Site-specific acetylation of the proteasome activator REGγ directs its heptameric structure and functions

Journal of Biological Chemistry

Volumn 288, Issue 23, 2013, Pages 16567-16578

  Liu, Jiang ^a,b,c   Wang, Ying ^a,b,c   Li, Lei ^a   Zhou, Li ^a   Wei, Haibin ^a   Zhou, Qingxia ^a   Liu, Jian ^c   Wang, Weicang ^a   Ji, Lei ^a   Shan, Peipei ^a   Wang, Yan ^a   Yang, Yuanyuan ^a   Jung, Sung Yun ^c   Zhang, Pei ^d   Wang, Chuangui ^a   Long, Weiwen ^c   Zhang, Bianhong ^a   Li, Xiaotao ^a,c  

^a EAST CHINA NORMAL UNIVERSITY   (China)

^b HANGZHOU NORMAL UNIVERSITY   (China)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d The Second Chengdu Municipal Hospital   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL ANALYSIS; CELL-CYCLE PROGRESSION; COMPARATIVE ANALYSIS; CREB BINDING PROTEINS; CYCLIN-DEPENDENT KINASE INHIBITORS; HEPATITIS C VIRUS; SITE DIRECTED MUTAGENESIS; STEROID RECEPTORS;

AMINO ACIDS; CELL PROLIFERATION; PROTEINS; TISSUE; VIRUSES;

ACETYLATION;

CORE PROTEIN; CYCLIC AMP RESPONSIVE ELEMENT BINDING PROTEIN BINDING PROTEIN; ENZYME ACTIVATOR; LYSINE; PROTEIN P21; REGGAMMA; SIRTUIN 1; UNCLASSIFIED DRUG;

ACETYLATION; ANIMAL CELL; ARTICLE; CELL CYCLE PROGRESSION; CELL PROLIFERATION; CONTROLLED STUDY; EMBRYO; ENZYME ACTIVITY; ENZYME REGULATION; ENZYME SUBSTRATE; HUMAN; HUMAN CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN DEGRADATION; PROTEIN PROTEIN INTERACTION; SITE DIRECTED MUTAGENESIS; STRUCTURE ACTIVITY RELATION;

ACETYLATION; CELL BIOLOGY; GENE REGULATION; HEPTAMERIZATION; K195; PROTEASOME; PROTEIN DEGRADATION; PROTEIN SELF-ASSEMBLY; PROTEIN-PROTEIN INTERACTIONS; REGΓ;

ACETYLATION; AMINO ACID SUBSTITUTION; ANIMALS; AUTOANTIGENS; CELL CYCLE; CREB-BINDING PROTEIN; HEK293 CELLS; HELA CELLS; HUMANS; MICE; MICE, KNOCKOUT; MUTATION, MISSENSE; PROTEASOME ENDOPEPTIDASE COMPLEX; PROTEIN MULTIMERIZATION; PROTEOLYSIS; UBIQUITIN;

HEPATITIS C VIRUS; MAMMALIA;

EID: 84878746494     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.437129     Document Type: Article

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