P38 MAPK- and Akt-mediated p300 phosphorylation regulates its degradation to facilitate nucleotide excision repair

Nucleic Acids Research

Volumn 41, Issue 3, 2013, Pages 1722-1733

  Wang, Qi En ^a,b   Han, Chunhua ^a   Zhao, Ran ^a   Wani, Gulzar ^a   Zhu, Qianzheng ^a   Gong, Li ^a   Battu, Aruna ^a   Racoma, Ira ^a   Sharma, Nidhi ^a   Wani, Altaf A ^a,b  

^a THE OHIO STATE UNIVERSITY WEXNER MEDICAL CENTER   (United States)

^b OHIO STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

E1A ASSOCIATED P300 PROTEIN; MITOGEN ACTIVATED PROTEIN KINASE P38; PROTEIN KINASE B; SERINE;

ARTICLE; CATALYSIS; CONTROLLED STUDY; DNA DAMAGE; DOUBLE STRANDED DNA BREAK; ENZYME REGULATION; ENZYME SUBSTRATE; EXCISION REPAIR; GENE LOCATION; HETEROCHROMATIN; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; UPREGULATION;

CELL LINE; CHROMATIN; CISPLATIN; CREB-BINDING PROTEIN; DNA DAMAGE; DNA REPAIR; DNA-BINDING PROTEINS; ETOPOSIDE; HUMANS; P300-CBP TRANSCRIPTION FACTORS; P38 MITOGEN-ACTIVATED PROTEIN KINASES; PHOSPHORYLATION; PROTEOLYSIS; PROTO-ONCOGENE PROTEINS C-AKT; RADIATION, IONIZING; SERINE; ULTRAVIOLET RAYS;

EID: 84873694093     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gks1312     Document Type: Article

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