The Escherichia coli PriA helicase has two nucleotide-binding sites differing dramatically in their affinities for nucleotide cofactors. 1. Intrinsic affinities, cooperativities, and base specificity of nucleotide cofactor binding

Biochemistry

Volumn 45, Issue 23, 2006, Pages 7202-7216

  Lucius, Aaron L ^a   Jezewska, Maria J ^a   Bujalowski, Wlodzimierz ^a  

^a University of Texas Medical Branch School of Medicine   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINETRIPHOSPHATE; ESCHERICHIA COLI; FLUORESCENCE; MONOMERS; PHOSPHATES; PROTEINS; TITRATION;

BINDING SITES; COFACTOR AFFINITY; NUCLEOTIDE; PRIA HELICASE; RIBOSE;

ENZYMES;

ADENOSINE DIPHOSPHATE; ADENOSINE TRIPHOSPHATE; HELICASE; HELICASE PRIA; MAGNESIUM ION; PHOSPHATE; UNCLASSIFIED DRUG;

ARTICLE; BINDING AFFINITY; ENZYME BINDING; ENZYME SPECIFICITY; ENZYME SUBSTRATE COMPLEX; ESCHERICHIA COLI; FLUORESCENCE ANALYSIS; MOLECULAR INTERACTION; NONHUMAN; NUCLEOTIDE BINDING SITE; PRIORITY JOURNAL; STOICHIOMETRY;

ADENOSINE DIPHOSPHATE; ADENOSINE TRIPHOSPHATASES; ADENOSINE TRIPHOSPHATE; BINDING SITES; DNA HELICASES; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; LIGANDS; SPECTROMETRY, FLUORESCENCE;

ESCHERICHIA COLI;

EID: 33745027664     PISSN: 00062960     EISSN: None     Source Type: Journal    
DOI: 10.1021/bi051826m     Document Type: Article

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