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Organism related
Word Map for Organism Aspergillus niger
- Aspergillus niger
- fumigatus
- esterase
- glucoamylase
- nidulans
- terreus
- xylanase
- versicolor
- phytase
- rhizopus
- aspergillosis
- mycotoxin
- mucor
- alternata
- endoglucanase
-
ochratoxin
- cellulases
- aflatoxin
- reesei
- crassa
- chrysogenum
-
aspergilli
- ochraceus
- carbonarius
- pastoris
- pectinase
- polygalacturonase
- beta-glucosidase
- viride
- aculeatus
- citrinum
- fumonisins
- itraconazole
- awamori
- lipases
- parasiticus
- voriconazole
- stolonifer
- bagasse
- endoxylanase
- lunata
- expansum
- notatum
- caspofungin
- alpha-galactosidase
-
feruloylated
- endoprotease
- arabinoxylans
- verrucosum
- catalases
-
bioleaching
TaxTree of Organism Aspergillus niger
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EC NUMBER 
COMMENTARY 
-
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
(1'S,5'S)-averufin biosynthesis
-
-
PWY-5954
(1,4)-beta-D-xylan degradation
-
-
PWY-6717
(3R)-linalool biosynthesis
-
-
PWY-7709
(3S)-linalool biosynthesis
-
-
PWY-7141
(4Z,7Z,10Z,13Z,16Z)-docosapentaenoate biosynthesis (6-desaturase)
-
-
PWY-7726
(5Z)-dodecenoate biosynthesis I
-
-
PWY0-862
(5Z)-dodecenoate biosynthesis II
-
-
PWY-7858
(8E,10E)-dodeca-8,10-dienol biosynthesis
-
-
PWY-7654
(aminomethyl)phosphonate degradation
-
-
PWY-7805
(R)- and (S)-3-hydroxybutanoate biosynthesis (engineered)
-
-
PWY-7216
(R)-camphor degradation
-
-
P601-PWY
(R)-cysteate degradation
-
-
PWY-6642
(S)-camphor degradation
-
-
PWY-6989
(S)-lactate fermentation to propanoate, acetate and hydrogen
-
-
PWY-8086
(S)-propane-1,2-diol degradation
-
-
PWY-7013
(S)-reticuline biosynthesis I
-
-
PWY-3581
1,3-beta-D-glucan biosynthesis
-
-
PWY-6773
1,3-propanediol biosynthesis (engineered)
-
-
PWY-7385
1,4-dichlorobenzene degradation
-
-
14DICHLORBENZDEG-PWY
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
2,3-dihydroxybenzoate biosynthesis
-
-
PWY-5901
2,4,5-trichlorophenoxyacetate degradation
-
-
PWY-6200
2,4,6-trichlorophenol degradation
-
-
PWY-6178
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-methylcitrate cycle I
-
-
PWY0-42
2-methylcitrate cycle II
-
-
PWY-5747
2-methylketone biosynthesis
-
-
PWY-6585
2-methylpropene degradation
-
-
PWY-7778
2-nitrobenzoate degradation II
-
-
PWY-5648
2-nitrotoluene degradation
-
-
PWY-5641
2-oxoglutarate decarboxylation to succinyl-CoA
-
-
PWY-5084
24-epi-campesterol, fucosterol, and clionasterol biosynthesis (diatoms)
-
-
PWY-8238
3,4,6-trichlorocatechol degradation
-
-
PWY-6094
3,5-dichlorocatechol degradation
-
-
PWY-6084
3,6-anhydro-alpha-L-galactopyranose degradation
-
-
PWY-7562
3,8-divinyl-chlorophyllide a biosynthesis I (aerobic, light-dependent)
-
-
CHLOROPHYLL-SYN
3,8-divinyl-chlorophyllide a biosynthesis III (aerobic, light independent)
-
-
PWY-7159
3-(4-hydroxyphenyl)pyruvate biosynthesis
-
-
PWY-5886
3-chlorocatechol degradation I (ortho)
-
-
PWY-6089
3-chlorocatechol degradation II (ortho)
-
-
PWY-6193
3-hydroxy-4-methyl-anthranilate biosynthesis II
-
-
PWY-7765
3-hydroxypropanoate/4-hydroxybutanate cycle
-
-
PWY-5789
3-methylbutanol biosynthesis (engineered)
-
-
PWY-6871
3-phenylpropanoate degradation
-
-
P281-PWY
3-phosphoinositide biosynthesis
-
-
PWY-6352
4,5-dichlorocatechol degradation
-
-
PWY-6093
4-aminobutanoate degradation I
-
-
PWY-6535
4-aminobutanoate degradation III
-
-
PWY-6536
4-aminobutanoate degradation IV
-
-
PWY-6473
4-aminobutanoate degradation V
-
-
PWY-5022
4-aminophenol degradation
-
-
PWY-7081
4-chlorobenzoate degradation
-
-
PWY-6215
4-chlorocatechol degradation
-
-
PWY-6087
4-coumarate degradation (aerobic)
-
-
PWY-8002
4-coumarate degradation (anaerobic)
-
-
PWY-7046
4-deoxy-L-threo-hex-4-enopyranuronate degradation
-
-
PWY-6507
4-ethylphenol degradation (anaerobic)
-
-
PWY-6080
4-hydroxy-2-nonenal detoxification
-
-
PWY-7112
4-hydroxyacetophenone degradation
-
-
PWY-7002
4-hydroxybenzoate biosynthesis I (eukaryotes)
-
-
PWY-5754
4-hydroxybenzoate biosynthesis III (plants)
-
-
PWY-6435
4-hydroxymandelate degradation
4-methylcatechol degradation (ortho cleavage)
-
-
PWY-6185
4-methylphenol degradation to protocatechuate
-
-
PWY-7700
4-nitrophenol degradation I
-
-
PWY-5487
4-nitrophenol degradation II
-
-
PWY-5488
4-oxopentanoate degradation
-
-
PWY-7948
4-sulfocatechol degradation
-
-
PWY-6041
6-gingerol analog biosynthesis (engineered)
-
-
PWY-6920
8-amino-7-oxononanoate biosynthesis I
-
-
PWY-6519
9-cis, 11-trans-octadecadienoyl-CoA degradation (isomerase-dependent, yeast)
-
-
PWY-7340
9-lipoxygenase and 9-allene oxide synthase pathway
-
-
PWY-5407
ABH and Lewis epitopes biosynthesis from type 1 precursor disaccharide
-
-
PWY-7832
ABH and Lewis epitopes biosynthesis from type 2 precursor disaccharide
-
-
PWY-7831
acetaldehyde biosynthesis I
-
-
PWY-6333
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
acrylonitrile degradation I
-
-
PWY-7308
adenine and adenosine salvage I
-
-
P121-PWY
adenine and adenosine salvage III
-
-
PWY-6609
adenine and adenosine salvage V
-
-
PWY-6611
adenosine nucleotides degradation I
-
-
PWY-6596
adenosine nucleotides degradation II
-
-
SALVADEHYPOX-PWY
adenosine ribonucleotides de novo biosynthesis
-
-
PWY-7219
adipate degradation
-
-
PWY-8354
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
ajmaline and sarpagine biosynthesis
-
-
PWY-5301
aldoxime degradation
-
-
P345-PWY
alkylnitronates degradation
-
-
PWY-723
all-trans-farnesol biosynthesis
-
-
PWY-6859
alliin metabolism
-
-
PWY-5706
alpha-linolenate metabolites biosynthesis
-
-
PWY-8398
alpha-tomatine degradation
-
-
PWY18C3-5
Amaryllidacea alkaloids biosynthesis
-
-
PWY-7826
ammonia assimilation cycle I
-
-
PWY-6963
ammonia assimilation cycle II
-
-
PWY-6964
ammonia assimilation cycle III
-
-
AMMASSIM-PWY
ammonia oxidation II (anaerobic)
-
-
P303-PWY
amygdalin and prunasin degradation
-
-
PWY-6011
anaerobic energy metabolism (invertebrates, cytosol)
-
-
PWY-7383
anaerobic energy metabolism (invertebrates, mitochondrial)
-
-
PWY-7384
anandamide biosynthesis I
-
-
PWY-8051
anandamide biosynthesis II
-
-
PWY-8053
anandamide lipoxygenation
-
-
PWY-8056
androstenedione degradation I (aerobic)
-
-
PWY-6944
androstenedione degradation II (anaerobic)
-
-
PWY-8152
anthranilate degradation I (aerobic)
-
-
PWY-6079
apratoxin A biosynthesis
-
-
PWY-8361
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
arsenic detoxification (mammals)
-
-
PWY-4202
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 II
-
-
SULFMETII-PWY
assimilatory sulfate reduction III
-
-
PWY-6683
assimilatory sulfate reduction IV
-
-
PWY1ZNC-1
ATP biosynthesis
-
-
PWY-7980
atromentin biosynthesis
-
-
PWY-7518
avenanthramide biosynthesis
-
-
PWY-8157
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
benzoyl-CoA biosynthesis
-
-
PWY-6458
beta-(1,4)-mannan degradation
-
-
PWY-7456
beta-alanine biosynthesis I
-
-
PWY-3981
beta-D-glucuronide and D-glucuronate degradation
-
-
PWY-7247
betanidin degradation
-
-
PWY-5461
Bifidobacterium shunt
-
-
P124-PWY
bile acid biosynthesis, neutral pathway
bisabolene biosynthesis (engineered)
-
-
PWY-7102
bisphenol A degradation
-
-
PWY-7757
brassicicene C biosynthesis
-
-
PWY-7517
bupropion degradation
-
-
PWY66-241
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
caffeine biosynthesis I
-
-
PWY-5037
caffeine biosynthesis II (via paraxanthine)
-
-
PWY-5038
caffeine degradation III (bacteria, via demethylation)
-
-
PWY-6538
Calvin-Benson-Bassham cycle
-
-
CALVIN-PWY
camalexin biosynthesis
-
-
CAMALEXIN-SYN
canavanine degradation
-
-
PWY-31
capsaicin biosynthesis
-
-
PWY-5710
carbaryl degradation
-
-
PWY-8111
carbofuran degradation I
-
-
PWY-8286
carbofuran degradation II
-
-
PWY-8287
carbofuran degradation III
-
-
PWY-8288
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
CDP-6-deoxy-D-gulose biosynthesis
-
-
PWY-8139
cellulose and hemicellulose degradation (cellulolosome)
-
-
PWY-6784
cellulose biosynthesis
-
-
PWY-1001
cellulose degradation II (fungi)
-
-
PWY-6788
cephalosporin C biosynthesis
-
-
PWY-5632
ceramide de novo biosynthesis
-
-
PWY3DJ-12
chanoclavine I aldehyde biosynthesis
-
-
PWY-6493
chitin biosynthesis
-
-
PWY-6981
chitin deacetylation
-
-
PWY-7118
chitin degradation I (archaea)
-
-
PWY-6855
chitin degradation II (Vibrio)
-
-
PWY-6902
chitin degradation III (Serratia)
-
-
PWY-7822
chitin derivatives degradation
-
-
PWY-6906
chlorogenic acid biosynthesis I
-
-
PWY-6039
chlorogenic acid degradation
-
-
PWY-6781
chlorosalicylate degradation
-
-
PWY-6107
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 II (via 24,25-dihydrolanosterol)
-
-
PWY66-3
cholesterol degradation to androstenedione I (cholesterol oxidase)
-
-
PWY-6945
cholesterol degradation to androstenedione II (cholesterol dehydrogenase)
-
-
PWY-6946
choline biosynthesis III
-
-
PWY-3561
choline degradation I
-
-
CHOLINE-BETAINE-ANA-PWY
chorismate biosynthesis from 3-dehydroquinate
-
-
PWY-6163
cichoriin interconversion
-
-
PWY-7057
cinnamoyl-CoA biosynthesis
-
-
PWY-6457
cis-geranyl-CoA degradation
-
-
PWY-6672
cis-zeatin biosynthesis
-
-
PWY-2781
CMP-legionaminate biosynthesis I
-
-
PWY-6749
CO2 fixation into oxaloacetate (anaplerotic)
-
-
PWYQT-4429
coenzyme A biosynthesis I (bacteria)
-
-
COA-PWY
coenzyme A biosynthesis III (archaea)
-
-
PWY-8342
coenzyme B biosynthesis
-
-
P241-PWY
coenzyme M biosynthesis II
-
-
PWY-6643
colanic acid building blocks biosynthesis
-
-
COLANSYN-PWY
colupulone and cohumulone biosynthesis
-
-
PWY-5133
coumarin biosynthesis (via 2-coumarate)
-
-
PWY-5176
coumarins biosynthesis (engineered)
-
-
PWY-7398
creatine phosphate biosynthesis
-
-
PWY-6158
crotonate fermentation (to acetate and cyclohexane carboxylate)
-
-
PWY-7401
crotonyl-CoA/ethylmalonyl-CoA/hydroxybutyryl-CoA cycle (engineered)
-
-
PWY-7854
curcuminoid biosynthesis
-
-
PWY-6432
cutin biosynthesis
-
-
PWY-321
cyanide detoxification II
-
-
PWY-7142
cycloartenol biosynthesis
-
-
PWY-8028
cyclobis-(1rarr6)-alpha-nigerosyl biosynthesis
-
-
PWY-8317
cytosolic NADPH production (yeast)
-
-
PWY-7268
D-altritol and galactitol degradation
-
-
PWY-7862
D-arabinitol degradation I
-
-
DARABITOLUTIL-PWY
D-arabinose degradation V
-
-
PWY-8334
D-fructuronate degradation
-
-
PWY-7242
D-galactonate degradation
-
-
GALACTCAT-PWY
D-galactose degradation I (Leloir pathway)
-
-
PWY-6317
D-galactose degradation IV
-
-
PWY-6693
D-galactose detoxification
-
-
PWY-3821
D-galacturonate degradation I
-
-
GALACTUROCAT-PWY
D-galacturonate degradation II
-
-
PWY-6486
D-galacturonate degradation III
-
-
PWY-8391
D-galacturonate degradation IV
-
-
PWY-6491
D-gluconate degradation
-
-
GLUCONSUPER-PWY
D-glucosaminate degradation
-
-
PWY-7310
D-glucuronate degradation I
-
-
PWY-5525
D-glucuronate degradation II
-
-
PWY-6501
D-glucuronate degradation III
-
-
PWY-8390
D-sorbitol biosynthesis I
-
-
PWY-5054
D-sorbitol degradation I
-
-
PWY-4101
D-xylose degradation I
-
-
XYLCAT-PWY
D-xylose degradation II
-
-
PWY-5516
D-xylose degradation IV
-
-
PWY-7294
D-xylose degradation to ethylene glycol (engineered)
-
-
PWY-7178
daphnin interconversion
-
-
PWY-7056
deacetylcephalosporin C biosynthesis
-
-
PWY-5631
degradation of aromatic, nitrogen containing compounds
-
-
detoxification of reactive carbonyls in chloroplasts
-
-
PWY-6786
dhurrin degradation
-
-
PWY-5976
di-homo-gamma-linolenate metabolites biosynthesis
-
-
PWY-8396
diethylphosphate degradation
-
-
PWY-5491
dimethyl sulfide biosynthesis from methionine
-
-
PWY-7793
dissimilatory sulfate reduction I (to hydrogen sufide))
-
-
DISSULFRED-PWY
divinyl ether biosynthesis II
-
-
PWY-5409
docosahexaenoate biosynthesis III (6-desaturase, mammals)
-
-
PWY-7606
docosahexaenoate metabolites biosynthesis
-
-
PWY-8400
dopamine degradation
-
-
PWY6666-2
dTDP-beta-L-rhamnose biosynthesis
-
-
DTDPRHAMSYN-PWY
dTMP de novo biosynthesis (mitochondrial)
-
-
PWY66-385
dZTP biosynthesis
-
-
PWY-8289
Entner-Doudoroff pathway I
-
-
PWY-8004
Entner-Doudoroff pathway II (non-phosphorylative)
-
-
NPGLUCAT-PWY
Entner-Doudoroff pathway III (semi-phosphorylative)
-
-
PWY-2221
Entner-Doudoroff shunt
-
-
ENTNER-DOUDOROFF-PWY
ephedrine biosynthesis
-
-
PWY-5883
epoxysqualene biosynthesis
-
-
PWY-5670
ergosterol biosynthesis I
-
-
PWY-6075
ergosterol biosynthesis II
-
-
PWY-7154
erythritol biosynthesis I
-
-
PWY-8372
erythritol biosynthesis II
-
-
PWY-8373
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 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
farnesylcysteine salvage pathway
-
-
PWY-6577
fatty acid beta-oxidation I (generic)
-
-
FAO-PWY
fatty acid beta-oxidation II (plant peroxisome)
-
-
PWY-5136
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 (type I)
-
-
PWY-5966-1
fatty acid elongation -- saturated
-
-
FASYN-ELONG-PWY
fatty acid salvage
-
-
PWY-7094
Fe(II) oxidation
-
-
PWY-6692
FeMo cofactor biosynthesis
-
-
PWY-7710
firefly bioluminescence
-
-
PWY-7913
flavonoid biosynthesis
-
-
PWY1F-FLAVSYN
flavonoid biosynthesis (in equisetum)
-
-
PWY-6787
flavonoid di-C-glucosylation
-
-
PWY-7897
fluoroacetate and fluorothreonine biosynthesis
-
-
PWY-6644
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
formate oxidation to CO2
-
-
PWY-1881
fructan biosynthesis
-
-
PWY-822
fructan degradation
-
-
PWY-862
fructose 2,6-bisphosphate biosynthesis
-
-
PWY66-423
fusicoccin A biosynthesis
-
-
PWY-6659
GABA shunt I
-
-
GLUDEG-I-PWY
GABA shunt II
-
-
PWY-8346
gallate degradation III (anaerobic)
-
-
P3-PWY
gamma-glutamyl cycle
-
-
PWY-4041
gamma-hexachlorocyclohexane degradation
-
-
GAMMAHEXCHLORDEG-PWY
gamma-resorcylate degradation I
-
-
PWY-7773
gamma-resorcylate degradation II
-
-
PWY-7772
GDP-alpha-D-glucose biosynthesis
-
-
PWY-5661
GDP-mannose biosynthesis
-
-
PWY-5659
geraniol and geranial biosynthesis
-
-
PWY-5829
geranyl diphosphate biosynthesis
-
-
PWY-5122
geranylgeranyl diphosphate biosynthesis
-
-
PWY-5120
ginsenoside degradation I
-
-
PWY-6411
ginsenoside degradation III
-
-
PWY-6413
ginsenosides biosynthesis
-
-
PWY-5672
gliotoxin biosynthesis
-
-
PWY-7533
glucocorticoid biosynthesis
-
-
PWY66-381
gluconeogenesis I
-
-
GLUCONEO-PWY
gluconeogenesis II (Methanobacterium thermoautotrophicum)
-
-
PWY-6142
gluconeogenesis III
-
-
PWY66-399
glucose and glucose-1-phosphate degradation
-
-
GLUCOSE1PMETAB-PWY
glucose degradation (oxidative)
-
-
DHGLUCONATE-PYR-CAT-PWY
glucosinolate activation
-
-
PWY-5267
glucosylglycerol biosynthesis
-
-
PWY-7902
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
glycerol degradation I
-
-
PWY-4261
glycerol degradation II
-
-
PWY-6131
glycerol degradation to butanol
-
-
PWY-7003
glycerol degradation V
-
-
GLYCEROLMETAB-PWY
glycerol-3-phosphate shuttle
-
-
PWY-6118
glycerol-3-phosphate to fumarate electron transfer
-
-
PWY0-1582
glycine betaine biosynthesis I (Gram-negative bacteria)
-
-
BETSYN-PWY
glycogen biosynthesis I (from ADP-D-Glucose)
-
-
GLYCOGENSYNTH-PWY
glycogen biosynthesis III (from alpha-maltose 1-phosphate)
-
-
PWY-7900
glycogen degradation I
-
-
GLYCOCAT-PWY
glycogen degradation II
-
-
PWY-5941
glycogen degradation III (via anhydrofructose)
-
-
PWY-7662
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
glyoxylate assimilation
-
-
PWY-5744
glyoxylate cycle
-
-
GLYOXYLATE-BYPASS
glyphosate degradation III
-
-
PWY-7807
gondoate biosynthesis (anaerobic)
-
-
PWY-7663
gossypol biosynthesis
-
-
PWY-5773
guanine and guanosine salvage I
-
-
PWY-6620
guanine and guanosine salvage II
-
-
PWY-6599
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 V (aerobic)
-
-
HEME-BIOSYNTHESIS-II-1
heme degradation I
-
-
PWY-5874
heterolactic fermentation
-
-
P122-PWY
histamine degradation
-
-
PWY-6181
homocysteine and cysteine interconversion
-
-
PWY-801
hydrogen sulfide biosynthesis II (mammalian)
-
-
PWY66-426
hydrogen to fumarate electron transfer
-
-
PWY0-1576
hypoglycin biosynthesis
-
-
PWY-5826
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 V (bacteria and fungi)
-
-
PWY-5026
indole-3-acetate biosynthesis VI (bacteria)
-
-
TRPIAACAT-PWY
inosine 5'-phosphate degradation
-
-
PWY-5695
inulin degradation
-
-
PWY-8314
ipsdienol biosynthesis
-
-
PWY-7410
isopenicillin N biosynthesis
-
-
PWY-5629
isoprene biosynthesis II (engineered)
-
-
PWY-7391
isopropanol biosynthesis (engineered)
-
-
PWY-6876
itaconate biosynthesis I
-
-
PWY-5750
itaconate degradation
-
-
PWY-5749
jadomycin biosynthesis
-
-
PWY-6679
jasmonic acid biosynthesis
-
-
PWY-735
justicidin B biosynthesis
-
-
PWY-6824
ketogenesis
-
-
PWY66-367
ketogluconate metabolism
ketolysis
-
-
PWY66-368
L-alanine biosynthesis II
-
-
ALANINE-SYN2-PWY
L-alanine degradation II (to D-lactate)
-
-
ALACAT2-PWY
L-alanine degradation III
-
-
ALANINE-DEG3-PWY
L-alanine degradation IV
-
-
PWY1-2
L-alanine degradation V (oxidative Stickland reaction)
-
-
PWY-8189
L-alanine degradation VI (reductive Stickland reaction)
-
-
PWY-8188
L-arabinose degradation II
-
-
PWY-5515
L-arabinose degradation IV
-
-
PWY-7295
L-arginine biosynthesis I (via L-ornithine)
-
-
ARGSYN-PWY
L-arginine biosynthesis II (acetyl cycle)
-
-
ARGSYNBSUB-PWY
L-arginine biosynthesis IV (archaea)
-
-
PWY-7400
L-arginine degradation I (arginase pathway)
-
-
ARGASEDEG-PWY
L-arginine degradation II (AST pathway)
-
-
AST-PWY
L-arginine degradation III (arginine decarboxylase/agmatinase pathway)
-
-
PWY0-823
L-arginine degradation IV (arginine decarboxylase/agmatine deiminase pathway)
-
-
ARGDEG-III-PWY
L-arginine degradation IX (arginine:pyruvate transaminase pathway)
-
-
PWY-5742
L-arginine degradation VI (arginase 2 pathway)
-
-
ARG-PRO-PWY
L-arginine degradation VII (arginase 3 pathway)
-
-
ARG-GLU-PWY
L-arginine degradation VIII (arginine oxidase pathway)
-
-
ARGDEG-IV-PWY
L-arginine degradation X (arginine monooxygenase pathway)
-
-
ARGDEG-V-PWY
L-arginine degradation XI
-
-
PWY-5024
L-arginine degradation XII
-
-
PWY-7523
L-arginine degradation XIII (reductive Stickland reaction)
-
-
PWY-8187
L-arginine degradation XIV (oxidative Stickland reaction)
-
-
PWY-6344
L-ascorbate biosynthesis I (plants, L-galactose pathway)
-
-
PWY-882
L-ascorbate biosynthesis IV (animals, D-glucuronate pathway)
-
-
PWY3DJ-35471
L-ascorbate biosynthesis V (euglena, D-galacturonate pathway)
-
-
PWY-6415
L-ascorbate biosynthesis VI (plants, myo-inositol pathway)
-
-
PWY-8142
L-ascorbate biosynthesis VII (plants, D-galacturonate pathway)
-
-
PWY-8143
L-ascorbate biosynthesis VIII (engineered pathway)
-
-
PWY-7165
L-ascorbate degradation II (bacterial, aerobic)
-
-
PWY-6961
L-ascorbate degradation III
-
-
PWY-6960
L-ascorbate degradation IV
-
-
PWY-6704
L-asparagine biosynthesis I
-
-
ASPARAGINE-BIOSYNTHESIS
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 III (from L-homocysteine)
-
-
HOMOCYSDEGR-PWY
L-dopa and L-dopachrome biosynthesis
-
-
PWY-6481
L-fucose degradation II
-
-
PWY-8318
L-glucose degradation
-
-
PWY-7130
L-glutamate biosynthesis I
-
-
GLUTSYN-PWY
L-glutamate biosynthesis III
-
-
GLUTSYNIII-PWY
L-glutamate degradation I
-
-
GLUTAMATE-DEG1-PWY
L-glutamate degradation II
-
-
GLUTDEG-PWY
L-glutamate degradation V (via hydroxyglutarate)
-
-
P162-PWY
L-glutamate degradation VI (to pyruvate)
-
-
PWY-5087
L-glutamate degradation XI (reductive Stickland reaction)
-
-
PWY-8190
L-glutamine biosynthesis I
-
-
GLNSYN-PWY
L-glutamine degradation I
-
-
GLUTAMINDEG-PWY
L-histidine degradation V
-
-
PWY-5031
L-idonate degradation
-
-
IDNCAT-PWY
L-isoleucine biosynthesis I (from threonine)
-
-
ILEUSYN-PWY
L-isoleucine biosynthesis II
-
-
PWY-5101
L-isoleucine biosynthesis III
-
-
PWY-5103
L-isoleucine biosynthesis IV
-
-
PWY-5104
L-isoleucine biosynthesis V
-
-
PWY-5108
L-isoleucine degradation I
-
-
ILEUDEG-PWY
L-isoleucine degradation II
-
-
PWY-5078
L-leucine degradation III
-
-
PWY-5076
L-lysine biosynthesis IV
-
-
LYSINE-AMINOAD-PWY
L-lysine biosynthesis V
-
-
PWY-3081
L-lysine degradation II (L-pipecolate pathway)
-
-
PWY66-425
L-lysine degradation V
-
-
PWY-5283
L-lysine degradation XI
-
-
LYSINE-DEG1-PWY
L-lysine fermentation to acetate and butanoate
-
-
P163-PWY
L-malate degradation II
-
-
PWY-7686
L-methionine degradation I (to L-homocysteine)
-
-
METHIONINE-DEG1-PWY
L-methionine degradation III
-
-
PWY-5082
L-Ndelta-acetylornithine biosynthesis
-
-
PWY-6922
L-phenylalanine biosynthesis I
-
-
PHESYN
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 VI (reductive Stickland reaction)
-
-
PWY-8014
L-rhamnose degradation II
-
-
PWY-6713
L-rhamnose degradation III
-
-
PWY-6714
L-serine biosynthesis II
-
-
PWY-8011
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 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
lactose degradation III
-
-
BGALACT-PWY
lanosterol biosynthesis
-
-
PWY-6132
leukotriene biosynthesis
-
-
PWY66-375
linalool biosynthesis I
-
-
PWY-7182
linamarin degradation
-
-
PWY-3121
linoleate metabolites biosynthesis
-
-
PWY-8395
linustatin bioactivation
-
-
PWY-7091
lipid A-core biosynthesis (E. coli K-12)
-
-
LIPA-CORESYN-PWY
lipid IVA biosynthesis (2,3-diamino-2,3-dideoxy-D-glucopyranose-containing)
-
-
PWY2B4Q-4
lipid IVA biosynthesis (E. coli)
-
-
NAGLIPASYN-PWY
lipid IVA biosynthesis (generic)
-
-
PWY-8283
lipid IVA biosynthesis (H. pylori)
-
-
PWYI-14
lipid IVA biosynthesis (P. gingivalis)
-
-
PWY-8245
lipid IVA biosynthesis (P. putida)
-
-
PWY-8073
lipid IVA biosynthesis (Vibrio cholerae serogroup O1 El Tor)
-
-
PWY2G6Z-2
lipoxin biosynthesis
-
-
PWY66-392
lotaustralin degradation
-
-
PWY-6002
lupulone and humulone biosynthesis
-
-
PWY-5132
luteolin triglucuronide degradation
-
-
PWY-7445
m-cresol degradation
-
-
M-CRESOL-DEGRADATION-PWY
malate/L-aspartate shuttle pathway
-
-
MALATE-ASPARTATE-SHUTTLE-PWY
manganese oxidation I
-
-
PWY-6591
mangrove triterpenoid biosynthesis
-
-
PWY-6109
mannitol biosynthesis
-
-
PWY-3881
mannitol cycle
-
-
PWY-6531
mannitol degradation I
-
-
MANNIDEG-PWY
mannitol degradation II
-
-
PWY-3861
maresin biosynthesis
-
-
PWY-8356
matairesinol biosynthesis
-
-
PWY-5466
melatonin degradation I
-
-
PWY-6398
melatonin degradation II
-
-
PWY-6399
melibiose degradation
-
-
PWY0-1301
menaquinol-4 biosynthesis II
-
-
PWY-7998
Methanobacterium thermoautotrophicum biosynthetic metabolism
-
-
PWY-6146
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 phomopsenoate biosynthesis
-
-
PWY-7721
methyl tert-butyl ether degradation
-
-
PWY-7779
methylaspartate cycle
methylerythritol phosphate pathway I
-
-
NONMEVIPP-PWY
methylerythritol phosphate pathway II
-
-
PWY-7560
methylgallate degradation
-
-
METHYLGALLATE-DEGRADATION-PWY
methylglyoxal degradation I
-
-
PWY-5386
methylglyoxal degradation III
-
-
PWY-5453
methylglyoxal degradation IV
-
-
PWY-5459
methylglyoxal degradation V
-
-
PWY-5458
methylglyoxal degradation VI
-
-
MGLDLCTANA-PWY
methylglyoxal degradation VIII
-
-
PWY-5386-1
methylsalicylate degradation
-
-
PWY-6184, PWY18C3-24
mevalonate pathway I (eukaryotes and bacteria)
-
-
PWY-922
mevalonate pathway II (haloarchaea)
-
-
PWY-6174
mevalonate pathway III (Thermoplasma)
-
-
PWY-7524
mevalonate pathway IV (archaea)
-
-
PWY-8125
mineralocorticoid biosynthesis
-
-
PWY66-382
mitochondrial NADPH production (yeast)
-
-
PWY-7269
mixed acid fermentation
-
-
FERMENTATION-PWY
mono-trans, poly-cis decaprenyl phosphate biosynthesis
-
-
PWY-6383
mucin core 1 and core 2 O-glycosylation
-
-
PWY-7433
muropeptide degradation
-
-
PWY0-1546
mycolate biosynthesis
-
-
PWYG-321
mycolyl-arabinogalactan-peptidoglycan complex biosynthesis
-
-
PWY-6397
N-acetylglucosamine degradation I
-
-
GLUAMCAT-PWY
N-methylpyrrolidone degradation
-
-
PWY-7978
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 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
NADPH to cytochrome c oxidase via plastocyanin
-
-
PWY-8271
naringenin biosynthesis (engineered)
-
-
PWY-7397
neolinustatin bioactivation
-
-
PWY-7092
nepetalactone biosynthesis
-
-
PWY-8069
nicotinate degradation III
-
-
PWY-5055
nicotine degradation IV
-
-
PWY66-201
nicotine degradation V
-
-
PWY66-221
nitrate reduction I (denitrification)
-
-
DENITRIFICATION-PWY
nitrate reduction II (assimilatory)
-
-
PWY-381
nitrate reduction V (assimilatory)
-
-
PWY-5675
nitrate reduction VII (denitrification)
-
-
PWY-6748
nitrate reduction VIIIb (dissimilatory)
-
-
PWY0-1573
nitric oxide biosynthesis II (mammals)
-
-
PWY-4983
nitrifier denitrification
-
-
PWY-7084
nitrite-dependent anaerobic methane oxidation
-
-
PWY-6523
nitrogen remobilization from senescing leaves
-
-
PWY-6549
nocardicin A biosynthesis
-
-
PWY-7797
noradrenaline and adrenaline degradation
-
-
PWY-6342
nucleoside and nucleotide degradation (archaea)
-
-
PWY-5532
O-antigen building blocks biosynthesis (E. coli)
-
-
OANTIGEN-PWY
o-diquinones biosynthesis
-
-
PWY-6752
octanoyl-[acyl-carrier protein] biosynthesis (mitochondria, yeast)
-
-
PWY-7388
oleandomycin activation/inactivation
-
-
PWY-6972
oleate beta-oxidation
-
-
PWY0-1337
oleate beta-oxidation (isomerase-dependent, yeast)
-
-
PWY-7291
oleate biosynthesis II (animals and fungi)
-
-
PWY-5996
oleate biosynthesis IV (anaerobic)
-
-
PWY-7664
ophiobolin F biosynthesis
-
-
PWY-7720
ophthalmate biosynthesis
-
-
PWY-8043
orcinol degradation
-
-
P342-PWY
oxalate biosynthesis
oxalate degradation III
-
-
PWY-6696
oxalate degradation IV
-
-
PWY-6697
oxalate degradation V
-
-
PWY-6698
oxalate degradation VI
-
-
PWY-7985
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 IV (fungi and animals)
-
-
PWY3O-1801
partial TCA cycle (obligate autotrophs)
-
-
PWY-5913
paspaline biosynthesis
-
-
PWY-7492
patulin biosynthesis
-
-
PWY-7490
pectin degradation I
-
-
PWY-7246
pectin degradation II
-
-
PWY-7248
penicillin K biosynthesis
-
-
PWY-5630
pentachlorophenol degradation
-
-
PCPDEG-PWY
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 I (meso-diaminopimelate containing)
-
-
PEPTIDOGLYCANSYN-PWY
peptidoglycan biosynthesis II (staphylococci)
-
-
PWY-5265
peptidoglycan biosynthesis III (mycobacteria)
-
-
PWY-6385
peptidoglycan biosynthesis IV (Enterococcus faecium)
-
-
PWY-6471
peptidoglycan biosynthesis V (beta-lactam resistance)
-
-
PWY-6470
peptidoglycan maturation (meso-diaminopimelate containing)
-
-
PWY0-1586
peptidoglycan recycling I
-
-
PWY0-1261
peptidoglycan recycling II
-
-
PWY-7883
phenylethanol biosynthesis
-
-
PWY-5751
phenylethylamine degradation I
-
-
2PHENDEG-PWY
phenylpropanoid biosynthesis
-
-
PWY-361
phenylpropanoid biosynthesis, initial reactions
-
-
PWY1F-467
phenylpropanoids methylation (ice plant)
-
-
PWY-7498
pheomelanin biosynthesis
-
-
PWY-7917
phloridzin biosynthesis
-
-
PWY-6515
phosphate acquisition
-
-
PWY-6348
phosphatidate biosynthesis (yeast)
-
-
PWY-7411
phosphatidate metabolism, as a signaling molecule
-
-
PWY-7039
phosphatidylcholine acyl editing
-
-
PWY-6803
phospholipases
-
-
LIPASYN-PWY
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
photosynthesis light reactions
-
-
PWY-101
photosynthetic 3-hydroxybutanoate biosynthesis (engineered)
-
-
PWY-7218
phytate degradation I
-
-
PWY-4702
phytochromobilin biosynthesis
-
-
PWY-7170
phytol degradation
-
-
PWY66-389
phytosterol biosynthesis (plants)
-
-
PWY-2541
pinoresinol degradation
-
-
PWY-7982
plasmalogen biosynthesis I (aerobic)
-
-
PWY-7782
plasmalogen degradation
-
-
PWY-7783
platensimycin biosynthesis
-
-
PWY-8179
plaunotol biosynthesis
-
-
PWY-6691
poly-hydroxy fatty acids biosynthesis
-
-
PWY-6710
polybrominated dihydroxylated diphenyl ethers biosynthesis
-
-
PWY-7934
polyhydroxybutanoate biosynthesis
-
-
PWY1-3
polyhydroxydecanoate biosynthesis
-
-
PWY-6657
polyphosphate metabolism
-
-
PWY-8138
prenylated FMNH2 biosynthesis
-
-
PWY0-1597
propanethial S-oxide biosynthesis
-
-
PWY-5707
propanoate fermentation to 2-methylbutanoate
-
-
PWY-5109
propanoyl-CoA degradation II
-
-
PWY-7574
protectin biosynthesis
-
-
PWY-8357
protein N-glycosylation initial phase (eukaryotic)
-
-
MANNOSYL-CHITO-DOLICHOL-BIOSYNTHESIS
protein N-glycosylation processing phase (plants and animals)
-
-
PWY-7919
protein ubiquitination
-
-
PWY-7511
protocatechuate degradation I (meta-cleavage pathway)
-
-
P184-PWY
protocatechuate degradation II (ortho-cleavage pathway)
-
-
PROTOCATECHUATE-ORTHO-CLEAVAGE-PWY
purine deoxyribonucleosides degradation I
-
-
PWY-7179
purine deoxyribonucleosides degradation II
-
-
PWY-7179-1
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 III
-
-
PWY-0
pyrimidine deoxyribonucleosides degradation
-
-
PWY-7181
pyrimidine deoxyribonucleosides salvage
-
-
PWY-7199
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 dephosphorylation
-
-
PWY-7206
pyrimidine ribonucleosides degradation
-
-
PWY0-1295
pyrimidine ribonucleosides salvage I
-
-
PWY-7193
pyrimidine ribonucleosides salvage II
-
-
PWY-6556
pyrrolnitrin biosynthesis
-
-
PWY-6831
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 acetone
-
-
PWY-6588
pyruvate fermentation to butanoate
-
-
CENTFERM-PWY
pyruvate fermentation to butanol I
-
-
PWY-6583
pyruvate fermentation to butanol II (engineered)
-
-
PWY-6883
pyruvate fermentation to ethanol I
-
-
PWY-5480
pyruvate fermentation to ethanol II
-
-
PWY-5486
pyruvate fermentation to ethanol III
-
-
PWY-6587
pyruvate fermentation to hexanol (engineered)
-
-
PWY-6863
pyruvate fermentation to isobutanol (engineered)
-
-
PWY-7111
pyruvate fermentation to propanoate I
-
-
P108-PWY
reactive oxygen species degradation
-
-
DETOX1-PWY-1
rebeccamycin biosynthesis
-
-
PWY-6324
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
resorcinol degradation
retinol biosynthesis
-
-
PWY-6857
rhamnogalacturonan type I degradation II (bacteria)
-
-
PWY-6771
rosmarinic acid biosynthesis I
-
-
PWY-5048
Rubisco shunt
-
-
PWY-5723
rutin degradation
-
-
PWY-6848
rutin degradation (plants)
-
-
PWY-7134
S-adenosyl-L-methionine salvage II
-
-
PWY-5041
saframycin A biosynthesis
-
-
PWY-7671
salicylate biosynthesis I
-
-
PWY-6406
salicylate biosynthesis II
-
-
PWY-8321
salicylate degradation I
-
-
PWY-6183
salidroside biosynthesis
-
-
PWY-6802
salinosporamide A biosynthesis
-
-
PWY-6627
Salmonella enterica serotype O:13 O antigen biosynthesis
-
-
PWY-8230
scopoletin biosynthesis
-
-
PWY-6792
secologanin and strictosidine biosynthesis
-
-
PWY-5290
sedoheptulose bisphosphate bypass
-
-
PWY0-1517
selenate reduction
-
-
PWY-6932
seleno-amino acid detoxification and volatilization I
-
-
PWY-6931
seleno-amino acid detoxification and volatilization III
-
-
PWY-6933
serotonin degradation
-
-
PWY-6313
sesamin biosynthesis
-
-
PWY-5469
shikimate degradation II
-
-
PWY-6419
sitosterol degradation to androstenedione
-
-
PWY-6948
sophorosyloxydocosanoate deacetylation
-
-
SOPHOROSYLOXYDOCOSANOATE-DEG-PWY
sorbitol biosynthesis II
-
-
PWY-5530
sorgoleone biosynthesis
-
-
PWY-5987
spermidine biosynthesis I
-
-
BSUBPOLYAMSYN-PWY
spermidine biosynthesis III
-
-
PWY-6834
sphingolipid biosynthesis (plants)
-
-
PWY-5129
sphingolipid biosynthesis (yeast)
-
-
SPHINGOLIPID-SYN-PWY
spongiadioxin C biosynthesis
-
-
PWY-7935
sporopollenin precursors biosynthesis
-
-
PWY-6733
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
stellatic acid biosynthesis
-
-
PWY-7736
sterol:steryl ester interconversion (yeast)
-
-
PWY-7424
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 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
sulfate activation for sulfonation
-
-
PWY-5340
sulfite oxidation II
-
-
PWY-5279
sulfite oxidation III
-
-
PWY-5278
sulfolactate degradation III
-
-
PWY-6638
sulfur reduction I
-
-
PWY-5332
sulfur reduction II (via polysulfide)
-
-
PWY-5364
superoxide radicals degradation
-
-
DETOX1-PWY
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 photosynthetic hydrogen production
-
-
PWY-7731
superpathway of pyrimidine deoxyribonucleotides de novo biosynthesis (E. coli)
-
-
PWY0-166
superpathway of UDP-glucose-derived O-antigen building blocks biosynthesis
-
-
PWY-7328
syringate degradation
-
-
PWY-6339
taurine biosynthesis I
-
-
PWY-5331
taurine biosynthesis II
-
-
PWY-7850
taurine biosynthesis III
-
-
PWY-8359
TCA cycle I (prokaryotic)
-
-
TCA
TCA cycle II (plants and fungi)
-
-
PWY-5690
TCA cycle III (animals)
-
-
PWY66-398
TCA cycle IV (2-oxoglutarate decarboxylase)
-
-
P105-PWY
TCA cycle V (2-oxoglutarate synthase)
-
-
PWY-6969
TCA cycle VI (Helicobacter)
-
-
REDCITCYC
TCA cycle VII (acetate-producers)
-
-
PWY-7254
TCA cycle VIII (Chlamydia)
-
-
TCA-1
tea aroma glycosidic precursor bioactivation
-
-
PWY-7114
teichuronic acid biosynthesis (B. subtilis 168)
-
-
PWY-7820
tetradecanoate biosynthesis (mitochondria)
-
-
PWY66-430
tetrahydrofolate biosynthesis I
-
-
PWY-6614
tetrapyrrole biosynthesis II (from glycine)
-
-
PWY-5189
theobromine biosynthesis I
-
-
PWY-5039
theophylline degradation
-
-
PWY-6999
thioredoxin pathway
-
-
THIOREDOX-PWY
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
traumatin and (Z)-3-hexen-1-yl acetate biosynthesis
-
-
PWY-5410
trehalose biosynthesis I
-
-
TRESYN-PWY
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
tRNA charging
-
-
TRNA-CHARGING-PWY
tRNA processing
-
-
PWY0-1479
tunicamycin biosynthesis
-
-
PWY-7821
type I lipoteichoic acid biosynthesis (S. aureus)
-
-
PWY-7817
UDP-alpha-D-galactofuranose biosynthesis
-
-
PWY-7622
UDP-alpha-D-galactose biosynthesis
-
-
PWY-7344
UDP-alpha-D-glucose biosynthesis
-
-
PWY-7343
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
UMP biosynthesis I
-
-
PWY-5686
UMP biosynthesis II
-
-
PWY-7790
UMP biosynthesis III
-
-
PWY-7791
urate conversion to allantoin I
-
-
PWY-5691
urea cycle
urea degradation II
-
-
PWY-5704
UTP and CTP dephosphorylation II
-
-
PWY-7177
valproate beta-oxidation
-
-
PWY-8182
vancomycin resistance I
-
-
PWY-6454
vanillin and vanillate degradation I
-
-
PWY-7097
vanillin and vanillate degradation II
-
-
PWY-7098
vanillin biosynthesis I
-
-
PWY-5665
versicolorin B biosynthesis
-
-
PWY-5955
vicianin bioactivation
-
-
PWY-7093
viridicatumtoxin biosynthesis
-
-
PWY-7659
vitamin K-epoxide cycle
xanthine and xanthosine salvage
-
-
SALVPURINE2-PWY
xanthohumol biosynthesis
-
-
PWY-5135
xanthommatin biosynthesis
-
-
PWY-8249
xylitol degradation I
-
-
LARABITOLUTIL-PWY
xyloglucan degradation II (exoglucanase)
-
-
PWY-6807
xyloglucan degradation III (cellobiohydrolase)
-
-
PWY-6812
zymosterol biosynthesis
-
-
PWY-6074
4-hydroxymandelate degradation
-
-
4-HYDROXYMANDELATE-DEGRADATION-PWY
bile acid biosynthesis, neutral pathway
-
-
PWY-6061
ketogluconate metabolism
-
-
KETOGLUCONMET-PWY
methylaspartate cycle
-
-
PWY-6728
oxalate biosynthesis
-
-
PWY-6699
resorcinol degradation
-
-
P343-PWY
suberin monomers biosynthesis
-
-
PWY-1121
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
-
563, 2374, 2624, 3063, 3663, 3664, 3714, 3715, 3718, 3719, 3720, 4104, 4560, 4574, 4576, 4577, 4578, 4581, 4582, 4583, 4718, 5685, 23596, 24216, 26100, 26105, 30566, 30574, 33784, 34023, 35230, 35244, 37414, 80767, 80768, 80931, 80932, 94250, 94717, 94719, 94776, 114100, 114108, 114252, 114253, 114257, 114258, 114273, 114279, 134747, 134797, 135794, 135797, 135820, 135824, 135827, 135838, 135843, 135851, 136020, 136021, 136039, 136040, 136059, 136077, 136138, 136192, 136194, 136199, 136200, 136217, 136226, 136307, 136310, 136311, 136315, 136382, 136385, 136388, 136395, 136633, 136636, 136749, 136785, 136793, 136861, 136948, 136949, 171187, 171190, 171236, 171273, 171279, 171280, 171317, 171325, 171339, 171597, 171598, 171599, 171633, 171634, 171743, 171749, 171750, 171752, 171753, 171754, 171755, 171756, 171764, 171765, 207955, 208300, 208303, 208305, 208306, 208307, 208310, 208311, 208312, 208313, 208314, 208315, 208316, 208363, 208567, 208580, 208674, 208697, 208804, 208924, 208949, 209134, 209833, 210609, 210611, 210612, 210613, 210615, 246567, 285665, 285787, 286357, 286644, 286749, 286793, 287005, 287289, 287290, 288169, 288807, 288808, 288809, 288810, 288811, 288812, 288813, 288814, 288815, 288816, 288818, 288820, 288822, 288823, 288824, 288826, 288828, 288829, 288830, 288831, 288832, 288833, 288834, 288835, 288837, 288838, 288840, 288841, 288842, 288843, 288849, 289264, 289268, 289291, 326273, 326277, 326279, 326316, 326337, 326358, 326377, 326387, 348275, 349015, 389419, 389421, 389787, 389788, 389790, 389792, 389793, 389794, 389796, 389797, 389798, 389799, 389801, 389802, 389803, 389804, 389805, 389806, 389807, 389813, 389815, 389816, 389817, 389819, 389821, 389822, 389823, 389824, 389825, 389827, 389829, 389834, 389836, 389837, 390692, 391374, 391953, 393278, 393286, 393340, 393406, 393576, 393583, 393584, 393591, 393600, 393615, 393713, 393786, 394561, 394982, 438802, 438867, 438874, 438875, 438877, 438964, 439799, 439808, 440256, 440258, 440260, 440261, 488608, 488993, 488994, 489650, 586945, 640318, 640480, 641513, 641593, 643849, 646670, 646707, 646709, 648795, 649341, 649750, 650508, 650654, 650670, 650815, 651022, 651389, 651740, 653101, 654003, 654143, 654185, 654190, 654222, 654358, 654468, 654481, 654659, 654780, 654806, 654892, 654909, 655079, 655110, 655166, 655172, 655179, 655354, 655356, 655361, 655380, 655442, 655613, 655657, 655711, 655759, 656059, 656254, 656562, 656782, 656889, 656919, 657249, 657283, 657384, 657645, 658230, 658464, 658465, 658564, 658791, 659675, 659861, 663906, 664207, 664319, 664379, 664391, 664778, 664832, 665152, 665238, 665281, 665282, 665283, 665775, 665884, 666092, 666230, 666569, 666691, 666692, 666778, 666784, 666786, 667009, 667011, 667273, 668048, 668063, 671192, 672872, 675186, 675825, 677260, 677354, 677520, 677624, 677668, 677690, 677766, 677774, 677813, 678379, 679051, 679549, 679568, 679573, 679941, 679961, 679966, 680275, 680281, 680303, 680395, 680401, 680530, 680931, 680956, 680984, 680985, 681058, 681131, 681336, 681772, 681802, 682317, 682431, 682674, 682704, 682864, 683049, 683283, 683285, 683506, 684515, 684594, 684638, 684646, 684945, 686239, 686726, 686921, 690078, 690499, 691357, 691432, 691957, 692507, 693054, 693493, 693684, 693798, 695559, 695600, 695666, 695675, 695678, 695712, 695790, 696068, 696369, 696555, 696586, 696777, 696821, 696864, 696865, 696884, 696899, 696900, 697118, 697654, 698006, 698321, 698405, 699078, 699600, 699763, 699771, 699922, 699941, 700541, 700599, 701266, 701487, 701986, 702801, 702806, 703066, 704956, 705128, 705514, 706393, 706569, 707145, 707241, 707347, 707403, 708005, 708235, 708265, 708515, 708522, 708831, 709376, 709504, 710263, 710494, 710642, 710686, 710858, 710908, 710966, 712023, 712533, 712784, 712785, 712857, 713259, 713702, 713703, 713803, 713805, 713879, 714504, 714510, 714657, 714873, 716478, 717110, 717405, 717449, 718343, 721358, 722316, 723947, 723981, 723985, 723997, 724880, 724884, 725095, 725199, 725789, 726413, 727612, 727635, 729072, 729183, 729287, 729365, 729421, 729425, 729532, 729537, 729773, 729790, 729868, 730080, 730091, 730092, 730137, 730189, 730199, 730219, 730222, 730280, 730283, 730351, 730851, 730876, 730924, 731024, 731517, 732920, 735457, 735795, 736591, 737497, 737543, 738435, 738734, 739221, 739387, 739710, 740181, 740195, 740477, 741479, 741527, 742129, 742213, 742217, 743095, 743099, 743171, 743532, 743644, 743775, 746015, 746335, 746904, 748428, 748517, 749439, 749601, 749626, 749634, 749780, 749781, 750139, 750222, 750231, 750251, 750780, 751377, 751414, 751438, 751636, 752069, 752158, 752344, 753334, 753337, 753842, 754660, 755274, 756253, 757260, 757266, 757638, 760657, 760777, 761153, 763039, 763297, 763681, 763698, 763959, 763980, 764036, 765344
-
-
-
114251, 391951, 391953, 491169, 646670, 649347, 654519, 660943, 666369, 666820, 677293, 677627, 677744, 678084, 679050, 679061, 679840, 680967, 682613, 685428, 685429, 686060, 688784, 690105, 695717, 699073, 700255, 707241, 707832, 714497, 726565, 727055, 727205, 728045, 729418, 729456, 730728, 730886, 737333, 737802, 739566, 741835, 742144, 743105, 743277, 743283, 743744, 743857, 745143, 746067, 746771, 746773, 747341, 747343, 747675, 748768, 749503, 749519, 749631, 750226, 750231, 751164, 751703, 751980, 752083, 762536, 762774, 762986, 762993, 763123, 763332, 763385, 763464, 763686, 763687, 764280, 764471
A1XP58, O42807, O74641, P13006, P34752, P46882, P69328, Q00078, Q12556, Q8J219, Q8TFP1, Q8TG09, Q8WZI8, Q96VT7, Q9P8F4, Q9P8R5, Q9UR30
SwissProt
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135842, 288845, 288846, 641066, 649946, 666365, 671410, 671462, 671497, 681717, 687682, 692398, 693684, 696466, 696988, 702388, 708849, 709429, 709554, 710970, 712260, 713698, 713873, 716839, 718670, 719168, 722316, 729014, 734496, 735455, 735929, 737422, 739579, 741418, 741576, 741716, 742156, 742640, 743193, 743643, 743824, 744006, 744078, 744139, 744626, 747889, 747890, 749419, 749475, 749604, 749677, 749692, 750082, 750154, 750431, 750586, 750602, 750785, 750829, 750855, 750888, 750893, 751060, 751146, 751243, 751303, 751836, 751980, 752093, 752106, 752543, 753407, 753726, 754912, 757903, 758967, 761084, 761153, 763543, 763698
A0A023J5W7, A0A075EKG1, A0A0B4UL66, A0A1D8RK43, A0A221C6S1, A0A345K402, A0PCH8, A2QAC0, A2QH83, A2QIR3, A2QJF7, A2QKT4, A2QR21, A2QV36, A2QZI3, A2R3C7, A2R3L3, A2R4V5, A2R6M7, A2R7U3, A5ABL2, A7YN26, A8DRH7, A8DRH9, A9QXE0, B3VPB3, B6HYI9, B6V7E4, D6QST5, E3VW38, F5CI28, G3XPU3, G3XRE5, G3XZT7, G3Y419, G3Y683, G3Y8T6, G3YAL0, G3YE52, G5D7B5, G8GYH6, I3QKR9, O74705, O74706, P17549, P26213, P26214, P34754, P42254, P55329, P56526, P78985, P87160, Q0PGS3, Q2L887, Q5EC68, Q6T9Z6, Q7Z986, Q8J229, Q92407, Q96VT2, Q9C2Z0, Q9HFQ1, Q9P4W2, Q9UVS8, R9W5L0, T1SGS1, U4MZ33, W8R465
UniProt
2 methylglyoxylate reductases: MGR I and MGR II, similar enzyme with NADPH-requirement for methylglyoxal reduction, that is inactive with NAD+, NADH and NADP+
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a xerophilic strain isolated from the Mexican semi-desert
UniProt
Aspergillus niger responds to cell wall stress by transcriptional activation of cell wall reinforcing genes including agsA (encoding a alpha-1,3-glucan synthase) through an RIm1p-like transcription factor.
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ATCC 9142. 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.
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BCC18081 (TR170), 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 (3-phytase) or 1D-myo-inositol 1,2,3,5,6-pentakisphosphate (4-phytase) (i.e. 1L-myo-inositol 1,2,3,4,5-pentakisphosphate if 1L numbering is applied) has not been analyzed. The reaction was monitored by analyzing the released phosphate
UniProt
bifunctional alpha-galactosidase and alpha-N-acetylgalactosaminidase
UniProt
bifunctional alpha-N-acetylgalactosaminidase and alpha-N-acetylgalactosidase
UniProt
bifunctional enzyme: quinate (shikimate) dehydrogenase, different from EC 1.1.1.25
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coexpression of enzyme with Trichoderma reesei xylanayse II in Saccharomyces cerevisiae
SwissProt
enzyme is induced in the presence of galactofuranoside containing glycoconjugates
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FS-44, 5'-PDase hyperproductive mutant: bifunctional enzyme: cyclic-ribonucleotide phosphomutase-5'-phosphodiesterase
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GDH from Aspergillus terreus is kinetically distinct from GDH of Aspergilli niger
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iron-chlorin protein also catalyzes methyl viologen-linked reduction of hydroxylamine and that of nitrite at a slower rate
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isolated from soil samples collected in Northeast Parana State in Brazil
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locally isolated Aspergillus niger, wild-type and deoxy-D-glucose-resistant mutant
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NRRL 3135. 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.
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strain 92 and strain NRRL 3135. 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.
SwissPRot
strain MTCC 2425, and a strain isolated from a composite tannery effluent collected from a local tannery
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strain MYA 135, formerly strain 419, constitutive and inducible enzymes
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strain NRRL3135. The T213 phytase differs from NRRL 3135 phytase at 12 amino acid residues.S13 in NRRL 3135 and A14 in T213, S30 in NRRL 3135 and T14 in T213, E66 in NRRL 3135 and D66 in T213, D89 in NRRL 3135 and E89 in T213, A106 in NRRL 3135 and V106 in T213, V155 in NRRL 3135 and I155 in T213, K171 in NRRL 3135 and E171 in T213, V236 in NRRL 3135 and A236 in T213, N292 in NRRL 3135 and H292 in T213, Q297 in NRRL 3135 and R297 in T213, S345 in NRRL 3135 and N345 in T213, V438 in NRRL 3135 and I438 in T213. 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.
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strains CBS 513.88, NRRL3122, and N402, isozymes AgtA and AgtB encoded by genes agtA and agtB
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the CBS 141257 strain is obtained by transformation of strain N593.20 with uridine (pyrG) from Aspergillus oryzae
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The enzyme exhibits phytase and acid phosphatase activity. 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.
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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.
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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.
SwissProt
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. Growth and phosphorus nutrition of the plants supplied with phytate is improved significantly when the phytase gene from Aspergillus niger is introduced.The Aspergillus phytase is only effective when secreted as an extracellular enzyme by inclusion of the signal peptide sequence from the carrot extensin gene
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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 (3-phytase) or 1D-myo-inositol 1,2,3,5,6-pentakisphosphate (4-phytase) (i.e. 1L-myo-inositol 1,2,3,4,5-pentakisphosphate if 1L numbering is applied) has not been analyzed. The reaction was monitored by analyzing the released phosphate
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The T213 phytase differs from NRRL 3135 phytase at 12 amino acid residues.S13 in NRRL 3135 and A14 in T213, S30 in NRRL 3135 and T14 in T213, E66 in NRRL 3135 and D66 in T213, D89 in NRRL 3135 and E89 in T213, A106 in NRRL 3135 and V106 in T213, V155 in NRRL 3135 and I155 in T213, K171 in NRRL 3135 and E171 in T213, V236 in NRRL 3135 and A236 in T213, N292 in NRRL 3135 and H292 in T213, Q297 in NRRL 3135 and R297 in T213, S345 in NRRL 3135 and N345 in T213, V438 in NRRL 3135 and I438 in T213. 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.
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two amine oxidases isolated: the first one corresponds to the copper-dependent enzyme, the second one is an evolutionary prototype form of MAO-A and B
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van Teighem. 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.
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wild-type strain NIAB 280, and its derivative the catabolite-derepressed mutant strain M125
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SOURCE TISSUE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
SOURCE
additional information
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endoxylanase production is optimized using agricultural bagasses and cost 20 times less than enzyme production using synthetic xylan
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136395, 208785, 208798, 389796, 389797, 389798, 389801, 389802, 389804, 389816, 389821, 389834, 389837, 650815, 657384, 664207, 665281, 677260, 680931, 685428, 685429, 688784, 690105, 693493, 709554, 714025, 716930, 717110, 717405, 723947, 723981, 724884, 725789, 726413, 729537, 741479, 741835, 742144, 743105, 743283, 744006, 749631, 750231, 750251, 750602, 752083
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commercial preparation of Koch-Light Ltd. Colnbrook, England
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industrial strain, Aspergillus niger/Talaromyces emersonii enzyme mixture containing Aspergillus niger acetylxylan esterase and Tlaromyces emersonii acetyl esterase
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proctase powder, crude enzyme powder from waters of Koji cultures
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Sumizyme AC, Shin-Nippon Chemical Industries Co., Ltd., cellulase activity 2-5 unit/mg
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3714, 4560, 4576, 24216, 134747, 208564, 208567, 209833, 326377, 348275, 389805, 391951, 391953, 438875, 438877, 438964, 440256, 487424, 488074, 640318, 640480, 641513, 651740, 668063, 668812, 671410, 672872, 675825, 677764, 684638, 695790, 696865, 712784, 722316, 729072, 740181, 741576, 741716, 742213, 747418, 752543
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highest activity found in rapidly growing mycelium, glucose-NH4+ or glucose-peptone medium
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solid-state fermentation in double-surface bioreactor, fermentation method optimization, overview
additional information
activity of wild-type and mutant M12 GOx during fermentation, overview
additional information
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culture conditions for enzyme production, overview
additional information
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culture conditions of wild-type and mutant strains: preferred as carbohydrate and nitrogen sources are wheat bran and corn steep liquor, pH 5.5-6.5, optimal conditions, overview, fermentation kinetics of wild-type and mutant strains with different substrates in submerged fermentations, overview
additional information
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cultures are grown on agar plates at pH 4.0 with the cutinase model substrate polycaprolactone as a carbon source
additional information
extracellular enzyme activity and L-DOPA production are maximal when glucose and peptone are employed as carbon source and nitrogen source, respectively, in the medium, and are enhanced notably when Cu2+ is supplemented
additional information
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from submerged or solid-state cultures with higher enzyme activity in the latter
additional information
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inductive synthesis of levoglucosan kinase, the organism grows well on levoglucosan as sole carbon source, fermenting it into citric acid with a yield comparable to that on glucose
additional information
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optimization of growth conditions, enzyme expression depends on carbon source for growth, glucose nearly completely suppresses enzyme expression, while wheat bran, rice bran, and cellulose induce it, the enzyme prefers monosaccharides to disaccharides for growth, overview
additional information
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optimization of production of beta-glucanase with barley flour as the sole carbon source
additional information
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poor expression of MpdA in conidiospores, expression anaylsis
additional information
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production of high levels of L-asparaginase in solid state fermentation, using agro-wastes from three leguminous crops (bran of Cajanus cajan, Phaseolus mungo, and Glycine max)
additional information
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the enzyme production is increased by 3.6fold with statistically optimized medium when compared to the basal medium, optimization, overview
additional information
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the highest enzyme production by both the strains is 3% (w/v) sucrose and 3% (w/v) peptone, or 3.5% (w/v) total sugars present in cane molasses and 1.5% (w/v) yeast powder
additional information
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up to 23% of the total FAE activity is found in detergent extracts of the residues of leaf tissue of plants transformed with FAEA targeted to the endoplasmic reticulum or Golgi, particularly those plants which show higher activity in soluble extracts such as plants T36 and T38. 50%60% of the FAEA activity is found in apoplast extracts
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LOCALIZATION
ORGANISM
UNIPROT
COMMENTARY
GeneOntology No.
LITERATURE
SOURCE
recombinant protein in expressed in Arabidopsis thaliana
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recombinant protein, localization to cell suface of Pichia pastoris with a glycosylphosphatidylinositiol anchoring system
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isoform EroA is retained in the ER lumen by a C-terminal retention motif
additional information
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12% of glucose oxidase activity in the stationary phase and 16% of glucose oxidase activity in the mid-exponential phase is localised in the cytoplasm
A0A0G3ZA16, A0A140CTD1, A1XP58, A2QJF7, A5ABL2, B3VPB3, G5D7B5, O42807, O74641, O93838, P13006, P29853, P34752, P56526, Q0PGS3, Q8J219, Q8WZI8
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30556, 30572, 94776, 114253, 114258, 114264, 114279, 136307, 136315, 136638, 136639, 136785, 136948, 136949, 171236, 171762, 171763, 171764, 171765, 208697, 288813, 288816, 288824, 288826, 288829, 288830, 288834, 288836, 288837, 288841, 288842, 326273, 326358, 393286, 649347, 650588, 650907, 653165, 655657, 664391, 665152, 667046, 667273, 667274, 667461, 668048, 668555, 669831, 670723, 670762, 678084, 678756, 679965, 681772, 691357, 692398, 701882, 707347, 710686, 714025, 716839, 717004, 729450, 729532, 729656, 741835, 742213, 743105, 743193, 743857, 744075, 749475, 749601, 750893, 751536, 751980
18 amino acids in the Nterminus function as a signal peptide that aides in the secretion of the enzyme
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38% of glucose oxidase activity in the stationary phase and 46% of glucose oxidase activity in the mid-exponential phase is localised in the extracellular fluid
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the enzyme may be a 3-phytase, EC 3.1.3.8, or a 6-phytase, EC 3.1.3.26. The product of the hydrolysis of myo-inositol hexakisphosphate i.e. myo-inositol 1,2,3,4,5-pentakisphosphate or myo-inositol 1,3,4,5,6-pentakisphosphate has not been identified
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variation in the number of isoforms, depending on culture medium used, due to proteolytic cleveage of a single polypeptide
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26100, 208564, 208567, 288826, 288835, 288843, 389419, 389421, 389792, 393286, 393345, 649347, 672763, 678756, 749601
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34% of glucose oxidase activity in the stationary phase and 26% of glucose oxidase activity in the mid-exponential phase is localised in the membrane
the enzyme has no N-terminal membrane anchor in contrast to the microsomal epoxide hydrolase, 3.3.2.9
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additional information
N-terminal mitochondrial signal and C-terminal peroxisomal target sequence, unclear if both are functional
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LINKS TO OTHER DATABASES (specific for Aspergillus niger)
SILVA: 16S/18S rRNA, 23S/28S rRNA
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