A methylation-phosphorylation switch determines Plk1 kinase activity and function in DNA damage repair

Author:

Li Weizhe1ORCID,Wang Hong-Yan1ORCID,Zhao Xiaolu1,Duan Hongguo1,Cheng Binghua2,Liu Yafei1,Zhao Mengjie1,Shu Wenjie1,Mei Yuchao1,Wen Zengqi3,Tang Mingliang1,Guo Lin4ORCID,Li Guohong3,Chen Qiang2ORCID,Liu Xiaoqi56,Du Hai-Ning1ORCID

Affiliation:

1. Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Wuhan University, Wuhan, Hubei 430072, China.

2. Medical Research Institute, School of Medicine, Wuhan University, Wuhan 430071, China.

3. National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences ,Beijing 100101, China.

4. State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, Hubei 430072, China.

5. Department of Biochemistry, Purdue University, West Lafayette, IN, USA.

6. Center for Cancer Research, Purdue University, West Lafayette, IN, USA.

Abstract

Two types of small-group modifications on Plk1 control its activity and its cellular functions.

Funder

National Natural Science Foundation of China

Major State Basic Research Development Program of China

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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