Tag |
Content |
dbPAF ID |
dbPAF-0001571 |
Uniprot Accession |
O43543; XRCC2_HUMAN; B2R925; |
Genbank Protein ID |
NP_005422.1; |
Genbank Nucleotide ID |
NM_005431.1; |
Protein Name |
DNA repair protein XRCC2 |
Protein Synonyms/Alias |
X-ray repair cross-complementing protein 2; |
Gene Name |
XRCC2 |
Gene Synonyms/Alias |
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Organism |
Homo sapiens(Human) |
NCBI Taxa ID |
9606 |
Functional Description (View all) |
Involved in the homologous recombination repair (HRR) pathway of double-stranded DNA, thought to repair chromosomal fragmentation, translocations and deletions. 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.Functional Description
Involved in the homologous recombination repair (HRR) pathway of double-stranded DNA, thought to repair chromosomal fragmentation, translocations and deletions. 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.
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Phosphorylation Sites
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dbPAF PTMs: 6 |
Sequence (Fasta) | MCSAFHRAES GTELLARLEG RSSLKEIEPN LFADEDSPVH GDILEFHGPE GTGKTEMLYH 60 LTARCILPKS EGGLEVEVLF IDTDYHFDML RLVTILEHRL SQSSEEIIKY CLGRFFLVYC 120 SSSTHLLLTL YSLESMFCSH PSLCLLILDS LSAFYWIDRV NGGESVNLQE STLRKCSQCL 180 EKLVNDYRLV LFATTQTIMQ KASSSSEEPS HASRRLCDVD IDYRPYLCKA WQQLVKHRMF 240 FSKQDDSQSS NQFSLVSRCL KSNSLKKHFF IIGESGVEFC
281Fasta Sequence
>O43543|XRCC2|Homo sapiens(Human) MCSAFHRAESGTELLARLEGRSSLKEIEPNLFADEDSPVHGDILEFHGPEGTGKTEMLYHLTARCILPKSEGGLEVEVLFIDTDYHFDMLRLVTILEHRLSQSSEEIIKYCLGRFFLVYCSSSTHLLLTLYSLESMFCSHPSLCLLILDSLSAFYWIDRVNGGESVNLQESTLRKCSQCLEKLVNDYRLVLFATTQTIMQKASSSSEEPSHASRRLCDVDIDYRPYLCKAWQQLVKHRMFFSKQDDSQSSNQFSLVSRCLKSNSLKKHFFIIGESGVEFC
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Keyword |
KW-0181--Complete proteome KW-0963--Cytoplasm KW-0206--Cytoskeleton KW-0227--DNA damage KW-0233--DNA recombination KW-0234--DNA repair KW-0238--DNA-binding KW-0539--Nucleus KW-0621--Polymorphism KW-1185--Reference proteome
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Interpro |
IPR013632--DNA_recomb/repair_Rad51_C IPR027417--P-loop_NTPase IPR020588--RecA_ATP-bd IPR030547--XRCC2
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PROSITE |
PS50162--RECA_2
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Pfam |
PF08423--Rad51
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Gene Ontology |
GO:0005813--C:centrosome GO:0005737--C:cytoplasm GO:0005654--C:nucleoplasm GO:0033063--C:Rad51B-Rad51C-Rad51D-XRCC2 complex GO:0005657--C:replication fork GO:0005524--F:ATP binding GO:0008094--F:DNA-dependent ATPase activity GO:0003690--F:double-stranded DNA binding GO:0000150--F:recombinase activity GO:0003697--F:single-stranded DNA binding GO:0051297--P:centrosome organization GO:0006281--P:DNA repair GO:0006302--P:double-strand break repair GO:0000724--P:double-strand break repair via homologous recombination GO:0045003--P:double-strand break repair via synthesis-dependent strand annealing GO:0001701--P:in utero embryonic development GO:0000707--P:meiotic DNA recombinase assembly GO:0007126--P:meiotic nuclear division GO:0000278--P:mitotic cell cycle GO:0006312--P:mitotic recombination GO:0035264--P:multicellular organism growth GO:0043524--P:negative regulation of neuron apoptotic process GO:0050769--P:positive regulation of neurogenesis GO:0007131--P:reciprocal meiotic recombination GO:2000269--P:regulation of fibroblast apoptotic process GO:0010332--P:response to gamma radiation GO:0010212--P:response to ionizing radiation GO:0010165--P:response to X-ray GO:0001756--P:somitogenesis GO:0042148--P:strand invasion
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