Insights into the structure of the PmrD protein with molecular dynamics simulations

dc.contributor.authorTatsis, V. A.en
dc.contributor.authorTsoulos, I. G.en
dc.contributor.authorKrinas, C. S.en
dc.contributor.authorAlexopoulos, C.en
dc.contributor.authorΣταυρακούδης, Αθανάσιοςel
dc.date.accessioned2015-11-24T17:04:26Z
dc.date.available2015-11-24T17:04:26Z
dc.identifier.issn0141-8130-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/11176
dc.rightsDefault Licence-
dc.subjectbeta-barrelen
dc.subjectcomputer simulationen
dc.subjectleucine-rich hydrophobic clusteren
dc.subjectmolecular dynamicsen
dc.subjectpolymyxin resistanceen
dc.subjectpmrden
dc.subjectpeptideen
dc.subjectwateren
dc.subjectorientationen
dc.subjectsystemen
dc.subjectforceen
dc.subjectewalden
dc.titleInsights into the structure of the PmrD protein with molecular dynamics simulationsen
heal.abstractResistance to cationic antimicrobial peptide polymyxin B from Gram-negative bacteria is accomplished by two-component systems (TCSs), protein complexes PmrA/PmrB and PhoP/PhoQ. PmrD is the first protein identified to mediate the connectivity between two TCSs. The 3D structure of PmrD has been recently solved by NMR and its unique fold was revealed. Here, a molecular dynamics study is presented started from the NMR structure. Numerous hydrophobic and electrostatic interactions were identified to contribute to PmrD's 3D stability. Moreover, the mobility of the five loops that connect the protein's six beta-strands has been explored. Solvent-accessible surface area calculation revealed that a Leucine-rich hydrophobic cluster of the protein stabilized the protein's structure. (C) 2009 Elsevier B.V. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.ijbiomac.2009.02.006-
heal.identifier.secondary<Go to ISI>://000266712500003-
heal.journalNameInt J Biol Macromolen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2009-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Οικονομικών και Κοινωνικών Επιστημών. Τμήμα Οικονομικών Επιστημώνel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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