AMPylation of Rho GTPases by Vibrio VopS disrupts effector binding and downstream signaling.

Article Details

Citation

Yarbrough ML, Li Y, Kinch LN, Grishin NV, Ball HL, Orth K

AMPylation of Rho GTPases by Vibrio VopS disrupts effector binding and downstream signaling.

Science. 2009 Jan 9;323(5911):269-72. doi: 10.1126/science.1166382. Epub 2008 Nov 27.

PubMed ID
19039103 [ View in PubMed
]
Abstract

The Vibrio parahaemolyticus type III effector VopS is implicated in cell rounding and the collapse of the actin cytoskeleton by inhibiting Rho guanosine triphosphatases (GTPases). We found that VopS could act to covalently modify a conserved threonine residue on Rho, Rac, and Cdc42 with adenosine 5'-monophosphate (AMP). The resulting AMPylation prevented the interaction of Rho GTPases with downstream effectors, thereby inhibiting actin assembly in the infected cell. Eukaryotic proteins were also directly modified with AMP, potentially expanding the repertoire of posttranslational modifications for molecular signaling.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Ras-related C3 botulinum toxin substrate 1P63000Details
Transforming protein RhoAP61586Details
Cell division control protein 42 homologP60953Details