Summary for 9IGX
| Entry DOI | 10.2210/pdb9igx/pdb |
| EMDB information | 52861 |
| Descriptor | X-ray repair cross-complementing protein 6, X-ray repair cross-complementing protein 5, Histone H2A type 1-B/E, ... (9 entities in total) |
| Functional Keywords | dna-binding protein, nhej, ku70/80, nucleosome, dna binding protein |
| Biological source | Homo sapiens (human) More |
| Total number of polymer chains | 14 |
| Total formula weight | 420870.24 |
| Authors | |
| Primary citation | Hall, C.,Frit, P.,Kefala-Stavridi, A.,Pelletier, A.,Hardwick, S.W.,Amin, H.,Bilyard, M.K.,Maia De Oliviera, T.,Tariq, A.,Zahid, S.,Chirgadze, D.Y.,Balasubramanian, S.,Meek, K.,Ropars, V.,Charbonnier, J.B.,Modesti, M.,Calsou, P.,Britton, S.,Blundell, T.L.,Schalch, T.,Chaplin, A.K. Cryo-EM structures of NHEJ assemblies with nucleosomes. Nat Commun, 2025 Cited by PubMed Abstract: DNA double-strand breaks (DSBs) are highly deleterious lesions that can trigger cell death or carcinogenesis if unrepaired or misrepaired. In mammals, most DSBs are repaired by non-homologous end joining (NHEJ), which begins when Ku70/80 binds DNA ends and recruits DNA-PKcs to form the DNA-PK holoenzyme. Although recent cryo-EM studies have resolved several NHEJ assemblies, how these factors access DSBs within nucleosomes remains unclear. Here, we present cryo-EM structures of human Ku70/80 and DNA-PK bound to nucleosomes. Ku70/80 binds the DNA end and bends it away from the nucleosome core, while the Ku70 C-terminal SAP domain makes an additional, specific DNA contact. Our DNA-PK-nucleosome structure further reveals the opening of the Ku80 vWA domain, and we show that non-hydrolysable ATP promotes synapsis by stabilising the Ku80-mediated DNA-PK dimer. These structures reveal a model for DSB recognition on nucleosomal DNA and provide insights relevant to targeting NHEJ in cancer therapy. PubMed: 41444611DOI: 10.1038/s41467-025-67376-2 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (3.56 Å) |
Structure validation
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