+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-1708 | |||||||||
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Title | Cryo-EM structure of S. cerevisiae 10-subunit exosome | |||||||||
Map data | Cryo-EM map of S. cerevisiae 10-subunit exosome | |||||||||
Sample |
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Keywords | exosome / cryo-EM / RNA quality control / exoribonuclease | |||||||||
Biological species | Saccharomyces cerevisiae (brewer's yeast) | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 14.0 Å | |||||||||
Authors | Malet H / Topf M / Clare DK / Ebert J / Bonneau F / Basquin J / Drazkowska K / Tomecki R / Dziembowski A / Conti E ...Malet H / Topf M / Clare DK / Ebert J / Bonneau F / Basquin J / Drazkowska K / Tomecki R / Dziembowski A / Conti E / Saibil HR / Lorentzen E | |||||||||
Citation | Journal: EMBO Rep / Year: 2010 Title: RNA channelling by the eukaryotic exosome. Authors: Hélène Malet / Maya Topf / Daniel K Clare / Judith Ebert / Fabien Bonneau / Jerome Basquin / Karolina Drazkowska / Rafal Tomecki / Andrzej Dziembowski / Elena Conti / Helen R Saibil / Esben Lorentzen / Abstract: The eukaryotic exosome is a key nuclease for the degradation, processing and quality control of a wide variety of RNAs. Here, we report electron microscopic reconstructions and pseudo-atomic models ...The eukaryotic exosome is a key nuclease for the degradation, processing and quality control of a wide variety of RNAs. Here, we report electron microscopic reconstructions and pseudo-atomic models of the ten-subunit Saccharomyces cerevisiae exosome in the unbound and RNA-bound states. In the RNA-bound structures, extra density that is visible at the entry and exit sites of the exosome channel indicates that a substrate-threading mechanism is used by the eukaryotic exosome. This channelling mechanism seems to be conserved in exosome-like complexes from all domains of life, and might have been present in the most recent common ancestor. | |||||||||
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_1708.map.gz | 1.1 MB | EMDB map data format | |
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Header (meta data) | emd-1708-v30.xml emd-1708.xml | 22.5 KB 22.5 KB | Display Display | EMDB header |
Images | EMD-1708apoexosomecorrected.tif | 732.7 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-1708 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-1708 | HTTPS FTP |
-Validation report
Summary document | emd_1708_validation.pdf.gz | 185.8 KB | Display | EMDB validaton report |
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Full document | emd_1708_full_validation.pdf.gz | 184.9 KB | Display | |
Data in XML | emd_1708_validation.xml.gz | 5.5 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-1708 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-1708 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_1708.map.gz / Format: CCP4 / Size: 7.8 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Cryo-EM map of S. cerevisiae 10-subunit exosome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 2.6 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 : S. cerevisiae 10-subunit exosome
+Supramolecule #1000: S. cerevisiae 10-subunit exosome
+Macromolecule #1: Rrp41
+Macromolecule #2: Rrp42
+Macromolecule #3: Rrp43
+Macromolecule #4: Rrp44
+Macromolecule #5: Rrp45
+Macromolecule #6: Rrp46
+Macromolecule #7: Mtr3
+Macromolecule #8: Rrp4
+Macromolecule #9: Rrp40
+Macromolecule #10: Csl4
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 0.3 mg/mL |
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Buffer | pH: 7.5 / Details: 20 mM Tris-Hcl pH 7.5, 50 mM NaCl, 1 mM DTT |
Grid | Details: C-flat grid CF-2/2-4C-100 |
Vitrification | Cryogen name: ETHANE / Chamber temperature: 100 K / Instrument: HOMEMADE PLUNGER / Details: Vitrification instrument: Manual plunger / Method: Blot for 2 seconds before plunging |
-Electron microscopy
Microscope | FEI POLARA 300 |
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Temperature | Average: 100 K |
Alignment procedure | Legacy - Astigmatism: Objective lens astigmatism was corrected at 150,000 times magnification Legacy - Electron beam tilt params: 0 |
Image recording | Category: CCD / Film or detector model: GENERIC GATAN (4k x 4k) / Digitization - Sampling interval: 15 µm / Number real images: 250 / Average electron dose: 25 e/Å2 / Bits/pixel: 16 |
Tilt angle min | 0 |
Tilt angle max | 0 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Calibrated magnification: 121000 / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.3 mm / Nominal defocus max: 3.5 µm / Nominal defocus min: 1.5 µm / Nominal magnification: 121000 |
Sample stage | Specimen holder: Gatan helium / Specimen holder model: GATAN HELIUM |
Experimental equipment | Model: Tecnai Polara / Image courtesy: FEI Company |
-Image processing
CTF correction | Details: Phase flipping |
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Final reconstruction | Applied symmetry - Point group: C1 (asymmetric) / Algorithm: OTHER / Resolution.type: BY AUTHOR / Resolution: 14.0 Å / Resolution method: FSC 0.5 CUT-OFF / Software - Name: IMAGIC-5, SPIDER / Number images used: 15000 |
-Atomic model buiding 1
Initial model | PDB ID: Chain - #0 - Chain ID: C / Chain - #1 - Chain ID: D / Chain - #2 - Chain ID: E / Chain - #3 - Chain ID: F / Chain - #4 - Chain ID: H |
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Software | Name: Flex-EM |
Details | PDBEntryID_givenInChain. Protocol: Flexible fitting of rigid bodies. Homology models of yeast subunits have been calculated using MODELLER from the chains C, D, E, F and H of the PDB entry 2NN6. Resulting homology models have been used for flexible fitting into the cryo-EM map. |
Refinement | Space: REAL / Protocol: FLEXIBLE FIT / Target criteria: Cross-correlation, energy |
-Atomic model buiding 2
Initial model | PDB ID: Chain - #0 - Chain ID: A / Chain - #1 - Chain ID: B / Chain - #2 - Chain ID: J |
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Software | Name: Flex-EM |
Details | PDBEntryID_givenInChain. Protocol: Flexible fitting of rigid bodies |
Refinement | Space: REAL / Protocol: FLEXIBLE FIT / Target criteria: cross-correlation, energy |
-Atomic model buiding 3
Initial model | PDB ID: Chain - Chain ID: A |
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Software | Name: Flex-EM |
Details | PDBEntryID_givenInChain. Protocol: Flexible fitting of rigid body |
Refinement | Space: REAL / Protocol: FLEXIBLE FIT / Target criteria: cross-correlation, energy |