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dc.creatorGuimarães, Ana Paula-
dc.creatorRamalho, Teodorico Castro-
dc.creatorFrança, Tanos Celmar Costa-
dc.date.accessioned2020-05-24T22:42:41Z-
dc.date.available2020-05-24T22:42:41Z-
dc.date.issued2014-
dc.identifier.citationGUIMARÃES, A. P.; RAMALHO, T. C.; FRANÇA, T. C. C. Preventing the return of smallpox: molecular modeling studies on thymidylate kinase from Variola virus. Journal of Biomolecular Structure & Dynamics, [S.l.], v. 32, n. 10, p. 1601-1612, 2014. DOI: 10.1080/07391102.2013.830578.pt_BR
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/07391102.2013.830578pt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/41183-
dc.description.abstractSmallpox was one of the most devastating diseases in the human history and still represents a serious menace today due to its potential use by bioterrorists. Considering this threat and the non-existence of effective chemotherapy, we propose the enzyme thymidylate kinase from Variola virus (VarTMPK) as a potential target to the drug design against smallpox. We first built a homology model for VarTMPK and performed molecular docking studies on it in order to investigate the interactions with inhibitors of Vaccinia virus TMPK (VacTMPK). Subsequently, molecular dynamics (MD) simulations of these compounds inside VarTMPK and human TMPK (HssTMPK) were carried out in order to select the most promising and selective compounds as leads for the design of potential VarTMPK inhibitors. Results of the docking and MD simulations corroborated to each other, suggesting selectivity towards VarTMPK and, also, a good correlation with the experimental data.pt_BR
dc.languageen_USpt_BR
dc.publisherTaylor & Francispt_BR
dc.rightsrestrictAccesspt_BR
dc.sourceJournal of Biomolecular Structure & Dynamicspt_BR
dc.subjectSmallpoxpt_BR
dc.subjectVariola viruspt_BR
dc.subjectThymidylate kinasept_BR
dc.subjectDockingpt_BR
dc.subjectMolecular dynamicspt_BR
dc.titlePreventing the return of smallpox: molecular modeling studies on thymidylate kinase from Variola viruspt_BR
dc.typeArtigopt_BR
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