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Open data
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Basic information
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| Title | Localized reconstructed spike HCIV-1 | |||||||||
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Sample |
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| Biological species | Haloarcula californiae ATCC 33799 (Halophile) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 8.9 Å | |||||||||
Authors | Santos-Perez I / Charro D / Gil-Carton D / Azkargorta M / Elortza F / Bamford DH / Oksanen HM / Abrescia NGA | |||||||||
Citation | Journal: Nat Commun / Year: 2019Title: Structural basis for assembly of vertical single β-barrel viruses. Authors: Isaac Santos-Pérez / Diego Charro / David Gil-Carton / Mikel Azkargorta / Felix Elortza / Dennis H Bamford / Hanna M Oksanen / Nicola G A Abrescia / ![]() Abstract: The vertical double β-barrel major capsid protein (MCP) fold, fingerprint of the PRD1-adeno viral lineage, is widespread in many viruses infecting organisms across the three domains of life. The ...The vertical double β-barrel major capsid protein (MCP) fold, fingerprint of the PRD1-adeno viral lineage, is widespread in many viruses infecting organisms across the three domains of life. The discovery of PRD1-like viruses with two MCPs challenged the known assembly principles. Here, we present the cryo-electron microscopy (cryo-EM) structures of the archaeal, halophilic, internal membrane-containing Haloarcula californiae icosahedral virus 1 (HCIV-1) and Haloarcula hispanica icosahedral virus 2 (HHIV-2) at 3.7 and 3.8 Å resolution, respectively. Our structures reveal proteins located beneath the morphologically distinct two- and three-tower capsomers and homopentameric membrane proteins at the vertices that orchestrate the positioning of pre-formed vertical single β-barrel MCP heterodimers. The cryo-EM based structures together with the proteomics data provide insights into the assembly mechanism of this type of viruses and into those with membrane-less double β-barrel MCPs. | |||||||||
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Structure visualization
| Structure viewer | EM map: SurfView Molmil Jmol/JSmol |
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Downloads & links
-EMDB archive
| Map data | emd_0073.map.gz | 96.2 MB | EMDB map data format | |
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| Header (meta data) | emd-0073-v30.xml emd-0073.xml | 19.3 KB 19.3 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_0073_fsc.xml | 10.8 KB | Display | FSC data file |
| Images | emd_0073.png | 90.3 KB | ||
| Others | emd_0073_additional.map.gz emd_0073_half_map_1.map.gz emd_0073_half_map_2.map.gz | 52.8 MB 79.5 MB 79.5 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-0073 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-0073 | HTTPS FTP |
-Validation report
| Summary document | emd_0073_validation.pdf.gz | 377.2 KB | Display | EMDB validaton report |
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| Full document | emd_0073_full_validation.pdf.gz | 376.3 KB | Display | |
| Data in XML | emd_0073_validation.xml.gz | 16.2 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-0073 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-0073 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 0050C ![]() 0072C ![]() 0131C ![]() 0172C ![]() 0174C ![]() 6h82C ![]() 6h9cC C: citing same article ( |
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| Similar structure data |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_0073.map.gz / Format: CCP4 / Size: 103 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.4 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Additional map: local resolution estimation performed using the post-processing-like procedure...
| File | emd_0073_additional.map | ||||||||||||
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| Annotation | local resolution estimation performed using the post-processing-like procedure in RELION 2.1 | ||||||||||||
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| Density Histograms |
-Half map: #1
| File | emd_0073_half_map_1.map | ||||||||||||
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-Half map: #2
| File | emd_0073_half_map_2.map | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : Haloarcula californiae ATCC 33799
| Entire | Name: Haloarcula californiae ATCC 33799 (Halophile) |
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| Components |
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-Supramolecule #1: Haloarcula californiae ATCC 33799
| Supramolecule | Name: Haloarcula californiae ATCC 33799 / type: virus / ID: 1 / Parent: 0 / Details: Haloarcula californiae icosahedral virus - 1 / NCBI-ID: 662475 / Sci species name: Haloarcula californiae ATCC 33799 / Virus type: VIRION / Virus isolate: SPECIES / Virus enveloped: No / Virus empty: Yes |
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| Host (natural) | Organism: Haloarcula californiae ATCC 33799 (Halophile) |
| Virus shell | Shell ID: 1 / Diameter: 800.0 Å / T number (triangulation number): 28 |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 1.2 mg/mL | ||||||||||||||||||
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| Buffer | pH: 7.2 Component:
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| Vitrification | Cryogen name: ETHANE / Instrument: FEI VITROBOT MARK III |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Image recording | Film or detector model: FEI FALCON II (4k x 4k) / Detector mode: INTEGRATING / Digitization - Frames/image: 1-26 / Number grids imaged: 1 / Number real images: 3218 / Average electron dose: 36.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 3.9 µm / Nominal defocus min: 0.6 µm |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi




Haloarcula californiae ATCC 33799 (Halophile)
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Processing
FIELD EMISSION GUN

