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Results 1 - 6 of 6
EC Number Natural Substrates Commentary (Nat. Sub.)
Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.116-(2-amino-2-carboxyethyl)-7,8-dioxo-1,2,3,4,5,6,7,8,-octahydroquinoline-2,4-dicarboxylate + O2 -
Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.116-(2-amino-2-carboxyethyl)-7,8-dioxo-1,2,3,4,7,8-hexahydroquinoline-2,4-dicarboxylate + 3 O2 -
Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.11more catalyzes the final step of PQQ formation, which involves a ring closure and an overall eight-electron oxidation of 3a-(2-amino-2-carboxyethyl)-4,5-dioxo-4,5,6,7,8,9-hexahydroquinoline-7,9-dicarboxylic acid in the absence of a redox-active metal or cofactor
Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.11more PqqC/D produces the reduced pyrroloquinoline quinone from the intermediate in vivo
Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.113a-(2-amino-2-carboxyethyl)-4,5-dioxo-4,5,6,7,8,9-hexahydroquinoline-7,9-dicarboxylic acid + O2 synthesis of the pyrroloquinoline quinone (PQQ), that serves as prosthetic group for many bacterial enzymes
Display the word mapDisplay the reaction diagram Show all sequences 1.3.3.113a-(2-amino-2-carboxyethyl)-4,5-dioxo-4,5,6,7,8,9-hexahydroquinoline-7,9-dicarboxylic acid + O2 synthesis of the pyrroloquinoline quinone (PQQ), that serves as prosthetic group for many bacterial enzymes, PQQ might also be involved in the protection against reactive oxygen species during growth under stress conditions
Results 1 - 6 of 6