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XRCC5 / Ku80

X-ray repair complementing defective repair in Chinese hamster cells 5 (double-strand-break rejoining)

Single-stranded DNA-dependent ATP-dependent helicase. Has a role in chromosome translocation. The DNA helicase II complex binds preferentially to fork-like ends of double-stranded DNA in a cell cycle-dependent manner. It works in the 3'-5' direction. Binding to DNA may be mediated by XRCC6. Involved in DNA non-homologous end joining (NHEJ) required for double-strand break repair and V(D)J recombination. The XRCC5/6 dimer acts as regulatory subunit of the DNA-dependent protein kinase complex DNA-PK by increasing the affinity of the catalytic subunit PRKDC to DNA by 100-fold. The XRCC5/6 dimer is probably involved in stabilizing broken DNA ends and bringing them together. The assembly of the DNA-PK complex to DNA ends is required for the NHEJ ligation step. In association with NAA15, the XRCC5/6 dimer binds to the osteocalcin promoter and activates osteocalcin expression. The XRCC5/6 dimer probably also acts as a 5'-deoxyribose-5-phosphate lyase (5'-dRP lyase), by catalyzing the beta-elimination of the 5' deoxyribose-5-phosphate at an abasic site near double-strand breaks. XRCC5 probably acts as the catalytic subunit of 5'-dRP activity, and allows to 'clean' the termini of abasic sites, a class of nucleotide damage commonly associated with strand breaks, before such broken ends can be joined. The XRCC5/6 dimer together with APEX1 acts as a negative regulator of transcription.

Gene Name: X-ray repair complementing defective repair in Chinese hamster cells 5 (double-strand-break rejoining)
Synonyms: XRCC5, 86 kDa subunit of Ku antigen, CTC85, CTCBF, DNA repair protein XRCC5, G22P2, KARP-1, Ku autoantigen, 80kDa, NFIV, KARP1, Ku86, KUB2, TLAA, Nuclear factor IV, KU80, Thyroid-lupus autoantigen
Target Sequences: NM_021141 NP_066964.1 P13010

Publications (2)

1
Identification of cellular proteins that interact with the adeno-associated virus rep protein. Nash K, Chen W, Salganik M, Muzyczka N. Journal of virology. 2009 83:454-69. [PubMed:18971280] [PMC:PMC2612328]
2
Androgen modulation of coregulator expression in prostate cancer cells. Heemers HV, Regan KM, Schmidt LJ, Anderson SK, Ballman KV, Tindall DJ. Molecular endocrinology (Baltimore, Md.). 2009 23:572-83. [PubMed:19164447] [PMC:PMC2667711]

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Proteins (8)
Over-Expression Lysate (2)
Recombinant (6)
XRCC5 / Ku80 (8)
No (8)
10His, N-terminus + Myc, C-terminus (1)
GST (1)
His (2)
His-T7 (1)
MBP, N-terminus + 6His, C-terminus (1)
Myc-DDK (Flag) (2)
Human (6)
Mouse (1)
293T Cells (1)
Baculovirus (1)
E. coli (4)
HEK 293 Cells (1)
Wheat Germ Extract (1)
Purified (3)
XRCC5 / Ku80 Protein - Recombinant X-Ray Repair Cross Complementing 5 By SDS-PAGE
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E. coli
His
55.7 kDa
10 µg/$279; 50 µg/$430; 100 µg/$687; 200 µg/$857; 1 mg/$1,956; 500 µg/$1,499; 5 mg/$2,997; 2 mg/$2,142
XRCC5 / Ku80 Protein - (Tris-Glycine gel) Discontinuous SDS-PAGE (reduced) with 5% enrichment gel and 15% separation gel.
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Baculovirus
MBP, N-terminus + 6His, C-terminus
67.4 kDa
100 µg/$1,164; 20 µg/$475; 1 mg/$2,187
XRCC5 / Ku80 Protein - (Tris-Glycine gel) Discontinuous SDS-PAGE (reduced) with 5% enrichment gel and 15% separation gel.
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E. coli
10His, N-terminus + Myc, C-terminus
30.4 kDa
1 mg/$1,355; 100 µg/$420; 20 µg/$323
XRCC5 / Ku80 Protein - Western validation with an anti-DDK antibody * L: Control HEK293 lysate R: Over-expression lysate
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HEK 293 Cells
Myc-DDK (Flag)
82.5 kDa
100 µg/$494
XRCC5 / Ku80 Protein - 12.5% SDS-PAGE of human XRCC5 stained with Coomassie Blue
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Wheat Germ Extract
GST
106.26 kDa
2 µg/$439
XRCC5 / Ku80 Protein - Recombinant  X-Ray Repair Cross Complementing 5 By SDS-PAGE
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E. coli
His-T7
58.8 kDa
10 µg/$283; 50 µg/$457; 100 µg/$732; 200 µg/$912; 1 mg/$2,032; 500 µg/$1,567; 5 mg/$3,193; 2 mg/$2,219
XRCC5 / Ku80 Protein
Select
E. coli
His
27.53 kD
1 mg/$1,355; 100 µg/$420; 20 µg/$323
XRCC5 / Ku80 Protein - Western validation with an anti-DDK antibody * L: Control HEK293 lysate R: Over-expression lysate
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293T Cells
Myc-DDK (Flag)
82.5 kDa
20 µg/$150
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The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).