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Results 1 - 9 of 9
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EC Number Inhibitors Commentary Structure
Display the reaction diagram Show all sequences 1.5.1.381,10-phenanthroline 0.005 M, 14% inhibition Go to the Ligand Summary Page
Display the reaction diagram Show all sequences 1.5.1.38AMP 0.01 M, 28% inhibition Go to the Ligand Summary Page
Display the reaction diagram Show all sequences 1.5.1.38dicoumarol 0.000325 M, 15% inhibition Go to the Ligand Summary Page
Display the reaction diagram Show all sequences 1.5.1.38FMN when NADPH is supplied as pyrimidinic substrate, maximal reductase activity is obtained with 2.5-10 mM FMN, while higher FMN concentration led to 15% decrease in SsuE activity. When NADH is the pyrimidinic substrate, a distinct activity maximum is obtained at an FMN concentration of 0.5 mM, whereas concentrations higher than 2.5 mM led to more than 60% decrease in specific activity Go to the Ligand Summary Page
Display the reaction diagram Show all sequences 1.5.1.38KCN 0.01 M, 10% inhibition Go to the Ligand Summary Page
Display the reaction diagram Show all sequences 1.5.1.38more FMN at concentrations over 0.002 mM significantly inhibits the coupled reaction in both light intensity and quantum yield, and shows apparent noncompetitive and competitive inhibition patterns against NADPH and luciferase, respectively. No inhibition of the NADPH oxidation is detected under identical conditions Go to the Ligand Summary Page
Display the reaction diagram Show all sequences 1.5.1.38N-ethylmaleimide 0.001 M, 26% inhibition Go to the Ligand Summary Page
Display the reaction diagram Show all sequences 1.5.1.38p-hydroxymercuribenzoate 0.001 M, 80% inhibition Go to the Ligand Summary Page
Display the reaction diagram Show all sequences 1.5.1.38rotenone 0.0004 M, 30% inhibition Go to the Ligand Summary Page
Results 1 - 9 of 9
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