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1JWT

CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH A NOVEL BICYCLIC LACTAM INHIBITOR

Summary for 1JWT
Entry DOI10.2210/pdb1jwt/pdb
DescriptorProthrombin, 4-OXO-2-PHENYLMETHANESULFONYL-OCTAHYDRO-PYRROLO[1,2-A]PYRAZINE-6-CARBOXYLIC ACID [1-(N-HYDROXYCARBAMIMIDOYL)-PIPERIDIN-4-YLMETHYL]-AMIDE (2 entities in total)
Functional Keywordshydrolase
Biological sourceHomo sapiens (human)
Cellular locationSecreted, extracellular space: P00734
Total number of polymer chains1
Total formula weight35616.63
Authors
Levesque, S.,St-Denis, Y.,Bachand, B.,Preville, P.,Leblond, L.,Winocour, P.D.,Edmunds, J.J.,Rubin, J.R.,Siddiqui, M.A. (deposition date: 2001-09-05, release date: 2002-02-27, Last modification date: 2017-10-04)
Primary citationLevesque, S.,St-Denis, Y.,Bachand, B.,Preville, P.,Leblond, L.,Winocour, P.D.,Edmunds, J.J.,Rubin, J.R.,Siddiqui, M.A.
Novel bicyclic lactam inhibitors of thrombin: potency and selectivity optimization through P1 residues.
Bioorg.Med.Chem.Lett., 11:3161-3164, 2001
Cited by
PubMed: 11720865
DOI: 10.1016/S0960-894X(01)00661-8
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

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