In TFIIH, XPD helicase is exclusively devoted to DNA repair.
The eukaryotic XPD helicase is an essential subunit of TFIIH involved in both transcription and nucleotide excision repair (NER). Mutations in human XPD are associated with several inherited diseases such as xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. We performed a comparativ...
Saved in:
Main Authors: | Jochen Kuper, Cathy Braun, Agnes Elias, Gudrun Michels, Florian Sauer, Dominik R Schmitt, Arnaud Poterszman, Jean-Marc Egly, Caroline Kisker |
---|---|
Format: | article |
Language: | EN |
Published: |
Public Library of Science (PLoS)
2014
|
Subjects: | |
Online Access: | https://doaj.org/article/88cc70ed5c364099a3152604a61d9dd6 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
In TFIIH the Arch domain of XPD is mechanistically essential for transcription and DNA repair
by: Stefan Peissert, et al.
Published: (2020) -
TFIIE orchestrates the recruitment of the TFIIH kinase module at promoter before release during transcription
by: Emmanuel Compe, et al.
Published: (2019) -
The structural and functional characterization of human RecQ4 reveals insights into its helicase mechanism
by: Sebastian Kaiser, et al.
Published: (2017) -
Functional interplay between TFIIH and KAT2A regulates higher-order chromatin structure and class II gene expression
by: Jérémy Sandoz, et al.
Published: (2019) -
Structural basis of TFIIH activation for nucleotide excision repair
by: Goran Kokic, et al.
Published: (2019)