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1MMJ

Porcine pancreatic elastase complexed with a potent peptidyl inhibitor, FR136706

Summary for 1MMJ
Entry DOI10.2210/pdb1mmj/pdb
Descriptorelastase 1, SULFATE ION, CALCIUM ION, ... (5 entities in total)
Functional Keywordschymotrypsin family, hydrolase
Biological sourceSus scrofa (pig)
Cellular locationSecreted: P00772
Total number of polymer chains1
Total formula weight26635.72
Authors
Kinoshita, T. (deposition date: 2002-09-04, release date: 2002-12-23, Last modification date: 2024-11-20)
Primary citationKinoshita, 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: 12467609
DOI: 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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