Publication date: Available online 28 February 2017
Source:Bioorganic & Medicinal Chemistry
Author(s): Xue Zhi Zhao, David Hymel, Terrence R. Burke
An important goal in the development of polo-like kinase 1 (Plk1) polo-box domain (PBD) binding inhibitors is selectivity for Plk1 relative to Plk2 and Plk3. In our current work we show that Plk1 PBD selectivity can be significantly enhanced by modulating interactions within a previously discovered "cryptic pocket" and a more recently identified proximal "auxiliary pocket."
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