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<< < Results 11 - 20 of 27 > >>
EC Number Inhibitors Commentary Structure
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.253,3',5'-L-triiodothyronine competitive inhibition Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.253,5,3'-L-triiodothyronine competitive inhibition Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.253,5-diiodothyronine competitive inhibition Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25L-thyroxine competitive inhibition Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25L-tyrosine competitive inhibition Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25picolinate competitive inhibition, picolinate is a much poorer inhibitor than pyrrole-2-carboxylate because it does not possess a ring -NH and relies on a relatively weak ring interaction Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25pyrrole-2-carboxylate competitive inhibition, pyrrole-2-carboxylate is an effective inhibitor of ketimine reductase/CRYM mainly as a result of the -NH hydrogen bonding to an active site residue Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25more in silico docking of substrates and inhibitors using ketimine reductase/CRYM cyrstal structure, PDB ID 4BVA, overview Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25Triton X-100 irreversible inactivation Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.253,5-diiodo-L-tyrosine low competitive inhibition Go to the Ligand Summary Page
<< < Results 11 - 20 of 27 > >>