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Yorodumi- EMDB-22794: Alpha2-macroglobulin family protein isolated from interphase chro... -
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Open data
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Basic information
| Entry | Database: EMDB / ID: EMD-22794 | |||||||||
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| Title | Alpha2-macroglobulin family protein isolated from interphase chromosome formed in Xenopus egg extract | |||||||||
Map data | Alpha2-macroglobulin family protein isolated from interphase chromosome formed in Xenopus egg extract | |||||||||
Sample |
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| Method | single particle reconstruction / cryo EM / Resolution: 8.07 Å | |||||||||
Authors | Arimura Y / Funabiki H | |||||||||
| Funding support | United States, Japan, 2 items
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Citation | Journal: Mol Cell / Year: 2021Title: Structural features of nucleosomes in interphase and metaphase chromosomes. Authors: Yasuhiro Arimura / Rochelle M Shih / Ruby Froom / Hironori Funabiki / ![]() Abstract: Structural heterogeneity of nucleosomes in functional chromosomes is unknown. Here, we devise the template-, reference- and selection-free (TRSF) cryo-EM pipeline to simultaneously reconstruct cryo- ...Structural heterogeneity of nucleosomes in functional chromosomes is unknown. Here, we devise the template-, reference- and selection-free (TRSF) cryo-EM pipeline to simultaneously reconstruct cryo-EM structures of protein complexes from interphase or metaphase chromosomes. The reconstructed interphase and metaphase nucleosome structures are on average indistinguishable from canonical nucleosome structures, despite DNA sequence heterogeneity, cell-cycle-specific posttranslational modifications, and interacting proteins. Nucleosome structures determined by a decoy-classifying method and structure variability analyses reveal the nucleosome structural variations in linker DNA, histone tails, and nucleosome core particle configurations, suggesting that the opening of linker DNA, which is correlated with H2A C-terminal tail positioning, is suppressed in chromosomes. High-resolution (3.4-3.5 Å) nucleosome structures indicate DNA-sequence-independent stabilization of superhelical locations ±0-1 and ±3.5-4.5. The linker histone H1.8 preferentially binds to metaphase chromatin, from which chromatosome cryo-EM structures with H1.8 at the on-dyad position are reconstituted. This study presents the structural characteristics of nucleosomes in chromosomes. | |||||||||
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Structure visualization
| Movie |
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| Structure viewer | EM map: SurfView Molmil Jmol/JSmol |
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_22794.map.gz | 118 MB | EMDB map data format | |
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| Header (meta data) | emd-22794-v30.xml emd-22794.xml | 17.1 KB 17.1 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_22794_fsc.xml | 11.2 KB | Display | FSC data file |
| Images | emd_22794.png | 104.3 KB | ||
| Masks | emd_22794_msk_1.map | 125 MB | Mask map | |
| Others | emd_22794_half_map_1.map.gz emd_22794_half_map_2.map.gz | 116 MB 116 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-22794 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-22794 | HTTPS FTP |
-Validation report
| Summary document | emd_22794_validation.pdf.gz | 662.5 KB | Display | EMDB validaton report |
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| Full document | emd_22794_full_validation.pdf.gz | 662 KB | Display | |
| Data in XML | emd_22794_validation.xml.gz | 18.4 KB | Display | |
| Data in CIF | emd_22794_validation.cif.gz | 23.9 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-22794 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-22794 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 7kbdC ![]() 7kbeC ![]() 7kbfC C: citing same article ( |
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| Similar structure data | |
| EM raw data | EMPIAR-10692 (Title: Oligo nucleosome fraction from interphase chromosome in Xenopus egg extract lot 1Data size: 634.3 Data #1: oligo nucleosome fraction from the interphase chromosome in Xenopus egg extract lot1 [micrographs - multiframe]) |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_22794.map.gz / Format: CCP4 / Size: 125 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | Alpha2-macroglobulin family protein isolated from interphase chromosome formed in Xenopus egg extract | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.5 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Mask #1
| File | emd_22794_msk_1.map | ||||||||||||
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| Density Histograms |
-Half map: Alpha2-macroglobulin family protein isolated from interphase chromosome formed...
| File | emd_22794_half_map_1.map | ||||||||||||
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| Annotation | Alpha2-macroglobulin family protein isolated from interphase chromosome formed in Xenopus egg extract | ||||||||||||
| Projections & Slices |
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| Density Histograms |
-Half map: Alpha2-macroglobulin family protein isolated from interphase chromosome formed...
| File | emd_22794_half_map_2.map | ||||||||||||
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| Annotation | Alpha2-macroglobulin family protein isolated from interphase chromosome formed in Xenopus egg extract | ||||||||||||
| Projections & Slices |
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| Density Histograms |
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Sample components
-Entire : alpha2-macroglobulin isolated from interphase chromosome formed i...
| Entire | Name: alpha2-macroglobulin isolated from interphase chromosome formed in Xenopus egg extract |
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| Components |
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-Supramolecule #1: alpha2-macroglobulin isolated from interphase chromosome formed i...
| Supramolecule | Name: alpha2-macroglobulin isolated from interphase chromosome formed in Xenopus egg extract type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#6 |
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| Source (natural) | Organism: |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 7.4 Component:
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| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | FEI TALOS ARCTICA |
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| Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: SUPER-RESOLUTION / Average electron dose: 33.11 e/Å2 |
| Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD |
| Experimental equipment | ![]() Model: Talos Arctica / Image courtesy: FEI Company |
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About Yorodumi


Authors
United States,
Japan, 2 items
Citation
UCSF Chimera






















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