|PROSITE documentation PDOC51771 [for PROSITE entry PS51771]|
Large bacterial protein toxins autotranslocate functional effector domains to the eukaryotic cell cytosol, resulting in alterations to cellular functions that ultimately benefit the infecting pathogen. Among these toxins, the clostridial glucosylating toxins (CGTs) produced by Gram-positive bacteria and the multifunctional-autoprocessing RTX (MARTX) toxins of Gram-negative bacteria have distinct mechanisms of post-translocation, but a shared mechanism of post-translocation autoprocessing that releases these functional domains from the large holotoxins. These toxins carry an embedded cysteine protease domain (CPD) that is regulated by a unique allosteric activation mechanism. Binding of the eukaryotic-specific small molecule inositol hexakisphosphate (InsP(6)) to a basic cleft within the CPD induces a structural rearrangement that exposes the protease active site to its substrates. The CGT and MARTX toxin CPDs form peptidase family C80 [E1] of clan CD [1,2,3,4].
The CGT/MARTX CPD domain consists of a central β-sheet that is surrounded by α-helices. Additional β-strands at the C-terminus form a subdomain known as the β-flap, that is loosely attached to the core protease (see <PDB:3EEB>). The CGT/MARTX CPD catalytic dyad is composed of one His and one Cys residue. The distance between the catalytic residues indicates that the Cys is not activated by protonation from His, but rather suggests that the Cys is substrate-activated by close alignment of the scissile bond, while the His functions solely to protonate the leaving group [1,3,4].
Some proteins known to contain a CGT/MARTX CPD domain are listed below:
The profile we developed covers the entire CGT/MARTX CPD domain.Last update:
August 2015 / First entry.
PROSITE method (with tools and information) covered by this documentation:
|1||Authors||Egerer M. Satchell K.J.F.|
|Title||Inositol hexakisphosphate-induced autoprocessing of large bacterial protein toxins.|
|Source||PLoS Pathog. 6:E1000942-E1000942(2010).|
|2||Authors||Sheahan K.-L. Cordero C.L. Satchell K.J.F.|
|Title||Autoprocessing of the Vibrio cholerae RTX toxin by the cysteine protease domain.|
|Source||EMBO J. 26:2552-2561(2007).|
|3||Authors||Lupardus P.J. Shen A. Bogyo M. Garcia K.C.|
|Title||Small molecule-induced allosteric activation of the Vibrio cholerae RTX cysteine protease domain.|
|4||Authors||Shen A. Lupardus P.J. Albrow V.E. Guzzetta A. Powers J.C. Garcia K.C. Bogyo M.|
|Title||Mechanistic and structural insights into the proteolytic activation of Vibrio cholerae MARTX toxin.|
|Source||Nat. Chem. Biol. 5:469-478(2009).|