The Cerebro-oculo-facio-skeletal Syndrome Point Mutation F231L in the ERCC1 DNA Repair Protein Causes Dissociation of the ERCC1-XPF Complex

The ERCC1-XPF heterodimer, a structure-specific DNA endonuclease, is best known for its function in the nucleotide excision repair (NER) pathway. The ERCC1 point mutation F231L, located at the hydrophobic interaction interface of ERCC1 (excision repair cross-complementation group 1) and XPF (xeroder...

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Vydáno v:J Biol Chem
Hlavní autoři: Faridounnia, Maryam, Wienk, Hans, Kovačič, Lidija, Folkers, Gert E., Jaspers, Nicolaas G. J., Kaptein, Robert, Hoeijmakers, Jan H. J., Boelens, Rolf
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society for Biochemistry and Molecular Biology 2015
Témata:
DNA and Chromosomes
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4536458/
https://ncbi.nlm.nih.gov/pubmed/26085086
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M114.635169
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