1MMJ
Porcine pancreatic elastase complexed with a potent peptidyl inhibitor, FR136706
Summary for 1MMJ
Entry DOI | 10.2210/pdb1mmj/pdb |
Descriptor | elastase 1, SULFATE ION, CALCIUM ION, ... (5 entities in total) |
Functional Keywords | chymotrypsin family, hydrolase |
Biological source | Sus scrofa (pig) |
Cellular location | Secreted: P00772 |
Total number of polymer chains | 1 |
Total formula weight | 26635.72 |
Authors | Kinoshita, T. (deposition date: 2002-09-04, release date: 2002-12-23, Last modification date: 2024-11-20) |
Primary citation | Kinoshita, T.,Nakanishi, I.,Sato, A.,Tada, T. True interaction mode of porcine pancreatic elastase with FR136706, a potent peptidyl inhibitor Bioorg.Med.Chem.Lett., 13:21-24, 2003 Cited by PubMed Abstract: The crystal structure of porcine pancreatic elastase (PPE) complexed with a potent peptidyl inhibitor, FR136706, was solved at 2.2A resolution. FR136706 fits snugly into the extended active site pocket. The benzene moiety of FR136706 induced dramatic movement of the side chain moiety of Arg217 and both moieties formed a pi-pi interaction, which has never been found previously in structures of PPE complexed with inhibitors. This novel interaction mode may lead to design of new types of inhibitors. PubMed: 12467609DOI: 10.1016/S0960-894X(02)00852-1 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.2 Å) |
Structure validation
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