GREP C00264

Selected compound(s)

C00264 3-Oxoacyl-CoA

Each orphan metabolite is emphasized in bold. Click [Fig] on the left hand, and the image of the reaction is shown.
[Suggested reactions | Reported reactions]

Suggested reactions

[Fig] 1.1.1.- : 3-Oxoacyl-CoA + NADPH + H+ = (3S)-3-Hydroxyacyl-CoA + NADP+
[Fig] 1.1.1.- : 3-Oxoacyl-CoA + NADPH + H+ = (3R)-3-Hydroxyacyl-CoA + NADP+
[Fig] 1.1.1.- : (3S)-3-Hydroxyacyl-CoA + NAD+ = 3-Oxoacyl-CoA + NADH + H+
[Fig] 1.1.1.- : (3R)-3-Hydroxyacyl-CoA + NAD+ = 3-Oxoacyl-CoA + NADH + H+
[Fig] 1.1.3.- : (3S)-3-Hydroxyacyl-CoA + O2 = 3-Oxoacyl-CoA + H2O2
[Fig] 1.1.3.- : (3R)-3-Hydroxyacyl-CoA + O2 = 3-Oxoacyl-CoA + H2O2
[Fig] 1.1.4.- : 3-Oxoacyl-CoA + 1,4-Dithiothreitol = (3S)-3-Hydroxyacyl-CoA + Oxidized dithiothreitol
[Fig] 1.1.4.- : 3-Oxoacyl-CoA + 1,4-Dithiothreitol = (3R)-3-Hydroxyacyl-CoA + Oxidized dithiothreitol
[Fig] 1.1.5.- : 3-Oxoacyl-CoA + Reduced thioredoxin = (3S)-3-Hydroxyacyl-CoA + Oxidized thioredoxin
[Fig] 1.1.5.- : 3-Oxoacyl-CoA + Reduced thioredoxin = (3R)-3-Hydroxyacyl-CoA + Oxidized thioredoxin
[Fig] 1.1.5.- : 3-Oxoacyl-CoA + CoQH2 = (3S)-3-Hydroxyacyl-CoA + CoQ
[Fig] 1.1.5.- : 3-Oxoacyl-CoA + CoQH2 = (3R)-3-Hydroxyacyl-CoA + CoQ
[Fig] 1.1.5.- : (3S)-3-Hydroxyacyl-CoA + Coenzyme F420 = 3-Oxoacyl-CoA + Reduced coenzyme F420
[Fig] 1.1.5.- : (3R)-3-Hydroxyacyl-CoA + Coenzyme F420 = 3-Oxoacyl-CoA + Reduced coenzyme F420
[Fig] 1.1.99.- : (3S)-3-Hydroxyacyl-CoA + FAD = 3-Oxoacyl-CoA + FADH2
[Fig] 1.1.99.- : (3R)-3-Hydroxyacyl-CoA + FAD = 3-Oxoacyl-CoA + FADH2
[Fig] 1.14.11.- : 2,3-Dehydroacyl-CoA + O2 + 2-Ketoglutaric acid = 3-Oxoacyl-CoA + CO2 + Butanedionic acid
[Fig] 1.14.11.- : trans-2,3-Dehydroacyl-CoA + O2 + 2-Ketoglutaric acid = 3-Oxoacyl-CoA + CO2 + Butanedionic acid
[Fig] 1.14.11.- : cis-2,3-Dehydroacyl-CoA + O2 + 2-Ketoglutaric acid = 3-Oxoacyl-CoA + CO2 + Butanedionic acid
[Fig] 1.14.11.- : cis-2-Enoyl-CoA + O2 + 2-Ketoglutaric acid = 3-Oxoacyl-CoA + CO2 + Butanedionic acid
[Fig] 1.14.13.- : 3-Oxoacyl-CoA + H2O + NAD+ = 2,3-Dehydroacyl-CoA + NADH + O2 + H+
[Fig] 1.14.13.- : 3-Oxoacyl-CoA + H2O + NAD+ = trans-2,3-Dehydroacyl-CoA + NADH + O2 + H+
[Fig] 1.14.13.- : 3-Oxoacyl-CoA + H2O + NAD+ = cis-2,3-Dehydroacyl-CoA + NADH + O2 + H+
[Fig] 1.14.13.- : 3-Oxoacyl-CoA + H2O + NAD+ = cis-2-Enoyl-CoA + NADH + O2 + H+
[Fig] 1.14.13.- : 3-Oxoacyl-CoA + H2O + NADP+ = 2,3-Dehydroacyl-CoA + NADPH + O2 + H+
[Fig] 1.14.13.- : 3-Oxoacyl-CoA + H2O + NADP+ = trans-2,3-Dehydroacyl-CoA + NADPH + O2 + H+
[Fig] 1.14.13.- : 3-Oxoacyl-CoA + H2O + NADP+ = cis-2,3-Dehydroacyl-CoA + NADPH + O2 + H+
[Fig] 1.14.13.- : 3-Oxoacyl-CoA + H2O + NADP+ = cis-2-Enoyl-CoA + NADPH + O2 + H+
[Fig] 1.14.16.- : 3-Oxoacyl-CoA + 6,7-Dihydrobiopterin + H2O = 2,3-Dehydroacyl-CoA + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
[Fig] 1.14.16.- : 3-Oxoacyl-CoA + 6,7-Dihydrobiopterin + H2O = trans-2,3-Dehydroacyl-CoA + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
[Fig] 1.14.16.- : 3-Oxoacyl-CoA + 6,7-Dihydrobiopterin + H2O = cis-2,3-Dehydroacyl-CoA + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
[Fig] 1.14.16.- : 3-Oxoacyl-CoA + 6,7-Dihydrobiopterin + H2O = cis-2-Enoyl-CoA + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
[Fig] 1.14.17.- : 2,3-Dehydroacyl-CoA + Vitamin C + O2 = 3-Oxoacyl-CoA + Dehydroascorbate + H2O
[Fig] 1.14.17.- : trans-2,3-Dehydroacyl-CoA + Vitamin C + O2 = 3-Oxoacyl-CoA + Dehydroascorbate + H2O
[Fig] 1.14.17.- : cis-2,3-Dehydroacyl-CoA + Vitamin C + O2 = 3-Oxoacyl-CoA + Dehydroascorbate + H2O
[Fig] 1.14.17.- : cis-2-Enoyl-CoA + Vitamin C + O2 = 3-Oxoacyl-CoA + Dehydroascorbate + H2O

Reported reactions

[Fig] EC 1.1.1.35 : (3S)-3-Hydroxyacyl-CoA + NAD+ = 3-Oxoacyl-CoA + NADH
[Fig] EC 1.1.1.211 : (3S)-3-Hydroxyacyl-CoA + NAD+ = 3-Oxoacyl-CoA + NADH
[Fig] EC 1.1.1.36 : (3R)-3-Hydroxyacyl-CoA + NADP+ = 3-Oxoacyl-CoA + NADPH
[Fig] EC 2.3.1.16 : Acyl-CoA + Acetyl-CoA = CoA + 3-Oxoacyl-CoA
[Fig] EC 2.8.3.5 : Succinyl-CoA + 3-Oxo acid = Butanedionic acid + 3-Oxoacyl-CoA

GREP v1.0.2 http://bisscat.org/GREP/
Developed by Masaaki Kotera (2008), Department of Biochemistry, Trinity College Dublin.
Science Foundation of Ireland is gratefully acknowledged.