The structure of the pro-apoptotic protease granzyme B reveals the molecular determinants of its specificity
Granzyme B is a serine protease of the chymotrypsin fold that mediates cell death by cytotoxic lymphocytes. It is a processing enzyme, requiring extended peptide substrates containing an Asp residue. The determinants that allow for this substrate specificity are revealed in the three-dimensional str...
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Veröffentlicht in: | Nature Structural Biology 2000-09, Vol.7 (9), p.762-765 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Granzyme B is a serine protease of the chymotrypsin fold that mediates cell death by cytotoxic lymphocytes. It is a processing enzyme, requiring extended peptide substrates containing an Asp residue. The determinants that allow for this substrate specificity are revealed in the three-dimensional structure of granzyme B in complex with a macromolecular inhibitor. The primary specificity for Asp occurs through a side-on interaction with Arg 226, a buried Arg side chain of granzyme B. An additional nine amino acids make contact with the substrate and define the granzyme B extended substrate specificity profile. The substrate determinants found in this structure are shared by other members of this protein class and help to reveal the properties that define substrate specificity. |
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ISSN: | 1072-8368 1545-9993 1545-9985 |
DOI: | 10.1038/78992 |