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.- : 3-Hydroxy-1,3,5(10)-estratrien-17-one + NADPH + H+ = 17alpha-Estradiol + NADP+
- [Fig] 1.1.1.- : 17alpha-Estradiol + NAD+ = 3-Hydroxy-1,3,5(10)-estratrien-17-one + NADH + H+
- [Fig] 1.1.3.- : 17alpha-Estradiol + O2 = 3-Hydroxy-1,3,5(10)-estratrien-17-one + H2O2
- [Fig] 1.1.4.- : 3-Hydroxy-1,3,5(10)-estratrien-17-one + 1,4-Dithiothreitol = 17alpha-Estradiol + Oxidized dithiothreitol
- [Fig] 1.1.5.- : 3-Hydroxy-1,3,5(10)-estratrien-17-one + Reduced thioredoxin = 17alpha-Estradiol + Oxidized thioredoxin
- [Fig] 1.1.5.- : 3-Hydroxy-1,3,5(10)-estratrien-17-one + CoQH2 = 17alpha-Estradiol + CoQ
- [Fig] 1.1.5.- : 17alpha-Estradiol + Coenzyme F420 = 3-Hydroxy-1,3,5(10)-estratrien-17-one + Reduced coenzyme F420
- [Fig] 1.1.99.- : 17alpha-Estradiol + FAD = 3-Hydroxy-1,3,5(10)-estratrien-17-one + FADH2
Reported reactions
- [Fig] EC 1.1.1.148 : 17alpha-Estradiol + NAD+ = 3-Hydroxy-1,3,5(10)-estratrien-17-one + NADH
- [Fig] EC 1.1.1.148 : 17alpha-Estradiol + NADP+ = 3-Hydroxy-1,3,5(10)-estratrien-17-one + NADPH
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.