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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Mcculloch, Andrew D. Boras, Britton W. Kornev, Alexandr Taylor, Susan S. |
| Description | Author Affiliation: Boras BW ( From the Departments of Bioengineering.); Kornev A ( Chemistry and Biochemistry.); Taylor SS ( Chemistry and Biochemistry, Pharmacology, and.); McCulloch AD ( From the Departments of Bioengineering, Medicine, University of California, San Diego, La Jolla, California 92093 amcculloch@ucsd.edu.) |
| Abstract | Protein kinase A (PKA) holoenzyme consists of two catalytic (C) subunits and a regulatory (R) subunit dimer (R(2)C(2)). The kinase is activated by the binding of cAMPs to the two cyclic nucleotide binding domains (CBDs), A and B, on each R-subunit. Despite extensive study, details of the allosteric mechanisms underlying the cooperativity of holoenzyme activation remain unclear. Several Markov state models of PKA-RI were developed to test competing theories of activation for the R(2)C(2) complex. We found that CBD-B plays an essential role in R-C interaction and promotes the release of the first C-subunit prior to the binding to CBD-A. This favors a conformational selection mechanism for release of the first C-subunit of PKA. However, the release of the second C-subunit requires all four cAMP sites to be occupied. These analyses elucidate R-C heterodimer interactions in the cooperative activation of PKA and cAMP binding and represent a new mechanistic model of R(2)C(2) PKA-RI activation. |
| ISSN | 00219258 |
| e-ISSN | 1083351X |
| Journal | Journal of Biological Chemistry |
| Issue Number | 43 |
| Volume Number | 289 |
| Language | English |
| Publisher | American Society for Biochemistry and Molecular Biology (United States) |
| Publisher Date | 2014-10-24 |
| Publisher Place | United States |
| Access Restriction | Open |
| Subject Keyword | Cyclic AMP-Dependent Protein Kinase RIalpha Subunit Metabolism Cyclic AMP Markov Chains Models, Molecular Chemistry Enzyme Activation Drug Effects Mutant Proteins Oligopeptides Pharmacology Protein Multimerization Protein Structure, Tertiary Reproducibility Of Results Research Support, N.I.H., Extramural Biochemistry Molecular Biology |
| Content Type | Text |
| Resource Type | Article |
| Subject | Cell Biology Biochemistry Molecular Biology |
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