Protein kinase inhibitor selectivity "hinges" on evolution.

Protein kinase inhibitor selectivity "hinges" on evolution.
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蛋白激酶抑制剂的选择性“取决于”进化。

DOI:
10.1016/j.str.2022.11.004
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发表时间:
2022
期刊:
Structure (London, England : 1993)
影响因子:
--
通讯作者:
Kannan,Natarajan
Kannan,Natarajan
中科院分区:
--
文献类型:
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作者:
Shrestha,Safal;Bendzunas,George;Kannan,Natarajan

文献摘要

相似文献

在这一期的结构中,Kelso等人。给出了与选择性抑制剂OTS964结合的未被研究的肿瘤相关细胞周期蛋白依赖性激酶11(CDK11)的晶体结构,说明了即使在密切相关的激酶之间,也可以利用激酶域的进化变异来实现抑制剂的选择性。
In this issue of Structure, Kelso et al. present the crystal structure of the understudied cancer-associated cyclin-dependent kinase 11 (CDK11) bound to the selective inhibitor OTS964, illuminating how evolutionary variations in the kinase domain can be exploited for inhibitor selectivity even among closely related kinases.