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Yorodumi- EMDB-1920: Improved ab initio 3D reconstruction of the EF-G containing E. co... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-1920 | |||||||||
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Title | Improved ab initio 3D reconstruction of the EF-G containing E. coli ribosome by SIMPLE | |||||||||
Map data | This is a volume of the EF-G containing E. coli ribosome reconstructed by SIMPLE | |||||||||
Sample |
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Keywords | ab initio | |||||||||
Biological species | Escherichia coli (E. coli) | |||||||||
Method | single particle reconstruction / cryo EM | |||||||||
Authors | Elmlund H | |||||||||
Citation | Journal: Ultramicroscopy / Year: 2001 Title: Strul--a method for 3D alignment of single-particle projections based on common line correlation in Fourier space. Authors: M Lindahl / Abstract: A central problem of 3D reconstruction in single-particle electron microscopy is the determination of relative orientations of the individual projections contributing to the reconstruction. This ...A central problem of 3D reconstruction in single-particle electron microscopy is the determination of relative orientations of the individual projections contributing to the reconstruction. This article describes an implementation of the method of common lines correlation in Fourier space that allows generation of common lines between an arbitrary number of projections which might posses an arbitrary point group symmetry. Based on this method, it is possible to optimize rotational and translational alignment parameters for individual single-particle projections. The underlying philosophy and details of implementation are discussed, and as an illustration a 3D reconstruction in ice of peroxisomal alcohol oxidase from Pichia pastoris, an octameric assembly with 422-symmetry and a molecular weight of 592 kDa is presented. | |||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_1920.map.gz | 7.4 MB | EMDB map data format | |
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Header (meta data) | emd-1920-v30.xml emd-1920.xml | 6.8 KB 6.8 KB | Display Display | EMDB header |
Images | EMD-1920.png | 99.9 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-1920 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-1920 | HTTPS FTP |
-Validation report
Summary document | emd_1920_validation.pdf.gz | 210.2 KB | Display | EMDB validaton report |
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Full document | emd_1920_full_validation.pdf.gz | 209.3 KB | Display | |
Data in XML | emd_1920_validation.xml.gz | 5.5 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-1920 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-1920 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Related items in Molecule of the Month |
-Map
File | Download / File: emd_1920.map.gz / Format: CCP4 / Size: 7.8 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | This is a volume of the EF-G containing E. coli ribosome reconstructed by SIMPLE | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 2.82 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Sample components
-Entire : EF-G ribosome test data
Entire | Name: EF-G ribosome test data |
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Components |
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-Supramolecule #1000: EF-G ribosome test data
Supramolecule | Name: EF-G ribosome test data / type: sample / ID: 1000 / Number unique components: 2 |
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-Supramolecule #1: Ribosome
Supramolecule | Name: Ribosome / type: complex / ID: 1 / Name.synonym: Ribosome / Recombinant expression: No / Ribosome-details: ribosome-prokaryote: ALL |
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Source (natural) | Organism: Escherichia coli (E. coli) |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Vitrification | Cryogen name: ETHANE / Instrument: OTHER |
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-Electron microscopy
Microscope | OTHER |
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Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: OTHER / Imaging mode: BRIGHT FIELD |
Sample stage | Specimen holder: Eucentric / Specimen holder model: GATAN LIQUID NITROGEN |
-Image processing
Final reconstruction | Applied symmetry - Point group: C1 (asymmetric) / Algorithm: OTHER / Software - Name: SIMPLE |
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