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Journal Abstract Search

197 related items for PubMed ID: 26519825

  • 1. Versatility in phospho-dependent molecular recognition of the XRCC1 and XRCC4 DNA-damage scaffolds by aprataxin-family FHA domains.
    Cherry AL, Nott TJ, Kelly G, Rulten SL, Caldecott KW, Smerdon SJ.
    DNA Repair (Amst); 2015 Nov; 35():116-25. PubMed ID: 26519825
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  • 2. Characterization of the APLF FHA-XRCC1 phosphopeptide interaction and its structural and functional implications.
    Kim K, Pedersen LC, Kirby TW, DeRose EF, London RE.
    Nucleic Acids Res; 2017 Dec 01; 45(21):12374-12387. PubMed ID: 29059378
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  • 4. Specific recognition of a multiply phosphorylated motif in the DNA repair scaffold XRCC1 by the FHA domain of human PNK.
    Ali AA, Jukes RM, Pearl LH, Oliver AW.
    Nucleic Acids Res; 2009 Apr 01; 37(5):1701-12. PubMed ID: 19155274
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  • 5. Species variations in XRCC1 recruitment strategies for FHA domain-containing proteins.
    London RE.
    DNA Repair (Amst); 2022 Feb 01; 110():103263. PubMed ID: 35026705
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  • 6. Identification and functional characterization of a Ku-binding motif in aprataxin polynucleotide kinase/phosphatase-like factor (APLF).
    Shirodkar P, Fenton AL, Meng L, Koch CA.
    J Biol Chem; 2013 Jul 05; 288(27):19604-13. PubMed ID: 23689425
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  • 7. An Intrinsically Disordered APLF Links Ku, DNA-PKcs, and XRCC4-DNA Ligase IV in an Extended Flexible Non-homologous End Joining Complex.
    Hammel M, Yu Y, Radhakrishnan SK, Chokshi C, Tsai MS, Matsumoto Y, Kuzdovich M, Remesh SG, Fang S, Tomkinson AE, Lees-Miller SP, Tainer JA.
    J Biol Chem; 2016 Dec 30; 291(53):26987-27006. PubMed ID: 27875301
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  • 8. The FHA domain of PNKP is essential for its recruitment to DNA damage sites and maintenance of genome stability.
    Tsukada K, Shimada M, Imamura R, Saikawa K, Ishiai M, Matsumoto Y.
    Mutat Res; 2021 Dec 30; 822():111727. PubMed ID: 33220551
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  • 9. The Rev1 interacting region (RIR) motif in the scaffold protein XRCC1 mediates a low-affinity interaction with polynucleotide kinase/phosphatase (PNKP) during DNA single-strand break repair.
    Breslin C, Mani RS, Fanta M, Hoch N, Weinfeld M, Caldecott KW.
    J Biol Chem; 2017 Sep 29; 292(39):16024-16031. PubMed ID: 28821613
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  • 10. The interaction between polynucleotide kinase phosphatase and the DNA repair protein XRCC1 is critical for repair of DNA alkylation damage and stable association at DNA damage sites.
    Della-Maria J, Hegde ML, McNeill DR, Matsumoto Y, Tsai MS, Ellenberger T, Wilson DM, Mitra S, Tomkinson AE.
    J Biol Chem; 2012 Nov 09; 287(46):39233-44. PubMed ID: 22992732
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  • 11. Independent mechanisms of stimulation of polynucleotide kinase/phosphatase by phosphorylated and non-phosphorylated XRCC1.
    Lu M, Mani RS, Karimi-Busheri F, Fanta M, Wang H, Litchfeld DW, Weinfeld M.
    Nucleic Acids Res; 2010 Jan 09; 38(2):510-21. PubMed ID: 19910369
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  • 13. Dual modes of interaction between XRCC4 and polynucleotide kinase/phosphatase: implications for nonhomologous end joining.
    Mani RS, Yu Y, Fang S, Lu M, Fanta M, Zolner AE, Tahbaz N, Ramsden DA, Litchfield DW, Lees-Miller SP, Weinfeld M.
    J Biol Chem; 2010 Nov 26; 285(48):37619-29. PubMed ID: 20852255
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  • 14. The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4.
    Clements PM, Breslin C, Deeks ED, Byrd PJ, Ju L, Bieganowski P, Brenner C, Moreira MC, Taylor AM, Caldecott KW.
    DNA Repair (Amst); 2004 Nov 02; 3(11):1493-502. PubMed ID: 15380105
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  • 17. APLF (C2orf13) facilitates nonhomologous end-joining and undergoes ATM-dependent hyperphosphorylation following ionizing radiation.
    Macrae CJ, McCulloch RD, Ylanko J, Durocher D, Koch CA.
    DNA Repair (Amst); 2008 Feb 01; 7(2):292-302. PubMed ID: 18077224
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