Phosphorylation of the p68 subunit of pol δ acts as a molecular switch to regulate its interaction with PCNA

Biochemistry

Volumn 51, Issue 1, 2012, Pages 416-424

  Rahmeh, Amal A ^a   Zhou, Yajing ^a   Xie, Bin ^a   Li, Hao ^a   Lee, Ernest Y C ^a   Lee, Marietta Y W T ^a  

^a NEW YORK MEDICAL COLLEGE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA POLYMERASE; DNA REPLICATIONS; FUNCTIONAL PROPERTIES; MOLECULAR SWITCHES; PHOSPHORYLATION SITES; PROCESSIVITY; REGULATORY MECHANISM;

DNA;

PHOSPHORYLATION;

CYCLINE; DNA DIRECTED DNA POLYMERASE DELTA; PROTEIN P68; SERINE;

ARTICLE; BINDING AFFINITY; ENZYME REGULATION; HUMAN; NONHUMAN; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN MOTIF; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; REGULATORY MECHANISM;

AMINO ACID MOTIFS; AMINO ACID SEQUENCE; ASPARTIC ACID; CYCLIC AMP-DEPENDENT PROTEIN KINASES; DNA POLYMERASE III; DOWN-REGULATION; HELA CELLS; HUMANS; MOLECULAR MIMICRY; MOLECULAR SEQUENCE DATA; MUTATION; PHOSPHORYLATION; PROLIFERATING CELL NUCLEAR ANTIGEN; PROTEIN BINDING; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTEIN SUBUNITS; SERINE;

EUKARYOTA;

EID: 84863012802     PISSN: 00062960     EISSN: 15204995     Source Type: Journal    
DOI: 10.1021/bi201638e     Document Type: Article

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