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<< < Results 11 - 20 of 20
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the word mapDisplay the reaction diagram Show all sequences 1.2.1.294-hydroxybenzaldehyde + NAD+ + H2O - Phanerodontia chrysosporium 4-hydroxybenzoic acid + NADH + H+ - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.2.1.29aromatic aldehydes + NAD+ + H2O - Oryctolagus cuniculus aromatic acids + NADH - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.2.1.29benzaldehyde + NAD+ + H2O - Phanerodontia chrysosporium benzoic acid + NADH + H+ - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.2.1.29gentisaldehyde + NAD+ - Oryctolagus cuniculus gentisic acid + NADH - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.2.1.29vanillin + NAD+ - Trametes cinnabarina vanillinic acid + NADH + H+ - r
Display the word mapDisplay the reaction diagram Show all sequences 1.2.1.29vanillin + NAD+ - Trametes cinnabarina MUCL 39533 vanillinic acid + NADH + H+ - r
Display the word mapDisplay the reaction diagram Show all sequences 1.2.1.294-hydroxy-3-methoxybenzaldehyde + NAD+ + H2O 4-hydroxy-3-methoxybenzaldehyde i.e. vanillin Phanerodontia chrysosporium 4-hydroxy-3-methoxybenzoic acid + NADH + H+ - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.2.1.29more ALDH catalysis involves acylation and deacylation. During acylation, a cysteine nucleophile interacts with the carbonyl carbon of aldehyde forming a thiohemiacetal intermediate, followed by hydride transfer from a tetrahedral thiohemiacetal intermediate to the pyridine ring of NAD(P)+. Then, deacylation occurs involving hydrolysis of the resulting thioester intermediate. Glu268 and Cys296 of PcALDH are potential active site residues Trametes cinnabarina ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.2.1.29more ALDH catalysis involves acylation and deacylation. During acylation, a cysteine nucleophile interacts with the carbonyl carbon of aldehyde forming a thiohemiacetal intermediate, followed by hydride transfer from a tetrahedral thiohemiacetal intermediate to the pyridine ring of NAD(P)+. Then, deacylation occurs involving hydrolysis of the resulting thioester intermediate. Glu268 and Cys296 of PcALDH are potential active site residues Trametes cinnabarina MUCL 39533 ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.2.1.29more the enzyme is capable of catalysing the oxidation of a number of aromatic aldehydes, but not aliphatic aldehydes Oryctolagus cuniculus ? - ?
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