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.- : Tabersonine + O2 + 2-Ketoglutaric acid = 19-Hydroxytabersonine + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : Tabersonine + O2 + 2-Ketoglutaric acid = 16-Hydroxytabersonine + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : Tabersonine + O2 + 2-Ketoglutaric acid = Lochnericine + CO2 + Butanedionic acid
- [Fig] 1.14.13.- : 19-Hydroxytabersonine + H2O + NAD+ = Tabersonine + NADH + O2 + H+
- [Fig] 1.14.13.- : 19-Hydroxytabersonine + H2O + NADP+ = Tabersonine + NADPH + O2 + H+
- [Fig] 1.14.13.- : 16-Hydroxytabersonine + H2O + NAD+ = Tabersonine + NADH + O2 + H+
- [Fig] 1.14.13.- : 16-Hydroxytabersonine + H2O + NADP+ = Tabersonine + NADPH + O2 + H+
- [Fig] 1.14.13.- : Lochnericine + H2O + NAD+ = Tabersonine + NADH + O2 + H+
- [Fig] 1.14.16.- : 19-Hydroxytabersonine + 6,7-Dihydrobiopterin + H2O = Tabersonine + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.16.- : 16-Hydroxytabersonine + 6,7-Dihydrobiopterin + H2O = Tabersonine + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.16.- : Lochnericine + 6,7-Dihydrobiopterin + H2O = Tabersonine + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.17.- : Tabersonine + Vitamin C + O2 = 19-Hydroxytabersonine + Dehydroascorbate + H2O
- [Fig] 1.14.17.- : Tabersonine + Vitamin C + O2 = 16-Hydroxytabersonine + Dehydroascorbate + H2O
- [Fig] 1.14.17.- : Tabersonine + Vitamin C + O2 = Lochnericine + Dehydroascorbate + H2O
- [Fig] 1.17.1.- : Tabersonine + H2O + NADP+ = 19-Hydroxytabersonine + NADPH + H+
- [Fig] 1.17.3.- : Tabersonine + H2O + O2 = 19-Hydroxytabersonine + H2O2
- [Fig] 1.17.4.- : Tabersonine + H2O + Oxidized thioredoxin = 19-Hydroxytabersonine + Reduced thioredoxin
- [Fig] 4.2.1.- 4.1.1.- : Tabersonine + H2O = Minovincinine
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.