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Results 1 - 5 of 5
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EC Number Natural Substrates Commentary (Nat. Sub.)
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + NADH + H+ + O2 -
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + NADH + H+ + O2 + alloxan -
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + O2 -
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + O2 FMNH2 reacts with oxygen to yield flavin hydroperoxide, which then undergoes a ring expansion with loss of a water molecule to produce intermediate A. This disintegrates further as a result of four hydrolysis reactions in which it is attacked by water molecules. The resulting diaminobenzene product undergoes two oxidation reactions, to form 5,6-dimethylbenzimidazole
Show all pathways known for 1.13.11.79Display the reaction diagram Show all sequences 1.13.11.79FMNH2 + O2 the rate of formation of the intermediate product unprotonated C4a-peroxyflavin is influenced by substitutions at C8 of FMN
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