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Yorodumi- PDB-9vnq: Bacillus Subtilis Ku core homodimer complexed with double strand DNA -
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Open data
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Basic information
| Entry | Database: PDB / ID: 9vnq | ||||||
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| Title | Bacillus Subtilis Ku core homodimer complexed with double strand DNA | ||||||
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Keywords | DNA BINDING PROTEIN / Non homologous end joining / DNA bridging | ||||||
| Function / homology | Function and homology informationdouble-strand break repair via nonhomologous end joining / double-stranded DNA binding / DNA recombination Similarity search - Function | ||||||
| Biological species | ![]() synthetic construct (others) | ||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.74 Å | ||||||
Authors | Kim, W.J. / Kim, M.S. | ||||||
| Funding support | 1items
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Citation | Journal: Nucleic Acids Res / Year: 2025Title: Structure of Bacillus subtilis Ku-mediated DNA synaptic complex. Authors: Whan-Jong Kim / Jieun Kim / Mingyu Jo / Youngjin Kim / Min-Sung Kim / ![]() Abstract: DNA double-strand breaks (DSBs) pose a severe threat to genomic integrity, and cells rely on two major pathways for repair: homologous recombination and non-homologous end joining (NHEJ). While ...DNA double-strand breaks (DSBs) pose a severe threat to genomic integrity, and cells rely on two major pathways for repair: homologous recombination and non-homologous end joining (NHEJ). While eukaryotic NHEJ requires a multi-component assembly including the Ku70/80 heterodimer, bacterial NHEJ operates with a simpler toolkit comprising a Ku homodimer and the multifunctional LigD. Despite this simplicity, the mechanism by which broken DNA ends are bridged together has remained unclear in bacterial NHEJ. Here, we present a cryo-electron microscopy structure of the Bacillus subtilis Ku (bsKu)-DNA complex at 2.74 Å resolution, capturing two blunt DNA ends bridged by a Ku protein alone. Supported by further biochemical assays, we propose an integrated model in which oligomeric arrays of Ku homodimers bridge and stabilize two DNA ends, facilitating efficient DSB repair in Bacillus subtilis. This work reveals a bsKu-mediated DNA bridging mechanism distinct from the eukaryotic system and provides critical structural insight into prokaryotic DNA repair. | ||||||
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 9vnq.cif.gz | 219.7 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9vnq.ent.gz | 173.9 KB | Display | PDB format |
| PDBx/mmJSON format | 9vnq.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 9vnq_validation.pdf.gz | 1.5 MB | Display | wwPDB validaton report |
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| Full document | 9vnq_full_validation.pdf.gz | 1.5 MB | Display | |
| Data in XML | 9vnq_validation.xml.gz | 44.8 KB | Display | |
| Data in CIF | 9vnq_validation.cif.gz | 65.4 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/vn/9vnq ftp://data.pdbj.org/pub/pdb/validation_reports/vn/9vnq | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 65215MC M: map data used to model this data C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
| #1: Protein | Mass: 26052.652 Da / Num. of mol.: 4 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() #2: DNA chain | | Mass: 9616.208 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) #3: DNA chain | | Mass: 9447.097 Da / Num. of mol.: 1 / Source method: obtained synthetically / Source: (synth.) synthetic construct (others) Has protein modification | N | |
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-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: Bacillus Subtilis Ku core homodimer complexed with double strand DNA Type: COMPLEX / Entity ID: all / Source: RECOMBINANT |
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| Source (natural) | Organism: ![]() |
| Source (recombinant) | Organism: ![]() |
| Buffer solution | pH: 7.5 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Cryogen name: ETHANE |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: TFS KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2000 nm / Nominal defocus min: 800 nm |
| Image recording | Electron dose: 60 e/Å2 / Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | |||||||||
| 3D reconstruction | Resolution: 2.74 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 156247 / Symmetry type: POINT |
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FIELD EMISSION GUN