Tyrosine phosphorylation of myosin heavy chain during skeletal muscle differentiation: an integrated bioinformatics approach
- PMID: 15790426
- PMCID: PMC1079951
- DOI: 10.1186/1742-4682-2-12
Tyrosine phosphorylation of myosin heavy chain during skeletal muscle differentiation: an integrated bioinformatics approach
Abstract
Background: Previously it has been shown that insulin-mediated tyrosine phosphorylation of myosin heavy chain is concomitant with enhanced association of C-terminal SRC kinase during skeletal muscle differentiation. We sought to identify putative site(s) for this phosphorylation event.
Results: A combined bioinformatics approach of motif prediction and evolutionary and structural analyses identified tyrosines163 and 1856 of the skeletal muscle heavy chain as the leading candidate for the sites of insulin-mediated tyrosine phosphorylation.
Conclusion: Our work is suggestive that tyrosine phosphorylation of myosin heavy chain, whether in skeletal muscle or in platelets, is a significant event that may initiate cytoskeletal reorganization of muscle cells and platelets. Our studies provide a good starting point for further functional analysis of MHC phosphor-signalling events within different cells.
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References
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- Sellers J. Myosins (Protein Profile S) Oxford University Press, Oxford; 1999.
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- Harney D, Cagney G, Thiede B, Treumann A, Fitzgerald DJ, Maguire PB. Proteomic analysis of platelets detects the May-Hegglin gene, non-muscle myosin heavy chain A in platelets and demonstrates its tyrosine phosphorylation following thrombin stimulation. [abstract] Circulation. 2003;108:s200.
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