Structure of the Helicase Domain of DNA Polymerase Theta Reveals a Possible Role in the Microhomology-Mediated End-Joining Pathway

Structure

Volumn 23, Issue 12, 2015, Pages 2319-2330

  Newman, Joseph A ^a   Cooper, Christopher D O ^a,b   Aitkenhead, Hazel ^a   Gileadi, Opher ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF HUDDERSFIELD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; DNA POLYMERASE; DNA POLYMERASE THETA; HELICASE; TETRAMER; UNCLASSIFIED DRUG; DNA; DNA DIRECTED DNA POLYMERASE; PROTEIN BINDING;

ARTICLE; CRYSTAL STRUCTURE; DNA BINDING; DNA TEMPLATE; ENZYME ACTIVITY; ENZYME STRUCTURE; NUCLEOTIDE BINDING SITE; PRIORITY JOURNAL; PROTEIN QUATERNARY STRUCTURE; AMINO ACID SEQUENCE; CHEMISTRY; DNA END JOINING REPAIR; ENZYME ACTIVE SITE; HUMAN; METABOLISM; MOLECULAR GENETICS;

AMINO ACID SEQUENCE; CATALYTIC DOMAIN; DNA; DNA END-JOINING REPAIR; DNA-DIRECTED DNA POLYMERASE; HUMANS; MOLECULAR SEQUENCE DATA; PROTEIN BINDING;

EID: 84949215325     PISSN: 09692126     EISSN: 18784186     Source Type: Journal    
DOI: 10.1016/j.str.2015.10.014     Document Type: Article

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