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Results 1 - 10 of 364 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.5more activity of less than 1% compared to the activity with madelonitrile: fumaronitrile, 3-hydroxyglutaronitrile, succinonitrile, 3-hydroxypropionitrile. The enzyme hydrolyzes nitriles with diverse structures. Arylacetonitriles are the optimal substrates Pseudomonas psychrotolerans ? - -
Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.5more 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 ? - -
Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.5more very low activity with: (R,S)-Mandelonitrile Trichoderma virens Gv29-8 ? - -
Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.5more very low activity with: benzonitrile, 2-cyanopyridine, 3-cyanopyridine Auricularia delicata ? - -
Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.5more very low activity with: benzonitrile, 2-cyanopyridine, 3-cyanopyridine, 4-cyanopyridine Aspergillus luchuensis ? - -
Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.5more very low activity with: benzonitrile, 2-cyanopyridine, 3-cyanopyridine, 4-cyanopyridine Macrophomina phaseolina ? - -
Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.5more 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 EBC191 ? - -
Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.5more very low activity with: benzonitrile, 2-cyanopyridine, 3-cyanopyridine, 4-cyanopyridine Macrophomina phaseolina MS6 ? - -
Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.5more very low activity with: benzonitrile, 2-cyanopyridine, 3-cyanopyridine Auricularia delicata TFB-10046 SS5 ? - -
Display the word mapDisplay the reaction diagram Show all sequences 3.5.5.5more very low activity with: benzonitrile, 2-cyanopyridine, 3-cyanopyridine, 4-cyanopyridine Aspergillus luchuensis IFO 4308 ? - -
Results 1 - 10 of 364 > >>