期刊
BIOCHEMISTRY
卷 57, 期 45, 页码 6387-6390出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.biochem.8b00729
关键词
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资金
- National Institute of Health (NIH) Director's New Innovator Award [1DP2CA186752-01]
- NIH MIRA award [1R35GM126940-01]
- NIH [R01GM097261]
Protein kinases achieve substrate selective phosphorylation through their conformational flexibility and dynamic interaction with the substrate. Designing substrate selective or kinase selective small molecule inhibitors remains a challenge because of a lack of understanding of the dynamic mechanism by which substrates are selected by the kinase. Using a combination of all-atom molecular dynamics simulations and FRET sensors, we have delineated an allosteric mechanism that results in interaction among the DFG motif, G-loop, and activation loop and structurally links the nucleotide and substrate binding interfaces in protein kinase C alpha and three other Ser/Thr kinases. ATP-competitive staurosporine analogues engage this allosteric switch region located just outside the ATP binding site to displace substrate binding to varying degrees. These inhibitors function as bitopic ligands by occupying the ATP binding site and interacting with the allosteric switch region. The conserved mechanism identified in this study can be exploited to select and design bitopic inhibitors for kinases.
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