The interaction between polynucleotide kinase phosphatase and the DNA repair protein XRCC1 is critical for repair of DNA alkylation damage and stable association at DNA damage sites

Journal of Biological Chemistry

Volumn 287, Issue 46, 2012, Pages 39233-39244

  Della Maria, Julie ^a   Hegde, Muralidhar L ^b   McNeill, Daniel R ^c   Matsumoto, Yoshihiro ^d   Tsai, Miaw Sheue ^e   Ellenberger, Tom ^f   Wilson Iii, David M ^c   Mitra, Sankar ^b   Tomkinson, Alan E ^d  

^a UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE   (United States)

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

^c NATIONAL INSTITUTES OF HEALTH   (United States)

^d UNIVERSITY OF NEW MEXICO   (United States)

^e UNIVERSITY OF CALIFORNIA   (United States)

^f WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

APRATAXIN; COMPLEMENTATION; DAMAGE REPAIR; DNA ALKYLATION AGENT; DNA ALKYLATIONS; DNA DAMAGES; DNA LIGASES; DNA REPAIR PROTEINS; ENZYMATIC ACTIVITIES; MUTANT CELLS; POLYNUCLEOTIDES; SINGLE-STRAND BREAKS; YEAST TWO HYBRID;

ALKYLATION; ASSOCIATION REACTIONS; NUCLEOTIDES; PHOSPHATASES; PROTEINS; REPAIR;

DNA;

ALANINE; ARGININE; GLYCINE; LEUCINE; POLYNUCLEOTIDE 5' HYDROXYL KINASE; PROLINE; SERINE; THREONINE; VALINE; XRCC1 PROTEIN;

ARTICLE; BINDING SITE; CELL SURVIVAL; DNA ALKYLATION; DNA DAMAGE; DNA REPAIR; ENZYME ACTIVITY; GENETIC COMPLEMENTATION; MUTANT; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DETERMINATION; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; REACTION TIME; WILD TYPE;

CELL SURVIVAL; DNA DAMAGE; DNA LIGASES; DNA REPAIR; DNA REPAIR ENZYMES; DNA-BINDING PROTEINS; GENE EXPRESSION REGULATION; HUMANS; KINETICS; MICROSCOPY, CONFOCAL; MUTATION; NUCLEAR PROTEINS; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); PROTEIN BINDING; PROTEIN INTERACTION MAPPING; PROTEIN STRUCTURE, TERTIARY; THREONINE; TWO-HYBRID SYSTEM TECHNIQUES;

EID: 84869074642     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.369975     Document Type: Article

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