A crystallographic study of the role of sequence context in thymine glycol bypass by a replicative DNA polymerase serendipitously sheds light on the exonuclease complex

Journal of Molecular Biology

Volumn 412, Issue 1, 2011, Pages 22-34

  Aller, Pierre ^a   Duclos, Stéphanie ^a   Wallace, Susan S ^a   Doublié, Sylvie ^a  

^a UNIVERSITY OF VERMONT COLLEGE OF MEDICINE   (United States)

Author keywords

bacteriophage RB69 gp43; DNA replication; lesion bypass; translesion synthesis

Indexed keywords

5,6 DIHYDRO 5,6 DIHYDROXYTHYMINE; DNA POLYMERASE; EXONUCLEASE; KLENOW FRAGMENT PROTEIN; THYMINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; CRYSTAL STRUCTURE; CRYSTALLOGRAPHY; DNA SEQUENCE; ENZYME ACTIVITY; ENZYME STRUCTURE; PRIORITY JOURNAL;

EID: 84860390395     PISSN: 00222836     EISSN: 10898638     Source Type: Journal    
DOI: 10.1016/j.jmb.2011.07.007     Document Type: Article

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