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Results 1 - 10 of 392 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Show all pathways known for 3.5.5.7Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.7more no activity with mandelonitrile, glycolonitrile Thermotoga maritima ? - -
Show all pathways known for 3.5.5.7Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.7more the enzyme shows a broad hydrolytic activity toward aliphatic and heterocyclic nitriles and shows high tolerance of 3-cyanopyridine. No activity with: benzonitrile, phenylacetonitrile, 4-chlorobenzyl cyanide, mandelonitrile, 2-chloromandelonitrile, alpha-methylphenylacetonitrile, 1,2-phenylenediacetonitrile, dodecanenitrile Cupriavidus necator ? - -
Show all pathways known for 3.5.5.7Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.7more the enzyme shows broad substrate specificity towards aliphatic, aromatic, and heterocyclic nitriles Pannonibacter carbonis ? - -
Show all pathways known for 3.5.5.7Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.7more the enzyme shows preference for unsaturated aliphatic substrates containing 5-6 carbon atoms. Increased reaction rates are also found for aliphatic nitriles carrying electron withdrawing substituents (e.g. chloro- or hydroxy-groups) close to the nitrile group. Aliphatic dinitriles are attacked only at one of the nitrile groups and with most of the tested dinitriles the monocarboxylates are detected as major products. Substrates converted with 1% less compared to the activity with 3-hexenedinitrile: 2-methylbutyronitrile, decanedinitrile, octanedinitrile, cis,trans-crotononitrile, popionitrile, isovaleronitrile, lactonitrile, butyronitrile Pseudomonas fluorescens ? - -
Show all pathways known for 3.5.5.7Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.7more the enzyme shows broad substrate specificity towards aliphatic, aromatic, and heterocyclic nitriles Pannonibacter carbonis Q4.6 ? - -
Show all pathways known for 3.5.5.7Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.7(E)-2-methyl-2-butenenitrile + H2O regioselective hydrolysis, no detectable conversion of (Z)-2-methyl-2-butenenitrile Acidovorax facilis (E)-2-methyl-2-butenoic acid + NH3 - ?
Show all pathways known for 3.5.5.7Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.7(E)-2-methyl-2-butenenitrile + H2O regioselective hydrolysis, no detectable conversion of (Z)-2-methyl-2-butenenitrile Acidovorax facilis 72W (E)-2-methyl-2-butenoic acid + NH3 - ?
Show all pathways known for 3.5.5.7Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.71,4-dicyano-2-butene + H2O 42.6% of the activity with crotononitrile Rhodococcus rhodochrous ? - ?
Show all pathways known for 3.5.5.7Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.71,4-dicyanobutane + H2O 114.3% activity compared to 3-cyanopyridine Cereibacter sphaeroides ? - ?
Show all pathways known for 3.5.5.7Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.71,8-dicyanooctane + H2O 114.3% activity compared to 3-cyanopyridine Cereibacter sphaeroides ? - ?
Results 1 - 10 of 392 > >>