NMR chemical shift and relaxation measurements provide evidence for the coupled folding and binding of the p53 transactivation domain

Nucleic Acids Research

Volumn 33, Issue 7, 2005, Pages 2061-2077

  Vise, Pamela D ^a   Baral, Bharat ^a   Latos, Andrew J ^a   Daughdrill, Gary W ^a  

^a UNIVERSITY OF IDAHO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; DOUBLE STRANDED DNA; PLASMID DNA; PROTEIN P53; PROTEIN SUBUNIT; REPLICATION PROTEIN A; TUMOR SUPPRESSOR PROTEIN; AMINO ACID; DNA BINDING PROTEIN; RPA1 PROTEIN, HUMAN; SINGLE STRANDED DNA; TRANSACTIVATOR PROTEIN;

AMINO TERMINAL SEQUENCE; ARTICLE; BINDING SITE; COMPLEX FORMATION; DNA REPAIR; HUMAN; NITROGEN NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN FOLDING; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; PROTEIN SECONDARY STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; TRANSACTIVATION; AMINO ACID SEQUENCE; CHEMISTRY; METABOLISM; MOLECULAR GENETICS; NUCLEAR MAGNETIC RESONANCE; PROTEIN TERTIARY STRUCTURE;

AMINO ACID SEQUENCE; AMINO ACIDS; BINDING SITES; DNA, SINGLE-STRANDED; DNA-BINDING PROTEINS; HUMANS; MOLECULAR SEQUENCE DATA; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PROTEIN FOLDING; PROTEIN STRUCTURE, TERTIARY; REPLICATION PROTEIN A; TRANS-ACTIVATORS; TUMOR SUPPRESSOR PROTEIN P53;

EID: 17544381252     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gki336     Document Type: Article

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