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XPA

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

XPA
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DNA repair protein complementing XP-A cells is a protein that in humans is encoded by the XPA gene.[4]

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Function

Nucleotide excision repair (NER) is a major pathway for repairing a variety of bulky DNA damages including those introduced by UV irradiation. The XPA protein appears to play a key role in NER at sites of damage as a scaffold for other repair proteins in order to ensure that the damages are appropriately excised.[5] Among the repair proteins with which XPA interacts is a protein complex (including the ERCC1 protein) that is capable of incising DNA at sites of damage.[6]

Xpa mutant individuals often show the severe clinical symptoms of xeroderma pigmentosum, a condition involving extreme sensitivity to sunlight and a high incidence of skin cancer.

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Interactions

XPA has been shown to interact with ERCC1,[6][7] Replication protein A1[8] and XAB2.[9]

References

Further reading

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