3WTD
Structure of PAXX
Summary for 3WTD
Entry DOI | 10.2210/pdb3wtd/pdb |
Related | 3WTF |
Descriptor | Uncharacterized protein C9orf142 (2 entities in total) |
Functional Keywords | dna repair, scaffold, nuclear protein |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 2 |
Total formula weight | 35706.32 |
Authors | Ochi, T.,Blundell, T.L. (deposition date: 2014-04-09, release date: 2015-01-21, Last modification date: 2024-03-20) |
Primary citation | Ochi, T.,Blackford, A.N.,Coates, J.,Jhujh, S.,Mehmood, S.,Tamura, N.,Travers, J.,Wu, Q.,Draviam, V.M.,Robinson, C.V.,Blundell, T.L.,Jackson, S.P. DNA repair. PAXX, a paralog of XRCC4 and XLF, interacts with Ku to promote DNA double-strand break repair. Science, 347:185-188, 2015 Cited by PubMed Abstract: XRCC4 and XLF are two structurally related proteins that function in DNA double-strand break (DSB) repair. Here, we identify human PAXX (PAralog of XRCC4 and XLF, also called C9orf142) as a new XRCC4 superfamily member and show that its crystal structure resembles that of XRCC4. PAXX interacts directly with the DSB-repair protein Ku and is recruited to DNA-damage sites in cells. Using RNA interference and CRISPR-Cas9 to generate PAXX(-/-) cells, we demonstrate that PAXX functions with XRCC4 and XLF to mediate DSB repair and cell survival in response to DSB-inducing agents. Finally, we reveal that PAXX promotes Ku-dependent DNA ligation in vitro and assembly of core nonhomologous end-joining (NHEJ) factors on damaged chromatin in cells. These findings identify PAXX as a new component of the NHEJ machinery. PubMed: 25574025DOI: 10.1126/science.1261971 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.35 Å) |
Structure validation
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