Computational Study of Gleevec and G6G Reveals Molecular Determinants of Kinase Inhibitor Selectivity
Gleevec is a potent inhibitor of Abl tyrosine kinase but not of the highly homologous c-Src kinase. Because the ligand binds to an inactive form of the protein in which an Asp-Phe-Gly structural motif along the activation loop adopts a so-called DFG-out conformation, it was suggested that binding sp...
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Veröffentlicht in: | Journal of the American Chemical Society 2014-10, Vol.136 (42), p.14753-14762 |
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Sprache: | eng |
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