1rhr
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(New page: 200px<br /> <applet load="1rhr" size="450" color="white" frame="true" align="right" spinBox="true" caption="1rhr, resolution 3.00Å" /> '''CRYSTAL STRUCTURE O...)
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Revision as of 16:57, 12 November 2007
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CRYSTAL STRUCTURE OF THE COMPLEX OF CASPASE-3 WITH A CINNAMIC ACID METHYL ESTER INHIBITOR
Overview
Caspases are cysteine proteases that specifically cleave Asp-Xxx bonds., They are key agents in inflammation and apoptosis and are attractive, targets for therapy against inflammation, neurodegeneration, ischemia, and, cancer. Many caspase structures are known, but most involve either peptide, or protein inhibitors, unattractive candidates for drug development. We, present seven crystal structures of inhibited caspase-3 that illustrate, several approaches to reducing the peptidyl characteristics of the, inhibitors while maintaining their potency and selectivity. The inhibitors, reduce the peptidyl nature of inhibitors while preserving binding potency, by (1). exploiting a hydrophobic binding site C-terminal to the cleavage, site, (2). replacing the negatively charged aspartyl residue at P4 with, neutral groups, and (3). using a peptidomimetic 5,6,7-tricyclic system or, a pyrazinone at P2-P3. In addition, we have found that two nicotinic acid, aldehydes induce a significant conformational change in the S2 and S3, subsites of caspase-3, revealing an unexpected binding mode. These results, advance the search for caspase-directed drugs by revealing how, unacceptable molecular features can be removed without loss of potency.
About this Structure
1RHR is a Protein complex structure of sequences from Homo sapiens with CNE as ligand. Full crystallographic information is available from OCA.
Reference
Reducing the peptidyl features of caspase-3 inhibitors: a structural analysis., Becker JW, Rotonda J, Soisson SM, Aspiotis R, Bayly C, Francoeur S, Gallant M, Garcia-Calvo M, Giroux A, Grimm E, Han Y, McKay D, Nicholson DW, Peterson E, Renaud J, Roy S, Thornberry N, Zamboni R, J Med Chem. 2004 May 6;47(10):2466-74. PMID:15115390
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