Selected compound(s)
- C11946 cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-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] 1.14.11.- : cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + O2 + 2-Ketoglutaric acid = 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + CO2 + Butanedionic acid
- [Fig] 1.14.13.- : 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + H2O + NAD+ = cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + NADH + O2 + H+
- [Fig] 1.14.13.- : 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + H2O + NADP+ = cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + NADPH + O2 + H+
- [Fig] 1.14.16.- : 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + 6,7-Dihydrobiopterin + H2O = cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.17.- : cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + Vitamin C + O2 = 2,6-Dimethyl-5-methylene-3-oxo-heptanoyl-CoA + Dehydroascorbate + H2O
- [Fig] 3.1.2.- : cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + H2O = CoA + cis-2-Methyl-5-isopropylhexa-2,5-dienoic acid
- [Fig] 4.2.1.- : cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + H2O = 3-Hydroxy-2,6-dimethyl-5-methylene-heptanoyl-CoA
- [Fig] 5.-.-.- : trans-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA = cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA
- [Fig] 6.2.1.- : CoA + cis-2-Methyl-5-isopropylhexa-2,5-dienoic acid + ATP = cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + ADP + Orthophosphate
- [Fig] 6.2.1.- : CoA + cis-2-Methyl-5-isopropylhexa-2,5-dienoic acid + ATP = cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + Diphosphate + 5'-AMP
Reported reactions
- [Fig] EC 6.2.1.- : cis-2-Methyl-5-isopropylhexa-2,5-dienoic acid + ATP + CoA = cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA + 5'-AMP + Orthophosphate
- [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
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.