RAD23A

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

UV excision repair protein RAD23 homolog A is a protein that in humans is encoded by the RAD23A gene.[5]

PDBOrtholog search: PDBe RCSB
AliasesRAD23A, HHR23A, HR23A, RAD23 homolog A, nucleotide excision repair protein
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RAD23A
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesRAD23A, HHR23A, HR23A, RAD23 homolog A, nucleotide excision repair protein
External IDsOMIM: 600061; MGI: 105126; HomoloGene: 48322; GeneCards: RAD23A; OMA:RAD23A - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001270362
NM_001270363
NM_005053

RefSeq (protein)

NP_001257291
NP_001257292
NP_005044

Location (UCSC)Chr 19: 12.95 – 12.95 MbChr 8: 85.56 – 85.57 Mb
PubMed search[3][4]
Wikidata
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Function

The protein encoded by this gene is one of two human homologs of Saccharomyces cerevisiae Rad23, a protein involved in nucleotide excision repair (NER). This protein was shown to interact with, and elevate the nucleotide excision activity of 3-methyladenine-DNA glycosylase (MPG), which suggested a role in DNA damage recognition in base excision repair. This protein contains an N-terminal ubiquitin-like domain, which was reported to interact with 26S proteasome, as well as with ubiquitin protein ligase E6AP, and thus suggests that this protein may be involved in the ubiquitin mediated proteolytic pathway in cells.[6]

RAD23A interacts with Y-family DNA polymerase iota (ι), DNA polymerase eta (η), DNA polymerase kappa and Y family DNA polymerase REV1.[7] These polymerases have roles in the DNA damage tolerance pathway of translesion synthesis that allows the replication fork to continue without stalling even when damage is present.[7]

Interactions

RAD23A has been shown to interact with:

References

Further reading

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