Residues in the RecQ C-terminal domain of the human Werner syndrome helicase are involved in unwinding G-quadruplex DNA

Journal of Biological Chemistry

Volumn 292, Issue 8, 2017, Pages 3154-3163

  Ketkar, Amit ^a   Voehler, Markus ^b   Mukiza, Tresor ^a   Eoff, Robert L ^a  

^a UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

^b VANDERBILT UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BINS; CELL PROLIFERATION;

ATP-ASE ACTIVITY; BIOPHYSICAL PROPERTIES; C-TERMINAL DOMAINS; DNA REPLICATIONS; PREFERENTIAL BINDING; SIGNIFICANT BLOCKS; WERNER SYNDROME HELICASE; WERNER SYNDROME PROTEIN;

DNA;

ADENOSINE TRIPHOSPHATASE; GUANINE QUADRUPLEX; MYC PROTEIN; RECQ HELICASE; WERNER SYNDROME ATP DEPENDENT HELICASE; DNA;

ARTICLE; BINDING AFFINITY; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; DNA DENATURATION; DNA SEQUENCE; ENZYME ACTIVITY; NUCLEAR MAGNETIC RESONANCE; PROTEIN DNA INTERACTION; PROTEIN EXPRESSION; RESIDUE ANALYSIS; SIGNAL TRANSDUCTION; CHEMISTRY; DNA REPAIR; DNA REPLICATION; ENZYMOLOGY; GENETICS; HUMAN; METABOLISM; MOLECULAR MODEL; MUTATION; PROTEIN DOMAIN; WERNER SYNDROME;

DNA; DNA REPAIR; DNA REPLICATION; G-QUADRUPLEXES; HUMANS; MODELS, MOLECULAR; MUTATION; PROTEIN DOMAINS; WERNER SYNDROME; WERNER SYNDROME HELICASE;

EID: 85013814402     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M116.767699     Document Type: Article

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