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Results 1 - 10 of 12 > >>
EC Number Inhibitors Commentary Structure
Show all pathways known for 1.13.11.57Display the word mapDisplay the reaction diagram Show all sequences 1.13.11.572,2'-dipyridyl 2 mM 2,2'-dipyridyl, a specific Fe2+-chelator, abolishes the gallate dioxygenase activity completely Go to the Ligand Summary Page
Show all pathways known for 1.13.11.57Display the word mapDisplay the reaction diagram Show all sequences 1.13.11.572-Methoxy-4-methylphenol 20.8% inhibition at 5 mM Go to the Ligand Summary Page
Show all pathways known for 1.13.11.57Display the word mapDisplay the reaction diagram Show all sequences 1.13.11.574-nitrocatechol 36.6% inhibition when the inhibitor is present in 5fold excess over substrate Go to the Ligand Summary Page
Show all pathways known for 1.13.11.57Display the word mapDisplay the reaction diagram Show all sequences 1.13.11.574-nitrocatechol 31.6% inhibition at 5 mM Go to the Ligand Summary Page
Show all pathways known for 1.13.11.57Display the word mapDisplay the reaction diagram Show all sequences 1.13.11.57EDTA complete inhibition at 0.5 mM, the oxygen consumption activity after EDTA treatment is completely recovered by addition of Fe2+ (119%) Go to the Ligand Summary Page
Show all pathways known for 1.13.11.57Display the word mapDisplay the reaction diagram Show all sequences 1.13.11.57EDTA complete inhibition at 1 mM, the activity is only fully recovered with Fe2+ Go to the Ligand Summary Page
Show all pathways known for 1.13.11.57Display the word mapDisplay the reaction diagram Show all sequences 1.13.11.57H2O2 hydrogen peroxide at 1 mM reduces the gallate dioxygenase activity to 15%, and the activity can be partially restored (50% activity of the untreated enzyme) upon addition of 10 mM ascorbate Go to the Ligand Summary Page
Show all pathways known for 1.13.11.57Display the word mapDisplay the reaction diagram Show all sequences 1.13.11.57protocatechuate most potent inhibitor with mixed (competitive and non-competitive) inhibition profile, 49% inhibition at 5 mM Go to the Ligand Summary Page
Show all pathways known for 1.13.11.57Display the word mapDisplay the reaction diagram Show all sequences 1.13.11.57syringaldehyde least potent inhibitor, 8.66% inhibition at 5 mM Go to the Ligand Summary Page
Show all pathways known for 1.13.11.57Display the word mapDisplay the reaction diagram Show all sequences 1.13.11.57syringate 16.3% inhibition at 5 mM Go to the Ligand Summary Page
Results 1 - 10 of 12 > >>