Display Settings:

Format

Send to:

Choose Destination
    Nat Struct Biol. 1996 Jul;3(7):619-25.

    The three-dimensional structure of apopain/CPP32, a key mediator of apoptosis.

    Source

    Department of Biochemistry, Merck Research Laboratories, Rahway, New Jersey 07065-0900, USA.

    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.

    PMID:
    8673606
    [PubMed - indexed for MEDLINE]

      Supplemental Content

      Save items

      loading

      Structures reported by this article

      Recent activity

      Your browsing activity is empty.

      Activity recording is turned off.

      Turn recording back on

      See more...
      Write to the Help Desk