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Yorodumi- PDB-9l8u: Cryo-EM structure of ASFV DNA polymerase in a DNA replication state -
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Open data
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Basic information
| Entry | Database: PDB / ID: 9l8u | ||||||||||||||||||||||||
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| Title | Cryo-EM structure of ASFV DNA polymerase in a DNA replication state | ||||||||||||||||||||||||
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Keywords | DNA BINDING PROTEIN/DNA / Virus / DNA polymerase / ASFV / DNA BINDING PROTEIN-DNA complex | ||||||||||||||||||||||||
| Function / homology | Function and homology informationviral DNA genome replication / DNA-directed DNA polymerase / DNA-directed DNA polymerase activity / DNA replication / nucleotide binding / DNA binding Similarity search - Function | ||||||||||||||||||||||||
| Biological species | Asfarviridae (virus) | ||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.53 Å | ||||||||||||||||||||||||
Authors | Hu, Z. / Yan, R. | ||||||||||||||||||||||||
| Funding support | China, 1items
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Citation | Journal: iScience / Year: 2025Title: Structural basis for DNA replication by the African swine fever virus polymerase. Authors: Ziwei Hu / Yongjie SunKang / Zhiheng Liu / Lihong Huang / Wenbao Qi / Renhong Yan / ![]() Abstract: African swine fever virus (ASFV) devastates swine herds and lacks widely available antivirals. We show that the ASFV DNA polymerase beta (Pol β; gene ) localizes to viral replication factories and ...African swine fever virus (ASFV) devastates swine herds and lacks widely available antivirals. We show that the ASFV DNA polymerase beta (Pol β; gene ) localizes to viral replication factories and is required for viral replication. Cryo-electron microscopy structures of Pol β in apo and double-stranded DNA (dsDNA)-bound states reveal pronounced conformational flexibility that enables transitions between functional states. Binding to dsDNA promotes higher-order oligomerization that is essential for catalytic activity, as demonstrated by structure-guided mutagenesis and biochemical assays. These findings define the structural basis of ASFV genome synthesis, highlight the functional significance of Pol β during viral replication, and provide a framework for polymerase-targeted antiviral discovery. | ||||||||||||||||||||||||
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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 | 9l8u.cif.gz | 230.3 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9l8u.ent.gz | 176.7 KB | Display | PDB format |
| PDBx/mmJSON format | 9l8u.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/l8/9l8u ftp://data.pdbj.org/pub/pdb/validation_reports/l8/9l8u | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 62891MC ![]() 9l8tC 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: 115127.031 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Details: Sequence reference for strain 'Asfarviridae' is not available in UniProt at the time of biocuration. Current sequence reference is from UniProt id A0A7D5JBM0. Source: (gene. exp.) Asfarviridae (virus) / Gene: G1211R / Production host: Eukaryota (eukaryotes)References: UniProt: A0A7D5JBM0, DNA-directed DNA polymerase | ||||||
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| #2: DNA chain | Mass: 5067.301 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Asfarviridae (virus) / Production host: Eukaryota (eukaryotes) | ||||||
| #3: DNA chain | Mass: 3229.125 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Asfarviridae (virus) / Production host: Eukaryota (eukaryotes) | ||||||
| #4: Chemical | | #5: Chemical | Has ligand of interest | N | Has protein modification | N | |
-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: ASFV DNA polymerase with dsDNA / Type: COMPLEX / Entity ID: #1-#3 / Source: RECOMBINANT |
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| Source (natural) | Organism: Asfarviridae (virus) |
| Source (recombinant) | Organism: Eukaryota (eukaryotes) |
| Buffer solution | pH: 7.5 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Cryogen name: NITROGEN |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Tecnai Polara / Image courtesy: FEI Company |
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| Microscopy | Model: FEI POLARA 300 |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 1800 nm / Nominal defocus min: 1400 nm / Calibrated defocus min: 1400 nm / Calibrated defocus max: 1800 nm / C2 aperture diameter: 70 µm |
| Specimen holder | Cryogen: NITROGEN / Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER |
| Image recording | Electron dose: 1.5625 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | |||||||||
| 3D reconstruction | Resolution: 2.53 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 696619 / Symmetry type: POINT |
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About Yorodumi



Asfarviridae (virus)
China, 1items
Citation



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FIELD EMISSION GUN