesis
-
-
PWY-8202
15-epi-lipoxin biosynthesis
-
-
PWY66-393
1D-myo-inositol hexakisphosphate biosynthesis I (from Ins(1,4,5)P3)
-
-
PWY-6361
1D-myo-inositol hexakisphosphate biosynthesis II (mammalian)
-
-
PWY-6362
1D-myo-inositol hexakisphosphate biosynthesis III (Spirodela polyrrhiza)
-
-
PWY-4661
1D-myo-inositol hexakisphosphate biosynthesis IV (Dictyostelium)
-
-
PWY-6372
1D-myo-inositol hexakisphosphate biosynthesis V (from Ins(1,3,4)P3)
-
-
PWY-6554
2'-deoxymugineic acid phytosiderophore biosynthesis
-
-
PWY-5912
2,3-cis-flavanols biosynthesis
-
-
PWY-6035
2,3-dihydroxybenzoate biosynthesis
-
-
PWY-5901
2,3-trans-flavanols biosynthesis
-
-
PWY-6029
2,4,5-trichlorophenoxyacetate degradation
-
-
PWY-6200
2,4-dichlorotoluene degradation
-
-
PWY-6190
2,4-dinitrotoluene degradation
-
-
PWY-5642
2,5-dichlorotoluene degradation
-
-
PWY-6191
2,5-xylenol and 3,5-xylenol degradation
-
-
PWY-7698
2-amino-3-carboxymuconate semialdehyde degradation to 2-hydroxypentadienoate
-
-
PWY-5654
2-amino-3-carboxymuconate semialdehyde degradation to glutaryl-CoA
-
-
PWY-5652
2-amino-3-hydroxycyclopent-2-enone biosynthesis
-
-
PWY-7536
2-aminoethylphosphonate degradation I
-
-
PHOSPHONOTASE-PWY
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-hydroxypenta-2,4-dienoate degradation
-
-
PWY-5162
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
2alpha,7beta-dihydroxylation of taxusin
-
-
PWY-7065
3,4,6-trichlorocatechol degradation
-
-
PWY-6094
3,4-dichlorotoluene degradation
-
-
PWY-6192
3,5-dichlorocatechol degradation
-
-
PWY-6084
3,5-dimethoxytoluene biosynthesis
-
-
PWY-7076
3,6-anhydro-alpha-L-galactopyranose degradation
-
-
PWY-7562
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-chlorobenzoate degradation III (via gentisate)
-
-
PWY-6228
3-chlorocatechol degradation I (ortho)
-
-
PWY-6089
3-chlorocatechol degradation II (ortho)
-
-
PWY-6193
3-chlorotoluene degradation II
-
-
PWY-6104
3-dehydroquinate biosynthesis I
-
-
PWY-6164
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-oxoadipate degradation
-
-
PWY-2361
3-phenylpropanoate degradation
-
-
P281-PWY
3-phosphoinositide biosynthesis
-
-
PWY-6352
3-phosphoinositide degradation
-
-
PWY-6368
4,5-dichlorocatechol degradation
-
-
PWY-6093
4-amino-2-methyl-5-diphosphomethylpyrimidine biosynthesis I
-
-
PWY-6890
4-amino-2-methyl-5-diphosphomethylpyrimidine biosynthesis II
-
-
PWY-7282
4-aminobenzoate biosynthesis I
-
-
PWY-6543
4-aminobenzoate biosynthesis II
-
-
PWY-8276
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-aminophenol degradation
-
-
PWY-7081
4-chlorobenzoate degradation
-
-
PWY-6215
4-chlorocatechol degradation
-
-
PWY-6087
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-hydroxy-4-methyl-L-glutamate biosynthesis
-
-
PWY-7701
4-hydroxybenzoate biosynthesis I (eukaryotes)
-
-
PWY-5754
4-hydroxybenzoate biosynthesis II (bacteria)
-
-
PWY-5755
4-hydroxybenzoate biosynthesis III (plants)
-
-
PWY-6435
4-hydroxyindole-3-carbonyl nitrile biosynthesis
-
-
PWY-8024
4-hydroxymandelate degradation
4-hydroxyphenylacetate degradation
4-methylcatechol degradation (ortho cleavage)
-
-
PWY-6185
4-methylphenol degradation to protocatechuate
-
-
PWY-7700
4-nitrophenol degradation I
-
-
PWY-5487
4-nitrophenol degradation II
-
-
PWY-5488
4-oxopentanoate degradation
-
-
PWY-7948
4-sulfocatechol degradation
-
-
PWY-6041
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-chloro-3-methyl-catechol degradation
-
-
PWY-6102
5-deoxystrigol biosynthesis
-
-
PWY-7101
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 II (Methanocaldococcus)
-
-
PWY-6797
6-hydroxymethyl-dihydropterin diphosphate biosynthesis III (Chlamydia)
-
-
PWY-7539
6-hydroxymethyl-dihydropterin diphosphate biosynthesis IV (Plasmodium)
-
-
PWY-7852
6-hydroxymethyl-dihydropterin diphosphate biosynthesis V (Pyrococcus)
-
-
PWY-7853
6-methylpretetramide biosynthesis
-
-
PWY-7811
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 II
-
-
PWY-7147
8-amino-7-oxononanoate biosynthesis III
-
-
PWY-6578
8-amino-7-oxononanoate biosynthesis IV
-
-
PWY-8203
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
abietic acid biosynthesis
-
-
PWY-5411
abscisic acid biosynthesis
-
-
PWY-695
Ac/N-end rule pathway
-
-
PWY-7800
acetaldehyde biosynthesis I
-
-
PWY-6333
acetaldehyde biosynthesis II
-
-
PWY-6330
acetate and ATP formation from acetyl-CoA I
-
-
PWY0-1312
acetate and ATP formation from acetyl-CoA III
-
-
PWY-8328
acetate conversion to acetyl-CoA
-
-
PWY0-1313
acetate formation from acetyl-CoA (succinate)
-
-
PWY-5536
acetoacetate degradation (to acetyl CoA)
-
-
ACETOACETATE-DEG-PWY
acetone degradation I (to methylglyoxal)
-
-
PWY-5451
acetone degradation III (to propane-1,2-diol)
-
-
PWY-7466
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
actinomycin D biosynthesis
-
-
PWY-7718
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 nucleotides degradation III
-
-
PWY-6617
adenosine ribonucleotides de novo biosynthesis
-
-
PWY-7219
adenosylcobinamide-GDP biosynthesis from cobyrinate a,c-diamide
-
-
PWY-7962
adenosylcobinamide-GDP salvage from assorted adenosylcobamides
-
-
PWY-8282
adenosylcobinamide-GDP salvage from cobinamide I
-
-
PWY-7971
adenosylcobinamide-GDP salvage from cobinamide II
-
-
PWY-7972
adipate biosynthesis
-
-
PWY-8347
adipate degradation
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
agarose degradation
-
-
PWY-6816
ajmaline and sarpagine biosynthesis
-
-
PWY-5301
alanine racemization
-
-
PWY-8072
aldoxime degradation
-
-
P345-PWY
alginate biosynthesis I (algal)
-
-
PWY-6073
alginate biosynthesis II (bacterial)
-
-
PWY-6082
alginate degradation
-
-
PWY-6986
alkane biosynthesis I
-
-
PWY-7032
alkane biosynthesis II
-
-
PWY-7033
alkane oxidation
-
-
PWY-2724
alkylnitronates degradation
-
-
PWY-723
all-trans-decaprenyl diphosphate biosynthesis
-
-
PWY-5806
all-trans-farnesol biosynthesis
-
-
PWY-6859
allantoin degradation IV (anaerobic)
-
-
PWY0-41
allantoin degradation to glyoxylate I
-
-
PWY-5694
allantoin degradation to glyoxylate II
-
-
PWY-5692
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
alpha-amyrin biosynthesis
-
-
PWY-5377
alpha-carotene biosynthesis
-
-
PWY-5946
alpha-dystroglycan glycosylation
-
-
PWY-7981
alpha-linolenate biosynthesis I (plants and red algae)
-
-
PWY-5997
alpha-linolenate biosynthesis II (cyanobacteria)
-
-
PWY-7598
alpha-linolenate metabolites biosynthesis
-
-
PWY-8398
alpha-tocopherol degradation
-
-
PWY-6377
alpha-tomatine degradation
-
-
PWY18C3-5
Amaryllidacea alkaloids biosynthesis
-
-
PWY-7826
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 I (aerobic)
-
-
AMMOXID-PWY
ammonia oxidation II (anaerobic)
-
-
P303-PWY
ammonia oxidation III
-
-
PWY-2242
amygdalin and prunasin degradation
-
-
PWY-6011
anaerobic aromatic compound degradation (Thauera aromatica)
-
-
BENZCOA-PWY
anaerobic energy metabolism (invertebrates, cytosol)
-
-
PWY-7383
anaerobic energy metabolism (invertebrates, mitochondrial)
-
-
PWY-7384
anandamide biosynthesis I
-
-
PWY-8051
anandamide biosynthesis II
-
-
PWY-8053
anandamide degradation
-
-
PWY6666-1
anandamide lipoxygenation
-
-
PWY-8056
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
anthocyanidin modification (Arabidopsis)
-
-
PWY-7450
anthocyanidin sambubioside biosynthesis
-
-
PWY-7678
anthocyanin biosynthesis
-
-
PWY-5125
anthocyanin biosynthesis (delphinidin 3-O-glucoside)
-
-
PWY-5153
anthocyanin biosynthesis (pelargonidin 3-O-glucoside)
-
-
PWY-7267
apigeninidin 5-O-glucoside biosynthesis
-
-
PWY-7253
apratoxin A biosynthesis
-
-
PWY-8361
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
archaetidylinositol biosynthesis
-
-
PWY-6350
Arg/N-end rule pathway (eukaryotic)
-
-
PWY-7799
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
arsenate reduction (respiratory)
-
-
PWY-4601
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
arsonoacetate degradation
-
-
P482-PWY
artemisinin and arteannuin B biosynthesis
-
-
PWY-5195
ascorbate glutathione cycle
-
-
PWY-2261
ascorbate recycling (cytosolic)
-
-
PWY-6370
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
aucuparin biosynthesis
-
-
PWY-7739
aureothin biosynthesis
-
-
PWY-8033
autoinducer AI-2 biosynthesis I
-
-
PWY-6153
autoinducer AI-2 biosynthesis II (Vibrio)
-
-
PWY-6154
avenacin A-1 biosynthesis
-
-
PWY-7473
avenanthramide biosynthesis
-
-
PWY-8157
bacilysin biosynthesis
backdoor pathway of androgen biosynthesis
-
-
PWY-8200
bacterial bioluminescence
-
-
PWY-7723
baicalein degradation (hydrogen peroxide detoxification)
-
-
PWY-7214
baicalein metabolism
-
-
PWY-7212
baruol biosynthesis
-
-
PWY-6008
base-degraded thiamine salvage
-
-
PWY-6899
benzoate biosynthesis I (CoA-dependent, beta-oxidative)
-
-
PWY-6443
benzoate biosynthesis II (CoA-independent, non-beta-oxidative)
-
-
PWY-6444
benzoate biosynthesis III (CoA-dependent, non-beta-oxidative)
-
-
PWY-6446
benzoate degradation I (aerobic)
-
-
PWY-2503
benzoate degradation II (aerobic and anaerobic)
-
-
PWY-283
benzoyl-CoA biosynthesis
-
-
PWY-6458
benzoyl-CoA degradation I (aerobic)
-
-
PWY-1361
benzoylanthranilate biosynthesis
-
-
PWY-6323
berberine biosynthesis
-
-
PWY-3901
bergamotene biosynthesis I
-
-
PWY-6243
bergamotene biosynthesis II
-
-
PWY-6244
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 degradation III
-
-
PWY-8120
beta-carboline biosynthesis
-
-
PWY-5877
beta-carotene biosynthesis
-
-
PWY-5943
beta-caryophyllene biosynthesis
-
-
PWY-6275
beta-D-glucuronide and D-glucuronate degradation
-
-
PWY-7247
beta-D-mannosyl phosphomycoketide biosynthesis
-
-
PWY-7740
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
biochanin A conjugates interconversion
-
-
PWY-2861
biosynthesis of Lewis epitopes (H. pylori)
-
-
PWY-7833
biotin biosynthesis from 8-amino-7-oxononanoate I
-
-
PWY0-1507
biotin biosynthesis from 8-amino-7-oxononanoate II
-
-
PWY-7380
biotin-carboxyl carrier protein assembly
-
-
PWY0-1264
biphenyl degradation
-
-
PWY5F9-12
bis(guanylyl molybdopterin) cofactor sulfurylation
-
-
PWY-8164
bisabolene biosynthesis (engineered)
-
-
PWY-7102
bisbenzylisoquinoline alkaloid biosynthesis
-
-
PWY-5472
bisphenol A degradation
-
-
PWY-7757
bisucaberin biosynthesis
-
-
PWY-6381
bombykol biosynthesis
-
-
PWY-7423
bornyl diphosphate biosynthesis
-
-
PWY-5813
botryococcenes and methylated squalene biosynthesis
-
-
PWY-6105
brassicicene C biosynthesis
-
-
PWY-7517
brassinolide biosynthesis I
-
-
PWY-699
brassinolide biosynthesis II
-
-
PWY-2582
bryostatin biosynthesis
-
-
PWY-8047
bupropion degradation
-
-
PWY66-241
butachlor degradation
-
-
PWY-7771
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
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
cadaverine biosynthesis
-
-
PWY0-1601
caffeine biosynthesis I
-
-
PWY-5037
caffeine biosynthesis II (via paraxanthine)
-
-
PWY-5038
caffeine degradation III (bacteria, via demethylation)
-
-
PWY-6538
caffeoylglucarate biosynthesis
-
-
PWY-6673
calonectrin biosynthesis
-
-
PWY-7711
Calvin-Benson-Bassham cycle
-
-
CALVIN-PWY
camalexin biosynthesis
-
-
CAMALEXIN-SYN
canavanine biosynthesis
-
-
PWY-5
canavanine degradation
-
-
PWY-31
cannabinoid biosynthesis
-
-
PWY-5140
capsaicin biosynthesis
-
-
PWY-5710
capsiconiate biosynthesis
-
-
PWY-6027
carbon tetrachloride degradation II
-
-
PWY-5372
cardenolide glucosides biosynthesis
-
-
PWY-6036
cardiolipin and phosphatidylethanolamine biosynthesis (Xanthomonas)
-
-
PWY-7509
cardiolipin biosynthesis I
-
-
PWY-5668
cardiolipin biosynthesis II
-
-
PWY-5269
cardiolipin biosynthesis III
-
-
PWY0-1545
carnosate bioynthesis
-
-
PWY-7680
carnosine biosynthesis
-
-
PWY66-420
carotenoid cleavage
-
-
PWY-6806
casbene biosynthesis
-
-
PWY-6304
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 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 II (fungi)
-
-
PWY-6788
cephalosporin C biosynthesis
-
-
PWY-5632
ceramide and sphingolipid recycling and degradation (yeast)
-
-
PWY-7119
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
chlorobactene biosynthesis
-
-
PWY-7939
chlorogenic acid biosynthesis I
-
-
PWY-6039
chlorogenic acid biosynthesis II
-
-
PWY-6040
chlorogenic acid degradation
-
-
PWY-6781
chlorophyll a biosynthesis I
-
-
PWY-5086
chlorophyll a biosynthesis II
-
-
PWY-5064
chlorophyll a biosynthesis III
-
-
PWY-7764
chlorophyll a degradation I
-
-
PWY-5098
chlorophyll a degradation II
-
-
PWY-6927
chlorophyll a degradation III
-
-
PWY-7164
chlorophyll a2 biosynthesis
-
-
PWY-8126
chlorophyll b2 biosynthesis
-
-
PWY-8127
chlorophyll cycle
-
-
PWY-5068
chlorosalicylate degradation
-
-
PWY-6107
chlorpyrifos degradation
-
-
PWY-8065
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
chondroitin biosynthesis
-
-
PWY-6566
chorismate biosynthesis from 3-dehydroquinate
-
-
PWY-6163
chrysin biosynthesis
-
-
PWY-5363
chrysoeriol biosynthesis
-
-
PWY-6232
cichoriin interconversion
-
-
PWY-7057
cinnamate esters biosynthesis
-
-
PWY-5968
cinnamoyl-CoA biosynthesis
-
-
PWY-6457
cis-abienol biosynthesis
-
-
PWY18C3-13
cis-geranyl-CoA degradation
-
-
PWY-6672
cis-vaccenate biosynthesis
cis-zeatin biosynthesis
-
-
PWY-2781
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-legionaminate biosynthesis I
-
-
PWY-6749
CMP-N-acetylneuraminate biosynthesis I (eukaryotes)
-
-
PWY-6138
CMP-N-acetylneuraminate biosynthesis II (bacteria)
-
-
PWY-6139
CO2 fixation into oxaloacetate (anaplerotic)
-
-
PWYQT-4429
cob(II)yrinate a,c-diamide biosynthesis I (early cobalt insertion)
-
-
PWY-7377
cob(II)yrinate a,c-diamide biosynthesis II (late cobalt incorporation)
-
-
PWY-7376
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 B biosynthesis
-
-
P241-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
costunolide biosynthesis
-
-
PWY-6540
coumarin biosynthesis (via 2-coumarate)
-
-
PWY-5176
coumarins biosynthesis (engineered)
-
-
PWY-7398
coumestrol biosynthesis
-
-
PWY-6332
creatine biosynthesis
-
-
GLYCGREAT-PWY
creatine phosphate biosynthesis
-
-
PWY-6158
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
curcuminoid biosynthesis
-
-
PWY-6432
cuticular wax biosynthesis
-
-
PWY-282
cutin biosynthesis
-
-
PWY-321
cyanate degradation
cyanide degradation
-
-
P401-PWY
cyanide detoxification I
-
-
ASPSYNII-PWY
cyanide detoxification II
-
-
PWY-7142
cyanophycin metabolism
-
-
PWY-7052
cyclic electron flow
-
-
PWY-8270
cycloartenol biosynthesis
-
-
PWY-8028
cyclobis-(1rarr6)-alpha-nigerosyl biosynthesis
-
-
PWY-8317
cyclohexanol degradation
cyclopropane fatty acid (CFA) biosynthesis
-
-
PWY0-541
cylindrospermopsin biosynthesis
-
-
PWY-8045
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
cytosolic NADPH production (yeast)
-
-
PWY-7268
D-altritol and galactitol degradation
-
-
PWY-7862
D-arabinitol degradation I
-
-
DARABITOLUTIL-PWY
D-arabinose degradation I
-
-
DARABCAT-PWY
D-arabinose degradation II
-
-
DARABCATK12-PWY
D-arabinose degradation III
-
-
PWY-5519
D-arabinose degradation IV
-
-
PWY-8331
D-arabinose degradation V
-
-
PWY-8334
D-cycloserine biosynthesis
D-fructuronate degradation
-
-
PWY-7242
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 I
-
-
GALACTUROCAT-PWY
D-galacturonate degradation II
-
-
PWY-6486
D-galacturonate degradation III
-
-
PWY-8391
D-galacturonate degradation IV
-
-
PWY-6491
D-glucarate degradation I
-
-
GLUCARDEG-PWY
D-glucarate degradation II
-
-
PWY-6499
D-gluconate degradation
-
-
GLUCONSUPER-PWY
D-glucosaminate degradation
-
-
PWY-7310
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-malate degradation
-
-
PWY0-1465
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-serine degradation
-
-
PWY0-1535
D-sorbitol biosynthesis I
-
-
PWY-5054
D-sorbitol degradation I
-
-
PWY-4101
D-sorbitol degradation II
-
-
SORBDEG-PWY
D-xylose degradation I
-
-
XYLCAT-PWY
D-xylose degradation II
-
-
PWY-5516
D-xylose degradation III
-
-
PWY-6760
D-xylose degradation IV
-
-
PWY-7294
D-xylose degradation to ethylene glycol (engineered)
-
-
PWY-7178
D-xylose degradation V
-
-
PWY-8020
D-xylose degradation VI
-
-
PWY-8330
daidzein conjugates interconversion
-
-
PWY-2343
daidzin and daidzein degradation
-
-
PWY-6996
dammara-20,24-diene biosynthesis
-
-
PWY-6095
daphnin interconversion
-
-
PWY-7056
daunorubicin biosynthesis
deacetylcephalosporin C biosynthesis
-
-
PWY-5631
degradation of aromatic, nitrogen containing compounds
-
-
dehydro-D-arabinono-1,4-lactone biosynthesis
-
-
PWY3O-6
dehydroabietic acid biosynthesis
-
-
PWY-5421
dehydroscoulerine biosynthesis
-
-
PWY-6337
delta-guaiene biosynthesis
-
-
PWY-6669
desferrioxamine B biosynthesis
-
-
PWY-6376
desferrioxamine E biosynthesis
-
-
PWY-6375
detoxification of reactive carbonyls in chloroplasts
-
-
PWY-6786
dhurrin degradation
-
-
PWY-5976
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
diazepinomicin biosynthesis
-
-
PWY-8382
DIBOA-glucoside biosynthesis
-
-
PWY-6949
dicranin biosynthesis
-
-
PWY-6603
diethylphosphate degradation
-
-
PWY-5491
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
dimorphecolate biosynthesis
-
-
PWY-5368
diphenyl ethers degradation
-
-
PWY-7747
diphthamide biosynthesis I (archaea)
-
-
PWY-6482
diphthamide biosynthesis II (eukaryotes)
-
-
PWY-7546
dipicolinate biosynthesis
-
-
PWY-8088
diploterol biosynthesis
-
-
PWY-6098
dissimilatory sulfate reduction I (to hydrogen sufide))
-
-
DISSULFRED-PWY
diterpene phytoalexins precursors 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
dolabralexins biosynthesis
-
-
PWY-7994
dolichol and dolichyl phosphate biosynthesis
dopamine degradation
-
-
PWY6666-2
drosopterin and aurodrosopterin biosynthesis
-
-
PWY-7442
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
dTMP de novo biosynthesis (mitochondrial)
-
-
PWY66-385
dZTP biosynthesis
-
-
PWY-8289
ecdysteroid metabolism (arthropods)
-
-
PWY-7321
echinatin biosynthesis
-
-
PWY-6325
ectoine biosynthesis
-
-
P101-PWY
ent-kaurene biosynthesis I
-
-
PWY-5032
enterobactin biosynthesis
Entner-Doudoroff pathway I
-
-
PWY-8004
Entner-Doudoroff pathway II (non-phosphorylative)
-
-
NPGLUCAT-PWY
Entner-Doudoroff pathway III (semi-phosphorylative)
-
-
PWY-2221
Entner-Doudoroff shunt
-
-
ENTNER-DOUDOROFF-PWY
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 and chloroethene degradation
-
-
PWY-7776
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
ethiin metabolism
-
-
PWY-5708
ethylbenzene degradation (anaerobic)
-
-
PWY-481
ethylene glycol degradation
-
-
PWY0-1280
ethylmalonyl-CoA pathway
-
-
PWY-5741
eumelanin biosynthesis
-
-
PWY-6498
even iso-branched-chain fatty acid biosynthesis
-
-
PWY-8175
extended VTC2 cycle
-
-
PWY4FS-13
factor 430 biosynthesis
-
-
PWY-5196
farnesene biosynthesis
-
-
PWY-5725
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 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 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
ferulate and sinapate biosynthesis
-
-
PWY-5168
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
flavonoid biosynthesis
-
-
PWY1F-FLAVSYN
flavonoid biosynthesis (in equisetum)
-
-
PWY-6787
flavonoid di-C-glucosylation
-
-
PWY-7897
flavonol biosynthesis
-
-
PWY-3101
flexixanthin biosynthesis
-
-
PWY-7947
fluoroacetate and fluorothreonine biosynthesis
-
-
PWY-6644
fluoroacetate degradation
-
-
PWY-6646
folate polyglutamylation
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 I
-
-
RUMP-PWY
formaldehyde oxidation II (glutathione-dependent)
-
-
PWY-1801
formaldehyde oxidation III (mycothiol-dependent)
-
-
PWY1G-170
formaldehyde oxidation IV (thiol-independent)
-
-
FORMASS-PWY
formaldehyde oxidation V (bacillithiol-dependent)
-
-
PWY-7908
formaldehyde oxidation VII (THF pathway)
-
-
PWY-7909
formate assimilation into 5,10-methylenetetrahydrofolate
-
-
PWY-1722
formate oxidation to CO2
-
-
PWY-1881
formate to nitrite electron transfer
-
-
PWY0-1585
formononetin biosynthesis
-
-
PWY-2321
formononetin conjugates interconversion
-
-
PWY-2904
free phenylpropanoid acid biosynthesis
-
-
PWY-2181
fructan biosynthesis
-
-
PWY-822
fructan degradation
-
-
PWY-862
fructose 2,6-bisphosphate biosynthesis
-
-
PWY66-423
fructose degradation
-
-
PWY0-1314
fumitremorgin A biosynthesis
-
-
PWY-7526
fumitremorgin C biosynthesis
-
-
PWY-7525
fusicoccin A biosynthesis
-
-
PWY-6659
GABA shunt I
-
-
GLUDEG-I-PWY
GABA shunt II
-
-
PWY-8346
gala-series glycosphingolipids biosynthesis
-
-
PWY-7840
galactolipid biosynthesis I
-
-
PWY-401
gallate biosynthesis
-
-
PWY-6707
gallate degradation I
-
-
GALLATE-DEGRADATION-II-PWY
gallate degradation II
-
-
GALLATE-DEGRADATION-I-PWY
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
gamma-resorcylate degradation I
-
-
PWY-7773
gamma-resorcylate degradation II
-
-
PWY-7772
ganglio-series glycosphingolipids biosynthesis
-
-
PWY-7836
GDP-6-deoxy-D-talose biosynthesis
-
-
PWY-5738
GDP-alpha-D-glucose biosynthesis
-
-
PWY-5661
GDP-D-perosamine biosynthesis
-
-
PWY-5739
GDP-D-rhamnose biosynthesis
-
-
GDPRHAMSYN-PWY
GDP-L-colitose biosynthesis
-
-
PWY-5740
GDP-L-fucose biosynthesis I (from GDP-D-mannose)
-
-
PWY-66
GDP-L-fucose biosynthesis II (from L-fucose)
-
-
PWY-6
GDP-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
genistein conjugates interconversion
-
-
PWY-2345
gentiodelphin biosynthesis
-
-
PWY-5307
gentisate degradation I
-
-
PWY-6223
gentisate degradation II
-
-
PWY-7469
geosmin biosynthesis
-
-
PWY-5950
geraniol and geranial biosynthesis
-
-
PWY-5829
geranyl acetate biosynthesis
-
-
PWY-5835
geranyl diphosphate biosynthesis
-
-
PWY-5122
geranylgeranyl diphosphate biosynthesis
-
-
PWY-5120
germacrene biosynthesis
-
-
PWY-5733
gibberellin biosynthesis III (early C-13 hydroxylation)
-
-
PWY-5035
gibberellin inactivation I (2beta-hydroxylation)
-
-
PWY-102
ginkgotoxin biosynthesis
-
-
PWY-8077
ginsenoside degradation I
-
-
PWY-6411
ginsenoside degradation III
-
-
PWY-6413
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 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 removal from folates
-
-
PWY-2161B
glutaminyl-tRNAgln biosynthesis via transamidation
-
-
PWY-5921
glutaryl-CoA degradation
-
-
PWY-5177
glutathione biosynthesis
-
-
GLUTATHIONESYN-PWY
glutathione degradation (DUG pathway)
-
-
PWY-7559
glutathione-mediated detoxification I
-
-
PWY-4061
glutathione-mediated detoxification II
-
-
PWY-6842
glutathione-peroxide redox reactions
-
-
PWY-4081
glutathionylspermidine biosynthesis
-
-
PWY-4121
glyceollin biosynthesis
-
-
PWY-2762
glycerol degradation I
-
-
PWY-4261
glycerol degradation II
-
-
PWY-6131
glycerol degradation III
-
-
PWY-6130
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
glycerophosphodiester degradation
-
-
PWY-6952
glycine betaine biosynthesis I (Gram-negative bacteria)
-
-
BETSYN-PWY
glycine betaine biosynthesis III (plants)
-
-
PWY1F-353
glycine betaine biosynthesis IV (from glycine)
-
-
P541-PWY
glycine betaine biosynthesis V (from glycine)
-
-
PWY-6004
glycine betaine degradation I
-
-
PWY-3661
glycine betaine degradation II (mammalian)
-
-
PWY-3661-1
glycine betaine degradation III
-
-
PWY-8325
glycine biosynthesis I
-
-
GLYSYN-PWY
glycine biosynthesis II
-
-
GLYCINE-SYN2-PWY
glycine biosynthesis III
-
-
GLYSYN-ALA-PWY
glycine biosynthesis IV
-
-
GLYSYN-THR-PWY
glycine cleavage
-
-
GLYCLEAV-PWY
glycine degradation (reductive Stickland reaction)
-
-
PWY-8015
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 I
-
-
GLYCOLATEMET-PWY
glycolate and glyoxylate degradation II
-
-
GLYOXDEG-PWY
glycolate and glyoxylate degradation III
-
-
PWY-6649
glycolipid desaturation
-
-
PWY-782
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-protein linkage region biosynthesis
-
-
PWY-6557
glycyrrhetinate biosynthesis
-
-
PWY-7066
glyoxylate assimilation
-
-
PWY-5744
glyoxylate cycle
-
-
GLYOXYLATE-BYPASS
glyphosate degradation I
-
-
PWY-7804
glyphosate degradation II
-
-
PWY-7806
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
heparan sulfate biosynthesis
-
-
PWY-6558
heparan sulfate degradation
-
-
PWY-7651
heparin degradation
-
-
PWY-7644
heptadecane biosynthesis
-
-
PWY-6622
heptaprenyl diphosphate biosynthesis
-
-
PWY-5807
heterolactic fermentation
-
-
P122-PWY
hexaprenyl diphosphate biosynthesis
-
-
HEXPPSYN-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
hopanoid biosynthesis (bacteria)
-
-
PWY-7072
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 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
hygromycin B biosynthesis
-
-
PWY-8367
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 glucosinolate activation (herbivore attack)
-
-
PWYQT-4476
indole glucosinolate activation (intact plant cell)
-
-
PWYQT-4477
indole-3-acetate biosynthesis I
-
-
PWYDQC-4
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
indole-3-acetate degradation II
-
-
PWY-8087
indole-3-acetate inactivation IX
-
-
PWY-1741
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
inulin degradation
-
-
PWY-8314
ipsdienol biosynthesis
-
-
PWY-7410
iron reduction and absorption
-
-
PWY-5934
isoflavonoid biosynthesis I
-
-
PWY-2002
isoflavonoid biosynthesis II
-
-
PWY-2083
isopenicillin N biosynthesis
-
-
PWY-5629
isopimaric acid biosynthesis
-
-
PWY-5422
isoprene biosynthesis I
-
-
PWY-6270
isoprene biosynthesis II (engineered)
-
-
PWY-7391
isoprene degradation
-
-
PWY-7777
isopropanol biosynthesis (engineered)
-
-
PWY-6876
isorenieratene biosynthesis I (actinobacteria)
-
-
PWY-7938
itaconate biosynthesis I
-
-
PWY-5750
itaconate degradation
-
-
PWY-5749
jadomycin biosynthesis
-
-
PWY-6679
jasmonic acid biosynthesis
-
-
PWY-735
jasmonoyl-amino acid conjugates biosynthesis I
-
-
PWY-6220
jasmonoyl-amino acid conjugates biosynthesis II
-
-
PWY-6233
jasmonoyl-L-isoleucine inactivation
-
-
PWY-7859
juniperonate biosynthesis
-
-
PWY-7619
justicidin B biosynthesis
-
-
PWY-6824
juvenile hormone III biosynthesis II
-
-
PWY-6650
K-252 biosynthesis
-
-
PWY-6345
kanamycin biosynthesis
kauralexin biosynthesis
-
-
PWY-6887
Kdo-lipid A biosynthesis (Vibrio cholerae serogroup O1 El Tor)
-
-
PWY-8378
ketogenesis
-
-
PWY66-367
ketogluconate metabolism
ketolysis
-
-
PWY66-368
kievitone detoxification
-
-
PWY-7635
kojibiose degradation
-
-
PWY-7459
L-alanine biosynthesis I
-
-
ALANINE-VALINESYN-PWY
L-alanine biosynthesis II
-
-
ALANINE-SYN2-PWY
L-alanine biosynthesis III
-
-
PWY0-1021
L-alanine degradation 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 I
-
-
ARABCAT-PWY
L-arabinose degradation II
-
-
PWY-5515
L-arabinose degradation IV
-
-
PWY-7295
L-arginine biosynthesis I (via L-ornithine)
-
-
ARGSYN-PWY
L-arginine biosynthesis II (acetyl cycle)
-
-
ARGSYNBSUB-PWY
L-arginine biosynthesis III (via N-acetyl-L-citrulline)
-
-
PWY-5154
L-arginine biosynthesis IV (archaea)
-
-
PWY-7400
L-arginine degradation I (arginase pathway)
-
-
ARGASEDEG-PWY
L-arginine degradation 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 V (euglena, D-galacturonate pathway)
-
-
PWY-6415
L-ascorbate biosynthesis VI (plants, myo-inositol pathway)
-
-
PWY-8142
L-ascorbate biosynthesis VII (plants, D-galacturonate pathway)
-
-
PWY-8143
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 degradation I
-
-
CYSTEINE-DEG-PWY
L-cysteine degradation II
-
-
LCYSDEG-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-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 biosynthesis V
-
-
PWY-4341
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 V
-
-
PWY-5031
L-histidine degradation VI
-
-
HISHP-PWY
L-homocysteine biosynthesis
-
-
PWY-5344
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 (aerobic)
-
-
PWY0-1317
L-lactaldehyde degradation (anaerobic)
-
-
PWY0-1315
L-leucine biosynthesis
-
-
LEUSYN-PWY
L-leucine degradation I
-
-
LEU-DEG2-PWY
L-leucine degradation II
-
-
PWY-5075
L-leucine degradation III
-
-
PWY-5076
L-leucine degradation IV (reductive Stickland reaction)
-
-
PWY-7767
L-leucine degradation V (oxidative Stickland reaction)
-
-
PWY-8185
L-lysine biosynthesis I
-
-
DAPLYSINESYN-PWY
L-lysine biosynthesis II
-
-
PWY-2941
L-lysine biosynthesis III
-
-
PWY-2942
L-lysine biosynthesis IV
-
-
LYSINE-AMINOAD-PWY
L-lysine biosynthesis V
-
-
PWY-3081
L-lysine biosynthesis VI
-
-
PWY-5097
L-lysine degradation I
-
-
PWY0-461
L-lysine degradation II (L-pipecolate pathway)
-
-
PWY66-425
L-lysine degradation III
-
-
LYSDEGII-PWY
L-lysine degradation IV
-
-
PWY-5280
L-lysine degradation V
-
-
PWY-5283
L-lysine degradation VI
-
-
PWY-5298
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-lyxose degradation
-
-
LYXMET-PWY
L-malate degradation I
-
-
PWY-7685
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 II
-
-
PWY-701
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-rhamnose degradation II
-
-
PWY-6713
L-rhamnose degradation III
-
-
PWY-6714
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-serine degradation
-
-
SERDEG-PWY
L-sorbose degradation
-
-
P302-PWY
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 II (via pyruvate)
-
-
TRYPDEG-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
labdane-type diterpenes biosynthesis
-
-
PWY-6645
labdenediol and sclareol biosynthesis
-
-
PWY18C3-18
lacinilene C biosynthesis
-
-
PWY-5828
lactate biosynthesis (archaea)
-
-
PWY-5197
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
lanosterol biosynthesis
-
-
PWY-6132
leucodelphinidin biosynthesis
-
-
PWY-5152
leucopelargonidin and leucocyanidin biosynthesis
-
-
PWY1F-823
leukotriene biosynthesis
-
-
PWY66-375
levopimaric acid biosynthesis
-
-
PWY-5412
limonene degradation IV (anaerobic)
-
-
PWY-8029
linalool biosynthesis I
-
-
PWY-7182
linamarin degradation
-
-
PWY-3121
lincomycin A biosynthesis
-
-
PWY-6955
linear furanocoumarin biosynthesis
-
-
PWY-5365
linezolid resistance
-
-
PWY-6828
linoleate biosynthesis I (plants)
-
-
PWY-5995
linoleate biosynthesis II (animals)
-
-
PWY-6001
linoleate biosynthesis III (cyanobacteria)
-
-
PWY-7593
linoleate metabolites biosynthesis
-
-
PWY-8395
linustatin bioactivation
-
-
PWY-7091
lipid A-core biosynthesis (E. coli K-12)
-
-
LIPA-CORESYN-PWY
lipid A-core biosynthesis (P. gingivalis)
-
-
PWY-8248
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
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
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
lovastatin biosynthesis
-
-
PWY-7535
lupanine biosynthesis
-
-
PWY-5468
lupeol biosynthesis
-
-
PWY-112
lupulone and humulone biosynthesis
-
-
PWY-5132
lutein biosynthesis
-
-
PWY-5947
luteolin biosynthesis
-
-
PWY-5060
luteolin triglucuronide degradation
-
-
PWY-7445
luteolinidin 5-O-glucoside biosynthesis
-
-
PWY-7252
lychnose and isolychnose biosynthesis
-
-
PWY-6524
m-cresol degradation
-
-
M-CRESOL-DEGRADATION-PWY
maackiain conjugates interconversion
-
-
PWY-2701
magnoflorine biosynthesis
-
-
PWY-5876
malate/L-aspartate shuttle pathway
-
-
MALATE-ASPARTATE-SHUTTLE-PWY
malbrancheamide biosynthesis
-
-
PWY-8345
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
mannosylglycerate biosynthesis I
-
-
PWY-5656
mannosylglycerate biosynthesis II
-
-
PWY-5658
maresin biosynthesis
-
-
PWY-8356
matairesinol biosynthesis
-
-
PWY-5466
medicarpin conjugates interconversion
-
-
PWY-2561
melatonin degradation I
-
-
PWY-6398
melatonin degradation II
-
-
PWY-6399
melibiose degradation
-
-
PWY0-1301
menaquinol-4 biosynthesis II
-
-
PWY-7998
menthol biosynthesis
-
-
PWY-3061
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 H2 and CO2
-
-
METHANOGENESIS-PWY
methanogenesis from methanol
-
-
CO2FORM-PWY
methanol oxidation to carbon dioxide
-
-
PWY-7616
methanol oxidation to formaldehyde II
-
-
PWY-6510
methanol oxidation to formaldehyde IV
-
-
PWY-5506
methiin metabolism
-
-
PWY-7614
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
methylaspartate cycle
methylerythritol phosphate pathway I
-
-
NONMEVIPP-PWY
methylerythritol phosphate pathway II
-
-
PWY-7560
methylgallate degradation
-
-
METHYLGALLATE-DEGRADATION-PWY
methylglyoxal degradation I
-
-
PWY-5386
methylglyoxal degradation III
-
-
PWY-5453
methylglyoxal degradation IV
-
-
PWY-5459
methylglyoxal degradation V
-
-
PWY-5458
methylglyoxal degradation VI
-
-
MGLDLCTANA-PWY
methylglyoxal degradation VII
-
-
PWY-5456
methylglyoxal degradation VIII
-
-
PWY-5386-1
methylhalides biosynthesis (plants)
-
-
PWY-6730
methylquercetin biosynthesis
-
-
PWY-6064
methylsalicylate biosynthesis
-
-
PWY18C3-22
methylsalicylate degradation
-
-
PWY-6184, PWY18C3-24
methylwyosine biosynthesis
-
-
PWY-7285
mevalonate degradation
-
-
PWY-5074
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
mineralocorticoid biosynthesis
-
-
PWY66-382
mitochondrial L-carnitine shuttle
-
-
PWY-6111
mitochondrial NADPH production (yeast)
-
-
PWY-7269
mixed acid fermentation
-
-
FERMENTATION-PWY
molybdenum cofactor biosynthesis
molybdopterin biosynthesis
-
-
PWY-6823
momilactone A biosynthesis
-
-
PWY-7477
mono-trans, poly-cis decaprenyl phosphate biosynthesis
-
-
PWY-6383
monoacylglycerol metabolism (yeast)
-
-
PWY-7420
monoterpene biosynthesis
-
-
PWY-3041
morphine 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
mupirocin biosynthesis
-
-
PWY-8012
muropeptide degradation
-
-
PWY0-1546
mycobacterial sulfolipid biosynthesis
-
-
PWY-7746
mycobactin biosynthesis
-
-
PWY185E-1
mycocyclosin biosynthesis
-
-
PWY-7236
mycolate biosynthesis
-
-
PWYG-321
mycolyl-arabinogalactan-peptidoglycan complex biosynthesis
-
-
PWY-6397
mycothiol biosynthesis
-
-
PWY1G-0
mycothiol-mediated detoxification
-
-
PWY1G-1
myo-, chiro- and scyllo-inositol degradation
-
-
PWY-7237
myo-inositol biosynthesis
myo-inositol degradation I
-
-
P562-PWY
myo-inositol degradation II
-
-
PWY-7241
myxol-2' fucoside biosynthesis
-
-
PWY-6279
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-hydroxy-L-pipecolate biosynthesis
-
-
PWY-7861
N-methylpyrrolidone degradation
-
-
PWY-7978
N1-methyl-N3-aminocarboxypropyl-pseudouridine-modified rRNA biosynthesis
-
-
PWY-8341
N6-L-threonylcarbamoyladenosine37-modified tRNA biosynthesis
-
-
PWY0-1587
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 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 (aerobic)
-
-
PWY-5427
naringenin biosynthesis (engineered)
-
-
PWY-7397
naringenin C-glucosylation
-
-
PWY-6602
neoabietic acid biosynthesis
-
-
PWY-5413
neolacto-series glycosphingolipids biosynthesis
-
-
PWY-7841
neolinustatin bioactivation
-
-
PWY-7092
neopentalenoketolactone and pentalenate biosynthesis
-
-
PWY-6919
nepetalactone biosynthesis
-
-
PWY-8069
nerol biosynthesis
-
-
PWY-8177
nicotinate degradation I
-
-
PWY-722
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 V (assimilatory)
-
-
PWY-5675
nitrate reduction VI (assimilatory)
-
-
PWY490-3
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
nitrilotriacetate degradation
-
-
PWY-6021
nitrite-dependent anaerobic methane oxidation
-
-
PWY-6523
nitroethane degradation
-
-
PWY-5355
nitrogen fixation I (ferredoxin)
-
-
N2FIX-PWY
nitrogen fixation II (flavodoxin)
-
-
PWY-7576
nitrogen remobilization from senescing leaves
-
-
PWY-6549
nocardicin A biosynthesis
-
-
PWY-7797
nonaprenyl diphosphate biosynthesis I
-
-
PWY-5805
nonaprenyl diphosphate biosynthesis II
-
-
PWY-6520
noradrenaline and adrenaline degradation
-
-
PWY-6342
norspermidine biosynthesis
-
-
PWY-6562
noscapine biosynthesis
-
-
PWY-7138
nucleoside and nucleotide degradation (archaea)
-
-
PWY-5532
O-antigen building blocks biosynthesis (E. coli)
-
-
OANTIGEN-PWY
o-diquinones biosynthesis
-
-
PWY-6752
octane oxidation
octanoyl-[acyl-carrier protein] biosynthesis (mitochondria, yeast)
-
-
PWY-7388
octaprenyl diphosphate biosynthesis
-
-
PWY-5783
octopamine biosynthesis
-
-
PWY-7297
odd iso-branched-chain fatty acid biosynthesis
-
-
PWY-8174
okenone biosynthesis
-
-
PWY-7591
oleandomycin activation/inactivation
-
-
PWY-6972
oleanolate biosynthesis
-
-
PWY-7069
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
oleoresin sesquiterpene volatiles biosynthesis
-
-
PWY-5425
ophiobolin F biosynthesis
-
-
PWY-7720
ophthalmate biosynthesis
-
-
PWY-8043
orientin and isoorientin biosynthesis I
-
-
PWY-7188
oryzalide A biosynthesis
-
-
PWY-7481
oxalate 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
p-HBAD biosynthesis
-
-
PWY-7745
palmatine biosynthesis
-
-
PWY-5470
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
palustric acid biosynthesis
-
-
PWY-5414
paraoxon degradation
-
-
PWY-5490
parathion degradation
-
-
PARATHION-DEGRADATION-PWY
parkeol biosynthesis
-
-
PWY-8027
paromamine biosynthesis I
-
-
PWY-7014
paromamine biosynthesis II
-
-
PWY-7022
partial TCA cycle (obligate autotrophs)
-
-
PWY-5913
paspaline biosynthesis
-
-
PWY-7492
patchoulol biosynthesis
-
-
PWY-6258
patulin biosynthesis
-
-
PWY-7490
pectin degradation I
-
-
PWY-7246
pectin degradation II
-
-
PWY-7248
pederin biosynthesis
-
-
PWY-8049
penicillin G and penicillin V biosynthesis
-
-
PWY-7716
pentachlorophenol degradation
-
-
PCPDEG-PWY
pentacyclic triterpene biosynthesis
-
-
PWY-7251
pentalenolactone biosynthesis
-
-
PWY-6915
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 (oxidative branch) II
-
-
PWY-7796
pentose phosphate pathway (partial)
-
-
P21-PWY
peptido-conjugates in tissue regeneration biosynthesis
-
-
PWY-8355
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
phaselate biosynthesis
-
-
PWY-6320
phenazine-1-carboxylate biosynthesis
-
-
PWY-5770
phenol degradation I (aerobic)
-
-
PWY-5418
phenolic malonylglucosides biosynthesis
-
-
PWY-6930
phenolphthiocerol biosynthesis
-
-
PWY-7742
phenylacetate degradation I (aerobic)
-
-
PWY0-321
phenylacetate degradation II (anaerobic)
-
-
PWY-1341
phenylethanol biosynthesis
-
-
PWY-5751
phenylethanol degradation
-
-
PWY-8162
phenylethylamine degradation I
-
-
2PHENDEG-PWY
phenylethylamine degradation II
-
-
PWY-6534
phenylmercury acetate degradation
phenylpropanoid biosynthesis
-
-
PWY-361
phenylpropanoid biosynthesis, initial reactions
-
-
PWY1F-467
phenylpropanoids methylation (ice plant)
-
-
PWY-7498
pheomelanin biosynthesis
-
-
PWY-7917
phloridzin biosynthesis
-
-
PWY-6515
phosalacine biosynthesis
-
-
PWY-7769
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
phosphatidylglycerol biosynthesis I
-
-
PWY4FS-7
phosphatidylglycerol biosynthesis II
-
-
PWY4FS-8
phosphatidylinositol biosynthesis I (bacteria)
-
-
PWY-6580
phosphatidylinositol biosynthesis II (eukaryotes)
-
-
PWY-7625
phosphatidylserine and phosphatidylethanolamine biosynthesis I
-
-
PWY-5669
phosphinothricin tripeptide biosynthesis
-
-
PWY-6322
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
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
phytate degradation I
-
-
PWY-4702
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
pinocembrin C-glucosylation
-
-
PWY-7189
pinolenate and coniferonate biosynthesis
-
-
PWY-7152
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
polybrominated phenols biosynthesis
-
-
PWY-7929
polyethylene terephthalate degradation
-
-
PWY-7794
polyhydroxybutanoate biosynthesis
-
-
PWY1-3
polyhydroxydecanoate biosynthesis
-
-
PWY-6657
polymethylated myricetin biosynthesis (tomato)
-
-
PWY-7160
polymethylated quercetin biosynthesis
-
-
PWY-7161
polymethylated quercetin glucoside biosynthesis I - quercetin series (Chrysosplenium)
-
-
PWY-7150
polymyxin resistance
-
-
PWY0-1338
polyphosphate metabolism
-
-
PWY-8138
polyvinyl alcohol degradation
-
-
PWY-6464
porphyran degradation
-
-
PWY-6815
ppGpp metabolism
-
-
PPGPPMET-PWY
preQ0 biosynthesis
-
-
PWY-6703
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
propanoyl CoA degradation I
-
-
PROPIONMET-PWY
propanoyl-CoA degradation II
-
-
PWY-7574
propene degradation
-
-
PWY-5534
protectin biosynthesis
-
-
PWY-8357
protective electron sinks in the thylakoid membrane (PSII to PTOX)
-
-
PWY1YI0-7
protein N-glycosylation (bacterial)
-
-
PWY-7031
protein N-glycosylation (Haloferax volcanii)
-
-
PWY-7661
protein N-glycosylation (Methanococcus voltae)
-
-
PWY-7658
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 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 II (ortho-cleavage pathway)
-
-
PROTOCATECHUATE-ORTHO-CLEAVAGE-PWY
PRPP biosynthesis
-
-
PWY0-662
prunasin and amygdalin biosynthesis
-
-
PWY-7824
pseudouridine degradation
-
-
PWY-6019
psilocybin biosynthesis
-
-
PWY-7936
punicate biosynthesis
-
-
PWY-5374
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
pyoverdine I biosynthesis
-
-
PWY-6409
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 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
pyrrolnitrin biosynthesis
-
-
PWY-6831
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 opines
-
-
PWY-7351
pyruvate fermentation to propanoate I
-
-
P108-PWY
pyruvate fermentation to propanoate II (acrylate pathway)
-
-
PWY-5494
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 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
rebeccamycin biosynthesis
-
-
PWY-6324
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
resorcinol degradation
resveratrol biosynthesis
-
-
PWY-84
retinoate biosynthesis I
-
-
PWY-6872
retinol biosynthesis
-
-
PWY-6857
rhamnogalacturonan type I degradation II (bacteria)
-
-
PWY-6771
ribitol degradation I
-
-
RIBITOLUTIL-PWY
ribose phosphorylation
-
-
RIBOKIN-PWY
ricinoleate biosynthesis
-
-
PWY-7618
rose anthocyanin biosynthesis II (via cyanidin 3-O-beta-D-glucoside)
-
-
PWY-7262
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 biosynthesis
-
-
PWY-5390
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 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
salicylate degradation III
-
-
PWY-6636
salicylate degradation IV
-
-
PWY-6640
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
sanguinarine and macarpine biosynthesis
-
-
PWY-5287
santalene biosynthesis II
-
-
PWY-6836
saponin biosynthesis II
-
-
PWY-5756
sciadonate biosynthesis
-
-
PWY-6598
scopoletin biosynthesis
-
-
PWY-6792
secologanin and strictosidine biosynthesis
-
-
PWY-5290
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
senecionine N-oxide biosynthesis
-
-
PWY-6852
serine racemization
-
-
PWY-8140
serotonin and melatonin biosynthesis
-
-
PWY-6030
serotonin degradation
-
-
PWY-6313
sesamin biosynthesis
-
-
PWY-5469
shikimate degradation I
-
-
SHIKIMATEDEG-PWY
shikimate degradation II
-
-
PWY-6419
shikonin biosynthesis
-
-
PWY-5701
sinapate ester biosynthesis
-
-
PWY-3301
siroheme biosynthesis
-
-
PWY-5194
sitosterol degradation to androstenedione
-
-
PWY-6948
solasodine glycosylation
-
-
PWY18C3-4
sophoraflavanone G biosynthesis
-
-
PWY-6914
sophorolipid biosynthesis
-
-
SOPHOROSYLOXYDOCOSANOATE-SYN-PWY
sophorosyloxydocosanoate deacetylation
-
-
SOPHOROSYLOXYDOCOSANOATE-DEG-PWY
sorbitol biosynthesis II
-
-
PWY-5530
sorgoleone biosynthesis
-
-
PWY-5987
soybean saponin I biosynthesis
-
-
PWY-5203
spectinabilin biosynthesis
-
-
PWY-8034
spermidine biosynthesis I
-
-
BSUBPOLYAMSYN-PWY
spermidine biosynthesis II
-
-
PWY-6559
spermidine biosynthesis III
-
-
PWY-6834
spermine and spermidine degradation I
-
-
PWY-6117
spermine and spermidine degradation III
-
-
PWY-6441
spermine biosynthesis
-
-
ARGSPECAT-PWY
sphingolipid biosynthesis (mammals)
-
-
PWY-7277
sphingolipid biosynthesis (plants)
-
-
PWY-5129
sphingolipid biosynthesis (yeast)
-
-
SPHINGOLIPID-SYN-PWY
sphingomyelin metabolism
-
-
PWY3DJ-11281
sphingosine and sphingosine-1-phosphate metabolism
-
-
PWY3DJ-11470
Spodoptera littoralis pheromone biosynthesis
-
-
PWY-7656
spongiadioxin C biosynthesis
-
-
PWY-7935
sporopollenin precursors biosynthesis
-
-
PWY-6733
stachyose biosynthesis
-
-
PWY-5337
stachyose degradation
-
-
PWY-6527
staphyloferrin A biosynthesis
-
-
PWY-7990
staphylopine biosynthesis
-
-
PWY-8007
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
staurosporine biosynthesis
-
-
PWY-6346
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
stearidonate biosynthesis (cyanobacteria)
-
-
PWY-7595
stellariose and mediose biosynthesis
-
-
PWY-6525
stellatic acid biosynthesis
-
-
PWY-7736
sterculate biosynthesis
-
-
PWY-4942
sterol biosynthesis (methylotrophs)
-
-
PWY-8026
sterol:steryl ester interconversion (yeast)
-
-
PWY-7424
stigma estolide biosynthesis
-
-
PWY-6453
streptomycin biosynthesis
-
-
PWY-5940
streptorubin B biosynthesis
-
-
PWY1A0-6120
strychnine biosynthesis
-
-
PWY-8216
styrene degradation
-
-
PWY-6941
suberin monomers biosynthesis
succinate fermentation to butanoate
-
-
PWY-5677
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
sulfide oxidation I (to sulfur globules)
-
-
P222-PWY
sulfide oxidation II (flavocytochrome c)
-
-
PWY-5274
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
sulfoacetaldehyde degradation IV
-
-
PWY-8062
sulfolactate degradation II
-
-
PWY-6637
sulfolactate degradation III
-
-
PWY-6638
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 adenosylcobalamin salvage from cobinamide I
-
-
COBALSYN-PWY
superpathway of adenosylcobalamin salvage from cobinamide II
-
-
PWY-6269
superpathway of anthocyanin biosynthesis (from cyanidin and cyanidin 3-O-glucoside)
-
-
PWY-5313
superpathway of C28 brassinosteroid biosynthesis
-
-
PWY-6544
superpathway of coenzyme A biosynthesis III (mammals)
-
-
COA-PWY-1
superpathway of fatty acid biosynthesis initiation
-
-
FASYN-INITIAL-PWY
superpathway of fermentation (Chlamydomonas reinhardtii)
-
-
PWY4LZ-257
superpathway of glucose and xylose degradation
-
-
PWY-6901
superpathway of glycolysis and the Entner-Doudoroff pathway
-
-
GLYCOLYSIS-E-D
superpathway of glycolysis, pyruvate dehydrogenase, TCA, and glyoxylate bypass
-
-
GLYCOLYSIS-TCA-GLYOX-BYPASS
superpathway of glyoxylate cycle and fatty acid degradation
-
-
PWY-561
superpathway of hyoscyamine (atropine) and scopolamine biosynthesis
-
-
PWY-7341
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 pterocarpan biosynthesis (via daidzein)
-
-
PWY-2055
superpathway of pyrimidine deoxyribonucleotides de novo biosynthesis (E. coli)
-
-
PWY0-166
superpathway of scopolin and esculin biosynthesis
-
-
PWY-7186
superpathway of UDP-glucose-derived O-antigen building blocks biosynthesis
-
-
PWY-7328
syringate degradation
-
-
PWY-6339
syringetin biosynthesis
-
-
PWY-5391
taurine biosynthesis I
-
-
PWY-5331
taurine biosynthesis II
-
-
PWY-7850
taurine biosynthesis III
-
-
PWY-8359
taurine degradation IV
-
-
PWY0-981
taxadiene biosynthesis (engineered)
-
-
PWY-7392
taxol biosynthesis
TCA cycle I (prokaryotic)
-
-
TCA
TCA cycle II (plants and fungi)
-
-
PWY-5690
TCA cycle III (animals)
-
-
PWY66-398
TCA cycle IV (2-oxoglutarate decarboxylase)
-
-
P105-PWY
TCA cycle V (2-oxoglutarate synthase)
-
-
PWY-6969
TCA cycle VI (Helicobacter)
-
-
REDCITCYC
TCA cycle VII (acetate-producers)
-
-
PWY-7254
TCA cycle VIII (Chlamydia)
-
-
TCA-1
tea aroma glycosidic precursor bioactivation
-
-
PWY-7114
teichuronic acid biosynthesis (B. subtilis 168)
-
-
PWY-7820
terminal O-glycans residues modification (via type 2 precursor disaccharide)
-
-
PWY-7434
testosterone and androsterone degradation to androstendione (aerobic)
-
-
PWY-6943
testosterone degradation (anaerobic)
-
-
PWY-8155
tetracenomycin C biosynthesis
-
-
PWY-7485
tetracycline and oxytetracycline biosynthesis
-
-
PWY-7812
tetradecanoate biosynthesis (mitochondria)
-
-
PWY66-430
tetrahydrofolate biosynthesis I
-
-
PWY-6614
tetrahydrofolate biosynthesis II
-
-
PWY2DNV-11
tetrahydrofolate salvage from 5,10-methenyltetrahydrofolate
-
-
PWY-6613
tetrahydromethanopterin biosynthesis
-
-
PWY-6148
tetrahydromonapterin biosynthesis
-
-
PWY0-1433
tetrahydropteridine recycling
-
-
PWY-8099
tetrahydroxyxanthone biosynthesis (from 3-hydroxybenzoate)
-
-
PWY-5002
tetrahydroxyxanthone biosynthesis (from benzoate)
-
-
PWY-5001
tetrapyrrole biosynthesis I (from glutamate)
-
-
PWY-5188
tetrapyrrole biosynthesis II (from glycine)
-
-
PWY-5189
thalianol and derivatives biosynthesis
-
-
PWY-5992
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
thiazole component of thiamine diphosphate biosynthesis II
-
-
PWY-6891
thiazole component of thiamine diphosphate biosynthesis III
-
-
PWY-6909
thioredoxin pathway
-
-
THIOREDOX-PWY
thiosulfate disproportionation I (thiol-dependent)
-
-
PWY-5277
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-caffeate degradation (aerobic)
-
-
PWY-8003
trans-lycopene biosynthesis II (oxygenic phototrophs and green sulfur bacteria)
-
-
PWY-6475
trans-zeatin biosynthesis
-
-
PWY-2681
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 III
-
-
PWY-2721
trehalose degradation IV
-
-
PWY-2722
trehalose degradation V
-
-
PWY-2723
trehalose degradation VI (periplasmic)
-
-
PWY0-1466
triacylglycerol degradation
-
-
LIPAS-PWY
trichome monoterpenes biosynthesis
-
-
PWY-6447
tricin biosynthesis
-
-
PWY-7995
triethylamine degradation
-
-
PWY-7085
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 (mammalian mitochondria)
-
-
PWY-7889
tRNA-uridine 2-thiolation and selenation (bacteria)
-
-
PWY-7892
tropane alkaloids biosynthesis
-
-
PWY-5317
trypanothione biosynthesis
-
-
TRYPANOSYN-PWY
tunicamycin biosynthesis
-
-
PWY-7821
tylosin biosynthesis
-
-
PWY-7415
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
UDP-3-acetamido-2-amino-2,3-dideoxy-alpha-D-glucopyranose biosynthesis
-
-
PWY-8273
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-alpha-D-xylose biosynthesis
-
-
PWY-4821
UDP-beta-L-arabinose biosynthesis I (from UDP-alpha-D-xylose)
-
-
PWY-63
UDP-beta-L-arabinose biosynthesis II (from beta-L-arabinose)
-
-
PWY-82
UDP-beta-L-rhamnose biosynthesis
-
-
PWY-3261
UDP-N-acetyl-alpha-D-mannosaminouronate biosynthesis
-
-
PWY-7335
UDP-N-acetyl-D-galactosamine biosynthesis I
-
-
PWY-5512
UDP-N-acetyl-D-galactosamine biosynthesis II
-
-
PWY-5514
UDP-N-acetyl-D-galactosamine biosynthesis III
-
-
PWY-8013
UDP-N-acetyl-D-glucosamine biosynthesis I
-
-
UDPNAGSYN-PWY
UDP-N-acetyl-D-glucosamine biosynthesis II
-
-
UDPNACETYLGALSYN-PWY
UDP-N-acetylmuramoyl-pentapeptide biosynthesis I (meso-diaminopimelate containing)
-
-
PWY-6387
UDP-N-acetylmuramoyl-pentapeptide biosynthesis II (lysine-containing)
-
-
PWY-6386
UDP-N-acetylmuramoyl-pentapeptide biosynthesis III (meso-diaminopimelate containing)
-
-
PWY-7953
ultra-long-chain fatty acid biosynthesis
-
-
PWY-8041
umbelliferone biosynthesis
-
-
PWY-6982
UMP biosynthesis I
-
-
PWY-5686
UMP biosynthesis II
-
-
PWY-7790
UMP biosynthesis III
-
-
PWY-7791
uracil degradation I (reductive)
-
-
PWY-3982
uracil degradation III
-
-
PWY0-1471
urate conversion to allantoin I
-
-
PWY-5691
urate conversion to allantoin II
-
-
PWY-7394
urate conversion to allantoin III
-
-
PWY-7849
urea cycle
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
valencene and 7-epi-alpha-selinene biosynthesis
-
-
PWY-6291
valproate beta-oxidation
-
-
PWY-8182
vancomycin resistance I
-
-
PWY-6454
vancomycin resistance II
-
-
PWY-6455
vanillin and vanillate degradation II
-
-
PWY-7098
vanillin biosynthesis I
-
-
PWY-5665
vernolate biosynthesis III
-
-
PWY-6917
versicolorin B biosynthesis
-
-
PWY-5955
very long chain fatty acid biosynthesis I
-
-
PWY-5080
very long chain fatty acid biosynthesis II
-
-
PWY-7036
vicianin bioactivation
-
-
PWY-7093
vindoline, vindorosine and vinblastine biosynthesis
-
-
PWY-5292
violacein biosynthesis
viridicatumtoxin biosynthesis
-
-
PWY-7659
vitamin B6 degradation I
-
-
PWY-5499
vitamin D3 biosynthesis
-
-
PWY-6076
vitamin E biosynthesis (tocopherols)
-
-
PWY-1422
vitamin K-epoxide cycle
volatile benzenoid biosynthesis I (ester formation)
-
-
PWY-4203
volatile esters biosynthesis (during fruit ripening)
-
-
PWY-6801
VTC2 cycle
-
-
PWY4FS-12
wax esters biosynthesis I
-
-
PWY-5884
wax esters biosynthesis II
-
-
PWY-5885
wighteone and luteone biosynthesis
-
-
PWY-4502
wogonin metabolism
-
-
PWY-7213
wybutosine biosynthesis
-
-
PWY-7283
xanthine and xanthosine salvage
-
-
SALVPURINE2-PWY
xanthohumol biosynthesis
-
-
PWY-5135
xanthommatin biosynthesis
-
-
PWY-8249
xylan biosynthesis
-
-
PWY-5800
xylitol degradation I
-
-
LARABITOLUTIL-PWY
xyloglucan degradation II (exoglucanase)
-
-
PWY-6807
xyloglucan degradation III (cellobiohydrolase)
-
-
PWY-6812
zealexin biosynthesis
-
-
PWY-6888
zerumbone biosynthesis
-
-
PWY-6265
zymosterol biosynthesis
-
-
PWY-6074
[2Fe-2S] iron-sulfur cluster biosynthesis
-
-
PWY-7250
(5R)-carbapenem carboxylate biosynthesis
-
-
PWY-5737
4-hydroxymandelate degradation
-
-
4-HYDROXYMANDELATE-DEGRADATION-PWY
4-hydroxyphenylacetate degradation
-
-
3-HYDROXYPHENYLACETATE-DEGRADATION-PWY
adipate degradation
-
-
PWY-8354
bacilysin biosynthesis
-
-
PWY-7626
bile acid biosynthesis, neutral pathway
-
-
PWY-6061
catecholamine biosynthesis
-
-
PWY66-301
cis-vaccenate biosynthesis
-
-
PWY-5973
cyanate degradation
-
-
CYANCAT-PWY
cyclohexanol degradation
-
-
CYCLOHEXANOL-OXIDATION-PWY
D-cycloserine biosynthesis
-
-
PWY-7274
daunorubicin biosynthesis
-
-
PWY-7352
diterpene phytoalexins precursors biosynthesis
-
-
PWY-2981
dolichol and dolichyl phosphate biosynthesis
-
-
PWY-6129
enterobactin biosynthesis
-
-
ENTBACSYN-PWY
folate polyglutamylation
-
-
PWY-2161
kanamycin biosynthesis
-
-
PWY-7000
ketogluconate metabolism
-
-
KETOGLUCONMET-PWY
methylaspartate cycle
-
-
PWY-6728
molybdenum cofactor biosynthesis
-
-
PWY-8171
morphine biosynthesis
-
-
PWY-5270
myo-inositol biosynthesis
-
-
PWY-2301
octane oxidation
-
-
P221-PWY
oxalate biosynthesis
-
-
PWY-6699
phenylmercury acetate degradation
-
-
P641-PWY
resorcinol degradation
-
-
P343-PWY
suberin monomers biosynthesis
-
-
PWY-1121
taxol biosynthesis
-
-
PWY-5660
thyroid hormone biosynthesis
-
-
PWY-6241
urea cycle
-
-
PWY-4984
violacein biosynthesis
-
-
PWY-7040
vitamin K-epoxide cycle
-
-
PWY-7999
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
ORGANISM
COMMENTARY
LITERATURE
UNIPROT
SEQUENCE DB
SOURCE
-
9, 11, 20, 22, 32, 39, 42, 50, 80, 82, 83, 86, 87, 90, 95, 96, 101, 102, 115, 117, 118, 122, 124, 133, 137, 138, 150, 151, 207, 254, 260, 273, 316, 320, 328, 329, 332, 334, 337, 340, 341, 342, 343, 364, 395, 399, 402, 424, 428, 458, 469, 472, 476, 496, 521, 529, 538, 542, 544, 550, 554, 556, 559, 561, 564, 566, 570, 577, 744, 949, 1023, 1092, 1161, 1188, 1197, 1199, 1267, 1370, 1385, 1397, 1419, 1505, 1526, 1538, 1570, 1600, 1602, 1603, 1604, 1609, 1611, 1612, 1623, 1625, 1723, 1769, 1773, 1792, 1796, 1800, 1906, 1907, 1908, 1909, 2225, 2229, 2232, 2236, 2238, 2282, 2283, 2285, 2286, 2309, 2311, 2344, 2524, 2526, 2528, 2560, 2575, 2584, 2624, 2775, 2793, 2806, 2807, 2811, 2816, 2817, 2828, 2839, 2857, 2858, 2932, 2935, 2939, 2953, 2956, 2957, 2958, 3074, 3080, 3083, 3094, 3097, 3213, 3214, 3215, 3230, 3231, 3239, 3240, 3257, 3258, 3281, 3283, 3289, 3324, 3349, 3553, 3569, 3571, 3572, 3573, 3591, 3592, 3599, 3601, 3603, 3604, 3605, 3608, 3609, 3615, 3689, 3699, 3702, 3705, 3706, 3707, 3793, 3808, 3812, 3833, 3854, 3870, 3874, 3877, 3878, 3894, 3900, 3902, 4018, 4042, 4169, 4172, 4173, 4176, 4179, 4181, 4182, 4184, 4185, 4186, 4188, 4190, 4362, 4371, 4406, 4443, 4597, 4617, 4618, 4619, 4620, 4624, 4627, 4668, 4671, 4676, 4779, 4783, 4784, 4785, 4848, 4855, 5121, 5468, 5532, 5533, 5534, 5543, 5546, 5549, 5554, 5555, 5560, 5596, 5599, 5659, 5663, 5675, 5677, 5679, 5821, 5822, 5823, 5843, 5855, 5856, 5860, 5885, 25144, 28283, 28284, 28285, 28286, 28287, 28288, 28289, 28290, 28292, 28293, 28294, 28295, 28296, 28297, 28298, 29355, 29356, 29360, 29417, 29419, 29420, 29422, 29423, 29424, 29672, 29808, 29813, 29815, 30696, 30697, 30698, 30699, 30700, 30701, 30702, 30703, 30704, 30706, 30707, 30709, 30711, 30712, 31230, 31314, 31355, 31382, 31383, 31384, 31385, 31389, 33283, 33478, 33487, 33488, 33489, 33490, 33492, 33496, 33499, 33507, 33618, 33640, 33642, 33745, 33749, 33769, 33772, 33784, 33789, 33969, 34423, 34458, 34463, 34464, 34467, 34476, 34480, 34510, 34786, 34933, 34946, 34956, 34973, 35924, 36045, 36212, 36260, 36448, 36455, 36713, 36715, 36895, 36896, 36897, 36898, 36899, 36900, 36901, 36902, 37329, 37413, 37421, 37431, 37433, 37434, 37437, 37439, 37446, 37450, 37451, 37452, 37455, 37583, 37593, 37613, 37622, 80769, 80771, 80874, 80875, 80990, 81019, 81020, 81108, 94059, 94373, 94375, 94486, 94489, 94590, 94687, 94698, 94708, 94726, 94844, 94847, 94872, 94878, 94928, 94931, 95054, 95200, 95506, 95507, 114122, 114284, 114286, 114291, 114293, 114294, 114299, 114300, 133775, 133856, 134054, 134068, 134076, 134078, 134098, 134174, 134180, 134196, 134317, 134323, 134327, 134330, 134363, 134381, 134382, 134383, 134415, 134436, 134437, 134438, 134448, 134589, 134590, 134619, 134718, 134721, 134750, 134824, 134866, 134878, 134892, 134895, 135143, 135181, 135840, 135972, 135979, 135981, 136008, 136011, 136019, 136063, 136065, 136069, 136071, 136075, 136076, 136083, 136084, 136085, 136086, 136090, 136092, 136107, 136113, 136122, 136123, 136131, 136135, 136140, 136144, 136158, 136162, 136165, 136174, 136175, 136182, 136347, 136362, 136428, 136441, 136642, 136648, 136649, 136656, 136664, 136705, 136805, 136853, 137135, 137137, 137182, 137347, 137350, 137359, 137360, 137363, 137364, 137373, 137612, 137624, 137659, 170719, 170720, 170729, 170750, 170799, 170816, 170817, 170821, 170824, 170948, 170956, 170957, 170966, 170967, 170968, 171190, 171365, 171367, 171370, 171389, 172116, 172118, 172142, 172179, 207955, 208939, 208949, 209492, 209493, 209494, 209506, 209507, 209644, 209653, 209656, 209659, 209669, 209697, 209736, 209739, 209836, 209837, 209845, 209846, 209847, 209849, 209852, 209865, 209907, 209937, 209938, 209959, 210041, 210056, 210057, 210233, 210234, 210237, 210248, 210262, 210382, 210404, 210407, 210413, 210414, 210415, 210416, 210417, 210418, 210419, 210436, 210437, 210438, 210439, 210440, 210441, 210463, 210468, 210495, 210500, 210502, 210511, 210514, 210515, 210516, 210534, 210546, 210548, 210549, 210559, 210560, 210567, 210572, 210576, 210577, 210578, 210579, 210582, 210584, 210585, 210587, 210588, 210591, 210592, 210594, 210596, 210597, 210598, 210599, 210600, 210601, 210602, 210603, 210604, 210605, 210708, 210725, 210798, 210820, 246397, 246399, 246401, 246409, 246410, 246413, 246428, 246577, 246581, 246601, 246643, 246755, 246767, 246781, 246800, 246932, 246933, 246936, 246938, 246941, 246942, 246943, 246944, 246946, 285344, 285345, 285346, 285347, 285348, 285351, 285352, 285354, 285558, 285641, 285643, 285644, 285645, 285649, 285660, 285697, 285763, 285774, 286103, 286104, 286105, 286107, 286280, 286558, 286560, 286566, 286604, 286696, 286749, 286770, 286771, 286772, 286835, 286839, 286843, 286863, 286876, 286877, 286878, 286880, 286904, 286987, 286990, 287235, 287297, 287325, 287328, 287330, 287349, 287359, 287801, 287864, 287894, 287899, 287931, 287937, 287943, 287952, 287954, 287967, 287975, 288037, 288052, 288053, 288085, 288132, 288189, 288191, 288196, 288197, 288198, 288199, 288201, 288344, 288494, 288550, 288563, 288567, 288586, 288663, 288664, 288675, 288884, 288893, 289000, 289020, 289067, 289082, 289083, 289186, 289187, 289188, 289189, 289190, 289191, 289192, 289193, 289194, 289221, 289225, 326358, 326394, 326395, 326396, 326397, 326398, 326399, 326402, 326403, 347723, 347725, 347726, 347730, 348057, 348058, 348061, 348062, 348063, 348064, 348065, 348066, 348069, 348070, 348071, 348072, 348073, 348074, 348075, 348076, 348077, 348724, 348789, 348793, 348794, 348795, 348919, 348958, 348959, 348999, 349030, 349032, 349038, 349041, 349042, 349080, 349081, 389623, 389624, 389625, 389744, 389745, 389746, 389747, 389748, 390182, 390187, 390188, 390189, 390197, 390198, 390284, 390285, 390286, 390290, 390515, 390720, 390845, 390846, 390847, 390848, 390927, 390937, 390957, 390960, 390974, 390981, 390982, 390983, 390997, 390999, 391001, 391006, 391008, 391013, 391054, 391115, 391140, 391183, 391191, 391382, 391460, 391475, 391485, 391493, 391541, 391684, 391742, 391874, 391886, 391896, 391899, 391900, 391995, 392057, 392083, 392091, 392092, 392118, 392119, 392222, 392248, 392313, 392314, 392365, 392369, 392375, 392545, 392679, 392700, 392718, 392955, 392956, 392957, 392969, 392971, 392972, 392973, 392974, 392987, 393060, 393062, 393067, 393082, 393215, 393216, 393220, 393221, 393294, 393295, 393312, 393506, 393975, 393984, 393993, 393996, 393999, 394098, 394253, 394629, 394630, 394631, 394723, 394764, 394766, 394929, 395014, 395015, 395016, 395915, 396002, 396004, 396006, 396058, 396072, 396093, 396094, 396095, 396116, 437838, 437839, 437840, 437904, 437918, 437948, 437984, 438096, 438110, 438205, 439808, 439942, 439943, 439945, 439948, 439963, 439972, 439973, 439974, 439984, 439988, 439990, 439997, 440002, 440005, 440006, 440008, 440009, 440011, 440015, 440018, 440023, 440030, 440031, 440042, 440353, 440355, 440356, 441299, 441326, 441328, 441357, 441383, 441384, 441385, 441386, 441388, 441389, 441413, 441420, 441427, 441615, 441617, 441642, 441643, 441644, 441645, 485022, 485023, 485029, 485092, 485166, 485321, 485324, 485328, 485330, 485332, 485333, 485340, 485404, 485477, 485482, 485803, 485837, 485880, 485899, 485991, 485998, 486018, 486027, 486081, 486169, 486391, 486418, 486431, 486494, 486651, 486659, 486675, 486676, 486779, 486795, 486801, 486803, 486806, 486807, 486820, 486835, 486850, 486852, 486854, 486863, 486974, 487161, 487560, 487562, 487564, 487574, 487600, 487603, 487604, 487608, 487609, 487610, 487614, 487618, 487664, 487735, 487736, 487737, 487743, 487744, 487745, 487747, 487752, 487755, 487757, 487758, 487776, 487952, 487970, 488013, 488022, 488095, 488098, 488101, 488103, 488115, 488117, 488131, 488134, 488137, 488138, 488146, 488149, 488150, 488153, 488171, 488172, 488178, 488253, 488254, 488257, 488291, 488405, 488409, 488431, 488449, 488491, 488495, 488496, 488507, 488508, 488510, 488515, 488605, 488610, 488613, 488617, 488635, 488640, 488644, 488654, 488659, 488666, 488669, 489023, 489057, 489063, 489074, 489075, 489076, 489077, 489078, 489113, 489242, 489426, 489427, 489428, 489444, 489446, 489449, 489715, 489717, 489734, 489826, 489827, 489828, 489829, 489830, 489831, 489832, 489833, 489837, 489843, 489844, 489845, 489846, 489856, 489951, 489958, 490801, 492165, 492172, 492175, 492179, 586911, 636513, 636514, 636519, 636520, 636534, 636537, 636543, 636544, 636545, 636546, 636614, 636758, 636921, 637084, 637327, 637329, 637331, 637332, 637344, 637446, 637486, 637505, 637507, 637516, 637559, 637560, 637561, 637563, 637570, 637756, 637763, 637827, 637838, 638007, 638031, 638063, 638066, 638072, 638074, 638077, 638078, 638081, 638131, 638135, 638171, 638331, 638332, 638343, 638365, 638394, 638401, 638475, 638479, 638485, 638487, 638490, 638572, 638595, 638599, 638600, 638666, 638697, 638856, 638857, 638858, 638859, 638862, 638864, 638868, 638973, 638974, 638975, 638976, 638977, 639050, 639051, 639092, 639134, 639138, 639139, 639140, 639147, 639363, 639472, 639719, 639721, 639725, 639728, 639729, 639785, 639864, 639921, 640225, 640249, 640288, 640313, 640320, 640321, 640421, 640469, 640983, 640985, 640986, 640987, 640988, 640989, 641100, 641105, 641115, 641185, 641202, 641217, 641218, 641219, 641221, 641236, 641281, 641287, 641297, 641351, 641361, 641363, 641374, 641376, 641377, 641379, 641403, 641430, 641432, 641437, 641445, 641452, 641468, 641469, 641570, 641572, 641620, 641654, 641657, 641708, 641713, 641717, 641727, 641775, 641784, 641785, 641795, 641803, 641827, 641841, 641843, 642053, 642062, 642064, 642065, 642066, 642241, 642243, 642245, 642246, 642248, 642251, 642254, 642255, 642259, 642265, 642282, 642283, 642285, 642293, 642294, 642300, 642495, 642549, 642558, 642574, 642661, 642691, 642692, 642693, 642696, 642701, 642702, 642742, 642752, 642754, 642800, 642806, 642807, 642811, 642827, 642838, 642879, 642918, 642958, 642973, 642980, 642987, 642989, 642990, 643001, 643055, 643059, 643060, 643062, 643249, 643258, 643269, 643270, 643290, 643301, 643309, 643310, 643321, 643328, 643454, 643455, 643462, 643470, 643471, 643472, 643507, 643508, 643509, 643510, 643528, 643554, 643555, 643577, 643578, 643580, 643581, 643607, 643608, 643625, 643649, 643650, 643664, 643666, 643748, 643862, 643863, 643864, 643865, 644113, 644115, 644117, 644119, 644131, 644137, 644139, 644278, 644283, 644288, 644298, 644301, 644303, 644306, 644347, 644353, 644361, 644372, 644415, 644538, 644539, 644541, 644543, 644846, 645058, 645061, 645064, 645124, 645149, 645173, 645191, 645199, 645240, 645246, 645250, 645316, 645358, 645415, 645581, 645615, 645622, 646096, 646323, 646326, 646329, 646333, 646334, 646336, 646337, 646400, 646593, 646594, 646595, 646599, 646613, 647007, 647010, 647012, 647013, 647015, 647037, 647038, 647040, 647041, 647042, 647046, 647048, 647049, 647053, 647072, 647075, 647191, 647192, 647206, 647218, 647223, 647224, 647225, 647226, 647227, 647228, 647229, 647230, 647232, 647236, 647398, 648107, 648619, 648639, 648671, 648675, 648683, 648688, 648771, 648931, 648936, 648973, 648975, 648976, 648978, 648994, 648999, 649040, 649041, 649113, 649135, 649199, 649249, 649331, 649431, 649432, 649441, 649452, 649458, 649479, 649542, 649561, 649625, 649656, 649667, 649746, 649758, 649814, 649817, 649847, 649851, 649858, 649859, 649910, 649915, 649921, 649953, 649970, 649971, 649975, 650019, 650049, 650079, 650080, 650128, 650144, 650151, 650152, 650161, 650216, 650234, 650238, 650255, 650258, 650289, 650314, 650356, 650372, 650379, 650408, 650479, 650513, 650541, 650545, 650602, 650640, 650671, 650700, 650779, 650904, 650908, 650916, 650961, 650962, 650966, 650973, 651002, 651089, 651094, 651104, 651126, 651176, 651226, 651283, 651423, 651424, 651427, 651481, 651541, 651674, 651741, 651786, 651810, 651850, 651889, 651895, 651936, 651942, 651963, 651995, 652109, 652123, 652127, 652171, 652203, 652228, 652230, 652260, 652270, 652295, 652380, 652385, 652438, 652455, 652477, 652487, 652508, 652511, 652523, 652540, 652551, 652561, 652597, 652603, 652611, 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-
-
5855, 5856, 5860, 33643, 33764, 36722, 36723, 394628, 394636, 395498, 439379, 441823, 441824, 441825, 485138, 485140, 485469, 485689, 486700, 487772, 487779, 488513, 490965, 490966, 490967, 490968, 490969, 490971, 490972, 490973, 490974, 491102, 491103, 491112, 491121, 491122, 491125, 491126, 491127, 491260, 491261, 491262, 491263, 491264, 491271, 491341, 491342, 491346, 491348, 491349, 491350, 491352, 491353, 491354, 491362, 491370, 491371, 491372, 491373, 491374, 491375, 491376, 491392, 491393, 491410, 491411, 491420, 491447, 491449, 491458, 491459, 491466, 491468, 491469, 491485, 491486, 491487, 491525, 491526, 491576, 491602, 491604, 491605, 491606, 491607, 491608, 491609, 491612, 491689, 491690, 491691, 491692, 491693, 491694, 491695, 491696, 491697, 491702, 491726, 491727, 491728, 491729, 491730, 491731, 491753, 491754, 491758, 491778, 491779, 491842, 491843, 491844, 491845, 491846, 491848, 491849, 491850, 491852, 491853, 491854, 491855, 491866, 491884, 491899, 491900, 491905, 491906, 492060, 532626, 532627, 532628, 532629, 532633, 532634, 532635, 532636, 532658, 532659, 532660, 532685, 532686, 532694, 532746, 532747, 532748, 532749, 532750, 532751, 532753, 532755, 532757, 532768, 532769, 532778, 532779, 532780, 532781, 532792, 532793, 532794, 532799, 532801, 532802, 532803, 532810, 532812, 636758, 636759, 636767, 637759, 637763, 638572, 638978, 639084, 639471, 640033, 640035, 640932, 640935, 640936, 640942, 640953, 642209, 644283, 647396, 647397, 648856, 648860, 648862, 648865, 649263, 650084, 650118, 650225, 650438, 653380, 653884, 654019, 654332, 656128, 656365, 656796, 657185, 657944, 658770, 659258, 659934, 659936, 661283, 662096, 662244, 663313, 663384, 663449, 663751, 664090, 664266, 664745, 665042, 665099, 665534, 666065, 666178, 666350, 666721, 666848, 666909, 669854, 670652, 671014, 671048, 671283, 671307, 672668, 673746, 673867, 674026, 674030, 674482, 674616, 674890, 676213, 676445, 676741, 676919, 677012, 677316, 677931, 679807, 680369, 680645, 680944, 681448, 681925, 682653, 682834, 682837, 684130, 684230, 684622, 684681, 684709, 685376, 685621, 685841, 686027, 686239, 686262, 686769, 687609, 687776, 687792, 687914, 687995, 688336, 688408, 688617, 688873, 689078, 689917, 689957, 690094, 690992, 691390, 692140, 692511, 692955, 693109, 694091, 695132, 695829, 696455, 697278, 697605, 698459, 698698, 700106, 704387, 704388, 704408, 704413, 704470, 704577, 704620, 704660, 705132, 705231, 705592, 706736, 707234, 707436, 707472, 707520, 707606, 708076, 708328, 708524, 708619, 708620, 708622, 708964, 708974, 709008, 709066, 710135, 710441, 710489, 710691, 711199, 711231, 711846, 711876, 712100, 712106, 712335, 712336, 712349, 712355, 712356, 712368, 712369, 712436, 712473, 712482, 712803, 713013, 713014, 713027, 713040, 713048, 713135, 713146, 713499, 713500, 713501, 713503, 713504, 714306, 714825, 714826, 715122, 715442, 715463, 716161, 716206, 716209, 716228, 716666, 718109, 718787, 719355, 719973, 721027, 721028, 721478, 722112, 722719, 722961, 723299, 723688, 723705, 725093, 725339, 726785, 726938, 726939, 726941, 727054, 727498, 727866, 727913, 728313, 728731, 728818, 729403, 729482, 729705, 729901, 729953, 730394, 730447, 730499, 730508, 730889, 730941, 732015, 732389, 733848, 734687, 735164, 735287, 735840, 736396, 736741, 736803, 736903, 737170, 737225, 737688, 738597, 739484, 739600, 739763, 740272, 741004, 741075, 741907, 742511, 744283, 744589, 745158, 745552, 745697, 745736, 746393, 746605, 747057, 747058, 747244, 747285, 747473, 749139, 749228, 749853, 749959, 750381, 750706, 751093, 751188, 751657, 751742, 752035, 752510, 752824, 752897, 753576, 753974, 754046, 754164, 755036, 755830, 756069, 756125, 756160, 756774, 756826, 756834, 756855, 756899, 757303, 757540, 757544, 757763, 757844, 757847, 757855, 757958, 758326, 758419, 758690, 759165, 759188, 759283, 759307, 759454, 759520, 759639, 759717, 759733, 759846, 760482, 760521, 760661, 760757, 761088, 761202, 761296, 761649, 762048, 762373, 762377, 763026, 764509, 764712, 765240
A6ZS09, P00431, P00546, P00890, P00924, P00925, P00958, P04806, P04807, P05694, P05986, P06169, P06242, P06243, P06244, P06245, P06782, P06784, P07251, P07263, P07267, P08018, P08417, P08456, P08458, P08524, P0CS90, P11154, P11792, P12688, P12866, P13185, P13186, P14680, P14681, P14743, P15565, P15700, P15807, P16622, P16892, P17157, P18961, P19881, P20051, P21264, P21592, P21954, P21965, P22204, P22209, P22211, P22216, P22517, P22543, P23291, P23292, P23293, P23561, P24583, P24719, P25087, P25297, P25333, P25360, P25627, P26637, P27466, P27514, P27636, P27680, P28274, P29295, P29465, P29509, P31115, P32048, P32264, P32327, P32328, P32350, P32356, P32361, P32377, P32378, P32461, P32469, P32477, P32485, P32490, P32491, P32528, P32562, P32581, P32600, P32622, P32783, P32785, P32795, P32796, P32801, P33317, P33333, P33734, P33767, P33775, P34227, P35127, P35169, P36002, P36022, P36088, P36159, P38147, P38179, P38205, P38230, P38238, P38242, P38332, P38615, P38622, P38623, P38691, P38698, P38720, P38793, P38840, P38891, P38913, P38961, P38986, P38990, P38991, P38993, P39007, P39009, P39010, P39073, P39535, P39683, P39928, P39962, P40025, P40028, P40034, P40051, P40086, P40341, P40345, P40351, P40493, P40537, P40545, P40566, P40991, P41543, P41695, P41808, P41939, P42836, P42934, P42938, P42941, P43565, P43567, P43568, P43636, P46655, P46964, P46971, P47096, P47116, P47154, P47176, P47190, P48439, P48562, P48567, P48570, P49017, P49367, P49957, P50076, P50861, P50873, P51979, P52867, P53065, P53086, P53090, P53095, P53104, P53123, P53128, P53164, P53167, P53177, P53178, P53215, P53259, P53294, P53323, P53341, P53550, P53599, P53629, P53720, P53730, P53759, P53848, P53868, P53894, P53930, P53954, P53972, P54199, P54781, P54860, Q00055, Q00772, Q01532, Q01919, Q02555, Q02648, Q02724, Q02783, Q02795, Q03289, Q03497, Q03957, Q04119, Q04120, Q04235, Q04751, Q05016, Q05902, Q06053, Q06063, Q06151, Q06244, Q06551, Q06644, Q06892, Q07560, Q07648, Q08548, Q08641, Q08647, Q12001, Q12069, Q12122, Q12178, Q12211, Q12263, Q12272, Q12291, Q12362, Q12383, Q12400, Q12429, Q12463, Q12469, Q12505, Q92316, Q99312, Q99321, Q99380
SwissProt
-
3216, 5205, 28299, 95018, 210229, 210733, 246396, 246402, 288201, 348078, 486433, 489711, 641066, 642299, 643068, 643295, 643327, 646596, 646601, 647233, 649101, 649757, 650068, 650088, 650977, 651339, 651660, 651857, 651909, 652496, 652559, 652693, 652790, 652799, 652888, 653899, 653921, 654505, 654766, 659501, 659711, 659731, 661101, 661395, 662663, 662830, 663501, 666040, 666716, 669890, 672263, 672419, 673183, 674616, 676225, 676853, 676854, 676880, 677160, 677164, 677228, 677824, 678649, 678730, 678829, 679055, 679077, 679172, 679464, 681525, 681766, 682951, 684586, 684644, 684928, 685100, 685104, 685107, 685117, 685174, 685201, 685327, 685773, 687859, 688286, 688383, 689960, 689967, 690211, 690681, 690879, 690961, 690968, 690970, 690984, 691005, 691085, 691129, 691133, 691265, 691390, 691806, 692020, 692067, 692071, 692493, 692638, 692945, 692979, 693088, 693121, 693133, 693139, 693208, 693616, 694160, 694345, 694464, 695273, 695827, 695890, 696145, 696302, 696883, 697473, 697669, 697905, 698128, 699019, 699140, 699526, 700098, 700152, 700203, 700205, 700492, 700586, 700955, 701402, 701558, 702234, 702515, 702710, 702932, 703814, 703856, 703858, 704189, 704472, 704764, 705108, 705155, 705168, 705183, 705680, 705681, 705978, 706525, 706643, 706715, 707596, 710768, 711153, 712045, 712759, 713846, 714071, 714159, 714189, 714686, 714975, 715475, 715537, 716340, 716366, 716929, 717588, 718878, 718924, 718993, 719186, 719370, 719378, 719809, 719810, 719840, 719954, 719999, 720254, 720410, 720412, 720417, 720450, 720947, 721537, 722112, 722277, 722978, 723287, 723557, 723760, 723805, 724219, 724344, 724358, 724359, 725492, 725703, 726040, 726066, 726785, 726887, 727358, 727895, 727950, 728154, 728426, 729034, 729263, 729302, 729499, 729632, 729976, 730026, 730034, 730045, 730064, 730075, 730322, 730653, 730884, 731698, 732012, 732505, 732670, 733178, 733375, 733582, 733604, 733755, 733855, 733876, 734004, 734124, 734132, 734140, 734196, 734214, 734303, 734337, 734683, 735012, 735179, 735196, 735257, 735343, 735390, 735555, 735708, 735721, 735780, 736030, 736393, 736396, 736474, 736483, 736721, 736926, 737610, 737721, 737738, 737753, 737766, 737920, 738000, 738240, 738443, 738612, 738614, 738987, 739197, 739457, 739502, 739667, 739699, 739760, 739803, 739958, 740061, 740558, 740649, 740657, 740757, 740936, 741051, 741062, 741182, 741343, 741519, 741780, 741962, 742717, 742884, 742910, 743232, 743420, 743895, 744304, 744348, 744589, 744932, 745150, 745151, 745362, 745552, 745760, 745765, 745855, 745881, 745884, 745918, 746216, 746322, 746464, 746572, 746588, 746605, 746625, 746644, 747089, 747102, 747127, 747139, 747170, 747185, 747186, 747212, 747306, 747339, 747383, 747460, 747483, 747751, 747764, 747802, 747807, 747809, 748024, 748029, 748037, 748038, 748039, 748045, 748101, 748122, 748124, 748142, 748144, 748150, 748155, 748188, 748252, 748566, 748596, 748652, 748934, 749092, 749143, 749156, 749253, 749367, 749467, 749824, 750363, 750387, 750390, 750405, 750624, 750703, 750856, 750885, 751057, 751097, 751113, 751120, 751188, 751193, 751549, 751694, 751722, 751733, 752036, 752170, 752503, 752537, 752576, 752663, 752789, 752803, 752822, 753050, 753413, 753721, 753739, 754027, 754049, 754050, 754078, 754102, 754138, 754237, 754588, 754676, 754812, 754922, 755042, 755059, 755317, 755343, 755478, 755542, 755543, 755668, 755681, 755716, 756124, 756125, 756195, 756382, 756463, 756475, 756719, 756723, 756755, 756826, 756850, 756866, 757126, 757164, 757202, 757358, 757635, 757664, 757734, 757987, 758217, 758241, 758377, 758491, 758562, 758668, 758951, 759307, 759312, 759455, 759459, 759463, 759480, 759494, 759680, 759777, 759789, 759820, 760376, 760464, 760470, 760645, 760709, 760758, 760825, 761007, 761106, 761208, 761212, 761296, 761414, 761424, 761439, 761456, 761867, 761868, 761894, 761957, 762019, 762030, 762083, 762546, 762641, 763285, 763355, 763375, 763438, 764022, 764441, 764878, 765027, 765242, 765436, 765801
A6ZSR0, A6ZZ16, B3LL85, B3LU11, C7GJD6, C7GJH6, C7GKE4, C7GM47, C7GP37, C7GRB2, C7GSG6, E3VL26, E9P8D2, I6WHP7, O13297, P00175, P00330, P00331, P00359, P00560, P00724, P00729, P00817, P00830, P00942, P00950, P02829, P03962, P04050, P04397, P04802, P04824, P05030, P05373, P06182, P06197, P06634, P06786, P07236, P07245, P07259, P07262, P07271, P07275, P07342, P07702, P07884, P08536, P09201, P09436, P09440, P09620, P09950, P0CZ17, P10614, P10963, P11353, P12612, P12683, P13188, P13298, P13586, P14020, P14540, P14682, P14742, P14904, P15019, P15367, P15442, P15454, P15496, P16120, P16467, P16603, P16661, P16862, P17119, P17709, P17898, P17967, P19358, P19414, P19812, P20048, P21243, P21269, P21372, P21373, P21524, P21734, P22434, P22515, P22936, P23254, P24521, P25582, P26263, P27616, P27796, P27882, P28273, P28625, P28777, P29029, P29340, P29468, P31116, P31688, P32178, P32179, P32318, P32329, P32340, P32347, P32449, P32501, P32567, P32573, P32579, P32582, P32639, P32656, P32660, P32861, P32906, P33299, P33300, P33315, P33327, P33334, P35187, P35196, P35731, P36051, P36059, P36107, P36126, P36421, P36775, P37303, P38013, P38115, P38137, P38158, P38169, P38218, P38221, P38225, P38274, P38286, P38287, P38319, P38340, P38703, P38715, P38820, P38954, P38992, P38995, P38998, P38999, P39006, P39107, P39109, P39518, P39524, P39708, P39714, P39875, P39940, P39956, P39976, P39979, P40152, P40318, P40347, P40353, P40354, P40363, P40495, P40562, P40825, P40857, P41338, P41734, P41735, P41921, P42826, P42884, P43122, P43123, P43534, P43619, P46367, P46677, P46957, P46969, P46995, P47016, P47047, P47156, P48016, P48236, P48561, P49435, P50264, P52893, P52910, P52917, P53051, P53114, P53144, P53184, P53199, P53200, P53204, P53208, P53228, P53230, P53615, P53632, P53686, P53893, P53915, P53934, P53942, P53965, P53973, P53981, P54115, P54783, P54861, P70500, Q00416, Q00764, Q00873, Q00955, Q01159, Q01217, Q01574, Q02159, Q02792, Q02890, Q03018, Q03034, Q03148, Q03175, Q03220, Q03266, Q03280, Q03305, Q03503, Q03529, Q03530, Q04066, Q04081, Q04089, Q04311, Q04430, Q04432, Q04585, Q04629, Q04740, Q05506, Q05549, Q05567, Q05788, Q05871, Q05874, Q06321, Q06408, Q06508, Q06592, Q06703, Q07471, Q07729, Q07747, Q07794, Q07830, Q07923, Q07993, Q08109, Q08162, Q08220, Q08225, Q08282, Q08649, Q08702, Q08911, Q08960, Q12006, Q12039, Q12051, Q12068, Q12284, Q12320, Q12382, Q12395, Q12452, Q12674, Q3E846, Q99190, Q99344, Q9H649
Uniprot
(Ferro-Novick et al., 1984), temperature sensitive mutants, mutants impaired in Sec59p (sec59-1), cells are defective in CTP-dependent dolichol kinase
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-
2 enzyme forms Acs1p and Acs2p. Under anaerobic glucose-limited conditions only the ACS2 gene is expressed. During carbon-limited growth on glucose, ethanol, and acetate under aerobic conditions both the ACS1 gene and the ACS2 gene are expressed
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-
2 genes grs1 and grs2 encoding GlyRS1, a mitochondrial and cytoplasmic isozyme, and GlyRS2, a dispensable mitochondrial isozyme
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-
2 isozymes FRDS1 and FRDS2 encoded by gene FRDS and OSM1, respectively
-
-
2 isozymes Thi20p and Thi21p encoded by 2 redundant genes THI20 and THI21
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-
3 enzyme forms, 1. alpha-isopropylmalate synthase I, isoenzyme encoded by LEU, subform Ia, MW 68000, which is imported into the mitochondrial matrix, and cytoplasmic synthase Ib, 2. alpha-isopropylmalate synthase II, minor enzyme form
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-
3 isoenzymes: PI, PII and PIIM: a posttranslational modified PII isoenzyme
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-
3 isozymes: mitochondrial IDP1, cytosolic IDP2, peroxisomal IDP3
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a heat-resistant enzyme from protoplast lysate and a thermosensitive tonoplast-bound enzyme
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a strain carrying the MES1 structure gene on a high copy number plasmid (pFL1)
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-
aerobically grown
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-
alignment of nucleotide-binding site from human MFE-2 with Saccharomyces cerevisiae and Candida tropicalis MFE-2 shown
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-
and strain ECY38-38A, isozymes CHS1p and CHS3p encoded by genes CHS1 and CHS3
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ARO 9 gene encoding aromatic aminotransferase II, expression is induced when aromaticc amino acids are present in the growth medium
SwissProt
ARO3-encoded isozyme is a phenylalanine-sensitive isozyme
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-
ARO4-encoded isozyme is a tyrosine-sensitive isozyme
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-
at least 3 components forming the enzyme complex: GPI1, GPI2 or PIG-C, GPI3 or PIG-A
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baker's yeast
30703, 35195, 136805, 171372, 171374, 171389, 209484, 209485, 209486, 209487, 209488, 209489, 209495, 209497, 209501, 209508, 246821, 286865, 394708, 394709, 394718, 394746, 396553, 396555, 396556, 396557, 396558, 396559, 396560, 396561, 396563, 396564, 396565, 396566, 396567, 396568, 396569, 437754, 437755, 437757, 485557, 485991, 485994, 485996, 485999, 486000, 486002, 486010, 486014, 486016, 486020, 486025, 487418, 487421, 487424, 487425, 487426, 487428, 487601, 487605, 488091, 488092, 488094, 488096, 488097, 488116, 490907, 637329, 637331, 637332, 637825, 637835, 640975, 642690, 642787, 642788, 642789, 642790, 645084, 647189, 647195, 647201, 647202, 647207, 647208, 647209, 647210, 647212, 647213, 647215, 647216, 647217, 647221, 647222, 648385, 649129, 652836
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-
baker's yeast, brewers' yeast, beer yeast, FAD1 nucleotide sequence
SwissProt
baker's yeast, strain D311-3A or B-7034 and cyc3-multi-copy mutant strain B-6868-1
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-
bakers' yeast, haploid strains MO-11-48A and X1049-2B, diploid strain F2, clonal isolate of commercial bakers' yeast
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-
bifunctional diacetyl reductase and (R)-2,3-butanediol dehydrogenase
-
-
bifunctional diacetyl reductase and (R)-2,3-butanediol dehydrogenase
UniProt
bifunctional enzyme with AIR synthetase activity and phosphoribosyl-glycinamide synthetase activity
-
-
bifunctional enzyme with hydroxyethylthiazole kinase and thiamine-phosphate pyrophosphorylase activity
-
-
bifunctional exo- and endopolyphosphatase, EC 3.6.1.11 and EC 3.6.1.10
SwissProt
bifunctional exo- and endopolyphosphatase, ECs 3.6.1.10 and 3.6.1.11
SwissProt
bifunctional hydroxymethylpyrimidine/phosphomethylpyrimidine kinase
SwissProt
brewer's yeast
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-
BY4741 and deletion mutant strain of ICT1 protein in BY4741-background
-
-
carboxypeptidase Y
-
-
carrying the gene PEP4 which encodes the prepro-proteinase A on multicopy plasmids, 7:3 mixture of two different forms of enzyme: 40000 MW and 42000 MW
-
-
CEP A stre, YC17, and TS141, the strains are isogenic to W303
UniProt
cerevisin precursor, vacuolar protease B, encoded by the PRB1 gene; after disruption of proteinase B termed MT8-1/delta-PrB
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-
chitin synthase 1 is examide in wild-type strain ATCC 26109 and D3C (MATalphaura3-52), chitin synthase 2 is investigated in a strain D3B freed of chitin synthase 1 by gene disruption
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-
cloned KEX2 gene introduced into the kex2 mutant cells and the KEX2 gene product expressed in these cells
-
-
comparison of wild-type enzyme and enzyme fused with N-terminal glutathione S-transferase
-
-
constructed strain contains a single ulp1-I615N mutation
SwissProt
construction of a chimeric enzyme, in which the C-terminal 136 residues of Escherichia coli enzyme are replaced by the corresponding residues of Saccharomyces cerevisae enzyme
-
-
construction of strain TMP 3044 with multiple genetic modifications for enhanced xylose growth, one of the modifications is the overexpression of ribulose 5-phosphate epimerase
-
-
CRN mutant with inactive PPN1 gene, which is deficient in endopolyphosphatase activity
-
-
crystallization: structure of Ufd2 in complex with the ubiquitin-like (UBL) and ubiquitin-associated (UBA) proteins Rad23 and Dsk2 domains, PDB-ID: 3M62 and 3M63, respectively; S288c
SwissProt
CTP transferase domain that is also present in CDS1-encoded CDP-diacylglycerolsynthase
-
-
cyclin-dependent protein kinase Pho85p controls the phosphorylation state of phosphorylase and thereby its activity
-
-
designed strain TMB 3045, carrying the XI gene from Thermus thermophilus
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-
different isoenzymes are elaborated under aerobic and nonaerobic conditions
-
-
different laboratory (S288c, BY4741, DTY1, EG103, SKY9, and YPH98) and wild type strains (RM11-1a and Fleischmanns), PCA1 allele in all laboratory yeast strains examined carries a missense mutation in a conserved residue resulting in loss of function, wild-type PCA1 allele confers cadmium resistance by an Cd2+ efflux mechanism
-
-
different wine yeast strains. Wine yeast can be distinguished in terms of ATPase activity and oleic acid and palmitoic acid in plasma membrane
-
-
DNA repair complex components Mre11 and Rad50 show adenylate kinase activity when in complex Mre11/Rad50
-
-
dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit OST6
SwissProt
dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit STT3
SwissProt
dual-specificity enzyme, activitiy of EC 2.7.8.1 and EC 2.7.8.2
-
-
dual-specificity enzyme, activity of EC 2.7.8.1 and EC 2.7.8.2
-
-
encoding subunits Lac1p, Lag1p, and Lip1p
UniProt
enzyme activity increases during post-diauxic growth, decrease of guanine may be required when cells shift from proliferation to quiescence
-
-
enzyme aggregate contains 5 activities: EC 1.1.1.25, EC 2.7.1.71, EC 4.2.1.10, EC 4.2.3.4 and 2.5.1.19
-
-
enzyme contains both RNA and single-stranded DNA 3-5-exonuclease activities
-
-
enzyme detected in wild type Saccharomaces cerevisiae not in a mutant defective in biotin-[acetyl-CoA-carboxylase] ligase
-
-
enzyme displays a rapid 5-10fold increase in activity when carbon-starved cells are exposed to glucose. Phosphorylation at S911and T921 is related to glucose activation
-
-
enzyme immunochemically related with Escherichia coli protease la
-
-
enzyme is a component of the sterol-4-demethylation multienzyme complex
-
-
expression of both small and catalytic subunit in Escherichia coli
-
-
full-length and truncated enzyme form lacking the NH2-terminal domain
-
-
gene chs3coding for the catalytic subunit of the chitin synthase III
SwissProt
gene MIP1 encoding DNA pol gamma, and gene POL1 encoding DNA polymerase alpha catalytic subunit A
UniProt
gene NPT1 at ocus YOR209C, eukaryotic type II enzyme
SwissProt
gene PH03 encoding thiamin-repressible acid phosphatase, gene PH05 encoding phosphate-repressible acid phosphatase
UniProt
genes CCT1-8 encoding subunits CCT-alpha, CCT-beta, CCT-gamma, CCT-delta, CCT-epsilon, CCT-zeta, CCT-eta, and CCT-theta
P12612, P39076, P39077, P39078, P40413, P39079, P42943, P47079
UniProt
genes SDHA, SDHB, SDHC, and SDHD encding the four subunits of the enzyme
-
-
GPP1; wild-type W303-1A, double mutant YA103, devoid of GPP1 and GPP2
SwissProt
GPP2; wild-type W303-1A, double mutant YA103, devoid of GPP1 and GPP2
SwissProt
haploid strain cat1.S3-14A of genotype a his MAL2-8c MAL3 SUC3, isoenzymes PI and PII
-
-
haploid strain expressing only one of three structural genes for pyruvate decarboxylase, PDC1
-
-
haploid wild-type strain (a-mating type) and met-auxotroph mutant strains 6,8,12,13,15, and 17
-
-
in complex with m-AAA protease Yta12p, EC 3.4.24.B18, complex is termed i-AAA protease
-
-
inactivation of DNL4 gene causes temperature-sensitive growth
SwissProt
involvement of thioredoxin reductase in the dimethyl sulphoxide reductase system
-
-
isoform Bna3 is not an formyl kynurenine formamidase, but kynurenine aminotransferase
UniProt
isozymes PAP1 and PAP2, encoded by genes PAH1, formerly known as SMP2, and DPP1 and LPP1, respectively
-
-
KEX1 gene from Saccharomyces cerevisiae expressed using the baculovirus/insect cell system
-
-
Like the yeast enzyme, mammalian, plant and fly orthologs share the capacity for the conversion of Ins(1,4,5)P3 to Ins(1,3,4,5,6)P5. Plant and fly IPMKs recapitulate the yeast enzyme's preference for D6-hydroxyl phoshorylation followed by D3-hydroxylphosphorylation, mammalian IPMKs appear to prefer the reverse order.
-
-
low enzyme activity is measured in mutants with increased adenylate cyclase activity
-
-
low molecular weight enzyme is the same protein as serine sulfhydrylase
-
-
MATa his3-DELTA200 leu2-3,112 lys2-801 DELTAste6::LEU2 trp1-DELTA63 ura3-52
-
-
MATalpha his3DELTA1 leu2DELTA0 lys2DELTA0 ura3DELTA0
SwissProt
metabolic engineering of a xylose-isomerase-expressing Saccharomyces cerevisiae strain for rapid anaerobic xylose fermentation. The overexpressed enzymes are EC 2.7.1.17, EC 5.3.1.6, EC 5.3.1.1, EC 2.2.1.1 and EC 2.2.1.2
-
-
mitochondrial and cytoplasmic isozymes encoded by a single nuclear gene ALA1
-
-
modulation of concentration of tyrosyl radicals is not involved in the regulation of enzyme activity
-
-
mutant resistant to 2-amino-4-methyl-5-beta-hydroxyethylthiazole, an antimetabolite of 4-methyl-5-beta-hydroxyethylthiazole, deficient in activity of both EC 2.5.1.3 and EC 2.7.1.50
-
-
mutant version of reverse trancriptase from retrotransposon Ty1, in which one of the three active site aspartates is changed to asparagine, D211N
-
-
mutant yBH strains and wild-type, features of the catalytic site of bleomycin hydrolase analyzed by mutagenesis of catalytic site residues
SwissProt
mutants with substituted His residues, expressed in Escherichia coli
-
-
NatE complex subunits Naa50, Naa10 (ARD1), and Naa15 (Nat1)
UniProt
native form and truncated form that has lost the first 50-64 residues
-
-
neutral trehalase and acid trehalase isozymes encoded by the NTH1 and ATH1 genes
-
-
NuA4 is a 13-subunit KAT complex containing the essential catalytic domain Esa1
Uniprot
only fungi where spermine synthase is found is the Saccharomycotina class of the Ascomycota
-
-
overexpression, wild-type and mutant lacking the 60 base pairs encoding the C-terminal peptide
-
-
overexprssion of glycerol-3-phosphate dehydrogenase results in the production of more glycerol and less ethanol during fermentation
-
-
overproducing transformed strain WAY.10-1C, isoenzymes PI and PII
-
-
P07149 i.e. subunit FAS1, P19097 i.e. subunit FAS2
UniProt
P07149 i.e.subunit FAS1, P19097 i.e. subunit FAS2
UniProt
P07149 i.e.subunit FAS1, P19097 i.e. subunit FAS2, Q12513 i.e. gamma-subunit Tma17
UniProt
P10507: mitochondrial-processing peptidase subunit beta (MAS1), P11914: mitochondrial-processing peptidase subunit alpha (MAS2)
SwissProt
P16658: subunit Sen2, P39707: subunit Sen34, Q04675: subunit Sen15, Q02825: subunit 54
SwissProt
P29703 i.e. alpha-subunit RAM2, P22007 i.e. beta-subunit RAM1
UniProt
P41543: dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit 1, P46964: dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit 2, P48439: dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit 3, Q99380: dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit 4, Q92316: dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit 5, P39007: dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit STT3 (catalytic subunit), P33767: dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit WBP1, Q02795: dolichyl-diphosphooligosaccharide-protein glycosyltransferase subunit SWP1
SwissProt
P46959: subunit Gcd14p (catalytic subunit), P41814: subunit Gcd10p (non-catalytic subunit)
P46959, P41814
SwissProt
parental control diploid strain KM91 obtained by crossing the haploid strain 777-3A with the haploid KL14-4A/60
-
-
Pda1, i.e. E1 component subunit alpha of pyruvate dehydrogenase complex, cf. EC 1.2.1.104
UniProt
Pda1, i.e. E1 component subunit alpha, cf. EC 1.2.4.1
UniProt
PEP4 deletion mutant, PEP4 gene disruption resulted in strongly decreased available nitrogen content after alcoholic fermentation
-
-
peroxisomal isozyme CS II and mitochondrial isozyme CS I
-
-
PPX1 mutant, two enzymes with different masses and biochemical properties
-
-
proteins SDH1, SDH2, SDH3, and SDH4
UniProt
RCSB Protein Data Bank: 1EX6, enzyme with a non-acetylated N terminus in its unligated form
Uniprot
RCSB Protein Data Bank: 1EX7, enzyme with a non-acetylated N terminus in a complex with GMP
Uniprot
recombinant enzyme
-
-
recombinant enzyme overexpressed in Saccharomyces cerevisiae and Zygosaccharomyces bailii
-
-
recombinant fusion protein of yeast citrate synthase and mitochondrial malate dehydrogenase
-
-
recombinant protein, using the Pichia pastoris expression system
-
-
recombinant wild-type and mutant Pap1 were expressed, using the T7 expression system
-
-
respiratory deficient mutants. The phenotype is a consequence of a mutation in a nuclear gene coding for mitochondrial leucyl-tRNA synthetase
-
-
Saccharomyces cerevisiae
30710, 95499, 95500, 95501, 95502, 95503, 95504, 95505, 95508, 95509, 95510, 95512, 95513, 95514, 95515, 390498
-
-
Saccharomyces cerevisiae /Homo sapiens chimeric protein
Uniprot
Saccharomyces cerevisiae genome database: U24437; overexpression corrects defects in dolichol-linked saccharide formation and protein glycosylation
SwissProt
sake strain Kyokai No 701 and diverse deletion mutants
UniProt
Sake yeast strain 2NF and 1-farnesylpyridinium-resistant strain A1. Alcohol acetyltransferase activity is high in strain A1, which further increases in response to isoamyl alcohol accumulation in medium
-
-
separase is part of the so called Cdc fourteen anaphase release network, that promotes Cdc14 release from the nucleolus during early anaphase
-
-
separase mediates Cdc14 release from nucleoli during meiosis through a mechanism that is indepenent of its protease activity
-
-
separate enzyme encoded by an independent gene, not associated with indole-3-glycerol-phosphate synthetase
-
-
sequence of strain S288c which is about 99% homologous to strain 38
UniProt
several strains, 5 genes IMA1 to IMA5, i.e. YGR287c, YIL172c, YJL216c, YJL221c and YOL157c. Gene IMA1/YGR287c encodes the major isomaltase
-
-
similar enzyme with NADPH-requirement for methylglyoxal reduction, that is inactive with NAD+, NADH and NADP+
-
-
small differences in amino acid composition and enzymatic properties between the enzyme from Danish yeast and the corresponding enzyme from Fleischmann yeast suggest the existence of more than 1 form of this enzyme
-
-
strain CRX, CRY, CRN, and CNX derived from strain W303-1A
SwissProt
strain D311-3A or B-7034, and cyc3-multi-copy mutant strain B-6868-1
-
-
strain TMB 3050, derived from strain TMB 3045, which carries the XI gene from Thermus thermophilus
-
-
strain TMB 3399 and mutant strain TMB 3400 derived from TMB399 and displaying improved ability to utilize xylose with higher expression of xylulokinase
-
-
strains 8973b and 8989c, mutant lys1, lacking LKR activity, used as expression system for enzyme from Arabidopsis thaliana, lysine-ketoglutarate reductase EC 1.5.1.8 and saccharopine dehydrogenase EC 1.5.1.9 are two separate proteins
-
-
strains BY4741, null mutant DELTAglo1, and overexpressed strain YEpGLO1
-
-
strains BY4742 and BY4741 and the YBR261C/tae1 deletion strain in each background, gene YBR261C/TAE1
-
-
strains BY4742, Sigma1278b, CENPK42, TCY1, FY23, L2323, VIN13,and W303
-
-
strains from BY strain background or isogenic to strain CEN.PK2, gene nep1
-
-
strains L40 and yAS1255, a pab1DELTA strain, and a pan3DELTA strain yME43
-
-
strains S288C variant M3750, strain BY4741, strain EY0986, strain Bio101 and strain INVSc1
-
-
strains W303, W303 pep4D::HIS3, W303 pDP34, W303 pDP34-PEP4, and W303 p416ADHPEP4-GFP enzyme, increased enzyme expression induced by oxidative damage prevents the accumulation of oxidized proteins, disruption of PEP4 results in strongly decreased degradation of oxidized proteins
-
-
substrate specific enzyme form, non specific enzyme form from structural gene PHO8, and particulate enzyme form from structural gene PHO8
-
-
temperature-sensitive mutant that is defect in trehalose 6-phosphate phosphohydrolase
-
-
temperature-sensitive Saccharomyces cerevisiae mutants, impaired in dolichol kinase (Sec59p) or dolichyl phosphate mannose synthase (Dpm1p) activity have an aberrant cell wall composition and ultrastructure
-
-
the enzyme consists of nine subunits. Five of them, Wbp1, Swp1, Stt3, Ost1, and Ost2, are essential for viability of the cell, whereas Ost4, Ost5, Ost3, and Ost6 are not essential but are required for maximal OST activity: Wbp1 (P33767 (SwissProt)), Swp1 (Q02795 (SwissProt)), Stt3 (P39007 (SwissProt)), Ost1 (P41543 (SwissProt)), Ost2 (P46964 (SwissProt)), Ost3 (P48439 (SwissProt)), Ost4 (Q99380 (SwissProt)), Ost5, and Ost6
SwissProt
the enzyme is also present in wild type yeast, although its level is ten to twenty times lower than those found in the mutant
-
-
The enzyme may be a 3-phytase (EC 3.1.3.8), or a 4-phytase (synonym 6-phytase, EC 3.1.3.26). The product of the hydrolysis of myo-inositol hexakisphosphate to 1D-myo-inositol 1,2,4,5,6-pentakisphosphate or alternatively 1D-myo-inositol 1,2,3,5,6-pentakisphosphate has not been identified.
-
-
the Leu4 gene encodes 2 forms: a short cytoplasmic form and a long form that is targeted to the mitochondria
-
-
the single-site mutation A122C and N124A/V (but not N124S/Y/C) restores the GST activity of Ure2p protein toward 1-chloro-2,4-dinitrobenzene, while causing a substantial reduction in glutathione peroxidase activity
-
-
this enzyme catalyses the reaction of EC 3.5.4.2 and EC 3.5.4.4; strain 23344c
SwissProt
this enzyme catalyses the reaction of EC 3.5.4.2. and EC 3.5.4.4; strain 23344c
SwissProt
trifunctional enzyme EC 3.5.99.2/EC 2.7.1.49/EC 2.7.4.7
SwissProt
trifunctional enzyme with 10-formyltetrahydrofolate synthetase, EC 6.3.4.3, 5,10-methenyltetrahydrofolate cyclohydrolase, EC 3.5.4.9, and 5,10-methylenetetrahydrofolate dehydrogenase activity, EC 1.5.1.5
-
-
trifunctional enzyme: EC 3.5.99.2/EC 2.7.1.49/EC 2.7.4.7
SwissProt
truncated KEX1 gene expressed in the baculovirus/insect cell system
-
-
two genes DPP1 and LPP1 encode Mg2+-independent phosphatidic acid phosphatase activities
-
-
two immunologically distinct enzyme forms are elaborated under aerobic and under nonaerobic conditions
-
-
two NADP+-dependent glutamate dehydrogenases encoded by GDH1 and GDH3
-
-
UDPgalactose 4-epimerase is a bifunctional enzyme with aldose 1-epimerase activity. The active sites for the two enzymatic activities are located in different regions of the epimerase homoenzyme
-
-
up-regulated expression by low doses of methymethane sulfonate in growth medium
-
-
W303-181, having the plasmid YEpPGK-G6P (built by coupling the vector YEPLAC 181 with the promoter phosphoglycerate kinase 1)
-
-
wild type and mutants lacking the acyl-CoA-independent acyltransferase activity
-
-
wild type and proteinase B deficiency strain, in wild-type strains, proPrA is activated to mature PrA with a molecular weight of 42000 Da, whereas in PrB-deficient strains PrA maturation is delayed and a mature pseudo-form of PrA with a molecular weight of 43000 Da is detected
SwissProt
wild type strain 2D-J809, strain 2A-J809 lacking the two genes encoding L24, strain L1726 lacking the single gene encoding L39, strain L1725 lacking the genes for both proteins L24 and L39
-
-
wild type strain BY4741, mutant strain yor090c lacking pyruvate dehydrogenase phosphatase
-
-
wild type strain YKS99-2A, strain YKS99-2C missing the protein L41, the two genes RPL41A and RPL41B
-
-
wild type strains IWD72 and BY4741 and enzyme knockout mutants, knockout mutant forms large, invasive filaments, activity increases at 5-6 h of cultivation in the presence of 0.5% isoamyl alcohol and then quickly declines to become undetectable after 8 h
-
-
wild type, mutants with resistance to inhibition by Leu, mutants with resistance to inhibition by CoA
-
-
wild-type and enzyme-deficient strain, nitrogen starvation-induced
-
-
wild-type and mutant strains CEN.PK 113-7D, CEN.PK 608-4B, CEN.PK 555-4A, CEN.PK 609-11A, CEN.PK 632-3B8
-
-
wild-type and mutants with mutagenesis of a portion of the SES1 gene encoding the motif 2 loop
-
-
wild-type strain MATaa and mutant derivatives, gene URH1
SwissProt
wild-type strain MB281-8B and MB1000 and mutant strain MB281-10C
-
-
yeast
1312, 29813, 133990, 134019, 135446, 135452, 136428, 172166, 209680, 209681, 209697, 209773, 209777, 209788, 209793, 209797, 209808, 209810, 209829, 286169, 286170, 286177, 286179, 286191, 286197, 286198, 286201, 286202, 286203, 286207, 286627, 286639, 286645, 286646, 286658, 286662, 286667, 286672, 286814, 287238, 287241, 288682, 288932, 289180, 390775, 390776, 390778, 390779, 392075, 392076, 392079, 392083, 392087, 392089, 392090, 438028, 438029, 438032, 485092, 485715, 485716, 485718, 485729, 485734, 485736, 485758, 486864, 487343, 487347, 487348, 489018, 642307, 642314, 642332, 644205, 645302, 645305, 645308, 645310, 645318, 645396, 645415, 646862, 646885, 648500, 648501, 649082, 649265, 649304, 649306, 649439, 649670, 649944, 650054, 650972, 651336, 651520, 651528, 651846, 651853, 651889, 651893, 651907, 651908, 652130, 652133, 652393, 653309, 653612, 653632, 653816, 653881, 653929
-
-
yeast TOP1 null strain, JEL1delta top1, strain BY4741, strain YOL006C-TAP
-
-
yeast, trifunctional enzyme
-
-
YR6a, YPH501, Bat1p, amino acid sequence accession number
SwissProt
YR6a, YPH501, Bat2p, amino acid sequence accession number
SwissProt
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SOURCE TISSUE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
SOURCE
-
xylulokinase activity is absent during glucose metabolism but is detectable during simultaneous utilization of xylulose and glucose
actively expressed in mitotically dividing cells
-
strains W303-1A,DY1457, ZHY6, ZHY3, SH304, SH303, SH307
additional information
-
3591, 133856, 135972, 135979, 136008, 136011, 136019, 136347, 207955, 209249, 209254, 246373, 246375, 286203, 390960, 390974, 390979, 439808, 490907, 640975, 641572, 644131, 664136, 671463, 687624, 687813, 692875
-
catalytically active soluble domain, released from endogenous proteases
-
cell culture growth conditions, optimization, partition factors, overview
Chs3p and Chs4p appear to co-localize at the neck region of the budding yeast
electrophoretic karyotyping and array-based comparative genomic hybridization (array-CGH), comparison of four different species derived from the Saccharomyces sensu stricto complex of 22 distillery strains, overview. The genomic diversity is mainly revealed within subtelomeric regions and the losses and/or gains of fragments of chromosomes I, III, VI and IX are the most frequently observed. Statistically significant differences in the gene copy number are documented in six functional gene categories: 1. telomere maintenance via recombination, DNA helicase activity or DNA binding, 2. maltose metabolism process, glucose transmembrane transporter activity, 3. asparagine catabolism, cellular response to nitrogen starvation, localized in cell wall-bounded periplasmic space, 4. siderophore transport, 5. response to copper ion, cadmium ion binding and 6. L-iditol 2-dehydrogenase activity. Distillery yeasts are diploid. Gene ontology overrepresentation profiles are species-specific
-
four different isoforms, beta-glucanases I, IIIB, IV and V
-
temperature-sensitive Saccharomyces cerevisiae mutants, impaired in dolichol kinase (Sec59p) or dolichyl phosphate mannose synthase (Dpm1p) activity have an aberrant cell wall composition and ultrastructure
-
286990, 655735, 661952, 662581, 665022, 669148, 677622, 678602, 678618, 681559, 685376, 685776, 691769, 707831, 708404, 714381, 714506, 717368, 721760, 727673, 730576, 735789, 735836, 736534, 738720, 752485, 760376, 762793
L-asparaginase-II is secreted in response to N starvation
-
the highest glucose 6-phosphate dehydrogenase activity occurrs when the glucose solution is fed into the fermenter through the decreasing linear mode
the production of the soluble HIS7 is highest at 25°C with 1 mM isopropyl beta-D-thiogalactopyranoside and this condition is used for the large-scale protein preparations
during the biological aging of sherry wines, where Saccharomyces bayanus has to grow on ethanol owing to the absence of glucose, this isoenzyme plays a prominent role by converting the ethanol into acetaldehyde and producing NADH in the process. Overexpression of the gene ADH2 (from Saccharomyces cerevisiae) during alcoholic fermentation has no effect on the proteomic profile or the net production of some metabolites associated with glycolysis and alcoholic fermentation such as ethanol, acetaldehyde, and glycerol. However, it affects indirectly glucose and ammonium uptakes, cell growth, and intracellular redox potential, which lead to an altered metabolome
-
grown in a fermenter in an inositol-deficient medium
additional information
-
AATase for ethyl acetate peaks at the beginning of the exponential growth phase and that for isoamylacetate at its end
additional information
-
ACH1 is present at low levels in D-glucose-containing medium, ACH1 expression is almost undetectable when lactate is the sole carbon source
additional information
actively expressed in mitotically dividing cells
additional information
-
activity dropps upon inoculation of stationary phase wild-type cells into a glucose medium
additional information
-
ARA1 can only be detected in yeast peptone dextrose 2-DE gel images, thus higher reductive efficiency and higher cofactor availability are obtained with the alternation of cultivation condition (mainly growth medium)
additional information
cells expressing only the Sip1 isoform of Snf1 kinase grow very poorly onmediawith glycerol/ethanol as the carbon source
additional information
-
chitin synthase II shows highest specific activities in extracts from logarithmically growing cultures. Chitin synthetase I, whether from growing cultures or stationary phase cultures, is only measurable after trypsin treatment, and levels of zymogen do not change
additional information
-
enzyme is expressed in a large number of different cell types and tissues
additional information
-
enzyme is synthezised in the cytosol as the precursor protein and then imported into the mitochondria matrix and cleaved to the mature enzyme, the targeting information is encoded in nonoverlapping regions of the presequence
additional information
-
expression of the two isoenzymes is differentially regulated and expressed during different growth conditions, expression of PYC1 and PYC2 is influenced by both the growth phase and carbon source, overview
additional information
-
expression, localization and degradation of Chs2 are cell cycle dependent
additional information
-
fairly constant levels of Hat1 protein throughout the cell cycle, soluble histone H4 Hat1-dependently acetylated on Lys12 is present in cells arrested at all cell cycle stages, G1, S, G2/M and also G0
additional information
glycerol production rates of different strains, overview
additional information
-
growth on trehalose leads to the Kluyver effect, in contrast to other yeasts
additional information
growth profile and ethanol production in isozyme knockout strains, overview
additional information
-
isozyme pattern of expression and localization, overview
additional information
-
level of chitin synthase 1 remains constant during vegetative growth in synchronised cells
additional information
molecular karyotyping reveals the diversity of chromosome patterns, four strains with the most accented genetic variabilities are selected and subjected to genome-wide array-based comparativ genomic hybridization (array-CGH) analysis. The differences in the gene copy number are found in five functional gene categories: (1) maltose metabolism and transport, (2) response to toxin, (3) siderophore transport, (4) cellular aldehyde metabolic process, and (5) L-iditol 2-dehydrogenase activity
additional information
-
most abundant in tissues which display active polysaccharide synthesis
additional information
mutants Cdc5-T238A and Cdc5-ad variants, as well as the wild-type protein, were detectable in late S and G2/M phases, but not in late G1 and early S, mirroring the expression of the CDK1-cyclin Clb2
additional information
-
permeabilized cells of Saccharomyces cerevisiae, with 0.01% (w/v) digitonin
additional information
-
screening of 102 pure yeast cultures isolated from wine ecosystems for enzyme activity
additional information
-
the enzyme activity is maximal during the logarithmic stage of growth and is decreased in the stationary phase
additional information
the enzyme is expressed preferentially during sporulation
additional information
-
the URA7 mRNA is 2-fold more abundant than the URA8 transcript
additional information
ubiquitous enzyme expression in mouse tissues
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LOCALIZATION
ORGANISM
UNIPROT
COMMENTARY
GeneOntology No.
LITERATURE
SOURCE
-
recombinant enzyme expressed in Escherichia coli
co-purifies with crude mitochondria during subcellular fractionation of organelles
-
Dim1 in eukaryotic organisms is an essential member of the processome, a multifactor assembly that does not exist in bacteria
-
-
integral membrane protein, tightly associated to luminal side of membrane
-
Cdc50p and Drs2p are localized to the trans-Golgi network and late endosome
additional information
subcellular localization of ABP140 to actin filaments is not involved in tRNA modification
-
subcellular localization of Abp140p to actin filaments
-
AP-1 is required, and GGA proteins, Golgi localized, gamma-ear containing, Arf-binding proteins acting as chlatrin adaptos, are dispensable, for efficient exclusion of Drs2p from exocytic vesicles targeted to the plasma membrane
-
enzyme variant with a deletion in the linker region
-
the extracellular enzyme is attached to the cell wall
-
in Schizosaccharomyces pombe the heterologous enzyme is secreted into the cell wall
-
the culture medium affects the relative abundance of chitin synthase 1 in chitosomes and plasma membrane populations
-
-
Rph1 is associated with a specific chromatin locus. Release of Rph1 from chromatin also required the phosphorylation at S652
E9P8D2, O13297, P00330, P00958, P09436, P21373, P26637, P29509, P31115, P32622, P32796, P36022, P38013, P38088, P38238, P38793, P40825, P46655, P53294, P53550, P53686, Q00055, Q02890, Q02979, Q03220, Q03305, Q04120, Q06504 AND Q12387, Q06817, Q06892, Q08641, Q12036, Q12320, Q12463, Q99321
-
70, 96, 109, 112, 316, 340, 341, 343, 370, 414, 538, 33749, 35924, 94561, 136441, 209731, 209732, 210600, 285774, 286627, 286645, 286646, 286672, 392079, 392083, 392090, 392091, 392333, 438096, 441420, 441427, 486864, 487952, 488095, 488096, 488101, 488103, 488115, 638066, 638074, 645191, 645405, 646096, 647037, 648860, 650151, 652038, 653192, 653816, 655130, 656757, 657645, 662300, 662307, 663236, 664954, 668182, 669589, 671048, 673963, 674616, 674764, 675961, 676064, 676123, 676213, 679593, 686262, 686967, 687514, 687609, 690063, 693109, 696455, 697267, 699019, 706503, 708328, 710544, 712349, 712762, 714826, 716929, 717822, 719075, 727593, 728297, 729626, 729721, 733796, 739927, 741300, 743567, 745346, 745362, 745765, 746265, 748150, 750703, 751012, 751690, 752035, 754027, 756069, 756855, 756931, 758326, 758836, 762030, 764878
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a nonessential RIND/PHD finger protein that constitutively shuttles between cytoplasm and nucelus
Bmt6 is localized predominantly in the cytoplasm
-
cytoplasmic isozyme has a zinc-finger motif and an insertion domain that divides the nucleotide-binding fold into 2 halves
-
during the normal cell cycle, the two large subunits Rnr1 and Rnr3 are predominantly localized to cytoplasm. Under genotoxic stress the subunits Rnr2 and Rnr4 become redistributed to the cytoplasm in a checkpoint-dependent manner
-
gene product of GRS1 has enzymic activity both in cytoplasm and mitochondria
Ire1p spans the ER membrane or the nuclear membrane with which the ER is continuous, with its kinase domain localized in the cytoplasm or in the nucleus
-
most of the Ach1p activity is distributed with mitochondria and little in the cytoplasm
-
subunits specified by nuclear genes and sythesized in the cytoplasm
the cytoplasmic C-terminal portion of the enzyme carries an essential protein kinase activity
-
the Leu4 gene encodes 2 forms: a short cytoplasmic form and a long form that is targeted to the mitochondria
-
translocates onto the cytosolic side of intracellular membranes
Trm7, Trm732, and Trm734 are localized to cytoplasm
-
Ulp1 localizes predominantly to nuclear pore complexes but also deconjugates sumoylated septins at the bud-neck of dividing cells. A 218-amino acid, substrate-trapping mutant of the catalytic domain of Ulp1, Ulp1(3) C580S is necessary and sufficient for septin localization
C7GKE4, P00942, P07245, P07347 AND P12945, P09440, P11353, P12612, P12612 AND P39076 AND P39077 AND P39078 AND P40413 AND P39079 AND P42943 AND P47079, P14743, P15454, P21269, P21373, P32356, P32567, P32622, P38137, P38225, P38623, P38715, P38891, P39518, P39976, P47095, P47176, P53215, P54115, Q00055, Q04430, Q06892, Q08689 AND P41227 AND P12945, Q12068
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1679, 2526, 4406, 5663, 80990, 134196, 134866, 134895, 209849, 210500, 210511, 210516, 210577, 210578, 210584, 246373, 246755, 286560, 286627, 286658, 286672, 288663, 288664, 288932, 289225, 390960, 392079, 392083, 392087, 392368, 437839, 437840, 485321, 485991, 486002, 488095, 488096, 488116, 491372, 492119, 492165, 586911, 639092, 640022, 640421, 641217, 641374, 641377, 642062, 642558, 642904, 649129, 649304, 649432, 649667, 651126, 654652, 654785, 654839, 654886, 655186, 656125, 665748, 666296, 667750, 667765, 668027, 668234, 668761, 669399, 669579, 670176, 670725, 671730, 672419, 673201, 674616, 675000, 676919, 677711, 681379, 685048, 685307, 687678, 688364, 689409, 690175, 690208, 691390, 692309, 693521, 694807, 694934, 695829, 696170, 696373, 699104, 701402, 703640, 705784, 706404, 710949, 711140, 711273, 714686, 717248, 718813, 720808, 721219, 724285, 724459, 731811, 733876, 734489, 738614, 738987, 740757, 744986, 749525, 749858, 749959, 750885, 751022, 751124, 751277, 752642, 758358, 758492, 758951, 759283, 759494, 759639, 759717, 759733, 761212, 761296, 762213, 762546, 763375, 764192, 764720, 765811
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aconitase in yeast is a single translation product, which is dual targeted and distributed between the mitochondria and the cytosol by a unique mechanism involving reverse translocation, dual localization, detailed overview
-
alcohol acetyltransferase 1 is located within the cellular vacuoles
Alg13p protein localizes both to the membrane and cytosol
-
during growth under isosmotic conditions, presence of Hog1, the Hog1-asmutant, and mutants K52R and D144A
-
enzyme is synthesized in the cytosol and subsequently imported into the peroxisome
-
heterologously expressed native and truncated protein
-
IDP2 carrying a type I peroxisomal targeting sequence, IDP2+CKL, is only partially localized to peroxisomes, the enzyme is able to function either instead of peroxisomal IDP3 or as cytosolic IDP2
-
isoform ACS2 is localized primarily to the nucleus, with a minor amount in the cytosol
-
localization of cytoplasmic GlnRS in mitochondrial Gln-tRNA synthesis
localized both to the cytosol and mitochondria by a reverse translocation mechanism
-
mitochondrial and cytosolic isoforms are derivatives of a single translation product and have identical amino termini
-
Pep4p is released from the vacuole into the cytosol in response to acetic acid treatment
-
Pex1p and Pex6p form a stable higher-molecular-mass complex in the cytosol
-
Pex6p and Pex1p form a stable higher-molecular-mass complex in the cytosol
-
Rho GTPase, partially cytosolic in association with guanine nucleotide dissociation inhibitor
small portion of enolase bound to vacuoles, in vitro stimulation of vacuole fusion determined
-
strict specificity avoids interference with plethora of phosphorylated metabolites in the metabolic network
the intracellular localization is changed depending on the growth phase. Distributed in the cytosol until the initial logarithmic phase (12 h), then delivered to an organelle with a granule structure in the middle logarithmic phase (14 h), and finally localized at the vacuole membranes in the stationary phase (18-20 h)
-
the Lcb1p and Lcb2p subunits of the SPT heterodimer may interact in the cytosol, as well as within the membrane and/or the lumen of the endoplasmic reticulum
-
the Pex1p/Pex6p complex exhibits a dual localization, with one fraction anchored to the peroxisomal membrane by its interaction to Pex15p and the second fraction located in the cytosol
the Pex1p/Pex6p-complex shows a dual localization in the cell as it is located in the cytosol as well as at the peroxisomal membrane
-
the zymogen remains in the cytoplasm and does not enter the secretory pathway
-
translation product of the FUM1 gene, distribution can be affected by hsp70 molecular chaperones
P17967, P22543, P28625, P32906, P38298, P39007, P40318, P43636, P50076, P53954, Q02896, Q03529, Q07830, Q08109, Q12284
-
3074, 3094, 170966, 170967, 210500, 210511, 210516, 210576, 210577, 210578, 390848, 394228, 394253, 485557, 485880, 488491, 638131, 638135, 638331, 638975, 638976, 646596, 650356, 650779, 652789, 656216, 656340, 657645, 658848, 662301, 662335, 679055, 681766, 682951, 687552, 687725, 691085, 696283, 704777, 707520, 708622, 708974, 716168, 718835, 719860, 722362, 723790, 730046, 733290, 735196, 742820, 742884, 745307, 749525, 750411, 752046, 752309, 753151, 753413, 753426, 753754, 754064, 754085, 754091, 754099, 754230, 754716, 754717, 756099, 757432, 759165, 760521, 761129, 761424, 763285
-
Alg 14 protein functions as a membrane anchor that recruits Alg 13 protein to the cytosolic face of the endoplasmic reticulum, where catalysis of GlcNAc2-PP-dol occurs. Alg 13 protein and Alg 14 protein physically interact and under normal conditions, are associated with the membrane of the endoplasmic reticulum
-
at Golgi-endoplasmic reticulum contact points
both the N and C termini are oriented toward the cytosol and have different catalytic roles. A highly conserved motif, 129YFP131, and a hydrophilic segment exclusive to yeast DGAT2 reside in a long endoplasmic reticulum luminal loop following the first transmembrane domain and play an essential role in enzyme catalysis. The strongly conserved residue His195 within the motif HPHG, which may play a role in the active site of DGAT2, is likely embedded in the membrane
-
cytosolic Alg13p is very short-lived, whereas membrane-associated Alg13 is relatively stable
-
distribution of Erg proteins between endoplasmic reticulum and liquid particles in wild-type and DELTAerg11-DELTAerg3 mutant, overview
-
endoplasmic reticulum-resident glycoprotein
enzyme contains the conserved His residue close to a short stretch of hydrophilic amino acids, which is intercalated between two potential transmembrane helices. The active site histidine resides in the lumen of the endoplasmic reticulum
-
enzyme exists as an interconvertible mixture of monomers and dimers
-
enzyme is closely associated with membranes of the endoplasmic reticulum
-
enzyme recycles between the Golgi and the endoplasmic reticulum, Och1p functions in the endoplasmic reticulum when allowed to accumulate there together with substrate proteins
ER, the predicted transmembrane domain localizes the N-terminus of Alg1 into the ER lumen. The N-terminal transmembrane domain including the following positively charged amino acids and an N-terminal amphiphilic-like alpha-helix domain exposed on the protein surface strictly coordinate the Alg1 orientation on the ER membrane. The N- and C-termini of Alg1 are located to luminal and cytosolic side of the ER, respectively. The conserved proline 20 residue has no effect on its membrane-spanning property. The positively charged amino acids (K35, K38, K39 and R40) downstream of the N-terminal transmembrane region are important for ER membrane attachment
highly enriched in a structure marking nuclear-vacuolar junctions
isoform Cds1 is an ER-resident protein
localized to the continuous endoplasmic reticulum and some dots associated with the endoplasmic reticulum
-
lumen, the Lcb1p and Lcb2p subunits of the SPT heterodimer may interact in the cytosol, as well as within the membrane and/or the lumen of the endoplasmic reticulum
-
many proteins are O-mannosylated inside the endoplasmic reticulum by an O-mannosyltransferase, the Pmt1p-Pmt2p complex
Mcd4 contains a large NH2-terminal ER lumenal domain
-
multiple oligosaccharyl transferase isoforms with different affinities for the translocon and ribosome and with heterogeneous subunit composition might exist in the endoplasmic reticulum membrane, thereby providing a means of regulating protein N-glycosylation
P41543 AND P46964 AND P48439 AND Q99380 AND Q92316 AND P39007 AND P33767 AND Q02795
N-linked glycosylation occurs in the endoplasmic reticulum lumen by the membrane associated oligosaccharyltransferase enzyme complex
-
N-terminal region of Alg14 is respnsible for its localization to the endoplasmic reticulum membrane
-
oligosaccharyl transferase has a large domain in the lumenal side of endoplasmic reticulum where the catalysis occurs. The lumenal domain mainly comprises the catalytic Stt3p, the donor substrate-recognizing Wbp1p, and the acceptor substrate-recognizing Ost1p
peripheral but tightly associated membrane protein, localized to a subregion of the endoplasmic reticulum membrane that is specialized for dolichol synthesis
-
physical interactions between the Alg1, Alg2, and Alg11 mannosyltransferases
protein accumulates at nucleus-vacuole junctions
-
the 18 N-terminal amino acids form the signal peptide responsible for enzyme entry into the endoplasmic reticulum lumen. Enzyme Rny1p requires entering into the endoplasmic reticulum first to become active by N-glycosylation and uses the adaptor protein Erv29p for packaging into COPII vesicles and transport to the Golgi apparatus, wich results in the further attachment of high-glycans
-
the endoplasmic reticulum localization of the enzyme in wild type cells depends on Redp for retrieval from an early Golgi compartment
-
the enzyme present in the endoplasmic reticulum lacks lipolytic as well as acyltransferase activity
-
the Erf2-Erf4 complex localizes to the endoplasmic reticulum where it palmitoylates Ras. Role of the quality control system in degrading Erf2 molecules that are not in complex with Erf4
-
the Mnn9p-containing multi-protein complexes cycle back and forth between the endoplasmic reticulum and Golgi, type II transmembrane protein
the most conserved motif containing the presumed active site histidine of isoform Slc1 is oriented in the the membrane towards the lumen, whereas other conserved motifs are cytosolic.embrane to the endereas other conserved motifs are cytosolic
-
the N terminus of Pca1 contains a targeting signal for ERAD. Degradation of Pca1 and cadmium sensing occur at the endoplasmic reticulum
the N- and C-terminal ends of Ypc1p are oriented towards the lumen and cytosol, respectively, cytosolic or lumenal loops
-
transmembrane protein with a luminally oriented active site
-
Tsc10p localizes to the yeast endoplasmic reticulum membrane
-
an integral membrane protein, the Scs7p core is composed of a helical catalytic cap domain that sits atop four transmembrane helices that anchor the enzyme in the endoplasmic reticulum
-
ERF2 encodes a protein with four predicted membrane-spanning domains
integral membrane protein
P28496 AND P38703 AND Q03579
Lac1p and Lag1p are integral membrane proteins with six to eight predicted transmembrane domains. Co-subunit Lip1 is also an integral membrane protein, with one transmembrane domain. Its short N-terminal part is cytoplasmic and not required for ceramide synthesis. Analysis of membrane topology of the heterotrimer for ceramide synthase catalytic activity, overview
membrane topology of enzyme Pis, overview. The enzyme central sequence contains 6 transmembrane helices
reaction takes place in the lumen
squalene synthase consists of both an N-terminal catalytic domain and a C-terminal domain which consists of a hinge region and a membrane spanning helix responsible for tethering the enzyme to the cytosolic face of the endoplasmic reticulum
-
the enzyme forms a demethylation complex in the ER together with the transmembrane protein Erg28p, and possibly the other C-4 demethylation proteins Erg26p, overview
P28496 AND P38703 AND Q03579
transmembrane topology of topology of the Lag1p and Lac1p subunits in yeast using insertion of glycosylation sites and factor Xa-cleavage sites in the loops between the predicted transmembrane segments, method, overview. The N- and C-termini of the proteins are in the cytoplasm and eight putative membrane-spanning domains are identified in Lag1p and Lac1p. The conserved Lag motif, potentially containing the active site, is most likely embedded in the membrane
-
210582, 656345, 668565, 670969, 674999, 676123, 688902, 718993, 723790, 737611, 752310, 760521, 760661
-
enzymes cycles between trans-Golgi network and late endosomes, facing the cytosol
-
loss of AP-1 markedly increases Drs2p trafficking to the plasma membrane, but does not perturb retrieval of Drs2p from the early endosome back to the trans Golgi network, AP-1 is required at the trans Golgi network to sort Drs2p out of the exocytic pathway, presumably for delivery to the early endosome
-
the C-terminal proline-rich domain of Bro1 participates in recruitment of the Doa4 ubiquitin hydrolase to the endosome
-
the important function of Doa4 in Gap1 endocytosis operates at the late endosome stage
-
when amino acids are scarce Gap1p is sorted to the plasma membrane, whereas when amino acids are abundant Gap1p is sorted from the trans-Golgi through the multivesicular endosome and to the vacuole requiring direct recognition of transport substrates
-
-
30805, 30806, 30807, 135837, 135847, 136071, 136187, 136642, 438096, 438110, 657645, 665274, 679566, 691434, 701558, 708558, 709373, 722310, 729344, 750624
-
the enzyme is secreted by the secretory pathway in active form
-
-
whereas modifications with glycans are dispensable for the nucleolytic activity of Rny1p, Golgi-mediated modifications are critical for its extracellular secretion
-
-
210576, 210577, 210578, 636762, 636764, 650257, 653329, 661239, 667421, 670969, 675000, 677233, 697976, 698771, 718993, 719999, 723790, 732218, 737738, 748170, 752046, 752309, 752310, 761208, 761957, 762019
-
at Golgi-endoplasmic reticulum contact points
-
distribution in multiple compartments
-
Drs2p and Dnf3p are localized in the trans Golgi network
-
Drs2p, which has multiple endocytosis signals, including two NPFXDs near the C terminus and PEST-like sequences near the N terminus that may mediate ubiquitin-dependent endocytosis, localizes to the trans-Golgi network in wild-type cells and accumulates on the plasma membrane when both the Ub- and NPFXD-dependent endocytic mechanisms are inactivated, the C-terminal and N-terminal NPFXD motifs ar functionally required by Drs2p and Drf1p, overview
-
enzyme recycles between the Golgi and the endoplasmic reticulum, but normally functions in the cis-Golgi
-
enzyme Rny1p requires entering into the endoplasmic reticulum first to become active by N-glycosylation and uses the adaptor protein Erv29p for packaging into COPII vesicles and transport to the Golgi apparatus, which results in the further attachment of high-glycans. Whereas modifications with glycans are dispensable for the nucleolytic activity of Rny1p, Golgi-mediated modifications are critical for its extracellular secretion. Function of Golgi glycosylation in a T2 RNase as a sorting and secretion signal
-
enzymes cycles between trans-Golgi network and late endosomes, facing the cytosol
-
excessive overexpression of GFP-tagged Env7 leads to additional localization to the Golgi apparatus
Q06346 and P36107
Kei1 localizes to mid-Golgi and is cleaved by protease Kex2
-
loss of AP-1 markedly increases Drs2p trafficking to the plasma membrane, but does not perturb retrieval of Drs2p from the early endosome back to the trans Golgi network, AP-1 is required at the trans Golgi network to sort Drs2p out of the exocytic pathway, presumably for delivery to the early endosome
-
Mnn9p, cis Golgi, the Mnn9p-containing multi-protein complexes cycle back and forth between the endoplasmic reticulum and Golgi, type II transmembrane protein
-
Mnn9p, primarily localized to the cis Golgi, type II transmembrane protein
the enzyme's active site is in the lumen
-
Vps74-Sac1 complexe is localised in the Golge apparatus
-
integral membrane protein Csg1 exhibits a membrane topology with its C-terminus in the cytosol and its mannosyltransferase domain in the lumen
integral membrane protein Csh1 exhibits a membrane topology with its C-terminus in the cytosol and its mannosyltransferase domain in the lumen
-
NSF requires a peripheral membrane protein to bind Golgi membranes
ScMnn9p enzyme is a type II membrane proteins, possessing a short cytosolic N-terminal domain followed by a transmembrane domain that is required for anchoring to the Golgi membrane
-
protease is inserted in the inner mitochondrial membrane
-
-
hydropathy analysis predicts multiple membrane spanning segments
-
-
Ste24 has a lumenal N-terminus and a cytosolic C-terminus indicativ of an odd number of transmembrane spans, hydropathy analysis suggests 7 membrane spans
-
-
-
membrane-bound vesicle, Chs3p is present in an active form
-
the enzyme activity is restricted to lipid droplets
Srt1p resides mostly in lipid particles
-
P07251, P14180, P20048, P29465, P33333, P33775, P36051, P38137, P38179, P38225, P38286, P39518, P43636, P46971, P47190, P53954, Q08548, Q12382
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29418, 29419, 29420, 29422, 34786, 94367, 94373, 133856, 134878, 135181, 135452, 135981, 210056, 210057, 210419, 289082, 392718, 438028, 438029, 439966, 439974, 440005, 440015, 440023, 440030, 485023, 485029, 486356, 486375, 487614, 488510, 489427, 489608, 489845, 638131, 638312, 638331, 638332, 638334, 638336, 638337, 638343, 640401, 642549, 644361, 645302, 645308, 645348, 651846, 651889, 653118, 655999, 656178, 656216, 656275, 656276, 658182, 659238, 659510, 659862, 669510, 672103, 672337, 672419, 674465, 685019, 686462, 686825, 687624, 687738, 687781, 688907, 689460, 690893, 692139, 696156, 696595, 697213, 697536, 698771, 707436, 707472, 707606, 708974, 709008, 711466, 712369, 714314, 716860, 719787, 719791, 719809, 720089, 722362, 723791, 724452, 733305, 735147, 736445, 736741, 737129, 751022, 754149, 757000, 758549, 759165, 761456, 761867
-
a membranespanning protein that traverses the membrane six times and has an N-terminus and C-terminus facing the cytosol
Alg13p protein localizes both to the membrane and cytosol
Alg14p protein is exclusively membrane-bound
-
an integral membrane protein with six transmembrane spanning regions
associated
bound to
-
DGPP phosphatase is an integral membrane protein with six transmembrane-spanning domains
-
enzyme is anchored with both its N-termini and C-termini in the membrane, while the main part of the protein is oriented towards the lumen of the endoplasmic reticulum
-
enzyme is closely associated with membranes of the endoplasmic reticulum
-
G970R mutation affects correct trafficking of the protein
Gpc1p is an intergral membrane protein with eight transmembrane helices
-
inner mitochondrial membrane and Golgi/vacuole membrane
integral membrane protein
-
integral membrane protein, at least a portion of the enzyme is exposed at the exocellular surface
-
integral membrane protein, destined for the vacuolar lumen
integral, multiple transmembranal domains
Ire1p spans the ER membrane or the nuclear membrane with which the ER is continuous, with its kinase domain localized in the cytoplasm or in the nucleus
-
lipid phosphate phosphatase enzymes possess a three-domain lipid phosphatase motif that is localized to the hydrophilic surface of the membrane
-
membrane protein complex. Ost2p and Stt3p have only their N terminus located in the cytosol. Ost3p and Swp1p have only their C terminus oriented in the cytosol. In the case of Ost5p and Ost6p, both their N and C termini are present in the cytosol
membrane topology of Alg1, overview. A conserved alpha-helix domain, Alg1 Nalpha3 domain, contributes to the membrane association of Alg1 protein
-
Mnn9p is a membrane-associated protein, type II transmembrane protein
-
multiple oligosaccharyl transferase isoforms with different affinities for the translocon and ribosome and with heterogeneous subunit composition might exist in the endoplasmic reticulum membrane, thereby providing a means of regulating protein N-glycosylation
-
Ndi1 is a peripheral membrane protein forming an intimate dimer, in which packing of the monomeric units within the dimer creates an amphiphilic membrane-anchor domain structure, membrane-anchor domain, overview
-
newly synthesized enzyme first travels to the cell surface via the secretory pathway, endoplasmic reticulum, Golgi, secretory vesicles, resides in the plasma membrane transiently and subsequently undergoes endocytosis and degradation in the vacuole
oligosaccharyl transferase consists of nine different subunits, all of which contain one or more predicted transmembrane segments
oligosaccharyl transferase consists of nine different subunits, all of which contain one or more predicted transmembrane segments. Ost4p is a minimembrane protein
oligosaccharyl transferase consists of nine different subunits, all of which contain one or more predicted transmembrane segments. Ost5p is a membrane protein
oligosaccharyl transferase consists of nine different subunits, all of which contain one or more predicted transmembrane segments. Swp1p probably possesses three transmembrane segments, with its N-terminus in the lumen and C-terminus in the cytosol
oligosaccharyl transferase consists of nine different subunits, all of which contain one or more predicted transmembrane segments. The functional domain of Ost1p is its membrane-anchored lumenal domain
oligosaccharyl transferase consists of nine different subunits, all of which contain one or more predicted transmembrane segments. The Ost2 protein possesses three transmembrane segments, with its N-terminus in the cytosol and C-terminus directed towards the lumen
oligosaccharyl transferase consists of nine different subunits, all of which contain one or more predicted transmembrane segments. The sequence of the lumen-oriented half of the transmembrane domain is important for the function of the Wbp1 protein
protein is predicted to have two hydrophobic domains, each capable of spanning the membrane twice, and has the HX(2-3)(XH)H motifs that are characteristic of membrane-bound fatty acid desaturases
-
proteolytic cleavage of the transmembrane form between residues Ala24 and Thr25 results in a soluble form
-
recruitment of the yeast lipin (Pah1p) is regulated by PA levels onto the nuclear/endoplasmic reticulum membrane. Recruitment requires the transmembrane protein phosphatase complex Nem1p-Spo7p
-
SDH is attached to the membrane through Sdh3 and Sdh4 subunits
-
soluble form is produced for comparison with the native membrane bound enzyme
-
sorting of integral membrane protein Cps1p into the luminal vesicles of multivesicular bodies
-
the acid trehalase contains either a transmembrane segment or a signal sequence at the N-terminus
-
the enzyme is an intramembrane serine protease, intramembrane rhomboid topology, modeling, overview
-
the enzyme's N-terminal Cys13 to -15 track is essential for Env7 vacuolar membrane anchoring and kinase activity
the intracellular localization is changed depending on the growth phase. Distributed in the cytosol until the initial logarithmic phase (12 h), then delivered to an organelle with a granule structure in the middle logarithmic phase (14 h), and finally localized at the vacuole membranes in the stationary phase (18-20 h)
the kinase contains a membrane-spanning domain
-
the Lcb1p and Lcb2p subunits of the SPT heterodimer may interact in the cytosol, as well as within the membrane and/or the lumen of the endoplasmic reticulum
-
two membrane-associated forms, 45000 Da and 104000 Da, of the Mg2+-dependent phosphatidate phosphatase
-
type II integral membrane glycoprotein with a short amino-terminal cytoplasmic domain, which is not sufficient for Golgi localization, a single transmembrane domain , and a large catalytic lumenal domain, which is required for activity
-
type II membrane protein with a single hydrophobic stretch acting as an uncleaved signal sequence and anchor to the membrane preceded by a short hydrophilic, cytosolic tail
-
type II transmembrane protein with a single hydrophobic domain, which acts as an uncleaved signal sequence and membrane anchor, and is preceded by a short hydrophilic cytosolic tail
-
type-II transmembrane protein
-
ubiquitinated Ste6 is associated with. Ubiquitination of Ste6 or of a trafficing factor is required for Ste6 sorting into the multivesivular bodies pathway. Ste6 recycles between an internal compartment and the plasma membrane
-
X-2180, equally distributed between particulate and supernatant fractions
P06197, P17898, P20048, P28496 AND P38703 AND Q03579, P33333, P38298, P43636, P48236, P54781, Q02896, Q08548, Q12063
-
-
3591, 3601, 3603, 3608, 5823, 134892, 170948, 285344, 285345, 285351, 285354, 288550, 288581, 289082, 289083, 393062, 438205, 485330, 486375, 486659, 486675, 486676, 487174, 488496, 488515, 489441, 489826, 489828, 489837, 489845, 489846, 638334, 640401, 641783, 645302, 645308, 645316, 645318, 645348, 654951, 656216, 658182, 672414, 681768, 687552, 687624, 690092, 716168, 733242, 733290, 733847, 733848, 734125, 737738, 737766, 738001, 753414, 753754, 756834, 757164, 757540, 759165, 759722
DPP1 is an integral membrane protein with six transmembrane helices, tightly associated with microsomal membranes
-
glycosylated N-terminal portion is located inside microsomes
-
-
subcellular localization of Gat1p and Gat2p are compared using fluorescence microscopy and subcellular fractionation using equilibrium density gradients. Gat1p and Gat2p overlap mostly in their localization and are microsomal GPATs, localized to both perinuclear and cortical endoplasmic reticula in actively proliferating cells
-
the N and C termini of the enzyme reside in the cytoplasm, and six putative membrane-spanning domains have been identified. The N-terminal domain including the first membrane-spanning segment contains sufficient information for targeting to the endoplasmic reticulum membrane
-
-
the spindle/microtubule association is specific for ScNep1p
-
29808, 29815, 94056, 653183, 653198, 659997, 674702, 681916, 686245, 687560, 689911, 692511, 694091, 700155, 718997, 738000
-
45% of CS II is bound to mitochondrial inner membrane and 2% of CS I
-
associated to on the matrix side
-
both subunit types span the membrane twice, integral, active at the matrix side of the inner membrane
Cox15p is a constituent of the mitochondrial inner membrane
-
exclusively in the inner mitochondrial membrane
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inner side, exposes catalytic sites to the mitochondrial matrix
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integral membrane protein, facing cytoplasmic surface
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integral, a large domain is exposed to the intermembrane space
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integral, active at the matrix side of the inner membrane
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integral, catalytic site facing the intermembrane space
Mrs2p contains two adjacent transmembrane domains near the C terminus of Mrs2p one of which ends with a F/Y-G-M-N motif
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oligomerization of ATP synthase is critical for the morphology of the inner mitochondrial membrane because it supports the generation of tubular cristae membrane domains, overview. Association of individual F1Fo-ATP synthase complexes is mediated by the membrane-embedded Fo-part
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only subunit type Yme1p spans the membrane once, integral, catalytic site facing the inter membrane space
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separation of mitochondrial inner and outer membrane on a sucrose gradient
Q00711 AND P21801 AND P33421 AND P37298
the catalytic domain (SDH1 and 2) is extrinsic on the matrix side, while the anchor subunits (SDH3 and 4) are intrinsic transmembrane proteins, allowing transfer of the electrons from succinate in the mitochondrial matrix to ubiquinone in the inner membrane
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the enzyme is found in monomeric, dimeric and higher oligomeric forms in the inner mitochondrial membrane. Two small proteins of the membrane-embedded Fo-domain subunits e and g are dimer-specific subunits of yeast ATP synthase and are required for stabilization of the dimers
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enzyme is transported into the intermembrane space via a direct sorting pathway, that can occur in absence of external energy sources
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high concentration of Evr1p
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29815, 486801, 486803, 486806, 487418, 487426, 645615, 645622, 651674, 661595, 662361, 686245, 687560, 687609, 689911, 715260, 716929, 759283
peripherally associated with the inner mitochondrial membrane on the matrix side
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94811, 392708, 396116, 485880, 643309, 643310, 645308, 648619, 687608, 696170, 700002, 714189, 718970, 718971, 733236, 734323, 734352
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the enzyme has a heme b-containing membrane-anchoring dimer, comprising the Sdh3p and Sdh4p subunits, overview
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the m-AAA protease is a conserved hetero-oligomeric complex in the inner membrane of mitochondria. m-AAA protease is preferentially localized in the inner boundary membrane compared to the cristae membrane
C7GJD6, C7GKE4, E9P8D2, P00830, P06182, P07236, P07245, P07262, P08417, P09440, P09950, P0CS90, P16387, P16622, P21373, P21954, P22936, P32048, P32622, P32785, P32796, P33327, P34227, P35731, P36059, P36775, P38071, P38088, P38891, P39006, P40051, P41735, P46367, P47176, P49017, P52893, P53123, P53259, P53294, Q00711 AND P21801 AND P33421 AND P37298, Q02783, Q06817, Q06892, Q07560
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334, 340, 341, 343, 443, 538, 5676, 29355, 29356, 31314, 31382, 31403, 33749, 33969, 94056, 134196, 134330, 134437, 134892, 209731, 210229, 210233, 210237, 210262, 286627, 286645, 286646, 286662, 286672, 286749, 287801, 289221, 348519, 348520, 389623, 389624, 389625, 389633, 389744, 389747, 390284, 390974, 390981, 390982, 390997, 391006, 392087, 392090, 392091, 392092, 392679, 392700, 392709, 392718, 394614, 395300, 438153, 439942, 439945, 439948, 439949, 439950, 439966, 439972, 439973, 439984, 439988, 439990, 439992, 439997, 440006, 440008, 440009, 440011, 440014, 440015, 440018, 440023, 440026, 440030, 441420, 441427, 441615, 485328, 485803, 485813, 486375, 486835, 486850, 487418, 487421, 487424, 487425, 487426, 487428, 488068, 640022, 640035, 642062, 643625, 643649, 644288, 644298, 644846, 645302, 645308, 649041, 649432, 649814, 650372, 650958, 650959, 651846, 651853, 651889, 651893, 651895, 651907, 651908, 652038, 652380, 652393, 653198, 653335, 653612, 653632, 653881, 654652, 654819, 655423, 656107, 656118, 656145, 656178, 656275, 656276, 656515, 657864, 658161, 659229, 659443, 659862, 659985, 661239, 662190, 662300, 665042, 665534, 666296, 666793, 666970, 667314, 667647, 668027, 668180, 668412, 668674, 668830, 669354, 669399, 669840, 672943, 673321, 673517, 673628, 673647, 673672, 673867, 673963, 674433, 674446, 674473, 674484, 674522, 674616, 674619, 674686, 674721, 674764, 675002, 675436, 675964, 676134, 676773, 676946, 677931, 678475, 679501, 680182, 681525, 681914, 682726, 682821, 682838, 683617, 684636, 684713, 685307, 685358, 685621, 686262, 686388, 686687, 686703, 687638, 687812, 689917, 691390, 692575, 692623, 692875, 693510, 694160, 695829, 696507, 697536, 697605, 698100, 698945, 700002, 700171, 701402, 703756, 703786, 704387, 704388, 704594, 704721, 705593, 705784, 706404, 706465, 708076, 708512, 709066, 710543, 710544, 710565, 710566, 712349, 712482, 712523, 712835, 715034, 716387, 718095, 718641, 718997, 719365, 719994, 721117, 721139, 721392, 721721, 722693, 722719, 723249, 723905, 724238, 724452, 724459, 727054, 727593, 727916, 727932, 728227, 728297, 728399, 728629, 728681, 729740, 730322, 730939, 732385, 733381, 734275, 734658, 734764, 736032, 738601, 738689, 739398, 739457, 740558, 743906, 744283, 745918, 746265, 747488, 747751, 747802, 748142, 748652, 749347, 751092, 751175, 752257, 752510, 752803, 754149, 755489, 755921, 757583, 758491, 758690, 758779, 759355, 759464, 759472, 759639, 759717, 759733, 760048, 761190, 761452, 761811, 761829, 762546, 762780, 762895, 763355, 763438, 763526, 764427, 765121, 765345
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aconitase in yeast is a single translation product, which is dual targeted and distributed between the mitochondria and the cytosol by a unique mechanism involving reverse translocation, dual localization, detailed overview
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active on the matrix side of the inner membrane
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alpha-isopropylmalate synthase Ia, MW 68000, is imported into the mitochondrial matrix
an N-terminal peptide, which is subsequently removed, is required to direct the protein to mitochondria in fungi
anchored to the inner mitochondrial membrane
autocatalytic processing in the mitochondrion
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cytosolic tRNAsLys tRK1 is partially targeted into mitochondria. Binding of tRK1 to the precursor of mitochondrial lysyl-tRNA synthetase preMsk1p, IIb class aminoacyl-tRNA synthetase, is a prerequisite of import. The hinge region of preMsk1p is essential to provide the import. The N-terminal domain of preMsk1p with the adjacent hinge region not only interacts with aminoacylated tRK1, but is also able to direct tRK1 import even in absence of the C-terminal domain. Enolase 2 participates as a putative RNA chaperone, suggesting that it may induce the import-active conformation in the tRNA
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D-lactate dehydrogenase is inserted into the inner membrane of mitochondria through its transmembrane domain located close to the N-terminus of the polypeptide chain in such a way that the protein globule is exposed in the intermembrane space
efficient and rapid targeting of Pus2p in yeast mitochondria
enzyme contains a mitochondrion targeting sequence
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enzyme is a component of mitochondrial DNA nucleoids
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enzyme is associated with both, the mitochondria and the endoplasmic reticulum
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Erv1 requires the redox-regulated receptor Mia40 for its import into mitochondria. Interacts via disulfide bonds with Mia40. It does not need two CX2C motifs for import into mitochondria
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gene product of GRS1 has enzymic activity both in cytoplasm and mitochondria
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Hfa1p is a mitochondrion-specific enzyme and contains a canonical mitochondrial targeting sequence with a matrix protease cleavage site
Icp55 behaves like a protein that is peripherally attached to the mitochondrial inner membrane from the matrix side
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in intact mitochondria, CO binds to two heme proteins, CytcO and flavohemoglobin yHb. yHb resides in the intermembrane space. In vesicles of the inner mitochondrial membranes the only CO-binding protein is CytcO
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in the intermembrane space, possibly associated with the outer membrane, minor enzyme portion
in yeast mitochondria two different DNA polymerases exist, pol gamma and pol NI, i.e. DNA polymerase alpha catalytic subunit A and its associated DNA polymerase subunit alphabeta, POL12
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inner membrane
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inner mitochondrial membrane
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integral membrane protein of inner membrane (facing cytoplasmic surface)
intermembrane space
internal surface of the inner mitochondrial membrane
isoenzyme, mutational loss of mitochondrial ACP has no effect on bulk cellular fatty acid synthesis
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isoform Gpd2p, contains mitochondrial presequence sufficient for targeting
isoform Tam41 directly catalyzes the formation of CDP-diacylglycerol from phosphatidic acid in the mitochondrial inner membrane
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localization of cytoplasmic GlnRS in mitochondrial Gln-tRNA synthesis. Saccharomyces cerevisiae imports the cytosolic pathway for Gln-tRNA synthesis into the mitochondrion
localized both to the cytosol and mitochondria by a reverse translocation mechanism
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matrix
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mitochondrial and cytosolic isoforms are derivatives of a single translation product and have identical amino termini
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mitochondrial ATP-dependent proteolytic activity is reduced by 35% in Deltapim1 cells. Oxidized proteins accumulate at elevated levels in mitochondria lacking pim1 activity
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mitochondrial isozyme contains no zinc-finger motif and no insertion domain in the nucleotide-binding fold
mitochondrial localization of Hmi1p is essential for its role in mtDNA metabolism
mitochondrial matrix
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mitochondrial Nfs1p is required for the biogenesis of both mitochondrial and extramitochondrial Fe/S proteins
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mitochondrial translation of the Saccharomyces cerevisiae Atp6p subunit of F1-F0 ATP synthase is regulated by the F1 ATPase
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most of the Ach1p activity is distributed with mitochondria and little in the cytoplasm
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Ndi1 protein from Saccharomyces cerevisiae is a monotopic membrane protein, directed to the matrix
NSUN3 has been shown to localize to the mitochondrial matrix, its mitochondrial import has not been determined
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part of alpha-ketoglutarate dehydrogenase complex
presence of mitochondrial FAD synthetase activity in strains transformed with FAD1 on a high-copy-number plasmid, but not in mitochondria of wild-type strains
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RNases P and MRP, enzyme consists of RNA component Rpm1r and protein component Rpm2p, the latter is required for the processing of the first
Sua5 catalyzes the first step leading to the threonyl-carbamoyl-AMP intermediate. Proteins Qri7 and Sua5 together constitute the mitochondrial pathway for the biosynthesis of N6-threonylcarbamoyladenosine. The import of cytoplasmic Sua5 into the mitochondria is required for this organelle to be functional
the 56 kDa precursor is processed upon import into mitochondria, leading to a 4 kDa alpha-subunit and a 47 kDa beta-subunit. Mutations in the conserved motif of the alpha-subunit affect processing and stability of Psd1, and consequently the enzyme's activity
the Coq3 polypeptide is peripherally associated with the matrix side of the inner membrane of yeast mitochondria
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the enzyme is localized and functions at the intermembrane space side of the inner membrane
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the enzyme requires integration into the inner mitochondrial membrane for full enzymatic activity
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the Leu4 gene encodes 2 forms: a short cytoplasmic form and a long form that is targeted to the mitochondria
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the presence of the enzyme in the mitochondrial fraction cannot be explained by the contamination of microsomes in this fraction
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the presequence of fumarase is exposed to the cytosol during import into mitochondria
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tightly associated with the inner mitochondrial membrane, oriented with the bulk of the protein facing the matrix
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translation product of the FUM1 gene, distribution can be affected by hsp70 molecular chaperones
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up to 7% of enolase activity associated with mitochondria, targeting towards the mitochondrial outer membrane, affinity to the mitochondrial surface more than 10fold higher for Eno2p than for Eno1p
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very poor mitochondrial targeting activity of the ALA1 leader peptide, mapping of the mitochondrial targeting signal, overview
yeast Lon protease localizes to mitochondrial nucleoids
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Yme1p is associated with the Mgr1 protein in mitochondria
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the NH2-terminal domain of the enzyme, residues between position 144 and 346, includes sequences necessary and sufficient to concentrate Ulp1 at nuclear envelope
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RanGTPase activating protein-Ran complex, stimulation of GTP hydrolysis, terminating export
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Ulp1 localizes predominantly to nuclear pore complexes but also deconjugates sumoylated septins at the bud-neck of dividing cells
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the N-terminal domain of the enzyme is important for its nucleolar localization
Rph1 associates with nucleosomes independently of H3 Lys36 methylation
C7GSG6, O13297, P06242, P06786, P22936, P23293, P31115, P32562, P32639, P38698, P38961, P39073, P39956, P39979, P40051, P40537, P46677, P46959 and P41814, P47156, P53114, P53204, P53942, Q00416, Q02724, Q02792, Q03220, Q03957, Q04089, Q04740, Q06592, Q07794
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3808, 134019, 134330, 134415, 134436, 134448, 210600, 210601, 391684, 441645, 488149, 488153, 638856, 640975, 642787, 643462, 643473, 644115, 645191, 648860, 654784, 655130, 656757, 656784, 657337, 657645, 661111, 661446, 661590, 661630, 661828, 661832, 662190, 662227, 662340, 662435, 663233, 663392, 664954, 665798, 666340, 666350, 668027, 669589, 675000, 675799, 680010, 681525, 682838, 686905, 692469, 692875, 694335, 694807, 695115, 696170, 702030, 702497, 703147, 703350, 703453, 703814, 705680, 705685, 705865, 705882, 705978, 706600, 708512, 709066, 710543, 710544, 712105, 715630, 716206, 716398, 716903, 716923, 719553, 720500, 726071, 727593, 729626, 730931, 730939, 735770, 737084, 737229, 739203, 740096, 740273, 741004, 741075, 743567, 744651, 746464, 750405, 751722, 753421, 754676, 754727, 754812, 755078, 756382, 756719, 756850, 758419, 758538, 762030, 763526
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a nonessential RIND/PHD finger protein that constitutively shuttles between cytoplasm and nucelus
beta subunit Gal83-containing isozyme after activation by alkaline stress, when the Gal83 isoform is activated by the other Snf1-activating kinases, Tos3 and Elm1, the Gal83 isoform is unable to translocate to the nucleus
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carbamoyl-phosphate-synthase/aspartate-transcarbamoylase complex
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distribution of TFIIB, TFIIH and RNA polymerase II at the URA2 locus, RNA polymerase II occupancy is increased on the URA2 open reading frame, overview
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during the normal cell cycle, the two small subunits Rnr2 and Rnr4 are predominantly localized to nucleus. Under genotoxic stress, Rnr2 and Rnr4 become redistributed to the cytoplasm in a checkpoint-dependent manner
Ire1p spans the ER membrane or the nuclear membrane with which the ER is continuous, with its kinase domain localized in the cytoplasm or in the nucleus
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isoform ACS2 is localized primarily to the nucleus, with a minor amount in the cytosol
isoform Rmt2 copurifies with the nucleoporins Nup49, Nup57 and Nup100
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Lag1 is uniquely required for the establishment of a lateral diffusion barrier in the nuclear envelope, which depends on phytoceramide
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Nma111p does not shuttle between the nucleus and cytoplasm
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nuclear exopolyphosphatase activity does not depend on the growth phase
overproduced Bub1 is found to localize to the cell nucleus
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Pik1 shuttles through the nucleus. Nuclear accumulation of Pik1 is promoted by nutrient, e.g. glucose, deprivation, a condition that also results in the release of PI4K effectors from Golgi membranes and slowing of the rate of secretion
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recruitment of Hat1p to chromatin is linked to DNA double-strand breaks, e.g. at the MAT locus, nuclear Hat1p-associated histone chaperone Hif1p is also recruited to an endonuclease HO-induced double-strand break with a similar distribution, the enzyme influences the chromatin structure at double-strand breaks, its recruitment to double-strand breaks is independent of recombinational repair, overview
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strong association of subunit Imd2 with actively transcribed genes, it is not recruited to nontranscribed regions. Serine 2 C-terminal domain phosphorylation of the elongating RNA polymerase II by Ctk1 kinase is required to recruit Imd2 to actively transcribed genes in vivo
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sumoylated Ntg1 accumulates in the nucleus following oxidative stress
the interaction of Ceg1 with RNA trisphophatase Cet1 essential for the nuclear localization of the Cet1-Ceg1 complex
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the m5U modification is found in unspliced tRNAs, suggesting that enzyme action is within the nucleus
the N-terminal domain is essential for Ulp2 function and is required for nuclear targeting
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while inhibiting separase, securin is able to promote nuclear accumulation of separase
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within 10 min after exposure to 1000 mM sorbitol, Hog1 and Hog1-asmutant almost exclusively present in the nucleus, nuclear import of activated Hog1 requires its catalytic function
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fructose-1,6-bisphosphatase is secreted into the periplasm during prolonged glucose starvation and is internalized into vacuole import and degradation vesicles/endosomes following glucose re-feeding. Fructose-1,6-bisphosphatase does not contain signal sequences required for the classical secretory and endocytic pathways, the secretion and internalization are mediated via the non-classical pathways and involves protein Vps34, which is involved in multiple protein trafficking events
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high-yield extraction of the periplasmic asparaginase produced by the recombinant Pichia pastoris strain habouring the Saccharomyes cerevisiae ASP3 gene. The use of six freeze-thaw cycles, folllowed by extraction with 20 mM potassium phosphate buffer pH 7.0 for 20 h, resulted in 85% enzyme recovery whereas the alkaline extraction using 500 mM potassium phosphate at pH 11.5 in the presence of 10 mM cysteine allows 100% enzyme recovery
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Pex15 is the membrane anchor required for Pex1/Pex6 recruitment to peroxisomes
the peroxisomal proteins Pex1 and Pex6 form a heterohexameric type II AAA+ ATPase complex
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the Pex1p/Pex6p complex exhibits a dual localization, with one fraction anchored to the peroxisomal membrane by its interaction to Pex15p and the second fraction located in the cytosol
the Pex1p/Pex6p-complex shows a dual localization in the cell as it is located in the cytosol as well as at the peroxisomal membrane. Association of this complex with the peroxisomal membrane is mediated by binding to Pex15p. The predominant part of the tail anchored protein Pex15p faces the cytosol and mediates the peroxisomal membrane association of the AAA-complex via a direct interaction with the N-terminal domain of Pex6p, assembly of the Pex1p/Pex6p-complex and recruitment to the peroxisomal membrane
the Pex1p/Pex6p-complex shows a dual localization in the cell as it is located in the cytosol as well as at the peroxisomal membrane. Association of this complex with the peroxisomal membrane is mediated by binding to Pex15p. The predominant part of the tail-anchored protein Pex15p faces the cytosol and mediates the peroxisomal membrane association of the AAA-complex via a direct interaction with the N-terminal domain of Pex6p, assembly of the Pex1p/Pex6p-complex and recruitment to the peroxisomal membrane
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two peroxisomal half ABC transporters Pxa1p and Pxa2p form a heterodimeric complex in the peroxisomal membrane
P07262, P22543, P24004, P32573, P33760, P34230, P38137, P38225, P39518, P41903, P41909, P53164, Q05871
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210404, 210407, 210411, 288675, 391054, 391061, 488068, 646193, 651339, 651909, 654332, 656347, 661257, 661258, 665707, 672419, 687492, 687638, 720022, 734571, 744209, 745264, 746625, 756224, 757772, 759455, 760661, 763355, 764331, 764720
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existence of two independent, Pex5p-mediated import pathways into peroxisomes in yeast: 1. a classical peroxisomal targeting signal 1 pathway and a novel, non-PTS1 pathway for Pox1p
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IDP3 contains a canonical type I peroxisomal targeting sequence, a carboxyl-terminal Cys-Lys-Leu tripeptide. IDP3 is normally strictly peroxisomal
peroxisomal matrix, the enzyme has a peroxisomal targeting signal type 1 (PTS1)
Pex1p is targeted to peroxisomes in a manner dependent on ATP hydrolysis, while Pex6p targeting requires ATP but not its hydrolysis
structural organization and localization of peroxisomal AAA+ ATPases. Dynamic Pex1p-Pex6p complex assembly at the peroxisomal membrane
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94367, 246932, 246933, 246936, 246941, 246942, 246943, 246944, 246946, 488654, 488663, 488666, 491612, 645308, 645316, 646105, 651541, 660950, 665607, 667643, 674435, 675890, 676123, 677233, 680603, 685327, 685369, 685408, 687558, 688899, 688902, 690150, 696144, 696476, 700356, 703874, 711852, 711983, 712599, 712954, 718753, 718781, 718835, 718949, 718993, 720413, 723790, 734628, 742820, 743271, 746901, 747157, 747611, 747788, 747805, 747894, 749049, 749181, 749334, 749867
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accumulates in the plasma membrane in a ubiquintinated form in endocytosis mutants
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at the nonpermissive temperature Ste6p-GFP is found exclusively at the plasma membrane
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both N-terminus and C-terminus of Alr1p and Alr2p are exposed to the inner side of the plasma membrane
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characteristics of phospholipid fatty acid composition of plasma membrane leading to the enhanced ethanol tolerance of the strain, are also efficicious to increase the percentage of activation of plasma membrane ATPase per unit of ethanol
chitin synthase III requires Chs4p-dependent translocation of Chs3p into the plasma membrane, Chs4p thus promotes Chs3p translocation into the plasma membrane in a stable and active form. In the absence of Chs4p, Chs3p is delivered to the plasma membrane but fails to accumulate there because it is rapidly endocytosed and accumulates in intracellular vesicles. The C-terminal region of Chs4p is required for its association with plasma membrane but not for biological function
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ERF2 encodes a protein with four predicted membrane-spanning domains
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Fet3p has 11 crystallographically mapped N-linked core glycan units. Assembly of four of these units is specifically required for localization of Fet3p to the plasma membrane. Fet3 protein lacking any one of these glycan units is found in an intracellular high-molecular mass species, overview
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Gap1 comprises 12 transmembrane domains flanked by cytosol-facing N- and C-terminal tails
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in the absence of cadmium, Pca1 is targeted for degradation before reaching the plasma membrane
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internalization of Dnf1p from the plasma membrane uses an NPFXD endocytosis signal and its recognition by Sla1p, part of an endocytic coat/adaptor complex with clathrin, Pan1p, Sla2p/End4p, and End3p
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loss of AP-1 markedly increases Drs2p trafficking to the plasma membrane, but does not perturb retrieval of Drs2p from the early endosome back to the trans Golgi network
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Pca1 contains a cytosolic cysteine-rich N-terminal extension of nearly 400 residue
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PHT1 transporters show a topology with 12 membrane-spanning domains, which are separated into two groups of six domains by a charged hydrophilic loop. Both C- and N-termini are expected to be oriented inside the cell, with the protein inserted in the plasma membrane
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the culture medium affects the relative abundance of chitin synthase 1 in chitosomes and plasma membrane populations
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when amino acids are scarce Gap1p is sorted to the plasma membrane, whereas when amino acids are abundant Gap1p is sorted from the trans-Golgi through the multivesicular endosome and to the vacuole requiring direct recognition of transport substrates
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54 S subunit of the yeast mitochondrial ribosome
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methionine aminopeptidase type 1 associates primarily with the 60S ribosome subunit, lower affinity or non-specific interaction with the 40S ribosome subunit
P07347 AND P12945, Q08689 AND P41227 AND P12945
near to
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oligosaccharyltransferase forms a binary complex with ribosomes. Reconstitution of a binary complex containing oligosaccharyltransferase and ribosomes and its electron microscopic images. Oligosaccharyltransferase, the Sec61 complex, and ribosomes form a ternary complex in vitro
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post-Golgi, Drs2p is incorporated into the low-density class of secretory vesicles
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9, 39, 42, 5823, 31383, 31384, 31385, 31389, 31390, 31403, 392969, 392971, 488022, 488405, 489717, 492119, 641784, 645084, 645240, 649910, 653632, 655610, 667596, 672761, 703622, 703756, 705747, 710639, 722153, 735723, 754084, 757987
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MAS1 becomes insoluble in the absence of MAS2, presumably by aggregation
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obtained by treating cells with lyophilized gastric juice of edible snails in 5% citric buffer with 0.8 M mannitol, pH 6.5
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-
the spindle/microtubule association is specific for ScNep1p
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detected by indirect immunofluorescence, fractionation technique
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-
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associated, the enzyme contains six putative transmembrane domains, the catalytic site is oriented to the cytosolic face of the vacuole membrane
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V-ATPase consists of a cytoplasmic domain V1 and a transmembrane domain V0. Both domains contain several subunits. The V0 transmembrane domain consists of subunits a, c, c', c'' and d
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28286, 28293, 95499, 95509, 95510, 95515, 136141, 136174, 136175, 209837, 209845, 289082, 487970, 643864, 647038, 647040, 647042, 649129, 653329, 657185, 660790, 665081, 668027, 670176, 670969, 677369, 679755, 680774, 681922, 681941, 682540, 683009, 688855, 691982, 696170, 700001, 707657, 712599, 713383, 717822, 718128, 719873, 730653, 731811, 733286, 734214, 748171, 749196, 754333, 755660, 756125
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at high amino acid concentrations, Gap1p-GFP is delivered to the vacuolar interior by the multivesicular endosome pathway in wild-type cells
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at late endosome and vacuole interface, GFP- and HA-tagged recombinant Env7s are vacuolar membrane proteins
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enters the secretory pathway and is transported to the vacuole by vesicular carriers
for the vacuolar-dependent degradation pathway, FBPase is imported into intermediate carriers know as Vid vesicles (vacuole import and degradation) vesicles
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Lap3 is spatially associated with Ape1 and selectively transported to the vacuole during nitrogen starvation. Gene products ATG11 and ATG19 are important for Lap3 transport. Lap3 is degraded within a couple of hours in the vacuole
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regulation of glutathione import into the vacuoles, kinetics
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role of a 17 amino acid prosequence in the transport process
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the cytosolic precursor is a protein of 732000-752000 MW (by glycerol density gradient centrifugation and native gel electrophoresis). After binding to membranes and formation of vesicles these are imported into the vacuoles and processed there into the mature enzyme
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the enzyme is imported into the vacuole by two different processes: cytoplasm to vacuole targeting pathway (Cvt) under vegetative growth conditions and a macroautophagy-like mechanism under starvation conditions
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the enzyme is synthesized as a cytosolic precursor of MW 61000 which, after incorporation in vacuoles, is proteolytically processed in two steps, first into an unstable intermediate of MW 55000 and subsequently into a mature enzyme of MW 50000
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the enzyme is synthesized on ribosomes and sorted into vacuoles. The vacuolar localization signal Gln24-Arg-Pro-Leu27 is loacetd near the NH2-terminus of the propeptide
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the localization determinant resides in the propeptide of the enzyme
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the precursor enzyme is transported into the vacuole via the non-classic Cvt pathway by cytoplasmic double-membrane vesicles, which fuse with the vacuole releasing a single-membrane autophagic body into the vacuolar lumen where it is proteolytically maturated, overview
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ubiquitination is required for the uptake of Ste6 into the lumen of the vacuole, uptake of Ste6 into the yeast vacuole is blocked in the doa4 mutant
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upon phosphate starvation, these low-affinity phosphate transporters, e.g. Pho87 and Pho90, are endocytosed and targeted to the vacuole. For Pho87, this process strictly depends on SPL2, another Pho4-dependent gene that encodes a protein known to interact with the N-terminal SPX domain of the transporter. In contrast, the vacuolar targeting of Pho90 upon phosphate starvation is independent of both Pho4 and Spl2, although it still requires its SPX domain. Both Pho87 and Pho90 are also targeted to the vacuole upon carbon-source starvation or upon treatment with rapamycin, which mimics nitrogen starvation, responses are independent of PHO pathway signalling requiring only the transporter N-terminal SPX domain. Spl2 mediates phosphate-starvation-induced vacuolar targeting of Pho87, but not of Pho90
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when amino acids are scarce Gap1p is sorted to the plasma membrane, whereas when amino acids are abundant Gap1p is sorted from the trans-Golgi through the multivesicular endosome and to the vacuole requiring direct recognition of transport substrates
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within microglobules in juvenile vacuoles, concept of vavuole biogenesis based on enzyme allocation
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Ste14p activity is lost in vesicles composed of 75-100 mol% C20BAS and 0-100 mol% C32BAS but retained in vesicles with 0-50 mol% C20BAS and 0-100 mol% C32phytBAS
additional information
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80% or more of the proteinase in the yeast cell is in the zymogen form and seems to be particle-bound
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activity is excluded from the nucleus
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altered localization to the mitochondria or peroxisomes prevents Gdh1, which was originally localized in the cytoplasm, from stationary phase-specific aggregation, suggesting that some cytosolic factors are involved in the process of Gdh1 aggregation
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amino acids govern the propensity of Gap1p to recycle from the multivesicular endosome to the plasma membrane. Gap1p redistributes from the multivesicular endosome to the plasma membrane and that this recycling relies on the same machinery required for vesicular trafficking between the trans-Golgi and the plasma membrane
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additional information
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Ape2 activity is found in allphases of growth
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additional information
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Ath1 possesses a transmembrane domain. Existence of a secretion sequence in Ath1
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biogenesis of mtHsp70 in mitochondria, analysis. mtHsp70 folds rapidly after its import into mitochondria. Both domains are independent folding units. The ATPase domain folds in the context of mtHsp70 only in presence of the interdomain linker, whereas the peptide-binding domain folds without the interdomain linker, model of the folding of mtHsp70, overview
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additional information
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budding yeast Esp1 is localized to the centrosomes and spindle before anaphase
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Chs4p is transported in vesicles in a polarized fashion independently of the other Chs proteins. Its association with membranes depends not only on prenylation, but also on its interaction with other proteins, mainly Chs3p, which is the catalytic subunit of CSIII and is able to properly direct Chs4p to the bud neck in the absence of prenylation
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complexed Csg1 functions in the Golgi and is then delivered to the vacuole for degradation
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enzyme non-mitochondrial, greatest activity in hard protein pellet, suggesting that enzyme is an insoluble protein
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enzyme undergoes endoplasmic reticulum-associated degradation which is physiologically regulated by sterol pathway signals
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eukaryotic cells may contain multiple RNase P activities, a nucear type as well as enzyme species in mitochondria and chloroplasts
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exosome, i.e. a macromolecule complex involved in RNA degradation
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Golgi localization
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in yeast, several plasma membrane nutrient transporters are inactivated and targeted to the vacuole in response to changes in the availability of nutrients
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influence of subcellular localization on isozyme activities, overview
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integral membrane protein, overview on localization
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isoform Rmt2 is not associated with ribosomes
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isozyme pattern of expression and localization, overview
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localization of Ntg1 is dynamically regulated in response to nuclear and mitochondrial oxidative stress
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mechanisms for copper-ATPase trafficking, detailed overview
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modeling of secondary structural elements of the scScs7p hydroxylase domain placed within a model lipid bilayer, overview
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molecular mechanisms controlling intra- and extracellular localization of enzyme Rny1p , overview. Failure of Golgi-specific glycosylation appears to direct the enzyme to the vacuole as an alternative destination and/or site of terminal degradation, the unglycosylated mutants are unable to be secreted
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additional information
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Nfs1 needs to be processed by MPP to be functional in the mitochondrion and the nucleus, the latter case requires a mechanism that involves reverse translocation of processed Nfs1, i.e. the retrograde movement of Nfs1
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additional information
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P4-ATPases Drs2p and Dnf1p cycle between the exocytic and endocytic pathways, and maintain a steady-state localization to internal organelles requiring endocytosis
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additional information
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Pab1p contains a non-essential leucine-rich nuclear export signal and shuttles in an Xpo1/Gsp-1-dependent manner between the nucleus and the cytoplasm
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Pca1 contains a cytosolic cysteine-rich N-terminal extension of nearly 400 residues
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phylogenetic analysis showed that plant PDAT can be grouped into four clades, two of which have one putative transmembrane domain (TMD) while the other two are predicted to be entirely soluble. The majority of PDAT in the database have the single-predicted TMD consisting of a small cytosolic N-terminus and a large C-terminal domain in the endoplasmic reticulum lumen. The N-terminal region is hydrophilic with arginine clusters similar to those observed in DGAT1
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additional information
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polyP metabolism in cytosol and mitochondria is substantially dependent on the carbon source, acid-soluble polyP accumulates mainly in cytosol using either glucose or ethanol. The level of the accumulation is lower during growth on ethanol compared to that on glucose. Increase in polyP content in mitochondria occurs during growth on glucose, but not on ethanol. In cytosol the activity of exopolyphosphatase PPN1 is increased and the activity of exopolyphosphatase PPX1 is decreased independently of the carbon source under phosphate surplus conditions, overview. Growth on ethanol induces exopolyphosphatase PPN1 in the soluble mitochondrial fraction, while during growth on glucose only exopolyphosphatase PPX1 is present in this fraction
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profiling of the location of the RNAPII phosphorylated isoforms in wild-type cells and mutants for most CTD modifying enzymes. The CTD cycle is uniform across genes
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subcellular localization analysis of CDP-diacylglycerol synthases in yeast
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subcellular localization analysis, overview
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subcellular localization of different enzyme forms
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subcellular localization of wild-type and mutant enzymes, overview
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subcellular localization study of isozymes, overview
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subcellular localization study, overview. All mutant aconitase protein molecules are partially imported into mitochondria, then the N-terminal mitochondrial targeting sequence is cleaved off by the mitochondrial processing peptidase. After the cleavage, a subpopulation of the protein molecules moves back into the cytosol by reverse translocation. The aconitase C-terminal domain confers dual targeting
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additional information
synthesized as an inactive precursor (zymogen), termed preproPrA, which transits to the endoplasmic reticulum where the protein is glycosylated and a hydrophobic signal peptide of the 22 amino acid is removed, the protein is then transported to the Golgi complex, where the carbohydrate side chains are modified by mannosyltransferases, the resulting 52 kDa proPrA is transported through the endosome to the vacuole, where a 54-amino acid propeptide is removed, yielding the mature 42 kDa proteinase
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additional information
the AAAdomains of Pex6p seem to influence the Pex6p/Pex15p-interaction and thereby regulate the recruitment of the cytosolic AAA-complex to the peroxisomal membrane, although in opposite fashion. In particular, ATP-binding to D1 of Pex6p stimulates association of the AAA-complex with Pex15p at the peroxisomal membrane while ATP-hydrolysis at D2 seems to trigger the release of the AAA-complex from Pex15p and thus from the membrane
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additional information
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the culture medium affects the relative abundance of chitin synthase 1 in chitosomes and plasma membrane populations
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the enzyme is colocalized with the septins at the mother-bud neck
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the recombinant enzyme expressed in Escherichia coli mostly exists in pellet in the absence of detergents, a low quantity of soluble enzyme is purified
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the tail-anchored protein Pex15p in yeast functions as membrane anchors responsible for the recruitment of the Pex1p-Pex6p complex to the peroxisomal membrane, the N-terminal domain of Pex6p interacts with the cytosolic part of Pex15p and mediates the attachment of the Pex1p-Pex6p complex to the membrane
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additional information
two of the seven NSUN proteins (NSUN3 and NSUN4) are synthesized on cytoplasmic ribosomes but localize to mitochondria
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uncomplexed Csh1 cannot exit from the endoplasmic reticulum. Complexed Csh1 functions in the Golgi and is then delivered to the vacuole for degradation
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additional information
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X-2180, equally distributed between particulate and supernatant fractions
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LINKS TO OTHER DATABASES (specific for Saccharomyces cerevisiae)
SILVA: 16S/18S rRNA, 23S/28S rRNA
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Release 2023.1 (January 2023)
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