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Entropy-driven cAMP-dependent Allosteric Control...
Journal article

Entropy-driven cAMP-dependent Allosteric Control of Inhibitory Interactions in Exchange Proteins Directly Activated by cAMP*

Abstract

Exchange proteins directly activated by cAMP (EPACs) are guanine nucleotide-exchange factors for the small GTPases Rap1 and Rap2 and represent a key receptor for the ubiquitous cAMP second messenger in eukaryotes. The cAMP-dependent activation of apoEPAC is typically rationalized in terms of a preexisting equilibrium between inactive and active states. Structural and mutagenesis analyses have shown that one of the critical determinants of the …

Authors

Das R; Mazhab-Jafari MT; Chowdhury S; SilDas S; Selvaratnam R; Melacini G

Journal

Journal of Biological Chemistry, Vol. 283, No. 28, pp. 19691–19703

Publisher

Elsevier

Publication Date

July 2008

DOI

10.1074/jbc.m802164200

ISSN

0021-9258