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- EMDB-1256: Structure of a hexameric RNA packaging motor in a viral polymeras... -
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Open data
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Basic information
Entry | Database: EMDB / ID: EMD-1256 | |||||||||
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Title | Structure of a hexameric RNA packaging motor in a viral polymerase complex. | |||||||||
![]() | Bacteriophage phi8 vertex with the hexameric packaging motor P4 reconstructed within the viral core without applying any symmetry | |||||||||
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Biological species | ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 15.0 Å | |||||||||
![]() | Huiskonen JT / Jaalinoja HT / Briggs JAG | |||||||||
![]() | ![]() Title: Structure of a hexameric RNA packaging motor in a viral polymerase complex. Authors: Juha T Huiskonen / Harri T Jäälinoja / John A G Briggs / Stephen D Fuller / Sarah J Butcher / ![]() Abstract: Packaging of the Cystovirus varphi8 genome into the polymerase complex is catalysed by the hexameric P4 packaging motor. The motor is located at the fivefold vertices of the icosahedrally symmetric ...Packaging of the Cystovirus varphi8 genome into the polymerase complex is catalysed by the hexameric P4 packaging motor. The motor is located at the fivefold vertices of the icosahedrally symmetric polymerase complex, and the symmetry mismatch between them may be critical for function. We have developed a novel image-processing approach for the analysis of symmetry-mismatched structures and applied it to cryo-electron microscopy images of P4 bound to the polymerase complex. This approach allowed us to solve the three-dimensional structure of the P4 in situ to 15-A resolution. The C-terminal face of P4 was observed to interact with the polymerase complex, supporting the current view on RNA translocation. We suggest that the symmetry mismatch between the two components may facilitate the ring opening required for RNA loading prior to its translocation. | |||||||||
History |
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Structure visualization
Movie |
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Structure viewer | EM map: ![]() ![]() ![]() |
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 3.6 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 8.2 KB 8.2 KB | Display Display | ![]() |
Images | ![]() | 15.3 KB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Validation report
Summary document | ![]() | 222.5 KB | Display | ![]() |
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Full document | ![]() | 221.6 KB | Display | |
Data in XML | ![]() | 5.1 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
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Links
EMDB pages | ![]() ![]() |
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Map
File | ![]() | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Bacteriophage phi8 vertex with the hexameric packaging motor P4 reconstructed within the viral core without applying any symmetry | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 2.8 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
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Sample components
-Entire : Bacteriophage phi8 core
Entire | Name: Bacteriophage phi8 core |
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Components |
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-Supramolecule #1000: Bacteriophage phi8 core
Supramolecule | Name: Bacteriophage phi8 core / type: sample / ID: 1000 / Number unique components: 1 |
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Molecular weight | Theoretical: 33 MDa |
-Supramolecule #1: Pseudomonas phage phi8
Supramolecule | Name: Pseudomonas phage phi8 / type: virus / ID: 1 / Name.synonym: Bacteriophage phi8 / NCBI-ID: 120086 / Sci species name: Pseudomonas phage phi8 / Virus type: VIRION / Virus isolate: SPECIES / Virus enveloped: Yes / Virus empty: No / Syn species name: Bacteriophage phi8 |
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Host (natural) | Organism: ![]() |
Molecular weight | Experimental: 33 MDa |
Virus shell | Shell ID: 1 / T number (triangulation number): 1 |
-Experimental details
-Structure determination
Method | cryo EM |
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![]() | single particle reconstruction |
Aggregation state | particle |
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Sample preparation
Buffer | pH: 7.5 Details: 10 mM potassium phosphate pH 7.5, 1 mM MgCl2, 50 mM NaCl |
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Grid | Details: 200 mesh holey carbon coated copper grid |
Vitrification | Cryogen name: ETHANE |
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Electron microscopy
Microscope | FEI TECNAI F20 |
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Image recording | Category: FILM / Film or detector model: KODAK SO-163 FILM / Digitization - Scanner: ZEISS SCAI / Digitization - Sampling interval: 7 µm / Number real images: 66 / Bits/pixel: 12 |
Electron beam | Acceleration voltage: 200 kV / Electron source: ![]() |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.0 mm / Nominal defocus max: 3.3 µm / Nominal defocus min: 0.7 µm / Nominal magnification: 50000 |
Sample stage | Specimen holder: Side entry liquid nitrogen-cooled cryo specimen holder Specimen holder model: OTHER |
Experimental equipment | ![]() Model: Tecnai F20 / Image courtesy: FEI Company |
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Image processing
CTF correction | Details: Each particle, phases flipped |
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Final reconstruction | Applied symmetry - Point group: C1 (asymmetric) / Algorithm: OTHER / Resolution.type: BY AUTHOR / Resolution: 15.0 Å / Resolution method: FSC 3 SIGMA CUT-OFF / Software - Name: Imagic5 |
Final two d classification | Number classes: 1267 |