Journal article
Crystal Structure of Human XLF: A Twist in Nonhomologous DNA End-Joining
Abstract
DNA double-strand breaks represent one of the most severe forms of DNA damage in mammalian cells. One pathway for repairing these breaks occurs via nonhomologous end-joining (NHEJ) and depends on XRCC4, LigaseIV, and Cernunnos, also called XLF. Although XLF stimulates XRCC4/LigaseIV to ligate mismatched and noncohesive DNA ends, the mechanistic basis for this function remains unclear. Here we report the structure of a partially functional 224 …
Authors
Andres SN; Modesti M; Tsai CJ; Chu G; Junop MS
Journal
Molecular Cell, Vol. 28, No. 6, pp. 1093–1101
Publisher
Elsevier
Publication Date
December 2007
DOI
10.1016/j.molcel.2007.10.024
ISSN
1097-2765
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
Amino Acid SequenceBinding SitesCrystallizationDNA Ligase ATPDNA LigasesDNA RepairDNA Repair EnzymesDNA-Binding ProteinsDimerizationElectrophoresis, Polyacrylamide GelElectrophoretic Mobility Shift AssayHumansModels, MolecularMolecular Sequence DataMutationProtein BindingProtein Structure, TertiarySequence Homology, Amino Acid