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Identification of a molecular target for the Yersinia protein kinase A.
Umeå University, Faculty of Science and Technology, Molecular Biology (Faculty of Science and Technology). (Wolf-Watz)
Umeå University, Faculty of Science and Technology, Molecular Biology (Faculty of Science and Technology). (Wolf-Watz)
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2007 (English)In: Mol Cell, ISSN 1097-2765, Vol. 26, no 4, 465-77 p.Article in journal (Refereed) Published
Abstract [en]

Pathogenic bacteria of the genus Yersinia employ a type III secretion system to inject bacterial effector proteins directly into the host cytosol. One of these effectors, the Yersinia serine/threonine protein kinase YpkA, is an essential virulence determinant involved in host actin cytoskeletal rearrangements and in inhibition of phagocytosis. Here we report that YpkA inhibits multiple Galphaq signaling pathways. The kinase activity of YpkA is required for Galphaq inhibition. YpkA phosphorylates Ser47, a key residue located in the highly conserved diphosphate binding loop of the GTPase fold of Galphaq. YpkA-mediated phosphorylation of Ser47 impairs guanine nucleotide binding by Galphaq. Y. pseudotuberculosis expressing wild-type YpkA, but not a catalytically inactive YpkA mutant, interferes with Galphaq-mediated signaling pathways. Identification of a YpkA-mediated phosphorylation site in Galphaq sheds light on the contribution of the kinase activity of YpkA to Yersinia pathogenesis.

Place, publisher, year, edition, pages
2007. Vol. 26, no 4, 465-77 p.
Keyword [en]
Actins/physiology, Bacterial Proteins/metabolism, Cell Line, Cyclic AMP-Dependent Protein Kinases/genetics/*metabolism, GTP-Binding Protein alpha Subunits; Gq-G11/metabolism/*physiology, Humans, Kidney, Phosphorylation, Phosphoserine/metabolism, Protein Binding, Recombinant Fusion Proteins/metabolism, Signal Transduction/*physiology, Stress; Mechanical, Transfection, Yersinia enterocolitica/enzymology/*physiology, Yersinia pestis/enzymology/*physiology, rhoA GTP-Binding Protein/metabolism
URN: urn:nbn:se:umu:diva-16674PubMedID: 17531806OAI: diva2:156347
Available from: 2007-10-08 Created: 2007-10-08 Last updated: 2011-01-11Bibliographically approved

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Nordfelth, RolandWolf-Watz, Hans
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Molecular Biology (Faculty of Science and Technology)

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