Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD - Wikidata - awgldk - TriplyDB

Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

http://www.wikidata.org/entity/Q27650943

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SF1 and SF2 helicases: family matters Subunit architecture of general transcription factor TFIIH The helicase XPD unwinds bubble structures and is not stalled by DNA lesions removed by the nucleotide excision repair pathway Xeroderma pigmentosum group C sensor: unprecedented recognition strategy and tight spatiotemporal regulation Disease-causing missense mutations in human DNA helicase disorders Double strand binding-single strand incision mechanism for human flap endonuclease: implications for the superfamily Nucleotide excision repair in eukaryotes Taking a molecular motor for a spin: helicase mechanism studied by spin labeling and PELDOR.Emerging critical roles of Fe-S clusters in DNA replication and repair.Functional and structural studies of the nucleotide excision repair helicase XPD suggest a polarity for DNA translocation Insights into Chi recognition from the structure of an AddAB-type helicase-nuclease complex Function of Conserved Topological Regions within the Saccharomyces cerevisiae Basal Transcription Factor TFIIH Near-atomic resolution visualization of human transcription promoter opening.Single-molecule analysis reveals differential effect of ssDNA-binding proteins on DNA translocation by XPD helicase Collaborative dynamic DNA scanning by nucleotide excision repair proteins investigated by single- molecule imaging of quantum-dot-labeled proteins.Mechanistic and biological aspects of helicase action on damaged DNA.Clinical and Molecular Heterogeneity of RTEL1 Deficiency Insight into the roles of helicase motif Ia by characterizing Fanconi anemia group J protein (FANCJ) patient mutations DNA-mediated charge transport in redox sensing and signaling Premature aging and cancer in nucleotide excision repair-disorders.The N-terminal domain of human DNA helicase Rtel1 contains a redox active iron-sulfur cluster.RTEL1: an essential helicase for telomere maintenance and the regulation of homologous recombination.On the traces of XPD: cell cycle matters - untangling the genotype-phenotype relationship of XPD mutations XPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase.Strand- and site-specific DNA lesion demarcation by the xeroderma pigmentosum group D helicase.In TFIIH, XPD helicase is exclusively devoted to DNA repair Fanconi anemia group J mutation abolishes its DNA repair function by uncoupling DNA translocation from helicase activity or disruption of protein-DNA complexes.Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability.Molecular and cellular functions of the FANCJ DNA helicase defective in cancer and in Fanconi anemia Impact of age-associated cyclopurine lesions on DNA repair helicases.Crystal structure of the Rad3/XPD regulatory domain of Ssl1/p44.Probing for DNA damage with β-hairpins: similarities in incision efficiencies of bulky DNA adducts by prokaryotic and human nucleotide excision repair systems in vitro Orchestral maneuvers at the damaged sites in nucleotide excision repair.ATP-stimulated, DNA-mediated redox signaling by XPD, a DNA repair and transcription helicase.The Association of the Xeroderma Pigmentosum Group D DNA Helicase (XPD) with Transcription Factor IIH Is Regulated by the Cytosolic Iron-Sulfur Cluster Assembly Pathway.Homozygous Wildtype of XPD K751Q Polymorphism Is Associated with Increased Risk of Nasopharyngeal Carcinoma in Malaysian Population DNA charge transport as a first step in coordinating the detection of lesions by repair proteins Tripartite DNA Lesion Recognition and Verification by XPC, TFIIH, and XPA in Nucleotide Excision Repair.Functional analyses of human DNA repair proteins important for aging and genomic stability using yeast genetics Mutations of the RTEL1 Helicase in a Hoyeraal-Hreidarsson Syndrome Patient Highlight the Importance of the ARCH Domain.

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Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

http://www.wikidata.org/entity/Q27650943

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2008 nî lūn-bûn

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2008 թուականի Յունիսին հրատարակուած գիտական յօդուած

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Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

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Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

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Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

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Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

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Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

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Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

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Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

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Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

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Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

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Crystal Structure of the FeS Cluster–Containing Nucleotide Excision Repair Helicase XPD

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Deborah L Croteau

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James J Truglio

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Stefanie C Wolski

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P2860

Trichothiodystrophy, a transcription syndrome

Distinct roles for the XPB/p52 and XPD/p44 subcomplexes of TFIIH in damaged DNA opening during nucleotide excision repair

Isolation and characterization of two human transcription factor IIH (TFIIH)-related complexes: ERCC2/CAK and TFIIH

Human cyclin-dependent kinase-activating kinase exists in three distinct complexes

Cockayne syndrome: defective repair of transcription?

Two related superfamilies of putative helicases involved in replication, recombination, repair and expression of DNA and RNA genomes

The comings and goings of nucleotide excision repair factors on damaged DNA

Improved methods for building protein models in electron density maps and the location of errors in these models

Crystal structures of complexes of PcrA DNA helicase with a DNA substrate indicate an inchworm mechanism

Mechanism of c-Myb-C/EBP beta cooperation from separated sites on a promoter

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e149

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6

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Caroline Kisker

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crystal structure

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