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dc.contributor.authorBann, James G.
dc.date.accessioned2012-04-18T14:48:10Z
dc.date.available2012-04-18T14:48:10Z
dc.date.issued2012-01
dc.identifier.citationBann, James G. 2012. “Anthrax toxin protective antigenuInsights into molecular switching from prepore to pore”. Protein Science.21 (1):1-12.en_US
dc.identifier.issn0961-8368
dc.identifier.issn1469-896X
dc.identifier.urihttp://hdl.handle.net/10057/5080
dc.identifier.urihttp://dx.doi.org/10.1002/pro.752
dc.descriptionClick on the DOI link below to access the article (may not be free).en_US
dc.description.abstractThe protective antigen is a key component of the anthrax toxin, as it allows entry of the enzymatic components edema factor and lethal factor into the host cell, through the formation of a membrane spanning pore. This event is absolutely critical for the pathogenesis of anthrax, and although we have yet to understand the mechanism of pore formation, recent developments have provided key insights into how this process may occur. Based on the available data, a model is proposed for the kinetic steps for protective antigen conversion from prepore to pore. In this model, the driving force for pore formation is the formation of the phi clamp, a region that forms a leak-free seal around the translocating polypeptide. Formation of the phi clamp elicits movements within the prepore that provide steric freedom for the subsequent conformational changes required to form the membrane spanning pore.en_US
dc.language.isoen_USen_US
dc.publisherCambridge University Pressen_US
dc.relation.ispartofseriesProtein Science;2012:, v.21, no.1
dc.titleAnthrax toxin protective antigenuInsights into molecular switching from prepore to poreen_US
dc.typeArticleen_US
dc.description.versionPeer reviewed
dc.rights.holderCopyright © 2011 The Protein Society


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