Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2050561 | FEBS Letters | 2007 | 5 Pages |
Abstract
Metacaspases are cysteine peptidases that are distantly related to the caspases, for which proteolytic processing is central to their activation. Here, we show that recombinant metacaspase 2 (MCA2) from Trypanosoma brucei has arginine/lysine-specific, Ca2+-dependent proteolytic activity. Autocatalytic processing of MCA2 occurred after Lys55 and Lys268; however, this was shown not to be required for the enzyme to be proteolytically active. The necessity of Ca2+, but not processing, for MCA2 enzymatic activity clearly distinguishes MCA2 from the caspases and would be consistent with different physiological roles.
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Authors
Catherine X. Moss, Gareth D. Westrop, Luiz Juliano, Graham H. Coombs, Jeremy C. Mottram,