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Structural Basis for Cyclic-Nucleotide Selectivity...
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