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Yorodumi- EMDB-8741: Thermoplasma acidophilum 20S Proteasome using 200keV with stage p... -
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Open data
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Basic information
| Entry | Database: EMDB / ID: EMD-8741 | |||||||||
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| Title | Thermoplasma acidophilum 20S Proteasome using 200keV with stage position | |||||||||
Map data | Final sharpened map of T. acidophilum 20S proteasome collected using stage position navigation | |||||||||
Sample |
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Keywords | Proteasome / hydrolase | |||||||||
| Function / homology | Function and homology informationproteasome endopeptidase complex / proteasome core complex, beta-subunit complex / threonine-type endopeptidase activity / proteasome core complex, alpha-subunit complex / proteasomal protein catabolic process / ubiquitin-dependent protein catabolic process / endopeptidase activity / cytoplasm Similarity search - Function | |||||||||
| Biological species | ![]() Thermoplasma acidophilum (acidophilic) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.1 Å | |||||||||
Authors | Herzik Jr MA / Wu M / Lander GC | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: Nat Methods / Year: 2017Title: Achieving better-than-3-Å resolution by single-particle cryo-EM at 200 keV. Authors: Mark A Herzik / Mengyu Wu / Gabriel C Lander / ![]() Abstract: Nearly all single-particle cryo-EM structures resolved to better than 4-Å resolution have been determined using 300-keV transmission electron microscopes (TEMs). We demonstrate that it is possible ...Nearly all single-particle cryo-EM structures resolved to better than 4-Å resolution have been determined using 300-keV transmission electron microscopes (TEMs). We demonstrate that it is possible to obtain reconstructions of macromolecular complexes of different sizes to better than 3-Å resolution using a 200-keV TEM. These structures are of sufficient quality to unambiguously assign amino acid rotameric conformations and identify ordered water molecules. | |||||||||
| History |
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Structure visualization
| Movie |
Movie viewer |
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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_8741.map.gz | 59.5 MB | EMDB map data format | |
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| Header (meta data) | emd-8741-v30.xml emd-8741.xml | 22.5 KB 22.5 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_8741_fsc.xml | 17.8 KB | Display | FSC data file |
| Images | emd_8741.png | 38.9 KB | ||
| Filedesc metadata | emd-8741.cif.gz | 6.6 KB | ||
| Others | emd_8741_additional.map.gz emd_8741_half_map_1.map.gz emd_8741_half_map_2.map.gz | 59 MB 409.8 MB 409.9 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-8741 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-8741 | HTTPS FTP |
-Validation report
| Summary document | emd_8741_validation.pdf.gz | 914.7 KB | Display | EMDB validaton report |
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| Full document | emd_8741_full_validation.pdf.gz | 914.3 KB | Display | |
| Data in XML | emd_8741_validation.xml.gz | 24.5 KB | Display | |
| Data in CIF | emd_8741_validation.cif.gz | 32.3 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-8741 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-8741 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 5vy3MC ![]() 8742C ![]() 8743C ![]() 5vy4C ![]() 5vy5C C: citing same article ( M: atomic model generated by this map |
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| Similar structure data | |
| EM raw data | EMPIAR-10185 (Title: T. acidophilum 20S proteasome core movies obtained using Talos Arctica operating at 200 kV equipped with a K2 – stage position used for exposure target navigationData size: 1.1 TB Data #1: Raw, unaligned movie stacks of T. acidophilum 20S proteasome core acquired on a Talos Arctica using a K2 direct electron detector - stage position used for exposure navigation [micrographs - multiframe]) |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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| Related items in Molecule of the Month |
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Map
| File | Download / File: emd_8741.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | Final sharpened map of T. acidophilum 20S proteasome collected using stage position navigation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.91 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Additional map: Unsharpened map of T. acidophilum 20S proteasome collected...
| File | emd_8741_additional.map | ||||||||||||
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| Annotation | Unsharpened map of T. acidophilum 20S proteasome collected using stage position navigation | ||||||||||||
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| Density Histograms |
-Half map: Thermoplasma acidophilum 20S Proteasome, odd half map
| File | emd_8741_half_map_1.map | ||||||||||||
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| Annotation | Thermoplasma acidophilum 20S Proteasome, odd half map | ||||||||||||
| Projections & Slices |
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| Density Histograms |
-Half map: Thermoplasma acidophilum 20S Proteasome, even half map
| File | emd_8741_half_map_2.map | ||||||||||||
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| Annotation | Thermoplasma acidophilum 20S Proteasome, even half map | ||||||||||||
| Projections & Slices |
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| Density Histograms |
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Sample components
-Entire : Thermoplasma acidophilum 20S proteasome
| Entire | Name: Thermoplasma acidophilum 20S proteasome |
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| Components |
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-Supramolecule #1: Thermoplasma acidophilum 20S proteasome
| Supramolecule | Name: Thermoplasma acidophilum 20S proteasome / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all Details: Thermoplasma acidophilum 20S proteasome purified from Escherichia coli |
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| Source (natural) | Organism: ![]() Thermoplasma acidophilum (acidophilic) |
| Molecular weight | Theoretical: 700 KDa |
-Macromolecule #1: Proteasome subunit alpha
| Macromolecule | Name: Proteasome subunit alpha / type: protein_or_peptide / ID: 1 / Number of copies: 14 / Enantiomer: LEVO / EC number: proteasome endopeptidase complex |
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| Source (natural) | Organism: ![]() Thermoplasma acidophilum (acidophilic) |
| Molecular weight | Theoretical: 24.776281 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: RAITVFSPDG RLFQVEYARE AVKKGSTALG MKFANGVLLI SDKKVRSRLI EQNSIEKIQL IDDYVAAVTS GLVADARVLV DFARISAQQ EKVTYGSLVN IENLVKRVAD QMQQYTQYGG VRPYGVSLIF AGIDQIGPRL FDCDPAGTIN EYKATAIGSG K DAVVSFLE ...String: RAITVFSPDG RLFQVEYARE AVKKGSTALG MKFANGVLLI SDKKVRSRLI EQNSIEKIQL IDDYVAAVTS GLVADARVLV DFARISAQQ EKVTYGSLVN IENLVKRVAD QMQQYTQYGG VRPYGVSLIF AGIDQIGPRL FDCDPAGTIN EYKATAIGSG K DAVVSFLE REYKENLPEK EAVTLGIKAL KSSLEEGEEL KAPEIASITV GNKYRIYDQE EVKKFL UniProtKB: Proteasome subunit alpha |
-Macromolecule #2: Proteasome subunit beta
| Macromolecule | Name: Proteasome subunit beta / type: protein_or_peptide / ID: 2 / Number of copies: 14 / Enantiomer: LEVO / EC number: proteasome endopeptidase complex |
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| Source (natural) | Organism: ![]() Thermoplasma acidophilum (acidophilic) |
| Molecular weight | Theoretical: 22.294848 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: TTTVGITLKD AVIMATERRV TMENFIMHKN GKKLFQIDTY TGMTIAGLVG DAQVLVRYMK AELELYRLQR RVNMPIEAVA TLLSNMLNQ VKYMPYMVQL LVGGIDTAPH VFSIDAAGGS VEDIYASTGS GSPFVYGVLE SQYSEKMTVD EGVDLVIRAI S AAKQRDSA ...String: TTTVGITLKD AVIMATERRV TMENFIMHKN GKKLFQIDTY TGMTIAGLVG DAQVLVRYMK AELELYRLQR RVNMPIEAVA TLLSNMLNQ VKYMPYMVQL LVGGIDTAPH VFSIDAAGGS VEDIYASTGS GSPFVYGVLE SQYSEKMTVD EGVDLVIRAI S AAKQRDSA SGGMIDVAVI TRKDGYVQLP TDQIESRIRK LGLIL UniProtKB: Proteasome subunit beta |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 0.5 mg/mL | |||||||||
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| Buffer | pH: 7.4 Component:
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| Grid | Model: Quantifoil, UltrAuFoil, R1.2/1.3 / Material: GOLD / Mesh: 300 / Pretreatment - Type: PLASMA CLEANING / Pretreatment - Time: 7 sec. / Pretreatment - Atmosphere: OTHER / Pretreatment - Pressure: 0.009000000000000001 kPa / Details: 15 Watts | |||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277.15 K / Instrument: HOMEMADE PLUNGER Details: 3 uL of sample/grid was manually blotted for 4 seconds prior to immediate plunge-freezing in liquid nitrogen-cooled ethane.. |
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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 / Digitization - Dimensions - Width: 7420 pixel / Digitization - Dimensions - Height: 7676 pixel / Digitization - Frames/image: 1-68 / Number grids imaged: 1 / Number real images: 629 / Average exposure time: 17.0 sec. / Average electron dose: 65.0 e/Å2 Details: Images were collected using stage position navigation to target exposure. |
| Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 70.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.8000000000000003 µm / Nominal defocus min: 0.8 µm / Nominal magnification: 45000 |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Talos Arctica / Image courtesy: FEI Company |
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Image processing
-Atomic model buiding 1
| Details | Starting model was generated by stripping PDB entry 1YAR of all ligands and alternate conformations, then refining into the EM density using imposed symmetry while adjusting weighting/scoring according to estimated map resolution. The top 10 generated models (ranked based on quality metrics) were real-space refined using Phenix software. |
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| Refinement | Space: REAL / Protocol: OTHER / Overall B value: 101 / Target criteria: Maximum Likelihood |
| Output model | ![]() PDB-5vy3: |
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About Yorodumi


Keywords
Thermoplasma acidophilum (acidophilic)
Authors
United States, 1 items
Citation
UCSF Chimera















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