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Yorodumi- EMDB-17411: Subtomogram averaging structure of the Vaccinia Virus core palisa... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-17411 | |||||||||
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Title | Subtomogram averaging structure of the Vaccinia Virus core palisade layer | |||||||||
Map data | Subtomogram averaging sharpened map (b-factor 2100) of Hexamers of Trimer from Vaccinia virus | |||||||||
Sample |
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Keywords | Poxvirus / Vaccinia Virus / core / cryo-electron tomography / AlphaFold / VIRAL PROTEIN | |||||||||
Biological species | Vaccinia virus Western Reserve | |||||||||
Method | subtomogram averaging / cryo EM / Resolution: 13.1 Å | |||||||||
Authors | Datler J / Hansen JM / Thader A / Schloegl A / Hodirnau VV / Schur FKM | |||||||||
Funding support | 1 items
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Citation | Journal: Nat Struct Mol Biol / Year: 2024 Title: Multi-modal cryo-EM reveals trimers of protein A10 to form the palisade layer in poxvirus cores. Authors: Julia Datler / Jesse M Hansen / Andreas Thader / Alois Schlögl / Lukas W Bauer / Victor-Valentin Hodirnau / Florian K M Schur / Abstract: Poxviruses are among the largest double-stranded DNA viruses, with members such as variola virus, monkeypox virus and the vaccination strain vaccinia virus (VACV). Knowledge about the structural ...Poxviruses are among the largest double-stranded DNA viruses, with members such as variola virus, monkeypox virus and the vaccination strain vaccinia virus (VACV). Knowledge about the structural proteins that form the viral core has remained sparse. While major core proteins have been annotated via indirect experimental evidence, their structures have remained elusive and they could not be assigned to individual core features. Hence, which proteins constitute which layers of the core, such as the palisade layer and the inner core wall, has remained enigmatic. Here we show, using a multi-modal cryo-electron microscopy (cryo-EM) approach in combination with AlphaFold molecular modeling, that trimers formed by the cleavage product of VACV protein A10 are the key component of the palisade layer. This allows us to place previously obtained descriptions of protein interactions within the core wall into perspective and to provide a detailed model of poxvirus core architecture. Importantly, we show that interactions within A10 trimers are likely generalizable over members of orthopox- and parapoxviruses. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_17411.map.gz | 10.6 MB | EMDB map data format | |
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Header (meta data) | emd-17411-v30.xml emd-17411.xml | 18 KB 18 KB | Display Display | EMDB header |
Images | emd_17411.png | 66 KB | ||
Masks | emd_17411_msk_1.map | 11.4 MB | Mask map | |
Filedesc metadata | emd-17411.cif.gz | 5.3 KB | ||
Others | emd_17411_half_map_1.map.gz emd_17411_half_map_2.map.gz | 10.4 MB 10.4 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-17411 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-17411 | HTTPS FTP |
-Validation report
Summary document | emd_17411_validation.pdf.gz | 768.8 KB | Display | EMDB validaton report |
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Full document | emd_17411_full_validation.pdf.gz | 768.4 KB | Display | |
Data in XML | emd_17411_validation.xml.gz | 9.5 KB | Display | |
Data in CIF | emd_17411_validation.cif.gz | 11 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-17411 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-17411 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_17411.map.gz / Format: CCP4 / Size: 11.4 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Annotation | Subtomogram averaging sharpened map (b-factor 2100) of Hexamers of Trimer from Vaccinia virus | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 2.762 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Mask #1
File | emd_17411_msk_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: Subtomogram averaging of Hexamers of Trimer from Vaccinia...
File | emd_17411_half_map_1.map | ||||||||||||
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Annotation | Subtomogram averaging of Hexamers of Trimer from Vaccinia virus half map odd | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Subtomogram averaging of Hexamers of Trimer from Vaccinia...
File | emd_17411_half_map_2.map | ||||||||||||
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Annotation | Subtomogram averaging of Hexamers of Trimer from Vaccinia virus half map even | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Vaccinia virus Western Reserve
Entire | Name: Vaccinia virus Western Reserve |
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Components |
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-Supramolecule #1: Vaccinia virus Western Reserve
Supramolecule | Name: Vaccinia virus Western Reserve / type: virus / ID: 1 / Parent: 0 / Macromolecule list: #1 Details: Purified from HeLa cells infected with Vaccinia virus Western Reserve. NCBI-ID: 696871 / Sci species name: Vaccinia virus Western Reserve / Virus type: VIRION / Virus isolate: STRAIN / Virus enveloped: No / Virus empty: No |
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-Experimental details
-Structure determination
Method | cryo EM |
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Processing | subtomogram averaging |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 9 / Component - Concentration: 1.0 mM / Component - Formula: Tris-HCl / Component - Name: Tris Hydrochloride Details: diluted 1:1 with 0.25% Trypsin (final concentration 0.125%) and 1:1 4% paraformaldehyde (final concentration 2%) in 1 mM Tris-HCl. |
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Grid | Model: Quantifoil R2/2 / Material: COPPER / Mesh: 300 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 180 sec. / Pretreatment - Atmosphere: AIR |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 80 % / Chamber temperature: 277 K / Instrument: LEICA EM GP / Details: Leica GP2. |
Details | Isolated Vaccinia Virus mature virus particles |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Specialist optics | Energy filter - Name: GIF Bioquantum / Energy filter - Slit width: 10 eV |
Details | Cryo-electron tomography data was collected with the SerialEM software package version 3.8 (Mastronarde 2005). New gain reference images were collected before data acquisition. DigitalMicrograph 3.4.3 as integrated into the Gatan Microscopy Suite v3.3 (Gatan) was used for filter tuning and SerialEM for microscope tuning. |
Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Digitization - Dimensions - Width: 5760 pixel / Digitization - Dimensions - Height: 4092 pixel / Average electron dose: 165.0 e/Å2 / Details: Images were collected in movie-mode with 10 frames |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | C2 aperture diameter: 50.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 8.0 µm / Nominal defocus min: 1.5 µm / Nominal magnification: 64000 |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Final reconstruction | Applied symmetry - Point group: C3 (3 fold cyclic) / Algorithm: BACK PROJECTION / Resolution.type: BY AUTHOR / Resolution: 13.1 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: Dynamo (ver. 1.1.333) / Number subtomograms used: 27922 |
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Extraction | Number tomograms: 15 / Number images used: 175095 / Software - Name: Dynamo (ver. 1.1.333) |
Final angle assignment | Type: PROJECTION MATCHING / Software - Name: Dynamo (ver. 1.1.333) |