The TATA-binding protein core domain in solution variably bends TATA sequences via a three-step binding mechanism

Biochemistry

Volumn 48, Issue 8, 2009, Pages 1801-1809

  Delgadillo, Roberto F ^a   Whittington, JoDell E ^a   Parkhurst, Laura K ^a   Parkhurst, Lawrence J ^a  

^a UNIVERSITY OF NEBRASKA LINCOLN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BEND ANGLES; BINDING MECHANISMS; CRYSTALLOGRAPHIC STUDIES; DNA BENDING; DNA BINDINGS; ENTROPY OF ACTIVATIONS; N-TERMINAL DOMAINS; ORDER OF MAGNITUDES; OSMOLYTE; OSMOLYTES; STRUCTURAL DIFFERENCES; TATA-BINDING PROTEINS; THREE-STEP MECHANISMS;

AMINES; AMINO ACIDS; DNA; NUCLEIC ACIDS; ORGANIC ACIDS; PROTEINS; RATE CONSTANTS; SEMICONDUCTOR DOPING; YEAST;

GENES;

CURVED DNA; DNA; TATA BINDING PROTEIN;

AMINO ACID SEQUENCE; ARTICLE; CRYSTALLOGRAPHY; DNA BINDING; ENERGY TRANSFER; ENTHALPY; ENTROPY; ENZYME ACTIVATION; ENZYME MECHANISM; HUMAN; NONHUMAN; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DOMAIN; PROTEIN STABILITY; PROTEIN VARIANT; TEMPERATURE;

BASE SEQUENCE; ENTROPY; FLUORESCENCE RESONANCE ENERGY TRANSFER; HUMANS; KINETICS; NUCLEIC ACID CONFORMATION; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SOLUTIONS; TATA BOX; TATA-BOX BINDING PROTEIN; TIME FACTORS;

EID: 64349107263     PISSN: 00062960     EISSN: None     Source Type: Journal    
DOI: 10.1021/bi8018724     Document Type: Article

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