Molecular dynamics simulations of an apoliprotein A-I derived peptide in explicit water

dc.contributor.authorΣταυρακούδης, Αθανάσιοςel
dc.date.accessioned2015-11-24T17:04:18Z
dc.date.available2015-11-24T17:04:18Z
dc.identifier.issn0009-2614-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/11156
dc.rightsDefault Licence-
dc.subjectmicroscopic viewen
dc.subjectalpha-helixen
dc.subjectpi-helixen
dc.subjectewalden
dc.subjectpropagationen
dc.subjecttransitionsen
dc.subjectproteinsen
dc.titleMolecular dynamics simulations of an apoliprotein A-I derived peptide in explicit wateren
heal.abstractMolecular dynamics simulations have been performed for the 104-117 alpha-helical fragment of apoliprotein A-I using the CHARMM22 force field and the NAMD simulation engine. Simulation ( 50 ns in explicit water) resulted in significant appearance of pi-helix conformation, which was totally diminished when the CMAP correction of the CHARMM force field was applied. This is consistent with other similar studies which suggest that the observation of pi-helix in peptide conformation was force field biased rather actually existed. This study suggests that the 104-117 fragment of apoliprotein A-I has a stable alpha-helical conformation in water. (C) 2008 Elsevier B.V. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.cplett.2008.07.007-
heal.identifier.secondary<Go to ISI>://000258395300026-
heal.journalNameChemical Physics Lettersen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2008-
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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