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Results 1 - 10 of 15 > >>
EC Number Natural Substrates Commentary (Nat. Sub.)
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4(2R,3R)-butane-2,3-diol + NAD+ preferred substrate
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4(2R,3R)-butane-2,3-diol + NAD+ Paenibacillus polymyxa ATCC 12321 has the ability to form almost exclusively the R isomer of 2,3-BDL (over 98%) when grown under anaerobic conditions
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4(2R,3R)-butane-2,3-diol + NAD+ -
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4(2R,3S)-butane-2,3-diol + NAD+ -
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4(2S)-acetoin + NADH + H+ the enzyme is not absolutely specific for (S)-acetoin, though this is the preferred substrate
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4(2S,3S)-butane-2,3-diol + NAD+ -
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4(R)-acetoin + NADH + H+ -
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4(R)-acetoin + NADH + H+ the activity of (R)-acetoin reduction is 7.7times higher than that of (2R,3R)-butane-2,3-diol oxidation at pH 7.0
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4(R)-acetoin + NADH + H+ high level production of (R,R)-butane-2,3-diol
Show all pathways known for 1.1.1.4Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.4(R,R)-butane-2,3-diol + NAD+ -
Results 1 - 10 of 15 > >>