Selected compound(s)
- C11947 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-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-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA + NAD+ = 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + NADH + H+
- [Fig] 1.1.1.- : 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + NADPH + H+ = 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA + NADP+
- [Fig] 1.1.3.- : 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA + O2 = 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + H2O2
- [Fig] 1.1.4.- : 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + 1,4-Dithiothreitol = 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA + Oxidized dithiothreitol
- [Fig] 1.1.5.- : 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA + Coenzyme F420 = 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + Reduced coenzyme F420
- [Fig] 1.1.5.- : 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + Reduced thioredoxin = 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA + Oxidized thioredoxin
- [Fig] 1.1.5.- : 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + CoQH2 = 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA + CoQ
- [Fig] 1.1.99.- : 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA + FAD = 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + FADH2
- [Fig] 4.2.1.- : trans-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + H2O = 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA
- [Fig] 4.2.1.- : cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + H2O = 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA
Reported reactions
- [Fig] EC 4.2.1.17 : cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + H2O = 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA
- [Fig] EC 4.2.1.17 : trans-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + H2O = 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA
- [Fig] EC 1.1.-.- : 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA + NAD+ = 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + NADH + H+
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.