Role of the insertion domain and the zinc-finger motif of Escherichia coli UvrA in damage recognition and ATP hydrolysis

DNA Repair

Volumn 10, Issue 5, 2011, Pages 483-496

  Wagner, Koen ^a   Moolenaar, Geri F ^a   Goosen, Nora ^a  

^a LEIDEN UNIVERSITY   (Netherlands)

Author keywords

Nucleotide excision repair; UvrABC

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ADENOSINE TRIPHOSPHATE; ARGININE; BACTERIAL PROTEIN; DEOXYRIBODIPYRIMIDINE PHOTOLYASE; DIMER; PHENYLALANINE; PHOSPHATE; PROTEIN UVRA; UNCLASSIFIED DRUG;

ARTICLE; COMPLEX FORMATION; CONTROLLED STUDY; DNA HELIX; ENZYME ACTIVATION; ESCHERICHIA COLI; EXCISION REPAIR; MOLECULAR RECOGNITION; MUTATION; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DNA BINDING; PROTEIN DOMAIN; PROTEIN FAMILY; SIGNAL TRANSDUCTION; ZINC FINGER MOTIF;

ADENOSINE TRIPHOSPHATASES; ADENOSINE TRIPHOSPHATE; AMINO ACID SEQUENCE; ARGININE; DEOXYRIBODIPYRIMIDINE PHOTO-LYASE; DNA DAMAGE; DNA REPAIR; DNA, BACTERIAL; DNA-BINDING PROTEINS; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; HYDROLYSIS; MICROBIAL VIABILITY; MOLECULAR SEQUENCE DATA; MUTANT PROTEINS; PROTEIN CONFORMATION; SEQUENCE ALIGNMENT; ULTRAVIOLET RAYS; ZINC FINGERS;

BACTERIA (MICROORGANISMS); ESCHERICHIA COLI;

EID: 79955098363     PISSN: 15687864     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dnarep.2011.02.002     Document Type: Article

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