Journal article
Structural Basis for Cyclic-Nucleotide Selectivity and cGMP-Selective Activation of PKG I
Abstract
Cyclic guanosine monophosphate (cGMP) and cyclic AMP (cAMP)-dependent protein kinases (PKG and PKA) are closely related homologs, and the cyclic nucleotide specificity of each kinase is crucial for keeping the two signaling pathways segregated, but the molecular mechanism of cyclic nucleotide selectivity is unknown. Here, we report that the PKG Iβ C-terminal cyclic nucleotide binding domain (CNB-B) is highly selective for cGMP binding, and we …
Authors
Huang GY; Kim JJ; Reger AS; Lorenz R; Moon E-W; Zhao C; Casteel DE; Bertinetti D; VanSchouwen B; Selvaratnam R
Journal
Structure, Vol. 22, No. 1, pp. 116–124
Publisher
Elsevier
Publication Date
January 2014
DOI
10.1016/j.str.2013.09.021
ISSN
0969-2126
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
Amino Acid SequenceArginineBinding SitesCatalytic DomainCrystallography, X-RayCyclic AMPCyclic GMPCyclic GMP-Dependent Protein Kinase Type IEscherichia coliGene ExpressionHEK293 CellsHumansKineticsLeucineModels, MolecularMolecular Sequence DataMutagenesis, Site-DirectedProtein BindingRecombinant ProteinsSequence AlignmentThermodynamics