Two human homologs of Rad23 are functionally interchangeable in complex formation and stimulation of XPC repair activity
about
Interaction of hHR23 with S5a. The ubiquitin-like domain of hHR23 mediates interaction with S5a subunit of 26 S proteasomeThe xeroderma pigmentosum group C protein complex XPC-HR23B plays an important role in the recruitment of transcription factor IIH to damaged DNA3-Methyladenine-DNA glycosylase (MPG protein) interacts with human RAD23 proteinsCentrosome protein centrin 2/caltractin 1 is part of the xeroderma pigmentosum group C complex that initiates global genome nucleotide excision repairCentrin 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 glycosylaseA novel regulation mechanism of DNA repair by damage-induced and RAD23-dependent stabilization of xeroderma pigmentosum group C proteinStructural determinants for the binding of ubiquitin-like domains to the proteasomeBinding surface mapping of intra- and interdomain interactions among hHR23B, ubiquitin, and polyubiquitin binding site 2 of S5aUV-induced ubiquitylation of XPC complex, the UV-DDB-ubiquitin ligase complex, and DNA repairA multistep damage recognition mechanism for global genomic nucleotide excision repairDevelopmental defects and male sterility in mice lacking the ubiquitin-like DNA repair gene mHR23BErythropoietic defect associated with reduced cell proliferation in mice lacking the 26S proteasome shuttling factor Rad23b.Critical DNA damage recognition functions of XPC-hHR23B and XPA-RPA in nucleotide excision repair.Ordered conformational changes in damaged DNA induced by nucleotide excision repair factors.Nuclear expression of dynamin-related protein 1 in lung adenocarcinomas.Molecular interaction map of the mammalian cell cycle control and DNA repair systems.Human papillomavirus type 16 E6 induces self-ubiquitination of the E6AP ubiquitin-protein ligaseIdentification of HHR23A as a substrate for E6-associated protein-mediated ubiquitination.USF-1 is critical for maintaining genome integrity in response to UV-induced DNA photolesions.DNA repair deficiency in neurodegeneration.p53 and DNA damage-inducible expression of the xeroderma pigmentosum group C gene.Rad23 promotes the targeting of proteolytic substrates to the proteasome.Proteogenomic analysis of human chromosome 9-encoded genes from human samples and lung cancer tissues.Efficient utilization of aerobic metabolism helps Tibetan locusts conquer hypoxia.Xeroderma pigmentosum complementation group E and UV-damaged DNA-binding protein.Orchestral maneuvers at the damaged sites in nucleotide excision repair.Oxidative stress during mitochondrial biogenesis compromises mtDNA integrity in growing hearts and induces a global DNA repair response.Pre-steady-state binding of damaged DNA by XPC-hHR23B reveals a kinetic mechanism for damage discrimination.HR23b expression is a potential predictive biomarker for HDAC inhibitor treatment in mesenchymal tumours and is associated with response to vorinostat.Nucleotide excision repair deficient mouse models and neurological disease.Tissue-specific accelerated aging in nucleotide excision repair deficiencyThe sequence dependence of human nucleotide excision repair efficiencies of benzo[a]pyrene-derived DNA lesions: insights into the structural factors that favor dual incisionsGene expression profiles in HPV-immortalized human cervical cells treated with the nicotine-derived carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone.Xeroderma pigmentosum complementation group C protein (XPC) serves as a general sensor of damaged DNA.A human XPC protein interactome--a resourceBinding of HIV-1 Vpr protein to the human homolog of the yeast DNA repair protein RAD23 (hHR23A) requires its xeroderma pigmentosum complementation group C binding (XPCB) domain as well as the ubiquitin-associated 2 (UBA2) domain.Molecular mechanisms of ultraviolet radiation-induced DNA damage and repair.Identification and characterization of XPC-binding domain of hHR23B.Thymine DNA glycosylase modulates DNA damage response and gene expression by base excision repair-dependent and independent mechanisms.
P2860
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P2860
Two human homologs of Rad23 are functionally interchangeable in complex formation and stimulation of XPC repair activity
description
1997 nî lūn-bûn
@nan
1997 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Two human homologs of Rad23 ar ...... ulation of XPC repair activity
@ast
Two human homologs of Rad23 ar ...... ulation of XPC repair activity
@en
Two human homologs of Rad23 ar ...... ulation of XPC repair activity
@en-gb
Two human homologs of Rad23 ar ...... ulation of XPC repair activity
@nl
type
label
Two human homologs of Rad23 ar ...... ulation of XPC repair activity
@ast
Two human homologs of Rad23 ar ...... ulation of XPC repair activity
@en
Two human homologs of Rad23 ar ...... ulation of XPC repair activity
@en-gb
Two human homologs of Rad23 ar ...... ulation of XPC repair activity
@nl
prefLabel
Two human homologs of Rad23 ar ...... ulation of XPC repair activity
@ast
Two human homologs of Rad23 ar ...... ulation of XPC repair activity
@en
Two human homologs of Rad23 ar ...... ulation of XPC repair activity
@en-gb
Two human homologs of Rad23 ar ...... ulation of XPC repair activity
@nl
P2093
P2860
P356
P1476
Two human homologs of Rad23 ar ...... ulation of XPC repair activity
@en
P2093
A Aboussekhra
C Masutani
J H Hoeijmakers
K Sugasawa
P2860
P304
P356
10.1128/MCB.17.12.6924
P407
P577
1997-12-01T00:00:00Z