Journal article
Mapping the Free Energy Landscape of PKA Inhibition and Activation: A Double-Conformational Selection Model for the Tandem cAMP-Binding Domains of PKA RIα
Abstract
Protein Kinase A (PKA) is the major receptor for the cyclic adenosine monophosphate (cAMP) secondary messenger in eukaryotes. cAMP binds to two tandem cAMP-binding domains (CBD-A and -B) within the regulatory subunit of PKA (R), unleashing the activity of the catalytic subunit (C). While CBD-A in RIα is required for PKA inhibition and activation, CBD-B functions as a "gatekeeper" domain that modulates the control exerted by CBD-A. Preliminary …
Authors
Akimoto M; McNicholl ET; Ramkissoon A; Moleschi K; Taylor SS; Melacini G
Journal
PLOS Biology, Vol. 13, No. 11,
Publisher
Public Library of Science (PLoS)
DOI
10.1371/journal.pbio.1002305
ISSN
1544-9173
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
Amino Acid SubstitutionAnimalsBinding SitesCattleCyclic AMPCyclic AMP-Dependent Protein Kinase Catalytic SubunitsCyclic AMP-Dependent Protein Kinase RIalpha SubunitCyclic AMP-Dependent Protein KinasesEnergy TransferEnzyme ActivationGene DeletionMiceModels, MolecularMutationPeptide FragmentsProtein ConformationProtein Interaction Domains and MotifsProtein Interaction MappingRecombinant Fusion ProteinsTandem Repeat Sequences