Homo sapiens Protein: RAD51D
Summary
InnateDB Protein IDBP-241284.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol RAD51D
Protein Name RAD51 homolog D (S. cerevisiae)
Synonyms BROVCA4; R51H3; RAD51L3; TRAD;
Species Homo sapiens
Ensembl Protein ENSP00000378090
InnateDB Gene IDBG-41136 (RAD51D)
Protein Structure
UniProt Annotation
Function Involved in the homologous recombination repair (HRR) pathway of double-stranded DNA breaks arising during DNA replication or induced by DNA-damaging agents. Bind to single- stranded DNA (ssDNA) and has DNA-dependent ATPase activity. Part of the Rad21 paralog protein complex BCDX2 which acts in the BRCA1-BRCA2-dependent HR pathway. Upon DNA damage, BCDX2 acts downstream of BRCA2 recruitment and upstream of RAD51 recruitment. BCDX2 binds predominantly to the intersection of the four duplex arms of the Holliday junction and to junction of replication forks. The BCDX2 complex was originally reported to bind single- stranded DNA, single-stranded gaps in duplex DNA and specifically to nicks in duplex DNA. Involved in telomere maintenance. The BCDX2 subcomplex XRCC2:RAD51D can stimulate Holliday junction resolution by BLM. {ECO:0000269PubMed:10871607, ECO:0000269PubMed:11751635, ECO:0000269PubMed:11834724, ECO:0000269PubMed:11842113, ECO:0000269PubMed:12975363, ECO:0000269PubMed:15109494, ECO:0000269PubMed:23149936}.
Subcellular Localization Nucleus {ECO:0000305}. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Chromosome, telomere.
Disease Associations Breast-ovarian cancer, familial, 4 (BROVCA4) [MIM:614291]: A condition associated with familial predisposition to cancer of the breast and ovaries. Characteristic features in affected families are an early age of onset of breast cancer (often before age 50), increased chance of bilateral cancers (cancer that develop in both breasts, or both ovaries, independently), frequent occurrence of breast cancer among men, increased incidence of tumors of other specific organs, such as the prostate. {ECO:0000269PubMed:21822267}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.
Tissue Specificity Expressed in colon, prostate, spleen, testis, ovary, thymus and small intestine. Weakly expressed in leukocytes.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 25 experimentally validated interaction(s) in this database.
Experimentally validated
Total 25 [view]
Protein-Protein 25 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0000400 four-way junction DNA binding
GO:0003677 DNA binding
GO:0003678 DNA helicase activity
GO:0003697 single-stranded DNA binding
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0008094 DNA-dependent ATPase activity
GO:0043015 gamma-tubulin binding
Biological Process
GO:0000723 telomere maintenance
GO:0000724 double-strand break repair via homologous recombination
GO:0006200 ATP catabolic process
GO:0006259 DNA metabolic process
GO:0006260 DNA replication
GO:0006281 DNA repair
GO:0007131 reciprocal meiotic recombination
GO:0042148 strand invasion
Cellular Component
GO:0000781 chromosome, telomeric region
GO:0005634 nucleus
GO:0005657 replication fork
GO:0005737 cytoplasm
GO:0005813 centrosome
GO:0033063 Rad51B-Rad51C-Rad51D-XRCC2 complex
Protein Structure and Domains
PDB ID
InterPro IPR003593 AAA+ ATPase domain
IPR007694 DNA helicase, DnaB-like, C-terminal
IPR013632 DNA recombination and repair protein Rad51, C-terminal
IPR014774 Circadian clock protein KaiC/DNA repair protein RadA
IPR016467 DNA recombination and repair protein, RecA-like
IPR020588 DNA recombination and repair protein RecA-like, ATP-binding domain
IPR027417 P-loop containing nucleoside triphosphate hydrolase
PFAM PF03796
PF08423
PF06745
PRINTS
PIRSF PIRSF005856
SMART SM00382
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt O75771
PhosphoSite PhosphoSite-O75771
TrEMBL Q7Z790
UniProt Splice Variant
Entrez Gene 5892
UniGene Hs.612360
RefSeq
HUGO HGNC:9823
OMIM 602954
CCDS CCDS11287
HPRD 04261
IMGT
EMBL AB013341 AB016223 AB016224 AB016225 AB018360 AB018361 AB018362 AB018363 AB020412 AC022916 AF034956 AK296241 AK301249 AL117459 AY623116 BC002723 BC014422 CH471147 Y15572
GenPept AAC39719 AAH02723 AAH14422 AAT38112 BAA25914 BAA31747 BAA31748 BAA31749 BAA33779 BAA33780 BAA33781 BAA33782 BAA34690 BAG58959 BAG62816 CAA75681 CAB55937 EAW80180 EAW80181 EAW80184 EAW80187 EAW80189 EAW80191 EAW80193 EAW80195 EAW80196