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] 1.1.1.- : 1,2,4-Benzenetriol + NAD+ = 2-Hydroxy-1,4-benzoquinone + NADH + H+
- [Fig] 1.1.1.- : 2-Hydroxy-1,4-benzoquinone + NADPH + H+ = 1,2,4-Benzenetriol + NADP+
- [Fig] 1.1.3.- : 1,2,4-Benzenetriol + O2 = 2-Hydroxy-1,4-benzoquinone + H2O2
- [Fig] 1.1.4.- : 2-Hydroxy-1,4-benzoquinone + 1,4-Dithiothreitol = 1,2,4-Benzenetriol + Oxidized dithiothreitol
- [Fig] 1.1.5.- : 2-Hydroxy-1,4-benzoquinone + CoQH2 = 1,2,4-Benzenetriol + CoQ
- [Fig] 1.1.99.- : 1,2,4-Benzenetriol + FAD = 2-Hydroxy-1,4-benzoquinone + FADH2
- [Fig] 1.1.99.- : 1,2,4-Benzenetriol + Coenzyme F420 = 2-Hydroxy-1,4-benzoquinone + Reduced coenzyme F420
- [Fig] 1.14.13.- : 1,2,4-Benzenetriol + H2O + NAD+ = 1,4-Benzenediol + NADH + O2 + H+
- [Fig] 1.14.13.- : 1,2,4-Benzenetriol + H2O + NAD+ = 1,3-Benzenediol + NADH + O2 + H+
- [Fig] 1.14.13.- : 1,2,4-Benzenetriol + H2O + NADP+ = 1,4-Benzenediol + NADPH + O2 + H+
- [Fig] 1.14.13.- : 1,2,4-Benzenetriol + H2O + NADP+ = 1,3-Benzenediol + NADPH + O2 + H+
Reported reactions
- [Fig] EC 1.13.11.37 : 1,2,4-Benzenetriol + O2 = 2-Maleylacetate
- [Fig] EC 1.13.11.44 : 1,2,4-Benzenetriol + O2 = 2-Maleylacetate
- [Fig] EC 1.6.5.7 : 2-Hydroxy-1,4-benzoquinone + NADH + H+ = 1,2,4-Benzenetriol + NAD+
- [Fig] EC 1.14.-.- : 4-Nitrocatechol + O2 + 3 H+ = 1,2,4-Benzenetriol + Nitrite + H2O
- [Fig] EC 1.14.13.7 : 1,3-Benzenediol + O2 + NADPH = 1,2,4-Benzenetriol + NADP+ + H2O
- [Fig] EC 1.13.11.- : 3,4-Dihydroxybenzoate + O2 + NADH = 1,2,4-Benzenetriol + CO2 + NAD+ + H2O
- [Fig] EC 1.13.11.37 : 1,2,4-Benzenetriol + O2 = 3-Hydroxy-cis,cis-muconate
- [Fig] EC 1.14.13.7 : 1,4-Benzenediol + NADPH + H+ + O2 = 1,2,4-Benzenetriol + NADP+ + H2O
- [Fig] EC 1.1.-.- : 1,2,4-Benzenetriol = 2-Hydroxy-1,4-benzoquinone
- [Fig] EC 1.13.11.- : 3,4-Dihydroxybenzoate + O2 + NADPH = 1,2,4-Benzenetriol + CO2 + 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.