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Computational Study of Gleevec and G6G Reveals Molecular Determinants of Kinase Inhibitor Selectivity

[Image: see text] 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 suggest...

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Main Authors: Lin, Yen-Lin, Meng, Yilin, Huang, Lei, Roux, Benoît
פורמט: Artigo
שפה:Inglês
יצא לאור: American Chemical Society 2014
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC4210138/
https://ncbi.nlm.nih.gov/pubmed/25243930
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ja504146x
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