+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-16256 | |||||||||
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Title | Cryo-EM structure of the BUS complex - domain IV lattice | |||||||||
Map data | ||||||||||
Sample |
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Keywords | DnaA / cryo-EM / BUS complex / replication initiation / REPLICATION | |||||||||
Biological species | Bacillus subtilis (bacteria) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 5.4 Å | |||||||||
Authors | Pelliciari S / Bodet-Lefevre S / Murray H / Ilangovan A | |||||||||
Funding support | United Kingdom, 1 items
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Citation | Journal: To Be Published Title: Cryo-EM structure of the bacterial replication origin opening basal unwinding system Authors: Pelliciari S / Bodet-Lefevre S / Murray H / Ilangovan A | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_16256.map.gz | 62.8 MB | EMDB map data format | |
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Header (meta data) | emd-16256-v30.xml emd-16256.xml | 11.6 KB 11.6 KB | Display Display | EMDB header |
Images | emd_16256.png | 15.4 KB | ||
Filedesc metadata | emd-16256.cif.gz | 3.6 KB | ||
Others | emd_16256_half_map_1.map.gz emd_16256_half_map_2.map.gz | 116 MB 116 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-16256 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-16256 | HTTPS FTP |
-Validation report
Summary document | emd_16256_validation.pdf.gz | 679.3 KB | Display | EMDB validaton report |
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Full document | emd_16256_full_validation.pdf.gz | 678.8 KB | Display | |
Data in XML | emd_16256_validation.xml.gz | 13.8 KB | Display | |
Data in CIF | emd_16256_validation.cif.gz | 16.3 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-16256 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-16256 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_16256.map.gz / Format: CCP4 / Size: 125 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: 1.072 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #1
File | emd_16256_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #2
File | emd_16256_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Basal unwinding complex
Entire | Name: Basal unwinding complex |
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Components |
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-Supramolecule #1: Basal unwinding complex
Supramolecule | Name: Basal unwinding complex / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#4 / Details: Nucleoprotein complex |
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Source (natural) | Organism: Bacillus subtilis (bacteria) |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Buffer | pH: 7.5 |
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Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 48.3 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: SPOT SCAN / Imaging mode: BRIGHT FIELD / Nominal defocus max: 3.0 µm / Nominal defocus min: 0.7000000000000001 µm |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Startup model | Type of model: OTHER / Details: Abinitio |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 5.4 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 1192717 |
Initial angle assignment | Type: MAXIMUM LIKELIHOOD |
Final angle assignment | Type: MAXIMUM LIKELIHOOD |