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(R)-camphor degradation
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P601-PWY
(S)-camphor degradation
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PWY-6989
(S)-reticuline biosynthesis
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(S)-reticuline biosynthesis I
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PWY-3581
(S)-reticuline biosynthesis II
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PWY-6133
1,5-anhydrofructose degradation
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PWY-6992
acetone degradation I (to methylglyoxal)
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PWY-5451
acetone degradation III (to propane-1,2-diol)
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PWY-7466
Amaryllidacea alkaloids biosynthesis
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PWY-7826
Aminobenzoate degradation
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aminopropylcadaverine biosynthesis
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PWY0-1303
Arachidonic acid metabolism
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arachidonic acid metabolism
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Biosynthesis of secondary metabolites
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bisucaberin biosynthesis
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PWY-6381
bupropion degradation
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PWY66-241
cadaverine biosynthesis
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PWY0-1601
cyclopropane fatty acid (CFA) biosynthesis
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PWY0-541
degradation of sugar alcohols
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desferrioxamine B biosynthesis
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PWY-6376
desferrioxamine E biosynthesis
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PWY-6375
Drug metabolism - cytochrome P450
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Fatty acid degradation
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formate to dimethyl sulfoxide electron transfer
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PWY0-1356
glucose and glucose-1-phosphate degradation
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GLUCOSE1PMETAB-PWY
glycerol degradation II
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PWY-6131
glycerol degradation V
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GLYCEROLMETAB-PWY
Glycerolipid metabolism
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Glycolysis / Gluconeogenesis
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histamine biosynthesis
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PWY-6173
hydrogen to dimethyl sulfoxide electron transfer
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PWY0-1577
hydroxycinnamic acid tyramine amides biosynthesis
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PWY-5474
Inositol phosphate metabolism
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Isoquinoline alkaloid biosynthesis
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L-lysine degradation I
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PWY0-461
L-lysine degradation X
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PWY-6328
Linoleic acid metabolism
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lupanine biosynthesis
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PWY-5468
melatonin degradation I
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PWY-6398
Metabolism of xenobiotics by cytochrome P450
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methanofuran biosynthesis
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PWY-5254
methanol oxidation to formaldehyde IV
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PWY-5506
Microbial metabolism in diverse environments
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Monoterpenoid biosynthesis
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mycolate biosynthesis
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PWYG-321
myo-inositol biosynthesis
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NADH to dimethyl sulfoxide electron transfer
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PWY0-1348
NADPH to cytochrome c oxidase via plastocyanin
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PWY-8271
nicotine degradation IV
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PWY66-201
nicotine degradation V
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PWY66-221
nocardicin A biosynthesis
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PWY-7797
octopamine biosynthesis
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PWY-7297
Other glycan degradation
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Penicillin and cephalosporin biosynthesis
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photosynthesis light reactions
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PWY-101
phytate degradation I
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PWY-4702
Propanoate metabolism
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retinol biosynthesis
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PWY-6857
salidroside biosynthesis
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PWY-6802
Sphingolipid metabolism
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sterculate biosynthesis
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PWY-4942
Steroid hormone biosynthesis
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triacylglycerol degradation
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LIPAS-PWY
Tropane, piperidine and pyridine alkaloid biosynthesis
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Tryptophan metabolism
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vanillin biosynthesis I
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PWY-5665
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UniProt
brenda
CinA, part of putative operon consisting of three open reading frames. CinB and cinC appear to encode the expected redox partners for a catalytically functional P450 system
UniProt
brenda
isolated from faecal samples of healthy humans of La Rioja region (Northern Spain), September to November 2010
UniProt
brenda
marked derepression of enzyme in synthetic medium by addition of tyramine
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brenda
The enzyme may be a 3-phytase (EC 3.1.3.8), or a 4-phytase (synonym 6-phytase, EC 3.1.3.26). The product of the hydrolysis of myo-inositol hexakisphosphate to 1D-myo-inositol 1,2,4,5,6-pentakisphosphate or alternatively 1D-myo-inositol 1,2,3,5,6-pentakisphosphate has not been identified.
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brenda
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