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Results 1 - 10 of 105 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Show all pathways known for 1.1.1.282Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2823-dehydroquinate + NADPH + H+ - Escherichia coli L-quinate + NADP+ - r
Show all pathways known for 1.1.1.282Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2823-dehydroquinate + NADPH + H+ may be responsible for the synthesis of quinic acid from the intermediate compound of the shikimate pathway, dehydroquinic acid Pinus taeda L-quinate + NADP+ - ?
Show all pathways known for 1.1.1.282Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2823-dehydroshikimate + NAD(P)H + H+ YdiB catalyzes the reduction of 3-dehydroshikimate to shikimate as part of the shikimate pathway Escherichia coli shikimate + NAD(P)+ - ?
Show all pathways known for 1.1.1.282Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.2823-dehydroshikimate + NADH + H+ - Escherichia coli shikimate + NAD+ - r
Show all pathways known for 1.1.1.282Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.282dihydroshikimate + NAD+ highly stereospecific with regard to hydroaromatic substrates, oxidizes only the axial hydroxyl group at C-3 of the (-)-enantiomer, 38% of the activity with (-)-quinate Rhodococcus rhodochrous (1S,3R,4S)-3,4-dihydroxy-5-oxocyclohexanecarboxylic acid + NADH + H+ (-)-enantiomer, reverse reaction: 3.3fold higher activity than with (-)-3-dehydroquinate r
Show all pathways known for 1.1.1.282Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.282dihydroshikimate + NAD+ highly stereospecific with regard to hydroaromatic substrates, oxidizes only the axial hydroxyl group at C-3 of the (-)-enantiomer, 38% of the activity with (-)-quinate Rhodococcus rhodochrous N75 (1S,3R,4S)-3,4-dihydroxy-5-oxocyclohexanecarboxylic acid + NADH + H+ (-)-enantiomer, reverse reaction: 3.3fold higher activity than with (-)-3-dehydroquinate r
Show all pathways known for 1.1.1.282Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.282L-quinate + 3-acetylpyridine adenine dinucleotide 67% of the activity with NAD+ Rhodococcus rhodochrous 3-dehydroquinate + ? - ?
Show all pathways known for 1.1.1.282Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.282L-quinate + 3-acetylpyridine adenine dinucleotide 67% of the activity with NAD+ Rhodococcus rhodochrous N75 3-dehydroquinate + ? - ?
Show all pathways known for 1.1.1.282Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.282L-quinate + beta-NAD+ highly stereospecific with regard to hydroaromatic substrates, oxidizes only the axial hydroxyl group at C-3 of the (-)-enantiomer, a single enzyme with both quinate and shikimate dehydrogenase activity Rhodococcus rhodochrous 3-dehydroquinate + beta-NADH + H+ (-)-enantiomer, reverse reaction: lower activity than with t-4,c-5-dihydroxy-3-oxocyclohexane-c-1-carboxylate or 4-hydroxy-3-oxocyclohexane-c-1-carboxylate r
Show all pathways known for 1.1.1.282Display the word mapDisplay the reaction diagram Show all sequences 1.1.1.282L-quinate + beta-NAD+ highly stereospecific with regard to hydroaromatic substrates, oxidizes only the axial hydroxyl group at C-3 of the (-)-enantiomer, a single enzyme with both quinate and shikimate dehydrogenase activity Rhodococcus rhodochrous N75 3-dehydroquinate + beta-NADH + H+ (-)-enantiomer, reverse reaction: lower activity than with t-4,c-5-dihydroxy-3-oxocyclohexane-c-1-carboxylate or 4-hydroxy-3-oxocyclohexane-c-1-carboxylate r
Results 1 - 10 of 105 > >>