Selected compound(s)
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.- : Myrcene + O2 + 2-Ketoglutaric acid = Geranial + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : Myrcene + O2 + 2-Ketoglutaric acid = Neral + CO2 + Butanedionic acid
- [Fig] 1.14.13.- : Geranial + H2O + NAD+ = Myrcene + NADH + O2 + H+
- [Fig] 1.14.13.- : Geranial + H2O + NADP+ = Myrcene + NADPH + O2 + H+
- [Fig] 1.14.13.- : Neral + H2O + NAD+ = Myrcene + NADH + O2 + H+
- [Fig] 1.14.13.- : Neral + H2O + NADP+ = Myrcene + NADPH + O2 + H+
- [Fig] 1.14.16.- : Geranial + 6,7-Dihydrobiopterin + H2O = Myrcene + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.16.- : Neral + 6,7-Dihydrobiopterin + H2O = Myrcene + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.17.- : Myrcene + Vitamin C + O2 = Geranial + Dehydroascorbate + H2O
- [Fig] 1.14.17.- : Myrcene + Vitamin C + O2 = Neral + Dehydroascorbate + H2O
- [Fig] 4.2.1.- : Myrcene + H2O = Geraniol
- [Fig] 4.2.1.- : Myrcene + H2O = 3,7-Dimethylocta-1,6-dien-3-ol
- [Fig] 4.2.1.- : Myrcene + H2O = Nerol
- [Fig] 4.2.1.- : Myrcene + H2O = (-)-Linalool
- [Fig] 4.2.3.- : Geranyl diphosphate = Myrcene + Diphosphate
- [Fig] 4.2.3.- : Polyprenyl phosphate = Orthophosphate + Myrcene
- [Fig] 4.2.3.- : Neryl diphosphate = Myrcene + Diphosphate
- [Fig] 4.2.3.- : poly-cis-Polyprenyl diphosphate = Myrcene + Diphosphate
- [Fig] 4.2.3.- : Linaloyl diphosphate = Myrcene + Diphosphate
- [Fig] 4.2.3.- : Polyprenyl diphosphate = Myrcene + Diphosphate
- [Fig] 5.3.3.- : beta-Ocimene = Myrcene
- [Fig] 5.5.1.- : Myrcene = (-)-(4S)-Limonene
- [Fig] 5.5.1.- : Myrcene = alpha-Terpinene
- [Fig] 5.5.1.- : Cajeputene = Myrcene
- [Fig] 5.5.1.- : (+)-(4R)-Limonene = Myrcene
- [Fig] 5.5.1.- : (+)-beta-Phellandrene = Myrcene
- [Fig] 5.5.1.- : gamma-Terpinene = Myrcene
- [Fig] 5.5.1.- : (-)-beta-Phellandrene = Myrcene
Reported reactions
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.