The structural location of DNA lesions in nucleosome core particles determines accessibility by base excision repair enzymes

Journal of Biological Chemistry

Volumn 288, Issue 19, 2013, Pages 13863-13875

  Rodriguez, Yesenia ^a   Smerdon, Michael J ^b  

^a Department of Pharmaceutical Sciences ^*  (United States)

^b WASHINGTON STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BASE EXCISION REPAIRS; CHROMATIN REMODELING; DNA LESIONS; HISTONE OCTAMERS; NUCLEOSOME CORE PARTICLES; NUCLEOSOMES; STRUCTURAL LOCATIONS; STRUCTURAL REQUIREMENTS;

BIOCHEMISTRY; BIOLOGY;

REPAIR;

DNA DIRECTED DNA POLYMERASE BETA; ENZYME; NUCLEOTIDE; URACIL; URACIL DNA GLYCOSIDASE;

ARTICLE; BIOACCUMULATION; CATALYSIS; CONTROLLED STUDY; DNA DAMAGE; DNA STRUCTURE; ENZYME ACTIVITY; ENZYME INHIBITION; EXCISION REPAIR; NUCLEOSOME; PRIORITY JOURNAL; PROTEIN DNA INTERACTION; STRUCTURE ANALYSIS;

BASE EXCISION REPAIR; DNA ENZYMES; DNA POLYMERASE; HISTONES; NUCLEOSOME;

ANIMALS; APURINIC ACID; CHICKENS; CROSS-LINKING REAGENTS; DNA; DNA DAMAGE; DNA POLYMERASE BETA; DNA REPAIR; DNA-(APURINIC OR APYRIMIDINIC SITE) LYASE; ERYTHROCYTES; ESCHERICHIA COLI PROTEINS; FORMALDEHYDE; HUMANS; HYDROLYSIS; KINETICS; MODELS, MOLECULAR; NUCLEIC ACID CONFORMATION; NUCLEOSOMES; PROTEIN BINDING; URACIL; URACIL-DNA GLYCOSIDASE;

EID: 84877696971     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.441444     Document Type: Article

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