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Structure and Dynamic Regulation of Abl Kinases
Authors:Shoghag Panjarian  Roxana E Iacob  Shugui Chen  John R Engen  Thomas E Smithgall
Institution:From the Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15219 and ;the §Department of Chemistry and Chemical Biology, Northeastern University, Boston, Massachusetts 02115
Abstract:The c-abl proto-oncogene encodes a unique protein-tyrosine kinase (Abl) distinct from c-Src, c-Fes, and other cytoplasmic tyrosine kinases. In normal cells, Abl plays prominent roles in cellular responses to genotoxic stress as well as in the regulation of the actin cytoskeleton. Abl is also well known in the context of Bcr-Abl, the oncogenic fusion protein characteristic of chronic myelogenous leukemia. Selective inhibitors of Bcr-Abl, of which imatinib is the prototype, have had a tremendous impact on clinical outcomes in chronic myelogenous leukemia and revolutionized the field of targeted cancer therapy. In this minireview, we focus on the structural organization and dynamics of Abl kinases and how these features influence inhibitor sensitivity.
Keywords:Protein/Drug Interactions  Protein Dynamics  SH2 Domains  SH3 Domains  Tyrosine Protein Kinase (Tyrosine Kinase)  Chronic Myelogenous Leukemia  Hydrogen Exchange Mass Spectrometry  Imatinib
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