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Organism related
Word Map for Organism Glycine max
- Glycine max
- isoflavones
- japonicum
- peanut
- proteinases
- lectin
- lipoxygenase
- genistein
- bradyrhizobium
- agglutinin
- sunflower
- cotyledon
- cyst
- alfalfa
- flour
- allergen
- canola
- barley
- silage
- methionine
- ileal
- beef
-
holstein
- triacylglycerols
- chick
-
rapeseed
- glyphosate
- sorghum
- infant
- aphid
- hull
- cowpea
- carcass
- hydroperoxide
- pancreas
- rhizobia
-
extrude
- pisum
- chymotrypsin
- hypogaea
- mottle
- duodenum
-
gluten
-
digesta
- truncatula
- tocopherol
- sesame
- arachis
- ferritin
- chickpea
-
sti
TaxTree of Organism Glycine max
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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
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
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
(1,4)-beta-D-xylan degradation
-
-
PWY-6717
(3R)-linalool biosynthesis
-
-
PWY-7709
(3R)-N-[(2S)-1-hydroxy-6-[(3R)-3-isocyanobutanamido]hexan-2-yl]-3-isocyanobutanamide biosynthesis
-
-
PWY-8320
(3S)-linalool biosynthesis
-
-
PWY-7141
(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
(R)- and (S)-3-hydroxybutanoate biosynthesis (engineered)
-
-
PWY-7216
(R)-cysteate degradation
-
-
PWY-6642
(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
1,2-dichloroethane degradation
-
-
12DICHLORETHDEG-PWY
1,3-beta-D-glucan biosynthesis
-
-
PWY-6773
1,3-propanediol biosynthesis (engineered)
-
-
PWY-7385
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-amino-3-carboxymuconate semialdehyde degradation to 2-hydroxypentadienoate
-
-
PWY-5654
2-amino-3-carboxymuconate semialdehyde degradation to glutaryl-CoA
-
-
PWY-5652
2-amino-3-hydroxycyclopent-2-enone biosynthesis
-
-
PWY-7536
2-arachidonoylglycerol biosynthesis
-
-
PWY-8052
2-carboxy-1,4-naphthoquinol biosynthesis
-
-
PWY-5837
2-deoxy-D-glucose 6-phosphate degradation
-
-
PWY-8121
2-deoxy-D-ribose degradation II
-
-
PWY-8058
2-methyl-branched fatty acid beta-oxidation
-
-
PWY-8181
2-methylpropene degradation
-
-
PWY-7778
2-nitrobenzoate degradation I
-
-
PWY-5647
2-nitrotoluene degradation
-
-
PWY-5641
2-oxoglutarate decarboxylation to succinyl-CoA
-
-
PWY-5084
2-oxoisovalerate decarboxylation to isobutanoyl-CoA
-
-
PWY-5046
24-epi-campesterol, fucosterol, and clionasterol biosynthesis (diatoms)
-
-
PWY-8238
3,4-dichlorobenzoate degradation
-
-
PWY-6217
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 II (via protocatechuate)
-
-
PWY-6216
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-methyl-branched fatty acid alpha-oxidation
-
-
PWY66-387
3-methylbutanol biosynthesis (engineered)
-
-
PWY-6871
3-phenylpropanoate degradation
-
-
P281-PWY
3-phosphoinositide biosynthesis
-
-
PWY-6352
3-phosphoinositide degradation
-
-
PWY-6368
4-amino-2-methyl-5-diphosphomethylpyrimidine biosynthesis II
-
-
PWY-7282
4-aminobutanoate degradation I
-
-
PWY-6535
4-aminobutanoate degradation II
-
-
PWY-6537
4-aminobutanoate degradation III
-
-
PWY-6536
4-aminobutanoate degradation V
-
-
PWY-5022
4-chloronitrobenzene degradation
-
-
PWY-5645
4-coumarate degradation (aerobic)
-
-
PWY-8002
4-coumarate degradation (anaerobic)
-
-
PWY-7046
4-ethylphenol degradation (anaerobic)
-
-
PWY-6080
4-hydroxy-2(1H)-quinolone biosynthesis
-
-
PWY-6661
4-hydroxy-2-nonenal detoxification
-
-
PWY-7112
4-hydroxy-3-prenylbenzoate biosynthesis
-
-
PWY-7303
4-hydroxybenzoate biosynthesis I (eukaryotes)
-
-
PWY-5754
4-hydroxybenzoate biosynthesis III (plants)
-
-
PWY-6435
4-hydroxymandelate degradation
4-nitrotoluene degradation II
-
-
PWY-5644
4-oxopentanoate degradation
-
-
PWY-7948
4-sulfocatechol degradation
-
-
PWY-6041
5'-deoxyadenosine degradation II
-
-
PWY-8131
5-aminoimidazole ribonucleotide biosynthesis I
-
-
PWY-6121
5-aminoimidazole ribonucleotide biosynthesis II
-
-
PWY-6122
5-deoxystrigol biosynthesis
-
-
PWY-7101
6-gingerol analog biosynthesis (engineered)
-
-
PWY-6920
7-dehydroporiferasterol biosynthesis
-
-
PWY-7155
8-amino-7-oxononanoate biosynthesis I
-
-
PWY-6519
8-amino-7-oxononanoate biosynthesis IV
-
-
PWY-8203
8-oxo-(d)GTP detoxification I
-
-
PWY-6502
9-cis, 11-trans-octadecadienoyl-CoA degradation (isomerase-dependent, yeast)
-
-
PWY-7340
9-lipoxygenase and 9-allene oxide synthase pathway
-
-
PWY-5407
9-lipoxygenase and 9-hydroperoxide lyase pathway
-
-
PWY-5408
ABH and Lewis epitopes biosynthesis from type 1 precursor disaccharide
-
-
PWY-7832
ABH and Lewis epitopes biosynthesis from type 2 precursor disaccharide
-
-
PWY-7831
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 III
-
-
PWY-8328
acetate conversion to acetyl-CoA
-
-
PWY0-1313
acetoacetate degradation (to acetyl CoA)
-
-
ACETOACETATE-DEG-PWY
acetone degradation I (to methylglyoxal)
-
-
PWY-5451
acetone degradation 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
acrylonitrile degradation I
-
-
PWY-7308
acyl-CoA hydrolysis
-
-
PWY-5148
acyl-[acyl-carrier protein] thioesterase pathway
-
-
PWY-5142
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 salvage
-
-
PWY-6610
adenosine deoxyribonucleotides de novo biosynthesis I
-
-
PWY-7227
adenosine deoxyribonucleotides de novo biosynthesis II
-
-
PWY-7220
adenosine nucleotides degradation I
-
-
PWY-6596
adenosine nucleotides degradation II
-
-
SALVADEHYPOX-PWY
adenosine ribonucleotides de novo biosynthesis
-
-
PWY-7219
adipate biosynthesis
-
-
PWY-8347
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
aldoxime degradation
-
-
P345-PWY
alkane biosynthesis I
-
-
PWY-7032
alkane biosynthesis II
-
-
PWY-7033
alkane oxidation
-
-
PWY-2724
all-trans-farnesol biosynthesis
-
-
PWY-6859
allantoin degradation to glyoxylate II
-
-
PWY-5692
allantoin degradation to ureidoglycolate I (urea producing)
-
-
PWY-5697
allantoin degradation to ureidoglycolate II (ammonia producing)
-
-
PWY-5698
alliin metabolism
-
-
PWY-5706
allopregnanolone biosynthesis
-
-
PWY-7455
alpha-carotene biosynthesis
-
-
PWY-5946
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
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 energy metabolism (invertebrates, cytosol)
-
-
PWY-7383
anaerobic energy metabolism (invertebrates, mitochondrial)
-
-
PWY-7384
anandamide biosynthesis I
-
-
PWY-8051
anandamide biosynthesis II
-
-
PWY-8053
anandamide lipoxygenation
-
-
PWY-8056
androgen biosynthesis
-
-
PWY66-378
androstenedione degradation I (aerobic)
-
-
PWY-6944
androstenedione degradation II (anaerobic)
-
-
PWY-8152
anteiso-branched-chain fatty acid biosynthesis
-
-
PWY-8173
anthocyanidin modification (Arabidopsis)
-
-
PWY-7450
anthocyanin biosynthesis
-
-
PWY-5125
anthocyanin biosynthesis (delphinidin 3-O-glucoside)
-
-
PWY-5153
anthocyanin biosynthesis (pelargonidin 3-O-glucoside)
-
-
PWY-7267
apigenin glycosides biosynthesis
-
-
PWY-6010
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
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 III
-
-
PWY-8263
arsenic detoxification (mammals)
-
-
PWY-4202
arsenic detoxification (plants)
-
-
PWY-8259
arsenic detoxification (yeast)
-
-
PWY-4621
arsenite to oxygen electron transfer
-
-
PWY-4521
arsenite to oxygen electron transfer (via azurin)
-
-
PWY-7429
ascorbate 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
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
-
-
PWY-7626
backdoor pathway of androgen biosynthesis
-
-
PWY-8200
bacterial bioluminescence
-
-
PWY-7723
baicalein degradation (hydrogen peroxide detoxification)
-
-
PWY-7214
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
benzoyl-CoA biosynthesis
-
-
PWY-6458
benzoyl-CoA degradation I (aerobic)
-
-
PWY-1361
berberine biosynthesis
-
-
PWY-3901
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 IV
-
-
PWY-5760
beta-carboline biosynthesis
-
-
PWY-5877
beta-carotene biosynthesis
-
-
PWY-5943
beta-D-glucuronide and D-glucuronate degradation
-
-
PWY-7247
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
biotin-carboxyl carrier protein assembly
-
-
PWY0-1264
biphenyl degradation
-
-
PWY5F9-12
bis(guanylyl molybdopterin) cofactor sulfurylation
-
-
PWY-8164
bisabolene biosynthesis (engineered)
-
-
PWY-7102
bisucaberin biosynthesis
-
-
PWY-6381
bombykol biosynthesis
-
-
PWY-7423
bornyl diphosphate biosynthesis
-
-
PWY-5813
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
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
carbaryl degradation
-
-
PWY-8111
carbofuran degradation I
-
-
PWY-8286
carbofuran degradation II
-
-
PWY-8287
carbofuran degradation III
-
-
PWY-8288
cardenolide glucosides biosynthesis
-
-
PWY-6036
cardiolipin biosynthesis I
-
-
PWY-5668
cardiolipin biosynthesis II
-
-
PWY-5269
cardiolipin biosynthesis III
-
-
PWY0-1545
carnosate bioynthesis
-
-
PWY-7680
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
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
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
chlorinated phenols degradation
-
-
PWY-6197
chlorobactene biosynthesis
-
-
PWY-7939
chlorogenic acid biosynthesis I
-
-
PWY-6039
chlorogenic acid degradation
-
-
PWY-6781
chlorophyll a degradation I
-
-
PWY-5098
chlorophyll a degradation II
-
-
PWY-6927
chlorophyll a degradation III
-
-
PWY-7164
chlorophyll cycle
-
-
PWY-5068
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
choline degradation IV
-
-
PWY-7494
chondroitin sulfate degradation I (bacterial)
-
-
PWY-6572
chorismate biosynthesis from 3-dehydroquinate
-
-
PWY-6163
chrysin biosynthesis
-
-
PWY-5363
chrysoeriol biosynthesis
-
-
PWY-6232
cichoriin interconversion
-
-
PWY-7057
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-legionaminate biosynthesis I
-
-
PWY-6749
CO2 fixation into oxaloacetate (anaplerotic)
-
-
PWYQT-4429
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
coniferin metabolism
-
-
PWY-116
conversion of succinate to propanoate
-
-
PWY0-43
coptisine biosynthesis
-
-
PWY-8030
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
crotonosine biosynthesis
-
-
PWY-8100
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
cyclic electron flow
-
-
PWY-8270
cylindrospermopsin biosynthesis
-
-
PWY-8045
cytidylyl molybdenum cofactor sulfurylation
-
-
PWY-8165
cytochrome c biogenesis (system I type)
-
-
PWY-8147
cytokinin-O-glucosides biosynthesis
-
-
PWY-2902
cytosolic NADPH production (yeast)
-
-
PWY-7268
D-arabinitol degradation I
-
-
DARABITOLUTIL-PWY
D-arabinose degradation V
-
-
PWY-8334
D-cycloserine biosynthesis
-
-
PWY-7274
D-galactose degradation I (Leloir pathway)
-
-
PWY-6317
D-galactose degradation IV
-
-
PWY-6693
D-galactose detoxification
-
-
PWY-3821
D-glucuronate degradation I
-
-
PWY-5525
D-lactate to cytochrome bo oxidase electron transfer
-
-
PWY0-1565
D-mannose degradation I
-
-
MANNCAT-PWY
D-mannose degradation II
-
-
PWY3O-1743
D-myo-inositol (1,4,5)-trisphosphate biosynthesis
-
-
PWY-6351
D-myo-inositol (1,4,5)-trisphosphate degradation
-
-
PWY-6363
D-myo-inositol (1,4,5,6)-tetrakisphosphate biosynthesis
-
-
PWY-6366
D-myo-inositol (3,4,5,6)-tetrakisphosphate biosynthesis
-
-
PWY-6365
D-myo-inositol-5-phosphate metabolism
-
-
PWY-6367
D-phenylglycine degradation
-
-
PWY-8161
D-sorbitol biosynthesis I
-
-
PWY-5054
D-sorbitol degradation I
-
-
PWY-4101
D-xylose degradation I
-
-
XYLCAT-PWY
D-xylose degradation IV
-
-
PWY-7294
D-xylose degradation to ethylene glycol (engineered)
-
-
PWY-7178
daidzein conjugates interconversion
-
-
PWY-2343
daidzin and daidzein degradation
-
-
PWY-6996
daphnetin modification
-
-
PWY-7055
daphnin interconversion
-
-
PWY-7056
degradation of aromatic, nitrogen containing compounds
-
-
dehydroabietic acid biosynthesis
-
-
PWY-5421
dehydroscoulerine biosynthesis
-
-
PWY-6337
dermatan sulfate degradation I (bacterial)
-
-
PWY-7646
desferrioxamine B biosynthesis
-
-
PWY-6376
desferrioxamine E biosynthesis
-
-
PWY-6375
detoxification of reactive carbonyls in chloroplasts
-
-
PWY-6786
di-homo-gamma-linolenate metabolites biosynthesis
-
-
PWY-8396
di-myo-inositol phosphate biosynthesis
-
-
PWY-6664
diacylglycerol and triacylglycerol biosynthesis
-
-
TRIGLSYN-PWY
diacylglycerol biosynthesis (PUFA enrichment in oilseed)
-
-
PWY-6804
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
dipicolinate biosynthesis
-
-
PWY-8088
dissimilatory sulfate reduction I (to hydrogen sufide))
-
-
DISSULFRED-PWY
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 metabolites biosynthesis
-
-
PWY-8400
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
echinatin biosynthesis
-
-
PWY-6325
ectoine biosynthesis
-
-
P101-PWY
ent-kaurene biosynthesis I
-
-
PWY-5032
Entner-Doudoroff pathway I
-
-
PWY-8004
Entner-Doudoroff pathway II (non-phosphorylative)
-
-
NPGLUCAT-PWY
Entner-Doudoroff pathway III (semi-phosphorylative)
-
-
PWY-2221
ephedrine biosynthesis
-
-
PWY-5883
epiberberine biosynthesis
-
-
PWY-8031
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:86 O antigen biosynthesis
-
-
PWY-7290
ethanol degradation I
-
-
ETOH-ACETYLCOA-ANA-PWY
ethanol degradation II
-
-
PWY66-21
ethanol degradation III
-
-
PWY66-161
ethanol degradation IV
-
-
PWY66-162
ethanolamine utilization
-
-
PWY0-1477
ethene biosynthesis I (plants)
-
-
ETHYL-PWY
ethene biosynthesis II (microbes)
-
-
PWY-6853
ethene biosynthesis III (microbes)
-
-
PWY-6854
ethene biosynthesis IV (engineered)
-
-
PWY-7126
ethene biosynthesis V (engineered)
-
-
PWY-7124
ethylbenzene degradation (anaerobic)
-
-
PWY-481
ethylmalonyl-CoA pathway
-
-
PWY-5741
eumelanin biosynthesis
-
-
PWY-6498
even iso-branched-chain fatty acid biosynthesis
-
-
PWY-8175
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 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
FeMo cofactor biosynthesis
-
-
PWY-7710
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
flaviolin dimer and mompain biosynthesis
-
-
PWY-7513
flavonoid biosynthesis
-
-
PWY1F-FLAVSYN
flavonoid biosynthesis (in equisetum)
-
-
PWY-6787
flavonoid di-C-glucosylation
-
-
PWY-7897
flavonol acylglucoside biosynthesis I - kaempferol derivatives
-
-
PWY-7168
flavonol acylglucoside biosynthesis III - quercetin derivatives
-
-
PWY-7172
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 IV (thiol-independent)
-
-
FORMASS-PWY
formaldehyde oxidation VII (THF pathway)
-
-
PWY-7909
formate assimilation into 5,10-methylenetetrahydrofolate
-
-
PWY-1722
formate oxidation to CO2
-
-
PWY-1881
formate to 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
GABA shunt I
-
-
GLUDEG-I-PWY
GABA shunt II
-
-
PWY-8346
galactolipid biosynthesis I
-
-
PWY-401
gamma-glutamyl cycle
-
-
PWY-4041
gamma-linolenate biosynthesis II (animals)
-
-
PWY-6000
ganglio-series glycosphingolipids biosynthesis
-
-
PWY-7836
GDP-6-deoxy-D-talose biosynthesis
-
-
PWY-5738
GDP-alpha-D-glucose biosynthesis
-
-
PWY-5661
GDP-D-perosamine biosynthesis
-
-
PWY-5739
GDP-D-rhamnose biosynthesis
-
-
GDPRHAMSYN-PWY
GDP-L-colitose biosynthesis
-
-
PWY-5740
GDP-L-fucose biosynthesis I (from GDP-D-mannose)
-
-
PWY-66
GDP-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
geraniol and geranial biosynthesis
-
-
PWY-5829
geranyl diphosphate biosynthesis
-
-
PWY-5122
gibberellin biosynthesis III (early C-13 hydroxylation)
-
-
PWY-5035
gibberellin inactivation I (2beta-hydroxylation)
-
-
PWY-102
ginsenosides biosynthesis
-
-
PWY-5672
gliotoxin biosynthesis
-
-
PWY-7533
globo-series glycosphingolipids biosynthesis
-
-
PWY-7838
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-mediated detoxification I
-
-
PWY-4061
glutathione-mediated detoxification II
-
-
PWY-6842
glutathione-peroxide redox reactions
-
-
PWY-4081
glyceollin biosynthesis
-
-
PWY-2762
glycerol degradation I
-
-
PWY-4261
glycerol degradation to butanol
-
-
PWY-7003
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 II (Gram-positive bacteria)
-
-
PWY-3722
glycine betaine biosynthesis III (plants)
-
-
PWY1F-353
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 cleavage
-
-
GLYCLEAV-PWY
glycogen biosynthesis I (from ADP-D-Glucose)
-
-
GLYCOGENSYNTH-PWY
glycogen biosynthesis II (from UDP-D-Glucose)
-
-
PWY-5067
glycogen biosynthesis III (from alpha-maltose 1-phosphate)
-
-
PWY-7900
glycogen degradation I
-
-
GLYCOCAT-PWY
glycogen degradation II
-
-
PWY-5941
glycolate and glyoxylate degradation II
-
-
GLYOXDEG-PWY
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
glycyrrhetinate biosynthesis
-
-
PWY-7066
glyoxylate assimilation
-
-
PWY-5744
glyoxylate cycle
-
-
GLYOXYLATE-BYPASS
glyphosate degradation I
-
-
PWY-7804
glyphosate degradation III
-
-
PWY-7807
gondoate biosynthesis (anaerobic)
-
-
PWY-7663
gossypol biosynthesis
-
-
PWY-5773
grixazone biosynthesis
-
-
PWY-7153
guadinomine B biosynthesis
-
-
PWY-7693
guanine and guanosine salvage I
-
-
PWY-6620
guanine and guanosine salvage II
-
-
PWY-6599
guanosine deoxyribonucleotides de novo biosynthesis I
-
-
PWY-7226
guanosine deoxyribonucleotides de novo biosynthesis II
-
-
PWY-7222
guanosine nucleotides degradation I
-
-
PWY-6607
guanosine nucleotides degradation II
-
-
PWY-6606
guanosine nucleotides degradation III
-
-
PWY-6608
guanosine ribonucleotides de novo biosynthesis
-
-
PWY-7221
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
heme degradation II
-
-
PWY-7845
heparan sulfate degradation
-
-
PWY-7651
heparin degradation
-
-
PWY-7644
heptadecane biosynthesis
-
-
PWY-6622
heterolactic fermentation
-
-
P122-PWY
histamine biosynthesis
-
-
PWY-6173
histamine degradation
-
-
PWY-6181
homocysteine and cysteine interconversion
-
-
PWY-801
homoglutathione biosynthesis
-
-
PWY-6840
homospermidine biosynthesis I
-
-
PWY-5907
homospermidine biosynthesis II
-
-
PWY-8149
hyaluronan degradation
-
-
PWY-7645
hydrogen oxidation I (aerobic)
-
-
P283-PWY
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
hypoglycin biosynthesis
-
-
PWY-5826
hypotaurine degradation
-
-
PWY-7387
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 II
-
-
PWY-581
indole-3-acetate biosynthesis III (bacteria)
-
-
PWY-3161
indole-3-acetate biosynthesis IV (bacteria)
-
-
PWY-5025
indole-3-acetate biosynthesis VI (bacteria)
-
-
TRPIAACAT-PWY
indole-3-acetate degradation II
-
-
PWY-8087
inosine 5'-phosphate degradation
-
-
PWY-5695
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
isopimaric acid biosynthesis
-
-
PWY-5422
isoprene biosynthesis II (engineered)
-
-
PWY-7391
isopropanol biosynthesis (engineered)
-
-
PWY-6876
isorenieratene biosynthesis I (actinobacteria)
-
-
PWY-7938
itaconate biosynthesis II
-
-
PWY-8018
itaconate degradation
-
-
PWY-5749
jadomycin biosynthesis
-
-
PWY-6679
jasmonic acid biosynthesis
-
-
PWY-735
juniperonate biosynthesis
-
-
PWY-7619
justicidin B biosynthesis
-
-
PWY-6824
kaempferol gentiobioside biosynthesis
-
-
PWY-7143
kaempferol glycoside biosynthesis (Arabidopsis)
-
-
PWY-5320
kaempferol triglucoside biosynthesis
-
-
PWY-5348
ketogenesis
-
-
PWY66-367
ketolysis
-
-
PWY66-368
kievitone biosynthesis
-
-
PWY-4681
L-alanine biosynthesis II
-
-
ALANINE-SYN2-PWY
L-alanine biosynthesis III
-
-
PWY0-1021
L-alanine degradation II (to D-lactate)
-
-
ALACAT2-PWY
L-alanine degradation III
-
-
ALANINE-DEG3-PWY
L-alanine degradation IV
-
-
PWY1-2
L-alanine degradation V (oxidative Stickland reaction)
-
-
PWY-8189
L-alanine degradation VI (reductive Stickland reaction)
-
-
PWY-8188
L-arabinose degradation II
-
-
PWY-5515
L-arabinose degradation IV
-
-
PWY-7295
L-arginine biosynthesis I (via L-ornithine)
-
-
ARGSYN-PWY
L-arginine biosynthesis II (acetyl cycle)
-
-
ARGSYNBSUB-PWY
L-arginine biosynthesis III (via N-acetyl-L-citrulline)
-
-
PWY-5154
L-arginine biosynthesis IV (archaea)
-
-
PWY-7400
L-arginine degradation I (arginase pathway)
-
-
ARGASEDEG-PWY
L-arginine degradation 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 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 X (arginine monooxygenase pathway)
-
-
ARGDEG-V-PWY
L-arginine degradation XIII (reductive Stickland reaction)
-
-
PWY-8187
L-arginine degradation XIV (oxidative Stickland reaction)
-
-
PWY-6344
L-ascorbate biosynthesis I (plants, L-galactose pathway)
-
-
PWY-882
L-ascorbate biosynthesis IV (animals, D-glucuronate pathway)
-
-
PWY3DJ-35471
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 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 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 degradation II
-
-
PWY-3641
L-citrulline biosynthesis
-
-
CITRULBIO-PWY
L-citrulline degradation
-
-
CITRULLINE-DEG-PWY
L-cysteine biosynthesis I
-
-
CYSTSYN-PWY
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-dopa and L-dopachrome biosynthesis
-
-
PWY-6481
L-dopa degradation II (bacterial)
-
-
PWY-8110
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 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-homoserine biosynthesis
-
-
HOMOSERSYN-PWY
L-isoleucine biosynthesis I (from threonine)
-
-
ILEUSYN-PWY
L-isoleucine biosynthesis II
-
-
PWY-5101
L-isoleucine biosynthesis III
-
-
PWY-5103
L-isoleucine biosynthesis IV
-
-
PWY-5104
L-isoleucine biosynthesis V
-
-
PWY-5108
L-isoleucine degradation I
-
-
ILEUDEG-PWY
L-isoleucine degradation II
-
-
PWY-5078
L-leucine biosynthesis
-
-
LEUSYN-PWY
L-leucine degradation I
-
-
LEU-DEG2-PWY
L-leucine degradation III
-
-
PWY-5076
L-leucine degradation IV (reductive Stickland reaction)
-
-
PWY-7767
L-leucine degradation V (oxidative Stickland reaction)
-
-
PWY-8185
L-lysine biosynthesis I
-
-
DAPLYSINESYN-PWY
L-lysine biosynthesis II
-
-
PWY-2941
L-lysine biosynthesis III
-
-
PWY-2942
L-lysine biosynthesis IV
-
-
LYSINE-AMINOAD-PWY
L-lysine biosynthesis V
-
-
PWY-3081
L-lysine biosynthesis VI
-
-
PWY-5097
L-lysine degradation I
-
-
PWY0-461
L-lysine degradation II (L-pipecolate pathway)
-
-
PWY66-425
L-lysine degradation V
-
-
PWY-5283
L-lysine degradation X
-
-
PWY-6328
L-lysine degradation XI
-
-
LYSINE-DEG1-PWY
L-lysine fermentation to acetate and butanoate
-
-
P163-PWY
L-malate degradation II
-
-
PWY-7686
L-methionine biosynthesis I
-
-
HOMOSER-METSYN-PWY
L-methionine biosynthesis II
-
-
PWY-702
L-methionine biosynthesis III
-
-
HSERMETANA-PWY
L-methionine biosynthesis IV
-
-
PWY-7977
L-methionine degradation I (to L-homocysteine)
-
-
METHIONINE-DEG1-PWY
L-methionine degradation III
-
-
PWY-5082
L-methionine salvage 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-phenylalanine biosynthesis I
-
-
PHESYN
L-phenylalanine biosynthesis II
-
-
PWY-3462
L-phenylalanine biosynthesis III (cytosolic, plants)
-
-
PWY-7432
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 III (from L-ornithine)
-
-
PWY-3341
L-proline degradation I
-
-
PROUT-PWY
L-selenocysteine biosynthesis I (bacteria)
-
-
PWY0-901
L-selenocysteine biosynthesis II (archaea and eukaryotes)
-
-
PWY-6281
L-serine biosynthesis I
-
-
SERSYN-PWY
L-serine biosynthesis II
-
-
PWY-8011
L-threonine biosynthesis
-
-
HOMOSER-THRESYN-PWY
L-threonine degradation III (to methylglyoxal)
-
-
THRDLCTCAT-PWY
L-tryptophan biosynthesis
-
-
TRPSYN-PWY
L-tryptophan degradation I (via anthranilate)
-
-
TRPCAT-PWY
L-tryptophan degradation IV (via indole-3-lactate)
-
-
TRPKYNCAT-PWY
L-tryptophan degradation to 2-amino-3-carboxymuconate semialdehyde
-
-
PWY-5651
L-tryptophan degradation V (side chain pathway)
-
-
PWY-3162
L-tryptophan degradation VI (via tryptamine)
-
-
PWY-3181
L-tryptophan degradation VIII (to tryptophol)
-
-
PWY-5081
L-tryptophan degradation X (mammalian, via tryptamine)
-
-
PWY-6307
L-tryptophan degradation XI (mammalian, via kynurenine)
-
-
PWY-6309
L-tryptophan degradation 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 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 II
-
-
PWY-5057
lactate fermentation to acetate, CO2 and hydrogen (Desulfovibrionales)
-
-
PWY-8377
lacto-series glycosphingolipids biosynthesis
-
-
PWY-7839
lactose degradation III
-
-
BGALACT-PWY
lanosterol biosynthesis
-
-
PWY-6132
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
linoleate biosynthesis I (plants)
-
-
PWY-5995
linoleate biosynthesis II (animals)
-
-
PWY-6001
linoleate metabolites biosynthesis
-
-
PWY-8395
linustatin bioactivation
-
-
PWY-7091
lipid A-core biosynthesis (E. coli K-12)
-
-
LIPA-CORESYN-PWY
lipoxin biosynthesis
-
-
PWY66-392
long chain fatty acid ester synthesis (engineered)
-
-
PWY-6873
long-chain fatty acid activation
-
-
PWY-5143
lotaustralin degradation
-
-
PWY-6002
lupanine biosynthesis
-
-
PWY-5468
lupulone and humulone biosynthesis
-
-
PWY-5132
lutein biosynthesis
-
-
PWY-5947
luteolin biosynthesis
-
-
PWY-5060
luteolin glycosides biosynthesis
-
-
PWY-6239
luteolin triglucuronide degradation
-
-
PWY-7445
lychnose and isolychnose biosynthesis
-
-
PWY-6524
maackiain conjugates interconversion
-
-
PWY-2701
malate/L-aspartate shuttle pathway
-
-
MALATE-ASPARTATE-SHUTTLE-PWY
mandelate degradation I
-
-
PWY-1501
manganese oxidation I
-
-
PWY-6591
mangrove triterpenoid biosynthesis
-
-
PWY-6109
mannitol biosynthesis
-
-
PWY-3881
mannitol cycle
-
-
PWY-6531
mannitol degradation II
-
-
PWY-3861
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
Methanobacterium thermoautotrophicum biosynthetic metabolism
-
-
PWY-6146
methanofuran biosynthesis
-
-
PWY-5254
methanol oxidation to carbon dioxide
-
-
PWY-7616
methanol oxidation to formaldehyde IV
-
-
PWY-5506
methiin metabolism
-
-
PWY-7614
methyl indole-3-acetate interconversion
-
-
PWY-6303
methyl ketone biosynthesis (engineered)
-
-
PWY-7007
methyl parathion degradation
-
-
PWY-5489
methyl tert-butyl ether degradation
-
-
PWY-7779
methyl-coenzyme M reduction to methane
-
-
METHFORM-PWY
methylamine degradation I
-
-
PWY-6967
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 V
-
-
PWY-5458
methylglyoxal degradation VIII
-
-
PWY-5386-1
methylquercetin biosynthesis
-
-
PWY-6064
methylsalicylate biosynthesis
-
-
PWY18C3-22
methylsalicylate degradation
-
-
PWY18C3-24
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
mitochondrial L-carnitine shuttle
-
-
PWY-6111
mitochondrial NADPH production (yeast)
-
-
PWY-7269
mixed acid fermentation
-
-
FERMENTATION-PWY
molybdenum cofactor biosynthesis
molybdenum cofactor sulfulylation (eukaryotes)
-
-
PWY-5963
molybdopterin biosynthesis
-
-
PWY-6823
momilactone A biosynthesis
-
-
PWY-7477
mono-trans, poly-cis decaprenyl phosphate biosynthesis
-
-
PWY-6383
monoacylglycerol metabolism (yeast)
-
-
PWY-7420
monolignol glucosides biosynthesis
-
-
PWY-83
morphine biosynthesis
mRNA capping I
-
-
PWY-7375
mucin core 1 and core 2 O-glycosylation
-
-
PWY-7433
mucin core 3 and core 4 O-glycosylation
-
-
PWY-7435
mupirocin biosynthesis
-
-
PWY-8012
mycobacterial sulfolipid biosynthesis
-
-
PWY-7746
mycobactin biosynthesis
-
-
PWY185E-1
mycolate biosynthesis
-
-
PWYG-321
mycolyl-arabinogalactan-peptidoglycan complex biosynthesis
-
-
PWY-6397
mycothiol biosynthesis
-
-
PWY1G-0
myo-, chiro- and scyllo-inositol degradation
-
-
PWY-7237
myo-inositol biosynthesis
myo-inositol degradation I
-
-
P562-PWY
myo-inositol degradation II
-
-
PWY-7241
myricetin gentiobioside biosynthesis
-
-
PWY-7140
myxol-2' fucoside biosynthesis
-
-
PWY-6279
N-3-oxalyl-L-2,3-diaminopropanoate biosynthesis
-
-
PWY-8071
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 V (PNC V cycle)
-
-
PWY3O-4107
NAD(P)/NADPH interconversion
-
-
PWY-5083
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 to cytochrome c oxidase via plastocyanin
-
-
PWY-8271
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
nepetalactone biosynthesis
-
-
PWY-8069
nerol biosynthesis
-
-
PWY-8177
neurosporaxanthin biosynthesis
-
-
PWY-6681
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
nitrite-dependent anaerobic methane oxidation
-
-
PWY-6523
nitrobenzene degradation I
-
-
PWY-5637
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
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
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 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
ophthalmate biosynthesis
-
-
PWY-8043
orientin and isoorientin biosynthesis I
-
-
PWY-7188
oxalate biosynthesis
oxalate degradation III
-
-
PWY-6696
oxalate degradation IV
-
-
PWY-6697
oxalate degradation V
-
-
PWY-6698
oxalate degradation VI
-
-
PWY-7985
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
partial TCA cycle (obligate autotrophs)
-
-
PWY-5913
pectin degradation I
-
-
PWY-7246
pectin degradation II
-
-
PWY-7248
pederin biosynthesis
-
-
PWY-8049
pentachlorophenol degradation
-
-
PCPDEG-PWY
pentacyclic triterpene biosynthesis
-
-
PWY-7251
pentose phosphate pathway (non-oxidative branch) I
-
-
NONOXIPENT-PWY
pentose phosphate pathway (non-oxidative branch) II
-
-
PWY-8178
pentose phosphate pathway (oxidative branch) I
-
-
OXIDATIVEPENT-PWY
pentose phosphate pathway (partial)
-
-
P21-PWY
peptido-conjugates in tissue regeneration biosynthesis
-
-
PWY-8355
peptidoglycan biosynthesis II (staphylococci)
-
-
PWY-5265
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
periplasmic disulfide bond formation
-
-
PWY0-1599
petroselinate biosynthesis
-
-
PWY-5367
phaselate biosynthesis
-
-
PWY-6320
phenol degradation I (aerobic)
-
-
PWY-5418
phenolic malonylglucosides biosynthesis
-
-
PWY-6930
phenylacetate degradation I (aerobic)
-
-
PWY0-321
phenylethanol biosynthesis
-
-
PWY-5751
phenylethylamine degradation I
-
-
2PHENDEG-PWY
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
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
photorespiration I
-
-
PWY-181
photorespiration II
-
-
PWY-8362
photorespiration III
-
-
PWY-8363
photosynthesis light reactions
-
-
PWY-101
photosynthetic 3-hydroxybutanoate biosynthesis (engineered)
-
-
PWY-7218
phycocyanobilin biosynthesis
-
-
PWY-5917
phycoerythrobilin biosynthesis I
-
-
PWY-5915
phycoerythrobilin biosynthesis II
-
-
PWY-7580
phycourobilin biosynthesis
-
-
PWY-7579
phycoviolobilin biosynthesis
-
-
PWY-7578
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
pinitol biosynthesis II
-
-
PWY-6739
pinobanksin biosynthesis
-
-
PWY-5059
pinocembrin C-glucosylation
-
-
PWY-7189
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
poly-hydroxy fatty acids biosynthesis
-
-
PWY-6710
polyhydroxybutanoate biosynthesis
-
-
PWY1-3
polyhydroxydecanoate biosynthesis
-
-
PWY-6657
polymethylated quercetin biosynthesis
-
-
PWY-7161
polyphosphate metabolism
-
-
PWY-8138
ponciretin biosynthesis
-
-
PWY-5118
ppGpp metabolism
-
-
PPGPPMET-PWY
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
protectin biosynthesis
-
-
PWY-8357
protective electron sinks in the thylakoid membrane (PSII to PTOX)
-
-
PWY1YI0-7
protein citrullination
-
-
PWY-4921
protein N-glycosylation initial phase (eukaryotic)
-
-
MANNOSYL-CHITO-DOLICHOL-BIOSYNTHESIS
protein N-glycosylation processing phase (endoplasmic reticulum, yeast)
-
-
PWY-7918
protein N-glycosylation processing phase (plants and animals)
-
-
PWY-7919
protein 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 S-nitrosylation and denitrosylation
-
-
PWY-7798
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
psilocybin biosynthesis
-
-
PWY-7936
purine deoxyribonucleosides degradation I
-
-
PWY-7179
purine deoxyribonucleosides degradation II
-
-
PWY-7179-1
purine deoxyribonucleosides salvage
-
-
PWY-7224
purine nucleobases degradation I (anaerobic)
-
-
P164-PWY
purine nucleobases degradation II (anaerobic)
-
-
PWY-5497
purine ribonucleosides degradation
-
-
PWY0-1296
putrescine biosynthesis I
-
-
PWY-40
putrescine biosynthesis II
-
-
PWY-43
putrescine biosynthesis III
-
-
PWY-46
putrescine degradation I
-
-
PUTDEG-PWY
putrescine degradation III
-
-
PWY-0
putrescine degradation IV
-
-
PWY-2
putrescine degradation V
-
-
PWY-3
pyridoxal 5'-phosphate biosynthesis I
-
-
PYRIDOXSYN-PWY
pyridoxal 5'-phosphate salvage I
-
-
PLPSAL-PWY
pyridoxal 5'-phosphate salvage II (plants)
-
-
PWY-7204
pyrimidine deoxyribonucleosides degradation
-
-
PWY-7181
pyrimidine deoxyribonucleosides salvage
-
-
PWY-7199
pyrimidine deoxyribonucleotide phosphorylation
-
-
PWY-7197
pyrimidine deoxyribonucleotides biosynthesis from CTP
-
-
PWY-7210
pyrimidine deoxyribonucleotides de novo biosynthesis I
-
-
PWY-7184
pyrimidine deoxyribonucleotides de novo biosynthesis II
-
-
PWY-7187
pyrimidine deoxyribonucleotides de novo biosynthesis III
-
-
PWY-6545
pyrimidine deoxyribonucleotides de novo biosynthesis IV
-
-
PWY-7198
pyrimidine deoxyribonucleotides dephosphorylation
-
-
PWY-7206
pyrimidine nucleobases salvage II
-
-
PWY-7194
pyrimidine ribonucleosides degradation
-
-
PWY0-1295
pyrimidine ribonucleosides salvage I
-
-
PWY-7193
pyrimidine ribonucleosides salvage II
-
-
PWY-6556
pyrimidine ribonucleosides salvage III
-
-
PWY-7195
pyruvate decarboxylation to acetyl CoA I
-
-
PYRUVDEHYD-PWY
pyruvate decarboxylation to acetyl CoA II
-
-
PWY-6970
pyruvate 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 V
-
-
PWY-5537
pyruvate fermentation to acetate VI
-
-
PWY-5538
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 to cytochrome bo oxidase electron transfer
-
-
PWY-7544
quercetin gentiotetraside biosynthesis
-
-
PWY-7137
quercetin glucoside biosynthesis (Allium)
-
-
PWY-7129
quercetin glucoside degradation (Allium)
-
-
PWY-7133
quercetin glycoside biosynthesis (Arabidopsis)
-
-
PWY-5321
quercetin sulfate biosynthesis
-
-
PWY-6199
quercetin triglucoside biosynthesis
-
-
PWY-7173
raspberry ketone biosynthesis
-
-
PWY-5393
reactive oxygen species degradation
-
-
DETOX1-PWY-1
reductive acetyl coenzyme A pathway I (homoacetogenic bacteria)
-
-
CODH-PWY
reductive glycine pathway of autotrophic CO2 fixation
-
-
PWY-8303
reductive TCA cycle I
-
-
P23-PWY
reductive TCA cycle II
-
-
PWY-5392
resolvin D biosynthesis
-
-
PWY66-397
resveratrol biosynthesis
-
-
PWY-84
retinol biosynthesis
-
-
PWY-6857
rhamnogalacturonan type I degradation II (bacteria)
-
-
PWY-6771
ribose phosphorylation
-
-
RIBOKIN-PWY
ricinoleate biosynthesis
-
-
PWY-7618
rose anthocyanin biosynthesis II (via cyanidin 3-O-beta-D-glucoside)
-
-
PWY-7262
rosmarinic acid biosynthesis I
-
-
PWY-5048
rosmarinic acid biosynthesis II
-
-
PWY-5049
Rubisco shunt
-
-
PWY-5723
rutin biosynthesis
-
-
PWY-5390
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 IV
-
-
PWY0-1391
S-methyl-L-methionine cycle
-
-
PWY-5441
salicylate biosynthesis I
-
-
PWY-6406
salicylate biosynthesis II
-
-
PWY-8321
salidroside biosynthesis
-
-
PWY-6802
salinosporamide A biosynthesis
-
-
PWY-6627
Salmonella enterica serotype O:13 O antigen biosynthesis
-
-
PWY-8230
salvigenin biosynthesis
-
-
PWY-7325
sanguinarine and macarpine biosynthesis
-
-
PWY-5287
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
serotonin and melatonin biosynthesis
-
-
PWY-6030
serotonin degradation
-
-
PWY-6313
sesamin biosynthesis
-
-
PWY-5469
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
spermidine biosynthesis I
-
-
BSUBPOLYAMSYN-PWY
spermidine biosynthesis II
-
-
PWY-6559
spermidine biosynthesis III
-
-
PWY-6834
spermine and spermidine degradation I
-
-
PWY-6117
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
sporopollenin precursors biosynthesis
-
-
PWY-6733
stachyose biosynthesis
-
-
PWY-5337
stachyose degradation
-
-
PWY-6527
starch biosynthesis
-
-
PWY-622
starch degradation I
-
-
PWY-842
starch degradation II
-
-
PWY-6724
starch degradation III
-
-
PWY-6731
starch degradation IV
-
-
PWY-6735
starch degradation V
-
-
PWY-6737
stearate biosynthesis I (animals)
-
-
PWY-5972
stearate biosynthesis II (bacteria and plants)
-
-
PWY-5989
stearate biosynthesis III (fungi)
-
-
PWY3O-355
stearate biosynthesis IV
-
-
PWY-8280
stearidonate biosynthesis (cyanobacteria)
-
-
PWY-7595
stellariose and mediose biosynthesis
-
-
PWY-6525
stellatic acid biosynthesis
-
-
PWY-7736
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
suberin monomers biosynthesis
succinate to chytochrome c oxidase via cytochrome c6
-
-
PWY1YI0-2
succinate to cytochrome bd oxidase electron transfer
-
-
PWY0-1353
succinate to cytochrome bo oxidase electron transfer
-
-
PWY0-1329
succinate to cytochrome c oxidase via plastocyanin
-
-
PWY1YI0-3
succinate to plastoquinol oxidase
-
-
PWY1YI0-8
sucrose biosynthesis I (from photosynthesis)
-
-
SUCSYN-PWY
sucrose biosynthesis II
-
-
PWY-7238
sucrose biosynthesis III
-
-
PWY-7347
sucrose degradation I (sucrose phosphotransferase)
-
-
SUCUTIL-PWY
sucrose degradation II (sucrose synthase)
-
-
PWY-3801
sucrose degradation III (sucrose invertase)
-
-
PWY-621
sucrose degradation IV (sucrose phosphorylase)
-
-
PWY-5384
sucrose degradation V (sucrose alpha-glucosidase)
-
-
PWY66-373
sucrose degradation VII (sucrose 3-dehydrogenase)
-
-
SUCROSEUTIL2-PWY
sulfate activation for sulfonation
-
-
PWY-5340
sulfide oxidation IV (mitochondria)
-
-
PWY-7927
sulfite oxidation II
-
-
PWY-5279
sulfite oxidation III
-
-
PWY-5278
sulfolactate degradation III
-
-
PWY-6638
sulfur volatiles biosynthesis
-
-
PWY-6736
superoxide radicals degradation
-
-
DETOX1-PWY
superpathway of 5-aminoimidazole ribonucleotide biosynthesis
-
-
PWY-6277
superpathway of anthocyanin biosynthesis (from cyanidin and cyanidin 3-O-glucoside)
-
-
PWY-5313
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 glyoxylate cycle and fatty acid degradation
-
-
PWY-561
superpathway of L-aspartate and L-asparagine biosynthesis
-
-
ASPASN-PWY
superpathway of methylsalicylate metabolism
-
-
PWY18C3-25
superpathway of ornithine degradation
-
-
ORNDEG-PWY
superpathway of phospholipid biosynthesis II (plants)
-
-
PHOSLIPSYN2-PWY
superpathway of photosynthetic hydrogen production
-
-
PWY-7731
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
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
tetradecanoate biosynthesis (mitochondria)
-
-
PWY66-430
tetrahydrofolate biosynthesis I
-
-
PWY-6614
tetrahydrofolate salvage from 5,10-methenyltetrahydrofolate
-
-
PWY-6613
tetrahydropteridine recycling
-
-
PWY-8099
tetrapyrrole biosynthesis I (from glutamate)
-
-
PWY-5188
tetrapyrrole biosynthesis II (from glycine)
-
-
PWY-5189
theobromine biosynthesis I
-
-
PWY-5039
theophylline degradation
-
-
PWY-6999
thiamine diphosphate biosynthesis III (Staphylococcus)
-
-
PWY-6907
thiamine diphosphate biosynthesis IV (eukaryotes)
-
-
PWY-6908
thiamine diphosphate salvage III
-
-
PWY-6898
thiamine diphosphate salvage IV (yeast)
-
-
PWY-7356
thiazole component of thiamine diphosphate biosynthesis I
-
-
PWY-6892
thiazole component of thiamine diphosphate biosynthesis II
-
-
PWY-6891
thioredoxin pathway
-
-
THIOREDOX-PWY
thiosulfate disproportionation IV (rhodanese)
-
-
PWY-5350
threo-tetrahydrobiopterin biosynthesis
-
-
PWY-6983
thymine degradation
-
-
PWY-6430
thyroid hormone biosynthesis
thyroid hormone metabolism I (via deiodination)
-
-
PWY-6260
thyroid hormone metabolism II (via conjugation and/or degradation)
-
-
PWY-6261
toluene degradation II (aerobic) (via 4-methylcatechol)
-
-
TOLUENE-DEG-3-OH-PWY
toluene degradation to 2-hydroxypentadienoate (via toluene-cis-diol)
-
-
TOLUENE-DEG-DIOL-PWY
toluene degradation to 2-hydroxypentadienoate I (via o-cresol)
-
-
TOLUENE-DEG-2-OH-PWY
trans, trans-farnesyl diphosphate biosynthesis
-
-
PWY-5123
trans-caffeate degradation (aerobic)
-
-
PWY-8003
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 IV
-
-
PWY-2722
trehalose degradation V
-
-
PWY-2723
trehalose degradation VI (periplasmic)
-
-
PWY0-1466
triacylglycerol degradation
-
-
LIPAS-PWY
tricin biosynthesis
-
-
PWY-7995
trigonelline biosynthesis
-
-
PWY-5110
tRNA charging
-
-
TRNA-CHARGING-PWY
tRNA processing
-
-
PWY0-1479
tRNA splicing I
-
-
PWY-6689
tRNA splicing II
-
-
PWY-7803
tRNA-uridine 2-thiolation and selenation (bacteria)
-
-
PWY-7892
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
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-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
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
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
valproate beta-oxidation
-
-
PWY-8182
vancomycin resistance I
-
-
PWY-6454
vanillin and vanillate degradation II
-
-
PWY-7098
vanillin biosynthesis I
-
-
PWY-5665
vernolate biosynthesis III
-
-
PWY-6917
very long chain fatty acid biosynthesis I
-
-
PWY-5080
very long chain fatty acid biosynthesis II
-
-
PWY-7036
viridicatumtoxin biosynthesis
-
-
PWY-7659
vitamin D3 biosynthesis
-
-
PWY-6076
vitamin E biosynthesis (tocopherols)
-
-
PWY-1422
vitamin E biosynthesis (tocotrienols)
-
-
PWY-7436
vitamin K-epoxide cycle
volatile benzenoid biosynthesis I (ester formation)
-
-
PWY-4203
wax esters biosynthesis I
-
-
PWY-5884
wax esters biosynthesis II
-
-
PWY-5885
wighteone and luteone biosynthesis
-
-
PWY-4502
xanthine and xanthosine salvage
-
-
SALVPURINE2-PWY
xanthohumol biosynthesis
-
-
PWY-5135
xanthommatin biosynthesis
-
-
PWY-8249
xylitol degradation I
-
-
LARABITOLUTIL-PWY
xyloglucan biosynthesis
-
-
PWY-5936
xyloglucan degradation II (exoglucanase)
-
-
PWY-6807
xyloglucan degradation III (cellobiohydrolase)
-
-
PWY-6812
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
adipate degradation
-
-
PWY-8354
bile acid biosynthesis, neutral pathway
-
-
PWY-6061
catecholamine biosynthesis
-
-
PWY66-301
cis-vaccenate biosynthesis
-
-
PWY-5973
cyanate degradation
-
-
CYANCAT-PWY
dolichol and dolichyl phosphate biosynthesis
-
-
PWY-6129
folate polyglutamylation
-
-
PWY-2161
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
suberin monomers biosynthesis
-
-
PWY-1121
thyroid hormone biosynthesis
-
-
PWY-6241
urea cycle
-
-
PWY-4984
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
-
52, 335, 606, 845, 1416, 1672, 1716, 2153, 2813, 2993, 2994, 3072, 3203, 3725, 3734, 3739, 3741, 3743, 4091, 4094, 4318, 4402, 4691, 12301, 30314, 33559, 33784, 34334, 34340, 34342, 34346, 35335, 37288, 37297, 37456, 81096, 94495, 114098, 114127, 114128, 134704, 134906, 134920, 136130, 171690, 172122, 208594, 208595, 208600, 208611, 208615, 208616, 208637, 208638, 208639, 208923, 208986, 209153, 209161, 209401, 209404, 285635, 286307, 287320, 287427, 287540, 287902, 287920, 288079, 288541, 326371, 326373, 348370, 349008, 390057, 390058, 390060, 390061, 390062, 391697, 391698, 391871, 391944, 391948, 392012, 392110, 392125, 392244, 392245, 392290, 392374, 392727, 392844, 392886, 392909, 392918, 393485, 394141, 394180, 394373, 394511, 394512, 394513, 394514, 394593, 437707, 439385, 485143, 485935, 486141, 487451, 487459, 487861, 488690, 488691, 488896, 489068, 489372, 489561, 489764, 636890, 636986, 637946, 638494, 638640, 638657, 639238, 640818, 640888, 641486, 642039, 642744, 642753, 642821, 644287, 644351, 644366, 644372, 644454, 644455, 644456, 645354, 645356, 648903, 649418, 650400, 652633, 653195, 653502, 653551, 654503, 656397, 656943, 656944, 657047, 657084, 657200, 657774, 657880, 658243, 658263, 658269, 659637, 659680, 659863, 659977, 660091, 660111, 660540, 662093, 662941, 664178, 666557, 666648, 667753, 667788, 668777, 669662, 671596, 671684, 673571, 674922, 675754, 675895, 676354, 676403, 676646, 676689, 678426, 681135, 681143, 681849, 682139, 682346, 684413, 685512, 685546, 685558, 685589, 685598, 688069, 688469, 688651, 688825, 688915, 689429, 689608, 691390, 692295, 696627, 702247, 702394, 702550, 702635, 702638, 702672, 702924, 703847, 704118, 705797, 706001, 706032, 706219, 706329, 706929, 711173, 711183, 711277, 711723, 711726, 712022, 712218, 712419, 712481, 712526, 712603, 712782, 713231, 713233, 713275, 713610, 713812, 713936, 714099, 714565, 715002, 715222, 715233, 716573, 716586, 716642, 717456, 718200, 720714, 720736, 721261, 724444, 724511, 724673, 725119, 725179, 725925, 726129, 726208, 726240, 726340, 726427, 727161, 728199, 728526, 728825, 729615, 731012, 731382, 733293, 733684, 734981, 735042, 737014, 737276, 737588, 738406, 739827, 740027, 740956, 741040, 741199, 741845, 742602, 742812, 743845, 744281, 744827, 746088, 747401, 747893, 747908, 748904, 748980, 751269, 751876, 757574, 757756, 757967, 757983, 758161, 758276, 760005, 760167, 762908, 764048, 765152
-
-
-
394002, 485339, 491360, 640888, 656853, 657502, 661622, 663135, 666607, 671601, 676545, 676727, 680693, 685131, 688693, 689556, 696257, 700677, 704462, 715018, 726252, 734874, 736438, 740449, 744152, 744597, 745464, 745831, 746013, 746050, 747908, 748823, 757544, 758036, 758367, 759283, 764782, 765865
A7ISW5, D4Q9Z4, D4Q9Z5, I1KAE3, I1L3T1, I1LPA7, I1LVA5, I1MSF2, K7LNT1, K7LY64, O48926, O49857, O81413, P28583, P30080, P42347, P42348, Q08IT7, Q41266, Q43445, Q43758, Q53B70, Q53B74, Q5GKZ7, Q5MYA1, Q6TXD0, Q6X0M8, Q6YLS3, Q8H2B0, Q8SAG1, Q8W1A0, Q8W3Y5, Q93XE6, Q93XG4, Q9M6D6, Q9SWR5
SwissProt
-
656270, 664104, 666019, 678300, 682320, 684943, 688632, 689553, 690149, 693875, 702839, 703633, 703847, 704094, 704482, 704740, 706244, 706299, 712490, 714948, 722715, 727474, 730601, 730653, 732643, 734953, 734961, 737738, 737769, 741857, 742430, 743684, 744080, 744229, 745637, 745739, 745831, 747189, 747908, 750918, 751827, 755832, 756234, 756258, 756309, 756434, 756832, 758023, 758367, 758926, 759886, 759917, 759933, 759939, 760318, 762185, 762189, 762849, 762941, 764064, 764556, 764620, 765652, 765865
A0A068JE73, A0A0R0FIH2, A0A0R0H2W2, A0A0R0HRL5, A0A0R0INR5, A0A0R0JU82, A0A0R0K0I2, A0A1L7NRS0, A0A1X9JQM7, A0A2H4GW71, A3RM03, A3RM04, A3RM05, A3RM06, A5YT86, A5YT88, B0M1A6, B1B538, B6ETP1, B9A1Q4, C3UZD2, C3VD33, C4MH52, D3U591, I1J5P4, I1J5P9, I1JB12, I1JCA9, I1JFY8, I1JZJ1, I1K037, I1KH05, I1KXC2, I1KXS8, I1L6I6, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXA6, I1MXC3, I1NHV6, I1NJA2, K7K0Q1, K7K424, K7K808, K7KKZ9, K7KL00, K7KR69, M4WFN0, O22443, O82560, P09186, P10538, P13708, P48631, Q0EDG6, Q0GJK0, Q39810, Q3S3F6, Q5F2M7, Q76LA6, Q7XAC5, Q7XJB3, Q7XZQ1, Q8S3B9, Q9FQE8, Q9FUK4, Q9M6B9, Q9SEH8, Q9XEY7, Q9XHC6, Q9ZTT3, R4HEK6, U5ILS4
UniProt
3D homology model of the matured soybean PDF2 based on the X-ray structure of the homologous enzyme from Plasmodium falciparum
-
-
comparison of thermal stability with enzymes from Pseudomonas sp. strain 101, Moraxella sp. C1, Candida boidinii, and Arabidopsis thaliana, all recombinant proteins, expressed in Escherichia coli
-
-
cv. Pusa 9712, collected from the Division of Genetics, IARI, New Delhi
UniProt
cv. Pusa-16, grown in the fields of Division of Genetics, I.A.R.I, New Delhi
UniProt
cv. Wye, 33 Chinese soybean accessions including 16 Glycine soja and 17 Glycine max
UniProt
drought-tolerant (Jackson) and drought-sensitive (Williams) genotypes
A9GYV1
SwissProt
expression is induced by UV-B irradiation and subsequently stimulates accumulation of kaempferol glycones
UniProt
isoform RBOHB, member of group six of orthologues based on phylogenetic analysis with their Arabidopsis counterparts
UniProt
isoform RBOHL, member of group six of orthologues based on phylogenetic analysis with their Arabidopsis counterparts
UniProt
isoform RBOHP, member of group six of orthologues based on phylogenetic analysis with their Arabidopsis counterparts
UniProt
isoform RBOHQ, member of group six of orthologues based on phylogenetic analysis with their Arabidopsis counterparts
UniProt
L. Merr. cv RCAT Angora (3150 CHU) and cv Harovinton (3100 CHU)
SwissProt
L. Merr.. 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.
-
-
NADH:nitrate oxidoreductase is more active in young cotyledons, as cotyledons age NAD(P)H:nitrate oxidoreductase becomes more active
-
-
several different cultuvars, e.g. metal-tolerant cv. Chernyatka and the metal-sensitive cv. Kyivska 98
-
-
soybean
805, 814, 4457, 4459, 4468, 4488, 33152, 134641, 135444, 136361, 136911, 171217, 171249, 246651, 246654, 246668, 246669, 246670, 246701, 246702, 246808, 286891, 288820, 288831, 390730, 391064, 392106, 392554, 393652, 394439, 394508, 394509, 394510, 438433, 439855, 439864, 439869, 439872, 439878, 441222, 441407, 485052, 485058, 485980, 487453, 488893, 489878, 636362, 638639, 639714, 640398, 644256, 644269, 644454, 644456, 644602, 644609, 645301, 646833, 652653, 653429, 676669, 692050
-
-
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.
-
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
SOURCE TISSUE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
SOURCE
additional information
-
maximal activity is observed on day 5 in light-exposed calli or day 14 in day-exposed ones. After 5 d of salt exposure, NAD kinase activity is markedly lower than in control, but NAD kinase of dark-exposed and NaCl-exposed calli is 10times more active than that of both light-exposed and NaCl-exposed calli
-
-
606, 608, 34340, 34342, 135444, 137558, 288230, 288233, 390057, 390058, 390062, 437707, 489902, 489903, 645354, 740956
-
the tunicamycin resistant cells have a greater than 40fold increase in the activity of the enzyme UDP-GlcNAc:dolichyl-P GlcNAc1P transferase. Increase in enzyme activity is due to an increased production of the enzyme
-
34340, 34342, 137558, 285325, 347801, 347812, 485052, 485143, 485344, 485545, 487451, 487459, 488454, 488687, 488690, 488691, 488896, 489068, 489372, 642090, 734953
-
elicitor-challenged, unstimulated cell culture does not contain detectable cyclase activity
-
the specific activity increases with age of the culture, reaching a maximum late in the growth cycle
-
52, 335, 33152, 94785, 134704, 134920, 136361, 208094, 288820, 288831, 391114, 392554, 438433, 486496, 486497, 489371, 489372, 489902, 489903, 489904, 638494, 644256, 657502, 666648, 675754, 692295, 694783, 703847, 713812, 713936, 716502, 716586, 717392, 728199, 736973, 740956, 756315, 764782
-
distribution to the endoplasmic reticulum and protein storage vacuoles, PDIS-1 levels, but not PDIS-2 levels, are increased in cotyledons
-
expression of GmPDIL-3a and GmPDIL-3b in soybean cotyledons during maturation, overview
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
of 5-day-old plants
-
phytase synthesized early in germination persists for several days in the cotyledon
A0A068JE73, A0A068JF10, A7ISP6, D3Y5N8, I1K3K3, O81980, Q09WE7, Q53B70, Q53B75, Q7XAC5, Q93XE6, Q949H4
-
-
and pod, highest expression level of isoform IFS2. Embryos excised from developing soybean seeds also accumulate isoflavonoids from a synthetic medium. Developing soybean embryos have an ability to synthesize isoflavonoids de novo, but transport from maternal tissues may in part contribute to the accumulation of these natural products in the seed
expression patterns is higher at 70 d after pollination in both the cultivars. Expression of the gene coincides with the onset of accumulation of isoflavonoids in the embryos. CHS7 is expressed at significantly greater level in RCAT Angora than in Harovinton
expression patterns is higher at 70 d after pollination in both the cultivars. Expression of the gene coincides with the onset of accumulation of isoflavonoids in the embryos. CHS8 is expressed at significantly greater level in RCAT Angora than in Harovinton
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
of 5-day-old plants
A0A068JE73, A0A068JF10, A3RM03, A3RM04, A3RM05, A3RM06, A5YT86, A5YT88, A6BM07, A7ISP6, A7X665, I1K3K3, K7K424, O81980, Q39810, Q43445, Q53B70, Q53B75, Q5GKZ7, Q6YLS3, Q8W3Y5, Q93XE6, Q949H4
-
485339, 676545, 679799, 706244, 713233, 716569, 738332, 746245, 747908, 749029, 755047, 758367, 760244, 764783
low expression
moderate expression
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
young
-
4094, 134641, 136130, 489371, 489902, 642744, 642821, 666648, 670607, 678426, 690395, 704094, 716502, 736973, 740956, 744991
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
of 5-day-old plants
A0A068JE73, A0A068JF10, A3RM03, A3RM04, A3RM05, A3RM06, A5YT86, A5YT88, A7ISP6, A7ISW5, A9GYV1, C0LZ80, C4MH52, D2D5G3, D2D5G4, D3Y5N8, F5A0U7, I1K3K3, I1KEV6, I1NHV6, K7K424, O48926, O81413, O81980, Q0EDG6, Q39827, Q43445, Q53B70, Q53B75, Q5GKZ7, Q8SAG1, Q93XE6, Q949H4, Q94FX1, R4HEK6
-
1416, 2153, 2993, 3203, 4457, 4488, 33559, 35335, 208093, 209153, 246651, 246654, 246668, 246702, 287427, 326373, 391608, 392012, 392125, 392844, 392886, 394002, 394439, 438417, 485935, 487861, 489371, 636362, 638639, 638640, 638657, 644269, 653016, 657774, 658243, 666557, 670607, 671601, 676354, 676646, 676705, 682139, 688651, 688693, 688915, 688942, 689608, 692295, 700677, 701203, 703847, 706244, 706329, 713233, 716502, 720561, 720826, 723364, 725119, 728526, 733684, 734953, 735863, 737014, 741040, 741199, 746050, 747893, 747908, 748904, 749029, 755047, 758023, 758367, 760052
altered levels of polyunsaturated fatty acids in leaves treated with cold stress have no direct correlation with the expression of enzyme isoforms FAD2-3 and FAD2-2
AOX2 isoform is most abundant and is constitutively expressed either mainly in photosynthetic tissues (AOX2A) or throughout the whole plant (AOX2D)
-
during the early stretching of soybean leaves, removing cytokines or growth factors can induce Fe-SOD mRNA accumulation. In contrast, Fe-SOD mRNA accumulation is normal during any other stage by removing cytokines or growth factors. Fe-SOD expression is related to whether the development stage is leaf expansion or not
expression levels are the highest in leaves, followed by roots, and lowest in seeds and seed pods. Among the MsrB isoforms, transcripts of MSRB1 in the leaves are the highest
expression levels are the highest in leaves, followed by roots, and lowest in seeds and seed pods. Among the MsrB isoforms, transcripts of MSRB5 in the leaves are the lowest
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
of 14-day-old plants
-
-
substantial increase in specific activity over root level concomitant with development of effective nodules
-
A0A068JE73, A0A068JF10, A7ISP6, A7X665, A9GYV1, C4MH52, D3Y5N8, K7K424, O81413, O81980, P31531, P42347, P42348, Q08IT7, Q39810, Q53B70, Q53B75, Q5F2M7, Q5GKZ7, Q93XE6
-
1416, 326373, 392727, 394002, 489371, 489372, 640888, 646833, 656944, 660091, 666648, 675895, 676646, 679799, 680693, 681143, 689608, 703847, 704094, 704895, 713233, 713610, 716502, 720561, 720736, 723364, 730359, 730592, 734953, 738332, 740956, 742602, 747908, 749020, 749029, 757967, 758367, 760244, 761179, 764783
ATPS mRNA is most abundant in root tissue, cold treatment induces RNA accumulation and enhances the specific activity of ATPS in root tissue
-
chitinases are components of plant defence against higher concentrations of heavy metals. Accumulation of some isoforms in response to one but not to other metal ions suggests that these enzymes might also be involved in a more metal specific mechanism in affected plants
-
cold-treatment increases expression and the total activity of APS reductase in root tissues
enzyme expression occurs principally in the junction area between roots and young nodules
expression after cultivation on nitrate. Expression of the gene is reduced to very low levels within days after submitting the plants to a N-free medium. The subsequent return to a complete medium, containing nitrate restores expression of all three genes. High and low expression of genes in the roots are associated with high and low ratios of Asn/Asp transported to the shoot through xylem
expression levels are the highest in leaves, followed by roots, and lowest in seeds and seed pods
expression of isoforms SAS1, SAS2 after cultivation on nitrate. Expression of the genes is reduced to very low levels within days after submitting the plants to a N-free medium. The subsequent return to a complete medium, containing nitrate restores expression of all three genes. High and low expression of genes in the roots are associated with high and low ratios of Asn/Asp transported to the shoot through xylem
hairy roots, transformed with the soybean chalcone synthase (CHS6) or isoflavone synthase (IFS2) genes, with dramatically decreased capacity to synthesize isoflavones are produced to determine what effects these changes would have on susceptibility to a fungal pathogen. Blockage of isoflavone synthesis by constitutive expression of two key genes in the isoflavonoid pathway, chalcone synthase and isoflavone synthase leads to the inability to synthesize glyceollin in soybean hairy roots on root resistance to Fusarium solani f. sp. glycines
-
involvement of plasma membrane H+-ATPase in the adaptation to phosphorus starvation
-
much lower expression levels than in shoots of etiolated plants, light treatment decreases expression levels
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
of 5-day-old plants
the expression of UGT4, an isoflavone-specific 7-O-glucosyltransferase (UGT4), is decreased during the reproductive stages. Expression of UGT4 is high in the vegetative stages, and decreased by over 90% during the reproductive stages
-
1672, 4318, 33559, 286307, 392012, 392106, 392110, 392139, 392918, 394002, 394180, 394187, 394508, 394509, 394510, 394511, 394512, 489760, 659863, 688825, 720736, 726240, 738332, 744080, 746120, 747908, 757967, 758367, 759886, 760167
A0A068JE73, A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, A3RM03, A3RM04, A3RM05, A3RM06, A5YT86, A5YT88, A6BM07, A7X665, B2ZF64, I1JB12, I1JZJ1, I1K037, I1L4P1, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MRZ6, I1MSF2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69, K7LZ65, P09186, Q39810, Q43445, Q5GKZ7, Q84X83, Q84X84, Q8SAG1, Q93XE6, Q9FXK9
-
3725, 171690, 208600, 208614, 209161, 288820, 390730, 391607, 391948, 393485, 393652, 394141, 394373, 489371, 644256, 644351, 645301, 658827, 669662, 671601, 675895, 676689, 680270, 684413, 688651, 697056, 702247, 702924, 706244, 706645, 711277, 713275, 716502, 716569, 716642, 728825, 733684, 734874, 735249, 736973, 738332, 746120, 746245, 747908, 756309, 756881, 757032, 757544, 758276, 762167, 762402
-
changes in the levels of PDIS-1 and PDIS-2 during seed development, overview
Eu4 expression is more prominent in seeds one day after dormancy break whereas Eu1 predominates in developing seeds
expression levels are the highest in leaves, followed by roots, and lowest in seeds and seed pods
-
found in developing seeds, 15-50 days after flowering, not in germinated seeds
germinating seed, GAD1 protein is observed in seeds of various states such as developing, matured and soaking
GmDGAT1A is highly expressed in seeds, the expression pattern is consistent with oil accumulation
high expression level, the expression pattern is consistent with oil accumulation
mainly expressed in developing seeds
mature, dry seeds, high enzyme expression level at the very early stage of seed development 13 days after flowering, the expression decreases gradually duting seed development and is nearly ceased at the very late stage 58 days after flowering
-
maximal activity in seed line 9686 is around 40 days after flowering, maximal activity in seed line Wayne is around 30 days after flowering
phytase mRNA and phytase activity increases during seed development, consistent with the use of an embryonic promoter
-
protein is already present at the dormant stage and gradually activated during germination in soybean seeds
-
seed-specific expression of isoform GmMIPS-1 in the outer integumentary layer during early seed development. Enzyme is associated with oxalate crystal idioblasts
-
soybean contains an ubiquitous urease (encoded by Eu4) that is synthesized in all tissues, as well as an embryo-specific urease (encoded by the gene Eu1) that is confined to the developing embryo and is retained in mature seeds where its activity is roughly 1000fold higher than that of ubiquitous urease
spatio-temporal transcript profiling signified GmItpk2 to be seed-specific, with higher transcript levels in the early stage of seed development, GmItpk2 expression profiling overview
-
sulfur and phosphorus deprivation increases expression level, while nitrogen starvation represses APS reductase mRNA transcript and protein levels
-
and root, highest expression level of isoform IFS1. Developing soybean embryos have an ability to synthesize isoflavonoids de novo, but transport from maternal tissues may in part contribute to the accumulation of these natural products in the seed
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, A6BM07, A7X665, A9GYV1, B9A1Q4, C0LZ80, C6TER4, D2D5G3, D2D5G4, F5A0U7, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69, Q08IT7, Q9FQE8, Q9ZT38, U5TRK1
-
845, 4402, 134906, 208923, 209404, 288820, 288831, 390057, 390060, 392244, 392245, 392290, 485980, 489372, 636986, 640167, 640398, 642753, 658827, 660305, 666648, 680693, 689608, 690395, 704094, 706299, 715757, 716569, 720714, 720826, 723437, 725119, 736973, 737769, 744991, 756309, 760005, 760244, 761238
cAPX 2 is involved in flooding stress responses in young soybean seedlings
in five-day old dark-grown seedling, enzyme expression is strongly induced by light, weakly induced by methyl jasmonate and low temperature, and not induced by elicitor or UV-B treatment
A9GYV1
drought-tolerant and drought-sensitive genotypes, different water treatments
-
the gene for AS is predominantly expressed in shoots as compared to roots of etiolated plants, light treatment decreases expression levels
A0A068JE73, A0A068JF10, A7ISP6, A7X665, D3Y5N8, O49857, O81413, O81980, Q39827, Q53B70, Q53B75, Q8SAG1, Q93XE6
-
326373, 394002, 661622, 670607, 671601, 676646, 679799, 713233, 720561, 723364, 749029, 760244, 764783
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
of 14-day-old plants
additional information
analysis of temporal and spatial specificity of the expression of beta-AS
additional information
by northern blot analysis a decline in the ATPS transcript level during seed development can be found
additional information
constitutive expression in both vegetative tissues and developing seeds
additional information
-
expressed in all photosynthetic tissues except pod wall and root
additional information
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expression of four Galpha, four Gbeta, and two Ggamma proteins, expression profiles by quantitative PCR during different developmental stages, overview. In general, the expression of G-protein genes is lower in roots than in aerial tissues. Except for GmGalpha4, which is highly expressed in the primary stem and the first trifoliate leaves at V1 stage, the soybean G-protein genes are expressed at comparable levels in all different developmental stages and tissue types
additional information
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expression patterns of GmGalpha1-4 are differentially regulated in different tissues of soybean and at various growth and development phases, e.g. during seed development and seed germination
additional information
expression profile of GmIPK1 across different tissues and seed development stages
additional information
gene GmUGT3 encodes a UGT that is highly specific for isoflavones
additional information
gene GmUGT4 encodes a UGT that is highly specific for isoflavones and is mainly expressed in the lateral roots and seeds, followed by taproots, cotyledon, and hypocotyls
additional information
gene GmUGT9 encodes a UGT that is highly specific for isoflavones, the levels of the GmUGT9 transcripts are highest in roots, followed by taproots, cotyledon, and hypocotyls
additional information
GmDGAT1A is mainly expressed in seeds, but also in tissues like roots, leaves, flowers, at relatively lower levels
additional information
GmDGAT2D transcripts are high in flowers and seeds, but also present in other tissues at lower levels, such as roots, leaves and pods
additional information
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
GmHDACs fall into three major groups previously named RPD3/HDA1, SIR2, and HD2. Real-time quantitative PCR tissue distribution analysis, differential expression across various tissues
additional information
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GmPDIL-3a and GmPDIL-3b are ubiquitously expressed in the plant body
additional information
no activity detectable in lateral roots emergence region
additional information
-
no appreciable activity is detected in cotyledons and shoots
additional information
not found in stem, leaf, cotyledon, root and embryo
additional information
present in all tissues of germinating seedling and in vegetative tissues from 45 day old plants. Isoforms ALN1 and ALN2 are consistently expressed at higher levels than ALN3 and ALN4 in all samples
additional information
present in all tissues of germinating seedling and in vegetative tissues from 45 day old plants. Isoforms ALN1 and ALN2 are consistently expressed at higher levels than ALN3 and ALN4 in all samples. Similar levels of ALN4 are found only in nodules
additional information
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quantitative real-time RT-PCR tissue expression analysis, overview
additional information
real-time RT-PCR tissue expression analysis of GmIF7GT gene homologues 1-6, overview. The transcript level of a less known gene homologue of isoflavone 7-O-glucosyltransferase GmIF7GT4 is significantly higher by about 11fold, in the roots than the gene homologue mIF7GT1 and the other homologues. Transcript levels of other homologues of GmIF7GT are much lower than the transcript levels of GmIF7GT1 or GmIF7GT4, overview
additional information
the expression level of soybean DGAT1 is much higher relative to DGAT2 throughout seed development
additional information
the levels of the most abundant GmUGT1 transcripts in cotyledons are much higher than those in lateral roots
additional information
the levels of the most abundant GmUGT7 transcripts in cotyledons are much higher than those in lateral roots
additional information
-
tissue expression pattern of gene GmF3'H at different developmental stages
additional information
tissue-specific enzyme expression analysis by virtual expression analysis from RNASeq data
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LOCALIZATION
ORGANISM
UNIPROT
COMMENTARY
GeneOntology No.
LITERATURE
SOURCE
-
GmPDIL-3a and GmPDIL-3b form protein complexes in the endoplasmic reticulum
co-purifies with crude mitochondria during subcellular fractionation of organelles
-
additional information
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isoform CHI3
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA10
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA14
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA16
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA3
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA8
located on the surface or in the intermembrane space of chloroplasts
the enzyme has a plastid localization sequence (residues 1-48)
-
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA1
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA10
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA11
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA12
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA13
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA14
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA15
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA17
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA18
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA2
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA3
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA4
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA5
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA6
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA9
subcellular localization analysis in transgenic protoplasts
A0A1X9JQM7, A0A1Y9TFD9, A7X665, I1KAE3, I1LPA7, I1LVA5, K7LNT1, K7LY64, O82560, Q43758, Q76LA8, Q9FQE8, Q9FUK4
-
4691, 94495, 208923, 209404, 246808, 286307, 286655, 394508, 394510, 438433, 439855, 439864, 488555, 489371, 489372, 639714, 642090, 653195, 656853, 660305, 663275, 676689, 685131, 685177, 689427, 692050, 696257, 703847, 714099, 726208, 737769, 744080, 756832, 759283, 761179, 762167
cytosolic localization of GmITPK2 protein is predicted by CELLO tool with a reliability index of 2.976
A0A1X9JQM7, A0A1Y9TFD9, A9GYV1, K7K424, K7K808, P48631, Q39810, Q5GKZ7, Q9M6B9, Q9SEH8
-
645301, 675754, 682320, 689608, 692295, 713233, 744229, 744827, 745739, 749020, 756832, 758367, 762185
-
PDIS-1 and PDIS-2 lack the C-terminal, endoplasmic reticulum-retrieval signal, KDEL
-
different fusion proteins analyzed to determine if the portion of ManI located in the Golgi lumen plays a role in the targeting of this glycosidase to the Golgi and the ER membranes
-
occurs as a membrane-associated form as well as a soluble form
-
the protein contains a RING-H2 motif and an N-terminal transmembrane domain
C3VD33, I1KH05, I1MSF2, P48631, Q19AK7, Q19AK8, Q5GKZ7, Q6YLS3, Q84X83, Q84X84, Q9FXK9, Q9M6B9, Q9SWR5
-
-
37574, 134920, 246654, 285325, 390057, 390058, 390062, 394593, 486496, 486497, 489068, 636890, 640398, 644351, 645301, 645354, 654324, 675656, 676545, 685598, 686340, 704482, 716642, 735249, 737738, 744152, 744229, 745739, 757032, 758036
-
94495, 286655, 349008, 394002, 653498, 692050, 713936, 715002, 726208, 738302, 760005, 762941, 764782, 765865
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA13
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA1
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA11
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA12
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA15
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA16
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA17
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA18
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA2
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA5
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA6
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA7
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA8
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
isozyme GmHDA9
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limited to large peroxisomes in uninfected cells of root nodules of Glycine max inoculated with Bradyrhizobium japonicum
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enzyme localizes to the plasma mebrane in transgenic Arabidopsis thaliana and Xenopus laevis oocyte
protein sequence is led by a plastid targeting signal sequence
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sequence contains a N-terminal plastid targeting sequence, plastidial localization of green fluorescent protein fusion protein
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protein storage vacuoles in parenchyma cells of seedling cotyledons and maturing seeds
additional information
determination of the subcellular localization of GmDGAT-GFP performed by using tobacco leaf infiltration. Comparison of tissue expression patterns of isozymes GmDGAT1A and GmDGAT2D in nodules, roots, stems, leaves, flowers, pods, and seeds
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additional information
A0A0R0FIH2, A0A0R0H2W2, A0A0R0JU82, A0A0R0K0I2, I1JB12, I1JZJ1, I1K037, I1LFN1, I1LKU7, I1LTZ2, I1LWR2, I1MTD8, I1MUF8, I1MXC3, K7K0Q1, K7KKZ9, K7KL00, K7KR69
GmHDACs fall into three major groups previously named RPD3/HDA1, SIR2, and HD2
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additional information
immunohistochemic localization analysis, overview
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additional information
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PDIS-1 and PDIS-2 both possess a putative N-terminal secretory signal sequence and two tandem thioredoxin-like motifs, with a CGHC active site
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additional information
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the doublet in cytosolic enzyme activity observed in the native-PAGE of soybean leaf and root nodule extracts could represent either the products of two cytosolic soybean enzyme genes or a single gene product with some post-translational modification, the cultivar Roanoke has a single isozyme
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LINKS TO OTHER DATABASES (specific for Glycine max)
SILVA: 16S/18S rRNA, 23S/28S rRNA
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Release 2023.1 (January 2023)
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