Literature DB >> 17996738

Analysis of the minimal specificity of CED-3 using a yeast transcriptional reporter system.

Sarah J Westein1, Fiona L Scott, Christine J Hawkins.   

Abstract

Determination of the substrate specificity of site-specific proteases helps define their physiological roles. We developed a yeast-based system for defining the minimal substrate specificity of site-specific proteases, within the context of a protein. Using this system, we characterized the P4-P1 substrate specificity of the nematode apoptotic caspase CED-3. Apart from an absolute requirement for aspartate at the P1 position, CED-3 is a relatively promiscuous caspase capable of cleaving substrates bearing many amino acids at P4-P2 sites.

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Year:  2007        PMID: 17996738     DOI: 10.1016/j.bbamcr.2007.10.003

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  2 in total

1.  Analysis of the minimal specificity of caspase-2 and identification of Ac-VDTTD-AFC as a caspase-2-selective peptide substrate.

Authors:  Tanja Kitevska; Sarah J Roberts; Delara Pantaki-Eimany; Sarah E Boyd; Fiona L Scott; Christine J Hawkins
Journal:  Biosci Rep       Date:  2014-04-01       Impact factor: 3.840

2.  Versatile assays for high throughput screening for activators or inhibitors of intracellular proteases and their cellular regulators.

Authors:  Hideki Hayashi; Michael Cuddy; Vincent Chih-Wen Shu; Kenneth W Yip; Charitha Madiraju; Paul Diaz; Toshifumi Matsuyama; Muneshige Kaibara; Kohtaro Taniyama; Stefan Vasile; Eduard Sergienko; John C Reed
Journal:  PLoS One       Date:  2009-10-30       Impact factor: 3.240

  2 in total

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