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Results 1 - 10 of 962 > >>
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EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Show all pathways known for 1.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2(+)-camphorquinone + NADPH - Homo sapiens ? + NADP+ - ?
Show all pathways known for 1.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2(+)-camphorquinone + NADPH - Sus scrofa ? + NADP+ - ?
Show all pathways known for 1.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2(-)-camphorquinone + NADPH relative activity 2% Sus scrofa ? + NADP+ - ?
Show all pathways known for 1.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2(2E)-4-hydroxynon-2-enal + NADPH 30% of activity with cinnamaldehyde Saccharomyces cerevisiae (2E)-non-2-ene-1,4-diol + NADP+ - r
Show all pathways known for 1.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2(2E)-hex-2-enal + NADPH + H+ - Pelophylax perezi (2E)-2-hexen-1-ol + NADP+ - r
Show all pathways known for 1.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2(2E,4E)-hexa-2,4-dienal + NAD(P)H + H+ - Mus musculus (2E,4E)-6-hydroxyhexa-2,4-dienal + NAD(P)+ - ?
Show all pathways known for 1.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2(2R,3R)-2,3-butanediol + NADP+ the enzyme shows higher oxidation activities on the (2R,3R)-(-)-2,3-butanediol and meso-2,3-butanediol than on the (2S,3S)-(+)-2,3-butanediol, indicating that the enzyme predominantly oxidizes the R-hydroxyl group of 2,3-butanediol and minorly functions on the S-hydroxyl group. When meso-2,3-butanediol is oxidized, (S)-2-acetoin is the predominant product, with an enantiomeric excess (ee) of 88%, while oxidation of (2R,3R)-2,3-butanediol results in the production of (R)-2-acetoin with higher stereoselectivity (94% ee) Thermococcus guaymasensis (R)-2-acetoin + NADPH + H+ - r
Show all pathways known for 1.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2(2S)-methyl-1-butanol + NADP+ 39% activity compared to cinnamyl alcohol Saccharomyces cerevisiae (2S)-methylbutanal + NADPH - r
Show all pathways known for 1.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2(2S,3S)-2,3-butanediol + NADP+ the enzyme shows higher oxidation activities on the (2R,3R)-(-)-2,3-butanediol and meso-2,3-butanediol than on the (2S,3S)-(+)-2,3-butanediol, indicating that the enzyme predominantly oxidizes the R-hydroxyl group of 2,3-butanediol and minorly functions on the S-hydroxyl group. When meso-2,3-butanediol is oxidized, (S)-2-acetoin is the predominant product, with an enantiomeric excess (ee) of 88%, while oxidation of meso-2,3-butanediol results in the production of (R)-2-acetoin with higher stereoselectivity (94% ee) Thermococcus guaymasensis (S)-2-acetoin + NADPH + H+ - r
Show all pathways known for 1.1.1.2Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2(4-hydroxy-3-[3-methyl-3-butene-1-ynyl]benzaldehyde) + NADPH + H+ eutypine, a toxin produced by Eutypa lata, the causal agent of Eutypa dieback in the grapevine Vitis vinifera Vigna radiata (4-hydroxy-3-[3-methyl-3-butene-1-ynyl]benzyl alcohol) + NADP+ eutypinol, non-toxic metabolite ir
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