ArticleProtein science : a publication of the Protein Society2009
CPDadh: a new peptidase family homologous to the cysteine protease domain in bacterial MARTX toxins.
Article in Protein science : a publication of the Protein Society, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Host S-nitrosylation inhibits clostridial small molecule-activated glucosylating toxins.Nature medicine · 2011Article
- Inositol hexakisphosphate-induced autoprocessing of large bacterial protein toxins.PLoS pathogens · 2010Review
- Structure-function analysis of inositol hexakisphosphate-induced autoprocessing in Clostridium difficile toxin A.The Journal of biological chemistry · 2009Article
- Review
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Authors and funding
4 authors.
Funding
Abstract
A cysteine protease domain (CPD) has been recently discovered in a group of multifunctional, autoprocessing RTX toxins (MARTX) and Clostridium difficile toxins A and B. These CPDs (referred to as CPDmartx) autocleave the toxins to release domains with toxic effects inside host cells. We report identification and computational analysis of CPDadh, a new cysteine peptidase family homologous to CPDmartx. CPDadh and CPDmartx share a Rossmann-like structural core and conserved catalytic residues. In bacteria, domains of the CPDadh family are present at the N-termini of a diverse group of putative cell-cell interaction proteins and at the C-termini of some RHS (recombination hot spot) proteins. In eukaryotes, catalytically inactive members of the CPDadh family are found in cell surface protein NELF (nasal embryonic LHRH factor) and some putative signaling proteins.
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Registered trials
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