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.- : (-)-(4S)-Limonene + O2 + 2-Ketoglutaric acid = (-)-trans-Carveol + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : (-)-(4S)-Limonene + O2 + 2-Ketoglutaric acid = (-)-trans-Isopiperitenol + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : (-)-(4S)-Limonene + O2 + 2-Ketoglutaric acid = Geranial + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : (-)-(4S)-Limonene + O2 + 2-Ketoglutaric acid = (-)-Perillyl alcohol + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : (-)-(4S)-Limonene + O2 + 2-Ketoglutaric acid = Perillaldehyde + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : (-)-(4S)-Limonene + O2 + 2-Ketoglutaric acid = Neral + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : (-)-(4S)-Limonene + O2 + 2-Ketoglutaric acid = (+)-Piperitone + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : (-)-(4S)-Limonene + O2 + 2-Ketoglutaric acid = (+)-Pulegone + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : (-)-(4S)-Limonene + O2 + 2-Ketoglutaric acid = (+)-(S)-Carvone + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : (-)-(4S)-Limonene + O2 + 2-Ketoglutaric acid = (4R,6R)-cis-Carveol + CO2 + Butanedionic acid
- [Fig] 1.14.11.- : (-)-(4S)-Limonene + O2 + 2-Ketoglutaric acid = (1S,4S)-Dihydrocarvone + CO2 + Butanedionic acid
- [Fig] 1.14.13.- : Geranial + H2O + NAD+ = (-)-(4S)-Limonene + NADH + O2 + H+
- [Fig] 1.14.13.- : Geranial + H2O + NADP+ = (-)-(4S)-Limonene + NADPH + O2 + H+
- [Fig] 1.14.13.- : (-)-Perillyl alcohol + H2O + NAD+ = (-)-(4S)-Limonene + NADH + O2 + H+
- [Fig] 1.14.13.- : (-)-Perillyl alcohol + H2O + NADP+ = (-)-(4S)-Limonene + NADPH + O2 + H+
- [Fig] 1.14.13.- : Perillaldehyde + H2O + NAD+ = (-)-(4S)-Limonene + NADH + O2 + H+
- [Fig] 1.14.13.- : Perillaldehyde + H2O + NADP+ = (-)-(4S)-Limonene + NADPH + O2 + H+
- [Fig] 1.14.13.- : Neral + H2O + NAD+ = (-)-(4S)-Limonene + NADH + O2 + H+
- [Fig] 1.14.13.- : Neral + H2O + NADP+ = (-)-(4S)-Limonene + NADPH + O2 + H+
- [Fig] 1.14.13.- : (+)-Piperitone + H2O + NAD+ = (-)-(4S)-Limonene + NADH + O2 + H+
- [Fig] 1.14.13.- : (+)-Piperitone + H2O + NADP+ = (-)-(4S)-Limonene + NADPH + O2 + H+
- [Fig] 1.14.13.- : (+)-Pulegone + H2O + NAD+ = (-)-(4S)-Limonene + NADH + O2 + H+
- [Fig] 1.14.13.- : (+)-Pulegone + H2O + NADP+ = (-)-(4S)-Limonene + NADPH + O2 + H+
- [Fig] 1.14.13.- : (+)-(S)-Carvone + H2O + NAD+ = (-)-(4S)-Limonene + NADH + O2 + H+
- [Fig] 1.14.13.- : (+)-(S)-Carvone + H2O + NADP+ = (-)-(4S)-Limonene + NADPH + O2 + H+
- [Fig] 1.14.13.- : (1S,4S)-Dihydrocarvone + H2O + NAD+ = (-)-(4S)-Limonene + NADH + O2 + H+
- [Fig] 1.14.13.- : (1S,4S)-Dihydrocarvone + H2O + NADP+ = (-)-(4S)-Limonene + NADPH + O2 + H+
- [Fig] 1.14.16.- : Geranial + 6,7-Dihydrobiopterin + H2O = (-)-(4S)-Limonene + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.16.- : (-)-Perillyl alcohol + 6,7-Dihydrobiopterin + H2O = (-)-(4S)-Limonene + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.16.- : Perillaldehyde + 6,7-Dihydrobiopterin + H2O = (-)-(4S)-Limonene + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.16.- : Neral + 6,7-Dihydrobiopterin + H2O = (-)-(4S)-Limonene + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.16.- : (+)-Piperitone + 6,7-Dihydrobiopterin + H2O = (-)-(4S)-Limonene + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.16.- : (+)-Pulegone + 6,7-Dihydrobiopterin + H2O = (-)-(4S)-Limonene + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.16.- : (+)-(S)-Carvone + 6,7-Dihydrobiopterin + H2O = (-)-(4S)-Limonene + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.16.- : (1S,4S)-Dihydrocarvone + 6,7-Dihydrobiopterin + H2O = (-)-(4S)-Limonene + 2-Amino-6-(1,2-dihydroxypropyl)-5,6,7,8-tetrahydoro-4(1H)- pteridinone + O2
- [Fig] 1.14.17.- : (-)-(4S)-Limonene + Vitamin C + O2 = Geranial + Dehydroascorbate + H2O
- [Fig] 1.14.17.- : (-)-(4S)-Limonene + Vitamin C + O2 = (-)-Perillyl alcohol + Dehydroascorbate + H2O
- [Fig] 1.14.17.- : (-)-(4S)-Limonene + Vitamin C + O2 = Perillaldehyde + Dehydroascorbate + H2O
- [Fig] 1.14.17.- : (-)-(4S)-Limonene + Vitamin C + O2 = Neral + Dehydroascorbate + H2O
- [Fig] 1.14.17.- : (-)-(4S)-Limonene + Vitamin C + O2 = (+)-Piperitone + Dehydroascorbate + H2O
- [Fig] 1.14.17.- : (-)-(4S)-Limonene + Vitamin C + O2 = (+)-Pulegone + Dehydroascorbate + H2O
- [Fig] 1.14.17.- : (-)-(4S)-Limonene + Vitamin C + O2 = (+)-(S)-Carvone + Dehydroascorbate + H2O
- [Fig] 1.14.17.- : (-)-(4S)-Limonene + Vitamin C + O2 = (1S,4S)-Dihydrocarvone + Dehydroascorbate + H2O
- [Fig] 1.17.1.- : (-)-(4S)-Limonene + H2O + NADP+ = Perillaldehyde + NADPH + H+
- [Fig] 1.17.1.- : (-)-(4S)-Limonene + H2O + NADP+ = (+)-(S)-Carvone + NADPH + H+
- [Fig] 1.17.3.- : (-)-(4S)-Limonene + H2O + O2 = Perillaldehyde + H2O2
- [Fig] 1.17.3.- : (-)-(4S)-Limonene + H2O + O2 = (+)-(S)-Carvone + H2O2
- [Fig] 2.7.1.- : (-)-(4S)-Limonene + GDP = Polyprenyl phosphate + 3',5'-Cyclic GMP
- [Fig] 2.7.1.- : (-)-(4S)-Limonene + GTP = Geranyl diphosphate + 3',5'-Cyclic GMP
- [Fig] 2.7.1.- : (-)-(4S)-Limonene + GTP = Neryl diphosphate + 3',5'-Cyclic GMP
- [Fig] 2.7.1.- : (-)-(4S)-Limonene + GTP = poly-cis-Polyprenyl diphosphate + 3',5'-Cyclic GMP
- [Fig] 2.7.1.- : (-)-(4S)-Limonene + GTP = Polyprenyl diphosphate + 3',5'-Cyclic GMP
- [Fig] 2.7.1.- : 3',5'-Cyclic dAMP + Geranyl diphosphate = dATP + (-)-(4S)-Limonene
- [Fig] 3.7.1.- : (-)-(4S)-Limonene + H2O = Geraniol
- [Fig] 3.7.1.- : (-)-(4S)-Limonene + H2O = (R)-(+)-Citronellal
- [Fig] 3.7.1.- : (-)-(4S)-Limonene + H2O = Nerol
- [Fig] 3.7.1.- : (-)-(4S)-Limonene + H2O = (S)-(-)-Citronellal
- [Fig] 4.2.1.- : (-)-(4S)-Limonene + H2O = (R)-(+)-alpha-Terpineol
- [Fig] 4.2.1.- : (-)-(4S)-Limonene + H2O = (-)-alpha-Terpineol
- [Fig] 4.2.3.- : Geranyl diphosphate = Diphosphate + (-)-(4S)-Limonene
- [Fig] 4.2.3.- : Polyprenyl phosphate = Orthophosphate + (-)-(4S)-Limonene
- [Fig] 4.2.3.- : Neryl diphosphate = Diphosphate + (-)-(4S)-Limonene
- [Fig] 4.2.3.- : poly-cis-Polyprenyl diphosphate = Diphosphate + (-)-(4S)-Limonene
- [Fig] 4.2.3.- : Polyprenyl diphosphate = Diphosphate + (-)-(4S)-Limonene
- [Fig] 5.-.-.- : (-)-(4S)-Limonene = Cajeputene
- [Fig] 5.-.-.- : (-)-(4S)-Limonene = (+)-(4R)-Limonene
- [Fig] 5.3.3.- : (-)-(4S)-Limonene = (+)-beta-Phellandrene
- [Fig] 5.3.3.- : (-)-(4S)-Limonene = (-)-beta-Phellandrene
- [Fig] 5.3.3.- : (R)-(-)-alpha-Phellandrene = (-)-(4S)-Limonene
- [Fig] 5.3.3.- : (S)-(+)-alpha-Phellandrene = (-)-(4S)-Limonene
- [Fig] 5.5.1.- : Myrcene = (-)-(4S)-Limonene
- [Fig] 5.5.1.- : beta-Ocimene = (-)-(4S)-Limonene
- [Fig] 5.5.1.- : alpha-Pinene = (-)-(4S)-Limonene
Reported reactions
- [Fig] EC 1.14.13.49 : (-)-(4S)-Limonene + O2 + NADPH + H+ = (-)-Perillyl alcohol + NADP+ + H2O
- [Fig] EC 4.2.3.16 : Geranyl diphosphate = (-)-(4S)-Limonene + Diphosphate
- [Fig] EC 1.14.13.48 : (-)-(4S)-Limonene + O2 + NADPH + H+ = (-)-trans-Carveol + NADP+ + H2O
- [Fig] EC 1.14.13.47 : (-)-(4S)-Limonene + O2 + NADPH = (-)-trans-Isopiperitenol + NADP+ + H2O
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.