EC Number |
Reaction |
Reference |
---|
1.13.11.52 | D-tryptophan + O2 = N-formyl-D-kynurenine |
- |
- |
1.13.11.52 | L-tryptophan + O2 = N-formyl-L-kynurenine |
- |
- |
1.13.11.52 | L-tryptophan + O2 = N-formyl-L-kynurenine |
Criegee type rearrangement for ring opening |
695525 |
1.13.11.52 | L-tryptophan + O2 = N-formyl-L-kynurenine |
density functional theory calculations have been performed to elucidate the new reaction mechanism of oxidative cleavage of Trp |
687297 |
1.13.11.52 | L-tryptophan + O2 = N-formyl-L-kynurenine |
density functional theory calculations have been performed to elucidate the reaction mechanism of oxidative cleavage of Trp |
687297 |
1.13.11.52 | L-tryptophan + O2 = N-formyl-L-kynurenine |
electrophilic or radical addition reaction mechanism via formation of a transient ferryl intermediate, assigned as a Compound II (ferryl) species, during oxidation of L-Trp, 1-methyl-L-Trp, and a number of other substrate analogues, overview. A common reaction mechanism for indoleamine 2,3-dioxygenase-catalyzed oxidation of tryptophan and other tryptophan analogues is determined |
742885 |
1.13.11.52 | L-tryptophan + O2 = N-formyl-L-kynurenine |
steady-state kinetic catalytic mechanism of hIDO1 |
741770 |
1.13.11.52 | L-tryptophan + O2 = N-formyl-L-kynurenine |
substrate recognition and catalytic mechanism, overview |
725837 |