Characterization of a human DNA damage binding protein implicated in xeroderma pigmentosum E
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Characterization of a protein complex containing spliceosomal proteins SAPs 49, 130, 145, and 155DDB, a putative DNA repair protein, can function as a transcriptional partner of E2F1.Sequential binding of UV DNA damage binding factor and degradation of the p48 subunit as early events after UV irradiation.Turnover of hepatitis B virus X protein is regulated by damaged DNA-binding complex.The p127 subunit (DDB1) of the UV-DNA damage repair binding protein is essential for the targeted degradation of STAT1 by the V protein of the paramyxovirus simian virus 5Correction of the DNA repair defect in xeroderma pigmentosum group E by injection of a DNA damage-binding proteinHepatitis B virus X protein and simian virus 5 V protein exhibit similar UV-DDB1 binding properties to mediate distinct activitiesTumor-prone phenotype of the DDB2-deficient miceDNA damage in the nucleosome core is refractory to repair by human excision nuclease.Xeroderma pigmentosum group A protein loads as a separate factor onto DNA lesions.Recognition and repair of the cyclobutane thymine dimer, a major cause of skin cancers, by the human excision nuclease.Interaction between UV-damaged DNA binding activity proteins and the c-Abl tyrosine kinaseRelationship of the xeroderma pigmentosum group E DNA repair defect to the chromatin and DNA binding proteins UV-DDB and replication protein A.Xeroderma pigmentosum complementation group E protein (XPE/DDB2): purification of various complexes of XPE and analyses of their damaged DNA binding and putative DNA repair properties.Damaged DNA binding protein 2 plays a role in breast cancer cell growthPhysical and functional interaction between DDB and XPA in nucleotide excision repair.DDB2 complex-mediated ubiquitylation around DNA damage is oppositely regulated by XPC and Ku and contributes to the recruitment of XPA.The paramyxovirus simian virus 5 V protein slows progression of the cell cycle.α-N-methylation of damaged DNA-binding protein 2 (DDB2) and its function in nucleotide excision repair.Hepatitis B virus X protein interferes with cellular DNA repair.Damaged DNA-binding protein 2 (DDB2) protects against UV irradiation in human cells and Drosophila.RETRACTED: DDB2, an essential mediator of premature senescenceCancer models in Caenorhabditis elegans.The naturally occurring mutants of DDB are impaired in stimulating nuclear import of the p125 subunit and E2F1-activated transcription.The xeroderma pigmentosum group E gene product DDB2 is a specific target of cullin 4A in mammalian cells.Drosophila damage-specific DNA-binding protein 1 (D-DDB1) is controlled by the DRE/DREF system.The DDB1-CUL4ADDB2 ubiquitin ligase is deficient in xeroderma pigmentosum group E and targets histone H2A at UV-damaged DNA sites.The deubiquitinating protein USP24 interacts with DDB2 and regulates DDB2 stability.Drosophila damaged DNA-binding protein 1 is an essential factor for development.repE--the Dictyostelium homolog of the human xeroderma pigmentosum group E gene is developmentally regulated and contains a leucine zipper motifA novel UV-damaged DNA binding protein emerges during the chromatin-eliminating cleavage period in Ascaris suum.Expression of the p48 xeroderma pigmentosum gene is p53-dependent and is involved in global genomic repairXeroderma pigmentosum complementation group E and UV-damaged DNA-binding protein.The Caenorhabditis elegans replication licensing factor CDT-1 is targeted for degradation by the CUL-4/DDB-1 complexDefective ribosomal protein gene expression alters transcription, translation, apoptosis, and oncogenic pathways in Diamond-Blackfan anemia.Ubiquitylation-independent degradation of Xeroderma pigmentosum group C protein is required for efficient nucleotide excision repairManipulation of light signal transduction as a means of modifying fruit nutritional quality in tomato.DDB2 gene disruption leads to skin tumors and resistance to apoptosis after exposure to ultraviolet light but not a chemical carcinogen.Functional complementation of xeroderma pigmentosum complementation group E by replication protein A in an in vitro systemThe Cul4-Ddb1(Cdt)² ubiquitin ligase inhibits invasion of a boundary-associated antisilencing factor into heterochromatin
P2860
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P2860
Characterization of a human DNA damage binding protein implicated in xeroderma pigmentosum E
description
1993 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique Journal of Biological Chemistry
@fr
artículu científicu espublizáu en 1993
@ast
im Oktober 1993 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1993/10/05)
@sk
vědecký článek publikovaný v roce 1993
@cs
wetenschappelijk artikel (gepubliceerd op 1993/10/05)
@nl
наукова стаття, опублікована в жовтні 1993
@uk
name
Characterization of a human DN ...... ted in xeroderma pigmentosum E
@ast
Characterization of a human DN ...... ted in xeroderma pigmentosum E
@en
Characterization of a human DN ...... ted in xeroderma pigmentosum E
@nl
type
label
Characterization of a human DN ...... ted in xeroderma pigmentosum E
@ast
Characterization of a human DN ...... ted in xeroderma pigmentosum E
@en
Characterization of a human DN ...... ted in xeroderma pigmentosum E
@nl
prefLabel
Characterization of a human DN ...... ted in xeroderma pigmentosum E
@ast
Characterization of a human DN ...... ted in xeroderma pigmentosum E
@en
Characterization of a human DN ...... ted in xeroderma pigmentosum E
@nl
P2093
P1476
Characterization of a human DN ...... ted in xeroderma pigmentosum E
@en
P2093
P304
21293-21300
P407
P577
1993-10-01T00:00:00Z