Predicting the open conformations of protein kinases using molecular dynamics simulations

DC FieldValueLanguage
dc.contributor.authorBjarnadottir, Una-
dc.contributor.authorNielsen, Jens Erik-
dc.date.accessioned2011-10-14T14:28:23Z-
dc.date.available2011-10-14T14:28:23Z-
dc.date.copyright2011 Wiley Periodicals, Inc.en
dc.date.issued2012-01-
dc.identifier.citationBiopolymersen
dc.identifier.issn1097-0282-
dc.identifier.urihttp://hdl.handle.net/10197/3230-
dc.description.abstractProtein kinases (PK) control phosphorylation in eukaryotic cells, and thereby regulate metabolic pathways, cell cycle progression, apoptosis and transcription. Consequently there is significant interest in manipulating PK activity and treat diseases by using small-molecule drugs. All PK catalytic domains undergo large conformational changes as a result of substrate binding and phosphorylation. The “closed” state of a PK cataltic domain is the only state able to phosphorylate the target substrate, which makes the two other observed states (the “open” and the “intermediate” states) interesting drug targets. We investigate if MD simulations starting from the closed state of the catalytic domain of protein kinase A (C-PKA) can be used to produce realistic structures representing the intermediate and/or open conformation of C-PKA, since this would allow for drug docking calculations and drug design using MD snapshots. We perform 36 ten-nanosecond MD simulations starting from the closed conformation (PDB ID: 1ATP) of C-PKA in various liganded and phosphorylated states. The results show that MD simulations are capable of reproducing the open conformation of C-PKA with good accuracy within 1 ns of simulation as measured by Cα RMSDs and RMSDs of atoms defining the ATPbinding pocket. Importantly we are able to show that even without knowledge of the structure of the open form of C-PKA, we can identify the MD snapshots resembling the open conformation most using the open structure of a different protein kinase displaying only 23% sequence identity to C-PKA.en
dc.description.sponsorshipScience Foundation Irelanden
dc.description.sponsorshipHealth Research Boarden
dc.format.extent1244382 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoenen
dc.publisherWiley-Blackwellen
dc.relation.requiresConway Institute Research Collectionen
dc.rightsThis is the pre-peer reviewed version of the following article: Bjarnadottir, U. and Nielsen, J. E. (2011), Predicting the open conformations of protein kinases using molecular dynamics simulations. Biopolymers. doi: 10.1002/bip.21704 which has been published in final form at http://onlinelibrary.wiley.com/doi/10.1002/bip.21704/abstracten
dc.subjectProtein kinaseen
dc.subjectActivation processen
dc.subjectMolecular dynamics simulationsen
dc.subjectConformational changeen
dc.subjectProtein Dynamicsen
dc.subject.lcshProtein kinasesen
dc.subject.lcshMolecular dynamicsen
dc.subject.lcshProteins--Conformationen
dc.subject.meshProtein Kinasesen
dc.subject.meshProtein Conformationen
dc.subject.meshMolecular Dynamics Simulationen
dc.titlePredicting the open conformations of protein kinases using molecular dynamics simulationsen
dc.title.alternativeMD simulations of C-PKAen
dc.typeJournal Articleen
dc.internal.availabilityFull text availableen
dc.internal.webversionshttp://dx.doi.org/10.1002/bip.21704-
dc.statusPeer revieweden
dc.identifier.volume97en
dc.identifier.issue1en
dc.identifier.startpage65en
dc.identifier.endpage72en
dc.identifier.doi10.1002/bip.21704-
dc.neeo.contributorBjarnadottir|Una|aut|-
dc.neeo.contributorNielsen|Jens Erik|aut|-
dc.description.adminab,ke,SB-09/09/2011en
item.grantfulltextopen-
item.fulltextWith Fulltext-
Appears in Collections:Conway Institute Research Collection
Biomolecular and Biomedical Science Research Collection
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