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9IGX

Ku70/80 bound to 153 bp nucleosome

This is a non-PDB format compatible entry.
Summary for 9IGX
Entry DOI10.2210/pdb9igx/pdb
EMDB information52861
DescriptorX-ray repair cross-complementing protein 6, X-ray repair cross-complementing protein 5, Histone H2A type 1-B/E, ... (9 entities in total)
Functional Keywordsdna-binding protein, nhej, ku70/80, nucleosome, dna binding protein
Biological sourceHomo sapiens (human)
More
Total number of polymer chains14
Total formula weight420870.24
Authors
Hall, C.,Chaplin, A.K. (deposition date: 2025-02-20, release date: 2026-01-14)
Primary citationHall, 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: 41444611
DOI: 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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PDB entries from 2026-01-14

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