+
Open data
-
Basic information
Entry | Database: PDB / ID: 8xb5 | ||||||
---|---|---|---|---|---|---|---|
Title | Portal protein of SH-Ab15497 | ||||||
![]() | Portal protein | ||||||
![]() | VIRAL PROTEIN / dodecamer / DNA channel | ||||||
Function / homology | Domain of unknown function DUF4055 / Domain of unknown function (DUF4055) / Portal protein![]() | ||||||
Biological species | ![]() | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.2 Å | ||||||
![]() | Lin, J. / Zhao, S.W. | ||||||
Funding support | ![]()
| ||||||
![]() | ![]() Title: Portal protein of SH-Ab15497 Authors: Lin, J. / Zhao, S.W. | ||||||
History |
|
-
Structure visualization
Structure viewer | Molecule: ![]() ![]() |
---|
-
Downloads & links
-
Download
PDBx/mmCIF format | ![]() | 1011.3 KB | Display | ![]() |
---|---|---|---|---|
PDB format | ![]() | 855.5 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Arichive directory | ![]() ![]() | HTTPS FTP |
---|
-Related structure data
Related structure data | ![]() 38211MC M: map data used to model this data C: citing same article ( |
---|---|
Similar structure data | Similarity search - Function & homology ![]() |
-
Links
-
Assembly
Deposited unit | ![]()
|
---|---|
1 |
|
-
Components
#1: Protein | Mass: 57059.113 Da / Num. of mol.: 12 / Source method: isolated from a natural source / Source: (natural) ![]() Has protein modification | N | |
---|
-Experimental details
-Experiment
Experiment | Method: ELECTRON MICROSCOPY |
---|---|
EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
-
Sample preparation
Component | Name: Acinetobacter phage SH-Ab 15497 / Type: VIRUS / Entity ID: all / Source: NATURAL |
---|---|
Source (natural) | Organism: ![]() |
Details of virus | Empty: NO / Enveloped: NO / Isolate: OTHER / Type: VIRION |
Virus shell | Diameter: 650 nm / Triangulation number (T number): 7 |
Buffer solution | pH: 7.5 |
Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 100 % |
-
Electron microscopy imaging
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
---|---|
Microscopy | Model: TFS KRIOS |
Electron gun | Electron source: ![]() |
Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2500 nm / Nominal defocus min: 1200 nm / Cs: 2.7 mm |
Image recording | Electron dose: 40 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) / Num. of real images: 27057 |
-
Processing
EM software |
| ||||||
---|---|---|---|---|---|---|---|
CTF correction | Type: NONE | ||||||
Symmetry | Point symmetry: C12 (12 fold cyclic) | ||||||
3D reconstruction | Resolution: 3.2 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 36368 / Num. of class averages: 1 / Symmetry type: POINT | ||||||
Refinement | Highest resolution: 3.2 Å |