Human calcium-calmodulin dependent protein kinase I: cDNA cloning, domain structure and activation by phosphorylation at threonine-177 by calcium-calmodulin dependent protein kinase I kinase
| Autor: | E G Goldstein, Ralph Snyderman, Sara S. Hook, Bodduluri Haribabu, Arthur M. Edelman, Anthony R. Means, M A Selbert, Eric D. Tomhave |
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| Rok vydání: | 1995 |
| Předmět: |
Threonine
DNA Complementary Recombinant Fusion Proteins Molecular Sequence Data Mutant Biology General Biochemistry Genetics and Molecular Biology Cell Line Calmodulin Animals Humans Amino Acid Sequence Cloning Molecular Phosphorylation Protein kinase A Molecular Biology chemistry.chemical_classification Messenger RNA Cdna cloning Base Sequence General Immunology and Microbiology Kinase General Neuroscience Chromosome Mapping Amino acid Enzyme Activation Calcium-Calmodulin-Dependent Protein Kinase Type 1 Biochemistry chemistry Calcium-Calmodulin-Dependent Protein Kinases Mutation Calcium Chromosomes Human Pair 3 Research Article |
| Zdroj: | The EMBO Journal. 14:3679-3686 |
| ISSN: | 0261-4189 |
| DOI: | 10.1002/j.1460-2075.1995.tb00037.x |
| Popis: | Human Ca(2+)-calmodulin (CaM) dependent protein kinase I (CaMKI) encodes a 370 amino acid protein with a calculated M(r) of 41,337. The 1.5 kb CaMKI mRNA is expressed in many different human tissues and is the product of a single gene located on human chromosome 3. CaMKI 1-306, was unable to bind Ca(2+)-CaM and was completely inactive thereby defining an essential component of the CaM-binding domain to residues C-terminal to 306. CaMKI 1-294 did not bind CaM but was fully active in the absence of Ca(2+)-CaM, indicating that residues 295-306 are sufficient to maintain CaMKI in an auto-inhibited state. CaMKI was phosphorylated on Thr177 and its activity enhanced approximately 25-fold by CaMKI kinase in a Ca(2+)-CaM dependent manner. Replacement of Thr177 with Ala or Asp prevented both phosphorylation and activation by CaMKI kinase and the latter replacement also led to partial activation in the absence of CaMKI kinase. Whereas CaMKI 1-306 was unresponsive to CaMKI kinase, the 1-294 mutant was phosphorylated and activated by CaMKI kinase in both the presence and absence of Ca(2+)-CaM although at a faster rate in its presence. These results indicate that the auto-inhibitory domain in CaMKI gates, in a Ca(2+)-CaM dependent fashion, accessibility of both substrates to the substrate binding cleft and CaMKI kinase to Thr177. Additionally, CaMKI kinase responds directly to Ca(2+)-CaM with increased activity. |
| Databáze: | OpenAIRE |
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