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Results 1 - 10 of 12 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the reaction diagram Show all sequences 5.99.1.42-hydroxy-2H-chromene-2-carboxylate - Comamonas testosteroni (3E)-4-(2-hydroxyphenyl)-2-oxobut-3-enoate - ?
Display the reaction diagram Show all sequences 5.99.1.42-hydroxy-2H-chromene-2-carboxylate - Brevundimonas vesicularis (3E)-4-(2-hydroxyphenyl)-2-oxobut-3-enoate - ?
Display the reaction diagram Show all sequences 5.99.1.42-hydroxy-2H-chromene-2-carboxylate extracts of Escherichia coli JM109 carrying pRE718 catalyze the conversion of trans-o-hydroxybenzylidenepyruvate or 2-hydroxychromene-2-carboxylate to an equilibrium mixture that contained 55% 2-hydroxychromene-2-carboxylate and 45% trans-o-hydroxybenzylidenepyruvate at pH 7. At pH 10 the reaction occus entirely in on direction, the conversion of 2-hydroxychromene-2-carboxylate to trans-o-hydroxybenzylidenepyruvate. The product is identified by nuclear magnetic resonance spectroscopy. This isomerization occurs spontaneously, although at a slower rate than the enzyme-catalyzed reaction Pseudomonas putida (3E)-4-(2-hydroxyphenyl)-2-oxobut-3-enoate i.e. (E)-2'-hydroxybenzylidenepyruvate, i.e. trans-o-hydroxybenzylidenepyruvate r
Display the reaction diagram Show all sequences 5.99.1.42-hydroxy-2H-chromene-2-carboxylate glutathione (GSH)-dependent interconversion. The isomerization reaction involves a short-lived covalent adduct between the sulfur of GSH and C7 of the substrate Pseudomonas putida (3E)-4-(2-hydroxyphenyl)-2-oxobut-3-enoate i.e. (E)-2'-hydroxybenzylidenepyruvate, i.e. trans-o-hydroxybenzylidenepyruvate ?
Display the reaction diagram Show all sequences 5.99.1.42-hydroxy-2H-chromene-2-carboxylate the product trans-o-hydroxybenzylidenepyruvate is analyzed by 1H NMR spectrum Pseudomonas sp. (3E)-4-(2-hydroxyphenyl)-2-oxobut-3-enoate i.e. (E)-2'-hydroxybenzylidenepyruvate, i.e. trans-o-hydroxybenzylidenepyruvate ?
Display the reaction diagram Show all sequences 5.99.1.42-hydroxy-2H-chromene-2-carboxylate the product trans-o-hydroxybenzylidenepyruvate is analyzed by 1H NMR spectrum Pseudomonas sp. TA-2 (3E)-4-(2-hydroxyphenyl)-2-oxobut-3-enoate i.e. (E)-2'-hydroxybenzylidenepyruvate, i.e. trans-o-hydroxybenzylidenepyruvate ?
Display the reaction diagram Show all sequences 5.99.1.42-hydroxybenzo[g]chromene-2-carboxylate more unstable than 2-hydroxychromene-2-carboxylate Comamonas testosteroni ? - ?
Display the reaction diagram Show all sequences 5.99.1.42-hydroxybenzo[g]chromene-2-carboxylate more unstable than 2-hydroxychromene-2-carboxylate Brevundimonas vesicularis ? - ?
Display the reaction diagram Show all sequences 5.99.1.4more enzyme degrades naphthalenesulfonates Comamonas testosteroni ? - ?
Display the reaction diagram Show all sequences 5.99.1.4more enzyme degrades naphthalenesulfonates Brevundimonas vesicularis ? - ?
Results 1 - 10 of 12 > >>