Home LiteratureArticle Details
PMID: 16214430 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Review

Dynamics of signaling by PKA.

Biochimica et biophysica acta ·Vol. 1754 ·No. 1-2 ·2005-12-30 ·Pages 25-37

Taylor SS, Kim C, Vigil D, Haste NM, Yang J, Wu J, Anand GS

Abstract

The catalytic and regulatory subunits of cAMP-dependent protein kinase (PKA) are highly dynamic signaling proteins. In its dissociated state the catalytic subunit opens and closes as it moves through its catalytic cycle. In this subunit, the core that is shared by all members of the protein kinase family is flanked by N- and C-terminal segments. Each are anchored firmly to the core by well-defined motifs and serve to stabilize the core. Protein kinases are not only catalysts, they are also scaffolds. One of their major functions is to bind to other proteins. In addition to its interactions with the N- and C- termini, the catalytic subunit interacts with its inhibitor proteins, PKI and the regulatory subunits. Both bind with subnanomolar affinity. To achieve this tight binding requires docking of a substrate mimetic to the active site cleft as well as a peripheral docking site. The peripheral site used by PKI is distinct from that used by RIalpha as revealed by a recent structure of a C:RIalpha complex. Upon binding to the catalytic subunit, the linker region of RIalpha becomes ordered. In addition, cAMP-binding domain A undergoes major conformational changes. RIalpha is a highly malleable protein. Using small angle X-ray scattering, the overall shape of the regulatory subunits and corresponding holoenzymes have been elucidated. These studies reveal striking and surprising isoform differences.

MeSH Terms
Amino Acid Sequence Animals Catalytic Domain Crystallography, X-Ray Cyclic AMP-Dependent Protein Kinase RIalpha Subunit Cyclic AMP-Dependent Protein Kinases/chemistry,metabolism Holoenzymes Humans Kinetics Models, Molecular Molecular Sequence Data Protein Binding Protein Conformation Protein Isoforms/chemistry,metabolism Signal Transduction
Chemicals
Cyclic AMP-Dependent Protein Kinase RIalpha Subunit Holoenzymes PRKAR1A protein, human Protein Isoforms Cyclic AMP-Dependent Protein Kinases
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Taylor Susan S
Howard Hughes Medical Institute, Department of Chemistry and Biochemistry and Department of Pharmacology, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0654, USA. staylor@ucsd.edu
Kim Choel
Vigil Dominico
Haste Nina M
Yang Jie
Wu Jian
Anand Ganesh S
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
2005-12-30
Epub
2005-00-22
Pages
25-37
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
Grants
NIGMS NIH HHS · GM19301 · United States
NIGMS NIH HHS · GM34921 · United States
NIDDK NIH HHS · T32-DK07233 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com