Sliding of p53 along DNA can be modulated by its oligomeric state and by cross-talks between its constituent domains

Journal of Molecular Biology

Volumn 408, Issue 2, 2011, Pages 335-355

  Khazanov, Netaly ^a   Levy, Yaakov ^a  

^a WEIZMANN INSTITUTE OF SCIENCE   (Israel)

Author keywords

coarse grained model; nonspecific protein DNA interactions; p53; sliding

Indexed keywords

DIMER; DNA; OLIGOMER; PROTEIN P53; SODIUM CHLORIDE; TETRAMER;

AMINO TERMINAL SEQUENCE; ARTICLE; BINDING AFFINITY; CROSS LINKING; DIFFUSION; ELECTRIC POTENTIAL; MISSENSE MUTATION; MOLECULAR DYNAMICS; MOLECULAR MODEL; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN DNA BINDING; PROTEIN DNA INTERACTION; PROTEIN DOMAIN; PROTEIN PROCESSING; PROTEIN VARIANT;

EID: 79953695332     PISSN: 00222836     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jmb.2011.01.059     Document Type: Article

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