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DDB2 protein, human
Known as:
DDBb
, DNA Damage-Binding Protein 2
, XPE48 protein, human
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DNA damage-binding protein 2 (427 aa, ~48 kDa) is encoded by the human DDB2 gene. This protein plays a role in the mediation of DNA repair.
National Institutes of Health
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Related topics
Related topics
12 relations
DDB2 gene
DNA Repair
DNA Repair Gene
DNA repair protein
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Broader (2)
DDB2 wt Allele
DNA-Binding Proteins
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Chromatin retention of DNA damage sensors DDB2 and XPC through loss of p97 segregase causes genotoxicity
Marjo-Riitta Puumalainen
,
D. Lessel
,
+4 authors
H. Naegeli
Nature Communications
2014
Corpus ID: 9937988
DNA damage recognition subunits such as DDB2 and XPC protect the human skin from ultraviolet (UV) light-induced genome…
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Highly Cited
2012
Highly Cited
2012
PARP1 promotes nucleotide excision repair through DDB2 stabilization and recruitment of ALC1
A. Pines
,
Mischa G. Vrouwe
,
+12 authors
L. Mullenders
Journal of Cell Biology
2012
Corpus ID: 982188
PARP1-mediated poly(ADP-ribosyl)ation of DDB2 prolongs its occupation on UV-damaged chromatin and promotes the recruitment of the…
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Highly Cited
2012
Highly Cited
2012
DDB2 promotes chromatin decondensation at UV-induced DNA damage
M. S. Luijsterburg
,
M. Lindh
,
+5 authors
N. Dantuma
Journal of Cell Biology
2012
Corpus ID: 15925015
In addition to its role in DNA lesion recognition, the damaged DNA-binding protein DDB2 elicits unfolding of large-scale…
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Highly Cited
2011
Highly Cited
2011
The Molecular Basis of CRL4DDB2/CSA Ubiquitin Ligase Architecture, Targeting, and Activation
E. Fischer
,
A. Scrima
,
+11 authors
N. Thomä
Cell
2011
Corpus ID: 17915668
Highly Cited
2006
Highly Cited
2006
The DDB1-CUL4ADDB2 ubiquitin ligase is deficient in xeroderma pigmentosum group E and targets histone H2A at UV-damaged DNA sites.
M. Kapetanaki
,
Jennifer Guerrero-Santoro
,
Dawn C. Bisi
,
C. Hsieh
,
V. Rapić-Otrin
,
A. Levine
Proceedings of the National Academy of Sciences…
2006
Corpus ID: 42405259
Xeroderma pigmentosum (XP) is a heritable human disorder characterized by defects in nucleotide excision repair (NER) and the…
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Highly Cited
2006
Highly Cited
2006
Cullin 4A-mediated Proteolysis of DDB2 Protein at DNA Damage Sites Regulates in Vivo Lesion Recognition by XPC*
M. El-mahdy
,
Qianzheng Zhu
,
Qi-En Wang
,
G. Wani
,
M. Prætorius-Ibba
,
A. Wani
Journal of Biological Chemistry
2006
Corpus ID: 23997523
Xeroderma pigmentosum (XP) complementation group E gene product, damaged DNA-binding protein 2 (DDB2), is a subunit of the DDB…
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Highly Cited
2006
Highly Cited
2006
DNA damage binding protein component DDB1 participates in nucleotide excision repair through DDB2 DNA-binding and cullin 4A ubiquitin ligase activity.
Jinyou Li
,
Qi-En Wang
,
+4 authors
A. Wani
Cancer Research
2006
Corpus ID: 13051414
Functional defect in DNA damage binding (DDB) activity has a direct relationship to decreased nucleotide excision repair (NER…
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Highly Cited
2005
Highly Cited
2005
DDB1-DDB2 (Xeroderma Pigmentosum Group E) Protein Complex Recognizes a Cyclobutane Pyrimidine Dimer, Mismatches, Apurinic/Apyrimidinic Sites, and Compound Lesions in DNA*
Birgitte Ø. Wittschieben
,
S. Iwai
,
R. Wood
Journal of Biological Chemistry
2005
Corpus ID: 24148929
The DDB protein complex, comprising the subunits DDB1 and DDB2, binds tightly to UV light-irradiated DNA. Mutations in DDB2 are…
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Highly Cited
2004
Highly Cited
2004
UV radiation-induced XPC translocation within chromatin is mediated by damaged-DNA binding protein, DDB2.
Qi-En Wang
,
Qianzheng Zhu
,
G. Wani
,
Jianming Chen
,
A. Wani
Carcinogenesis
2004
Corpus ID: 11478710
The tumor suppressor p53 protein has been established as an important factor in modulating the efficiency of global genomic…
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Highly Cited
2003
Highly Cited
2003
True XP group E patients have a defective UV-damaged DNA binding protein complex and mutations in DDB2 which reveal the functional domains of its p48 product.
V. Rapić-Otrin
,
Valentina Navazza
,
+5 authors
M. Stefanini
Human Molecular Genetics
2003
Corpus ID: 8457101
Xeroderma pigmentosum (XP) is a skin cancer-prone autosomal recessive disease characterized by inability to repair UV-induced DNA…
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