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Cascleave 2.0, a new approach for predicting caspase and granzyme cleavage targets
Author(s) -
Mingjun Wang,
XingMing Zhao,
Hao Tan,
Tatsuya Akutsu,
James C. Whisstock,
Jiangning Song
Publication year - 2013
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btt603
Subject(s) - caspase , proteases , granzyme , cleavage (geology) , granzyme b , computational biology , biology , deubiquitinating enzyme , computer science , microbiology and biotechnology , programmed cell death , apoptosis , biochemistry , enzyme , cytotoxic t cell , in vitro , ubiquitin , paleontology , fracture (geology) , perforin , gene
Caspases and granzyme B (GrB) are important proteases involved in fundamental cellular processes and play essential roles in programmed cell death, necrosis and inflammation. Although a number of substrates for both types have been experimentally identified, the complete repertoire of caspases and granzyme B substrates remained to be fully characterized. Accordingly, systematic bioinformatics studies of known cleavage sites may provide important insights into their substrate specificity and facilitate the discovery of novel substrates.

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