Strong functional interactions of TFIIH with XPC and XPG in human DNA nucleotide excision repair, without a preassembled repairosome
about
Structural determinants for substrate binding and catalysis by the structure-specific endonuclease XPGCentrin 2 stimulates nucleotide excision repair by interacting with xeroderma pigmentosum group C protein.Xeroderma pigmentosum group C protein interacts physically and functionally with thymine DNA glycosylaseRole of the XPA protein in the NER pathway: A perspective on the function of structural disorder in macromolecular assemblyNucleotide excision repair in eukaryotesStructural basis for the recruitment of ERCC1-XPF to nucleotide excision repair complexes by XPAStructural and functional evidence that Rad4 competes with Rad2 for binding to the Tfb1 subunit of TFIIH in NERStructural and functional characterization of interactions involving the Tfb1 subunit of TFIIH and the NER factor Rad2The active site of the DNA repair endonuclease XPF-ERCC1 forms a highly conserved nuclease motif.Mammalian nucleotide excision repair proteins and interstrand crosslink repairMalfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemiaAssociation between the XPG Asp1104His and XPF Arg415Gln polymorphisms and risk of cancer: a meta-analysisAssociation between the ERCC5 Asp1104His polymorphism and cancer risk: a meta-analysis.p38 MAPK- and Akt-mediated p300 phosphorylation regulates its degradation to facilitate nucleotide excision repair.Xeroderma pigmentosum group A protein loads as a separate factor onto DNA lesions.Molecular anatomy of the human excision nuclease assembled at sites of DNA damage.Biochemical analysis of the damage recognition process in nucleotide excision repair.Ordered conformational changes in damaged DNA induced by nucleotide excision repair factors.Biochemical and structural domain analysis of xeroderma pigmentosum complementation group C protein.Sequence variations in DNA repair gene XPC is associated with lung cancer risk in a Chinese population: a case-control studyIn vivo destabilization and functional defects of the xeroderma pigmentosum C protein caused by a pathogenic missense mutationOther proteins interacting with XP proteins.Localization of xeroderma pigmentosum group A protein and replication protein A on damaged DNA in nucleotide excision repair.Impaired repair of cyclobutane pyrimidine dimers in human keratinocytes deficient in p53 and p63Stochastic and reversible assembly of a multiprotein DNA repair complex ensures accurate target site recognition and efficient repair.The role of XPC: implications in cancer and oxidative DNA damageDeficiency in the nuclease activity of xeroderma pigmentosum G in mice leads to hypersensitivity to UV irradiation.DDB1-DDB2 (xeroderma pigmentosum group E) protein complex recognizes a cyclobutane pyrimidine dimer, mismatches, apurinic/apyrimidinic sites, and compound lesions in DNA.HCMV-infected cells maintain efficient nucleotide excision repair of the viral genome while abrogating repair of the host genome.Oxidative DNA damage and nucleotide excision repair.GCN5 and E2F1 stimulate nucleotide excision repair by promoting H3K9 acetylation at sites of damage.Differential contributory roles of nucleotide excision and homologous recombination repair for enhancing cisplatin sensitivity in human ovarian cancer cellsStructure-function analysis of the EF-hand protein centrin-2 for its intracellular localization and nucleotide excision repairFunctional and mechanistic studies of XPC DNA-repair complex as transcriptional coactivator in embryonic stem cells.Domain swapping between FEN-1 and XPG defines regions in XPG that mediate nucleotide excision repair activity and substrate specificity.APE1, the DNA base excision repair protein, regulates the removal of platinum adducts in sensory neuronal cultures by NERUbiquitylation-independent degradation of Xeroderma pigmentosum group C protein is required for efficient nucleotide excision repairMolecular mechanisms of xeroderma pigmentosum (XP) proteins.DNA excision repair: where do all the dimers go?Calcium-binding capacity of centrin2 is required for linear POC5 assembly but not for nucleotide excision repair.
P2860
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P2860
Strong functional interactions of TFIIH with XPC and XPG in human DNA nucleotide excision repair, without a preassembled repairosome
description
2001 nî lūn-bûn
@nan
2001 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2001年の論文
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2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
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2001年学术文章
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2001年學術文章
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name
Strong functional interactions ...... out a preassembled repairosome
@ast
Strong functional interactions ...... out a preassembled repairosome
@en
Strong functional interactions ...... out a preassembled repairosome
@en-gb
Strong functional interactions ...... out a preassembled repairosome
@nl
type
label
Strong functional interactions ...... out a preassembled repairosome
@ast
Strong functional interactions ...... out a preassembled repairosome
@en
Strong functional interactions ...... out a preassembled repairosome
@en-gb
Strong functional interactions ...... out a preassembled repairosome
@nl
prefLabel
Strong functional interactions ...... out a preassembled repairosome
@ast
Strong functional interactions ...... out a preassembled repairosome
@en
Strong functional interactions ...... out a preassembled repairosome
@en-gb
Strong functional interactions ...... out a preassembled repairosome
@nl
P2093
P2860
P50
P921
P1476
Strong functional interactions ...... out a preassembled repairosome
@en
P2093
P2860
P304
P356
10.1128/MCB.21.7.2281-2291.2001
P407
P577
2001-04-01T00:00:00Z