Crystal structure of human caspase-1 in complex with 4-oxo-3-{6-[4-(quinoxalin-2-yloxy)-benzoylamino]-2-thiophen-2-yl-hexanoylamino}-butyric acid

File:1rwx.gif


1rwx, resolution 1.85Å

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OverviewOverview

Disulfide Tethering was applied to the active site of human caspase-1, resulting in the discovery of a novel, tricyclic molecular fragment that, selectively binds in S4. This fragment was developed into a class of, potent inhibitors of human caspase-1. Several key analogues determined the, optimal distance of the tricycle from the catalytic residues, the relative, importance of various features of the tricycle, and the importance of the, linker.

About this StructureAbout this Structure

1RWX is a Protein complex structure of sequences from Homo sapiens with as ligand. Active as Caspase-1, with EC number 3.4.22.36 Full crystallographic information is available from OCA.

ReferenceReference

Tethering identifies fragment that yields potent inhibitors of human caspase-1., Fahr BT, O'Brien T, Pham P, Waal ND, Baskaran S, Raimundo BC, Lam JW, Sopko MM, Purkey HE, Romanowski MJ, Bioorg Med Chem Lett. 2006 Feb;16(3):559-62. Epub 2005 Nov 4. PMID:16274992

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