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<< < Results 11 - 20 of 27 > >>
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EC Number Inhibitors Commentary Structure
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 1.5.1.253,5-L-diiodothyronine - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.254,5-dibromopyrrole-2-carboxylate - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 1.5.1.25DELTA1-piperideine 2-carboxylate substrate 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-thyroxine - 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 1.5.1.25L-tyrosine - 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 1.5.1.25more the P2C reductase activity is potently inhibited by thyroid hormones, thyroid hormones and analogues docked into the active site of the crystal structure of human KR, overview Go to the Ligand Summary Page
<< < Results 11 - 20 of 27 > >>
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