1bqi
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USE OF PAPAIN AS A MODEL FOR THE STRUCTURE-BASED DESIGN OF CATHEPSIN K INHIBITORS. CRYSTAL STRUCTURES OF TWO PAPAIN INHIBITOR COMPLEXES DEMONSTRATE BINDING TO S'-SUBSITES.
OverviewOverview
Papain has been used as a surrogate enzyme in a drug design effort to, obtain potent and selective inhibitors of cathepsin K, a new member of the, papain superfamily of cysteine proteases that is selectively and highly, expressed in osteoclasts and is implicated in bone resorption. Here we, report the crystal structures of two papain-inhibitor complexes and the, rational design of novel cathepsin K inhibitors. Unlike previously known, crystal structures of papain-inhibitor complexes, our papain structures, show ligand binding extending deep within the S'-subsites. The two, inhibitor complexes, carbobenzyloxyleucinyl-leucinyl-leucinal and, carbobenzyloxy-L-leucinyl-L-leucinyl methoxymethyl ketone, were refined to, 2.2- and 2.5-A resolution with R-factors of 0.190 and 0. 217, respectively. The S'-subsite interactions with the inhibitors are, dominated by an aromatic-aromatic stacking and an oxygen-aromatic ring, edge interaction. The knowledge of S'-subsite interactions led to a design, strategy for an inhibitor spanning both subsites and yielded a novel, symmetric inhibitor selective for cathepsin K. Simultaneous exploitation, of both S- and S'-sites provides a general strategy for the design of, cysteine protease inhibitors having high specificity to their target, enzymes.
About this StructureAbout this Structure
1BQI is a Single protein structure of sequence from Carica papaya with SBA as ligand. Full crystallographic information is available from OCA.
ReferenceReference
Use of papain as a model for the structure-based design of cathepsin K inhibitors: crystal structures of two papain-inhibitor complexes demonstrate binding to S'-subsites., LaLonde JM, Zhao B, Smith WW, Janson CA, DesJarlais RL, Tomaszek TA, Carr TJ, Thompson SK, Oh HJ, Yamashita DS, Veber DF, Abdel-Meguid SS, J Med Chem. 1998 Nov 5;41(23):4567-76. PMID:9804696
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