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Results 1 - 10 of 33

EC Number	Natural Substrates	Commentary (Nat. Sub.)
1.1.1.153	1'-oxo-2'-D-hydroxypropyl-tetrahydropterin + NADP+	-
1.1.1.153	1'-oxo-2'-D-hydroxypropyl-tetrahydropterin + NADPH	-
1.1.1.153	1'-oxo-2'-hydroxypropyl-tetrahydropterin + NADPH + H+	-
1.1.1.153	1'-oxo-2'-L-hydroxypropyl-tetrahydropterin + NADP+	-
1.1.1.153	1'-oxo-2'-L-hydroxypropyl-tetrahydropterin + NADPH	-
1.1.1.153	6-(S)-lactoyl-7,8-dihydropterin + NADPH	-
1.1.1.153	6-(S)-lactoyl-7,8-dihydropterin + NADPH	equilibrium lies much in favor of dihydrobiopterin formation
1.1.1.153	6-(S)-lactoyl-7,8-dihydropterin + NADPH	terminal step in the biosynthetic pathway for tetrahydrobiopterin
1.1.1.153	6-(S)-lactoyl-7,8-dihydropterin + NADPH	reverse reaction, L-erythro and L-threo-dihydroneopterin are also oxidized, the corresponding D-isomers are inactive
1.1.1.153	6-(S)-lactoyl-7,8-dihydropterin + NADPH	catalyzes the complete reduction of pyrovoyltetrahydropterin to tetrahydrobiopterin

Results 1 - 10 of 33

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Release 2023.1 (January 2023)