Editorials: Cell Cycle Features
Plugging PKA into ERK scaffolds
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Volume 10, Issue 5 March 1, 2011
Pages 731 - 732
http://dx.doi.org/10.4161/cc.10.5.14902
Keywords: AKAP, cancer, kinase, network, scaffold, signaling
Authors: F. Donelson Smith, Lorene K. Langeberg and John D. Scott
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- F. Donelson Smith
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Corresponding author: smithdon@uw.edu
Howard Hughes Medical Institute; Department of Pharmacology; University of Washington School of Medicine; Seattle, WA USA
- Lorene K. Langeberg
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Howard Hughes Medical Institute; Department of Pharmacology; University of Washington School of Medicine; Seattle, WA USA
- John D. Scott
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Corresponding author: scottjdw@uw.edu
Howard Hughes Medical Institute; Department of Pharmacology; University of Washington School of Medicine; Seattle, WA USA
Abstract:
Cancers often arise in part through derangements in protein kinase signaling. A striking example of this is the finding that approximately 30% of human tumors have mutations in Ras or B-Raf, leading to aberrant ERK kinase activation. Kinase signaling networks are often organized by scaffolding and anchoring proteins that help shape the dynamics of signal processing. AKAP-Lbc associates with the ERK scaffold protein KSR-1 to organize a growth factor and cAMP responsive signaling network. AKAP-Lbc also directs PKA phosphorylation of KSR-1 on a critical residue to ensure maximal signaling efficiency.
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