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dc.contributor.authorThwaites, Tristan
dc.contributor.authorNogueira, Ana T
dc.contributor.authorCampeotto, Ivan
dc.contributor.authorSilva, Ana P
dc.contributor.authorGrieshaber, Scott S
dc.contributor.authorCarabeo, Rey A
dc.date.accessioned2015-02-06T14:40:02Z
dc.date.available2015-02-06T14:40:02Z
dc.date.issued2014-10-31
dc.identifier.citationThwaites , T , Nogueira , A T , Campeotto , I , Silva , A P , Grieshaber , S S & Carabeo , R A 2014 , ' The Chlamydia Effector TarP Mimics the Mammalian LD Motif of Paxillin to Subvert the Focal Adhesion Kinase During Invasion ' The Journal of Biological Chemistry , vol. 289 , no. 44 , pp. 30426-30442 . DOI: 10.1074/jbc.M114.604876en
dc.identifier.issn0021-9258
dc.identifier.otherPURE: 42064604
dc.identifier.otherPURE UUID: c1342a83-cb53-4cd3-95d3-2273c9a32a12
dc.identifier.otherPubMed: 25193659
dc.identifier.otherScopus: 84908592806
dc.identifier.urihttp://hdl.handle.net/2164/4247
dc.descriptionCopyright © 2014, The American Society for Biochemistry and Molecular Biology. This work was supported by the Medical Research Council and the University of Aberdeen Knowledge Exchange and Transfer Fund (to R. A. C.).en
dc.format.extent17en
dc.language.isoeng
dc.relation.ispartofThe Journal of Biological Chemistryen
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/3.0/en
dc.subjectactinen
dc.subjectbacterial pathogenesisen
dc.subjectcell biologyen
dc.subjectchlamydiaen
dc.subjectPTK2 protein-tyrosine kinase 2 (PTK2) (focal adhesion kinase (FAK)en
dc.subjectsignalingen
dc.subjectvirulence factoren
dc.subjectQH301 Biologyen
dc.subjectMedical Research Council (MRC)en
dc.subjectG0900213en
dc.subject.lccQH301en
dc.titleThe Chlamydia Effector TarP Mimics the Mammalian LD Motif of Paxillin to Subvert the Focal Adhesion Kinase During Invasionen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen, Medical Sciencesen
dc.description.statusPeer revieweden
dc.description.versionPublisher PDFen
dc.identifier.doihttps://doi.org/10.1074/jbc.M114.604876


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