hCLP46 increases Smad3 protein stability via inhibiting its ubiquitin-proteasomal degradation.
10.1007/s13238-015-0174-0
- Author:
Yingying XING
1
;
Qiaoyun CHU
2
,
3
;
Run FENG
1
;
Wei WANG
4
;
Lixin LIU
5
;
Zhongbing LU
6
Author Information
1. College of Life Sciences, University of Chinese Academy of Science, Beijing, 100049, China.
2. 1. College of Life Sciences, University of Chinese Academy of Science, Beijing, 100049
3. 2. Department of Biochemistry and Molecular Biology, Capital Medical University, Beijing 100069 China.
4. School of Medical Science, Edith Cowan University, Joondalup, WA 6027, Australia.
5. 1.College of Life Sciences, University of Chinese Academy of Science, Beijing, 100049, China.2. Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, liulixin@mail.sysu.edu.cn
6. College of Life Sciences, University of Chinese Academy of Science, Beijing, 100049, China. luzhongbing@ucas.ac.cn.
- Publication Type:Letter
- MeSH:
Glucosyltransferases;
metabolism;
HEK293 Cells;
Humans;
Proteasome Endopeptidase Complex;
metabolism;
Protein Stability;
Proteolysis;
Smad3 Protein;
chemistry;
metabolism;
Ubiquitin;
metabolism
- From:
Protein & Cell
2015;6(10):767-770
- CountryChina
- Language:English
