How bacterial ADP-ribosylating toxins recognize substrates
- 15 August 2004
- journal article
- research article
- Published by Springer Nature in Nature Structural & Molecular Biology
- Vol. 11 (9) , 868-876
- https://doi.org/10.1038/nsmb818
Abstract
ExoS and ExoT are bifunctional type III cytotoxins of Pseudomonas aeruginosa that contain an N-terminal RhoGAP domain and a C-terminal ADP-ribosylation domain. Although they share 76% amino acid identity, ExoS and ExoT ADP-ribosylate different substrates. Using protein modeling and site-directed mutagenesis, the regions of ExoS and ExoT that define substrate specificity were determined. Regions B (active site loop), C (ARTT motif) and E (PN loop) on ExoS are necessary and sufficient to recognize ExoS targets, whereas regions B, C and E on ExoT are necessary but not sufficient to recognize ExoT targets, such as the Crk proteins. A specific Crk recognition motif on ExoT was defined as region A (helix α1). The electrostatic properties of regions A, B, C and E define the substrate specificity of ExoS and ExoT and these interactions can explain how other bacterial ADP-ribosylating toxins recognize their unique substrates.Keywords
This publication has 42 references indexed in Scilit:
- The Crystal Structure of C3stau2 from Staphylococcus aureus and Its Complex with NADJournal of Biological Chemistry, 2003
- SWISS-MODEL: an automated protein homology-modeling serverNucleic Acids Research, 2003
- NAD Binding Induces Conformational Changes in Rho ADP-ribosylating Clostridium botulinum C3 ExoenzymeJournal of Biological Chemistry, 2002
- Refined crystallographic structure of Pseudomonas aeruginosa exotoxin A and its implications for the molecular mechanism of toxicity 1 1Edited by D. ReesJournal of Molecular Biology, 2001
- Crystal structure and novel recognition motif of Rho ADP-ribosylating C3 exoenzyme from Clostridium botulinum: structural insights for recognition specificity and catalysisJournal of Molecular Biology, 2001
- Pseudomonas aeruginosa ExoT Is a Rho GTPase-Activating ProteinInfection and Immunity, 2000
- SWISS‐MODEL and the Swiss‐Pdb Viewer: An environment for comparative protein modelingElectrophoresis, 1997
- Identification of Glutamic Acid 381 as a Candidate Active Site Residue of Pseudomonas aeruginosa Exoenzyme SBiochemistry, 1996
- Refined Structure of Escherichia coli Heat-labile Enterotoxin, a Close Relative of Cholera ToxinJournal of Molecular Biology, 1993
- Comparison of the B-pentamers of heat-labile enterotoxin and verotoxin-1: two structures with remarkable similarity and dissimilarityBiochemistry, 1993