Publication:
Mode coupling points to functionally important residues in myosin II

dc.contributor.departmentDepartment of Computer Engineering
dc.contributor.departmentDepartment of Chemical and Biological Engineering
dc.contributor.departmentDepartment of Physics
dc.contributor.kuauthorVarol, Onur
dc.contributor.kuauthorYüret, Deniz
dc.contributor.kuauthorErman, Burak
dc.contributor.kuauthorKabakçıoğlu, Alkan
dc.contributor.kuprofileFaculty Member
dc.contributor.kuprofileFaculty Member
dc.contributor.kuprofileFaculty Member
dc.contributor.otherDepartment of Computer Engineering
dc.contributor.otherDepartment of Chemical and Biological Engineering
dc.contributor.otherDepartment of Physics
dc.contributor.schoolcollegeinstituteGraduate School of Sciences and Engineering
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.contributor.yokidN/A
dc.contributor.yokid179996
dc.contributor.yokid179997
dc.contributor.yokid49854
dc.date.accessioned2024-11-09T11:45:30Z
dc.date.issued2014
dc.description.abstractRelevance of mode coupling to energy/information transfer during protein function, particularly in the context of allosteric interactions is widely accepted. However, existing evidence in favor of this hypothesis comes essentially from model systems. We here report a novel formal analysis of the near-native dynamics of myosin II, which allows us to explore the impact of the interaction between possibly non-Gaussian vibrational modes on fluctutational dynamics. We show that an information-theoretic measure based on mode coupling alone yields a ranking of residues with a statistically significant bias favoring the functionally critical locations identified by experiments on myosin II.
dc.description.fulltextYES
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue9
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuTÜBİTAK
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TÜBİTAK)
dc.description.sponsorshipNational Center for High Performance Computing of Turkey (UYBHM)
dc.description.versionAuthor's final manuscript
dc.description.volume82
dc.formatpdf
dc.identifier.doi10.1002/prot.24531
dc.identifier.eissn1097-0134
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR00276
dc.identifier.issn0887-3585
dc.identifier.linkhttps://doi.org/10.1002/prot.24531
dc.identifier.quartileQ3
dc.identifier.scopus2-s2.0-84906320335
dc.identifier.urihttps://hdl.handle.net/20.500.14288/474
dc.identifier.wos340940300009
dc.keywordsMode coupling
dc.keywordsMolecular dynamics
dc.keywordsAnharrnoincity
dc.keywordsAllostery
dc.keywordsMyosin II
dc.languageEnglish
dc.publisherWiley
dc.relation.grantnoMFAG-113F092
dc.relation.grantno4001752012
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/1301
dc.sourceProteins-Structure Function and Bioinformatics
dc.subjectBiochemistry and molecular biology
dc.subjectBiophysics
dc.titleMode coupling points to functionally important residues in myosin II
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authoridN/A
local.contributor.authorid0000-0002-7039-0046
local.contributor.authorid0000-0002-2496-6059
local.contributor.authorid0000-0002-9831-3632
local.contributor.kuauthorVarol, Onur
local.contributor.kuauthorYüret, Deniz
local.contributor.kuauthorErman, Burak
local.contributor.kuauthorKabakçıoğlu, Alkan
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relation.isOrgUnitOfPublication.latestForDiscovery89352e43-bf09-4ef4-82f6-6f9d0174ebae

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