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...
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: | English |
Published: |
Public Library of Science (PLoS)
2014-09-01
|
Series: | PLoS Biology |
Online Access: | https://doi.org/10.1371/journal.pbio.1001954 |
Similar Items
-
In TFIIH the Arch domain of XPD is mechanistically essential for transcription and DNA repair
by: Stefan Peissert, et al.
Published: (2020-04-01) -
The structure of the TFIIH p34 subunit reveals a von Willebrand factor A like fold.
by: Dominik R Schmitt, et al.
Published: (2014-01-01) -
Crystal structure of the FeS cluster-containing nucleotide excision repair helicase XPD.
by: Stefanie C Wolski, et al.
Published: (2008-06-01) -
Distinct regions of MAT1 regulate cdk7 kinase and TFIIH transcription activities.
by: Busso, D, et al.
Published: (2000) -
DNA translocation mechanism of an XPD family helicase
by: Kaiying Cheng, et al.
Published: (2018-12-01)