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Results 1 - 10 of 13 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the reaction diagram Show all sequences 1.3.1.1122 cyanidin + 4 NADPH + 4 H+ - Vitis vinifera (+)-epicatechin + (-)-catechin + 4 NADP+ - ?
Display the reaction diagram Show all sequences 1.3.1.1122 cyanidin + 4 NADPH + 4 H+ - Vitis vinifera (+)-epicatechin + (-)-catechin + 4 NADP+ at pH 7.5 and 30°C, the first hydride transfer to anthocyanidin is irreversible, and no intermediate is released during catalysis ir
Display the reaction diagram Show all sequences 1.3.1.1122 cyanidin + 4 NADPH + 4 H+ - Vitis vinifera (+)-epicatechin + (-)-catechin + 4 NADP+ the relative concentration of catechin versus epicatechin remains nearly constant and is close to 1 ?
Display the reaction diagram Show all sequences 1.3.1.1122 delphinidin + 4 NADPH + 4 H+ - Vitis vinifera (-)-gallocatechin + (+)-epigallocatechin + 4 NADP+ - ir
Display the reaction diagram Show all sequences 1.3.1.1122 pelargonidin + 4 NADPH + 4 H+ - Vitis vinifera (-)-afzelechin + (+)-epiafzelechin + 4 NADP+ - ir
Display the reaction diagram Show all sequences 1.3.1.112cyanidin + 2 NADPH + 2 H+ - Vitis vinifera epicatechin + 2 NADP+ - ?
Display the reaction diagram Show all sequences 1.3.1.112delphinidin + 2 NADPH + 2 H+ - Vitis vinifera epigallocatechin + 2 NADP+ - ?
Display the reaction diagram Show all sequences 1.3.1.112pelargonidin + 2 NADPH + 2 H+ - Vitis vinifera epiafzelechin + 2 NADP+ - ?
Display the reaction diagram Show all sequences 1.3.1.112peonidin + 2 NADPH + 2 H+ - Vitis vinifera (2S,3S)-3,5,7-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydro-1-benzopyran-1-ium + 2 NADP+ - ?
Display the reaction diagram Show all sequences 1.3.1.112petunidin + 2 NADPH + 2 H+ - Vitis vinifera ? + 2 NADP+ - ?
Results 1 - 10 of 13 > >>