| Literature DB >> 8673606 |
J Rotonda1, D W Nicholson, K M Fazil, M Gallant, Y Gareau, M Labelle, E P Peterson, D M Rasper, R Ruel, J P Vaillancourt, N A Thornberry, J W Becker.
Abstract
Cysteine proteases related to mammalian interleukin-1 beta converting enzyme (ICE) and to its Caenorhabditis elegans homologue, CED-3, play a critical role in the biochemical events that culminate in apoptosis. We have determined the three-dimensional structure of a complex of the human CED-3 homologue CPP32/apopain with a potent tetrapeptide-aldehyde inhibitor. The protein resembles ICE in overall structure, but its S4 subsite is strikingly different in size and chemical composition. These differences account for the variation in specificity between the ICE- and CED-3-related proteases and enable the design of specific inhibitors that can probe the physiological functions of the proteins and disease states with which they are associated.Entities:
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Year: 1996 PMID： 8673606 DOI： 10.1038/nsb0796-619
Source DB: PubMed Journal: Nat Struct Biol ISSN： 1072-8368