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Yorodumi- PDB-9s4q: Cryo-EM structure of the Saccharomyces cerevisiae KMN junction co... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 9s4q | |||||||||||||||
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| Title | Cryo-EM structure of the Saccharomyces cerevisiae KMN junction complex lacking the Mis12c(Mtw1c) head 2 domain | |||||||||||||||
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Keywords | CELL CYCLE / Kinetochore / chromosome segregation / mitosis | |||||||||||||||
| Function / homology | Function and homology informationregulation of meiosis I spindle assembly checkpoint / Knl1/Spc105 complex / positive regulation of meiosis I spindle assembly checkpoint / homologous chromosome orientation in meiotic metaphase I / centromere clustering / MIS12/MIND type complex / Ndc80 complex / mitotic sister chromatid biorientation / spindle attachment to meiosis I kinetochore / sister chromatid biorientation ...regulation of meiosis I spindle assembly checkpoint / Knl1/Spc105 complex / positive regulation of meiosis I spindle assembly checkpoint / homologous chromosome orientation in meiotic metaphase I / centromere clustering / MIS12/MIND type complex / Ndc80 complex / mitotic sister chromatid biorientation / spindle attachment to meiosis I kinetochore / sister chromatid biorientation / attachment of spindle microtubules to kinetochore / meiotic sister chromatid cohesion, centromeric / kinetochore assembly / outer kinetochore / protein localization to kinetochore / mitotic spindle assembly checkpoint signaling / mitotic sister chromatid segregation / chromosome, centromeric region / Neutrophil degranulation / chromosome segregation / kinetochore / spindle pole / microtubule binding / cell division / mitochondrion / identical protein binding / nucleus Similarity search - Function | |||||||||||||||
| Biological species | ![]() | |||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 4.9 Å | |||||||||||||||
Authors | Turner, N.N. / Barford, D. | |||||||||||||||
| Funding support | United Kingdom, 3items
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Citation | Journal: To Be PublishedTitle: Assembly and phospho-regulatory mechanisms of the budding yeast outer kinetochore KMN complex Authors: Turner, N.N. / Zhang, Z. / Muir, K.W. / McLaughlin, S.H. / Morgan, T. / Barford, D. | |||||||||||||||
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 9s4q.cif.gz | 442.6 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb9s4q.ent.gz | Display | PDB format | |
| PDBx/mmJSON format | 9s4q.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/s4/9s4q ftp://data.pdbj.org/pub/pdb/validation_reports/s4/9s4q | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 54579MC ![]() 9s53C ![]() 9s5nC C: citing same article ( M: map data used to model this data |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
-Kinetochore-associated protein ... , 4 types, 4 molecules NnMtDsNs
| #1: Protein | Mass: 23668.541 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: P47149 |
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| #2: Protein | Mass: 33291.180 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: P39731 |
| #5: Protein | Mass: 65777.023 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: P40568 |
| #8: Protein | Mass: 25448.398 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: Q12143 |
-Outer kinetochore KNL1 complex subunit ... , 2 types, 2 molecules ZwKl
| #3: Protein | Mass: 48468.273 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Details: Fused to a C-terminal TEV protease cleavage site and twin-strep-tag II affinity tag. Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: Q04431 |
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| #4: Protein | Mass: 55581.047 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Details: N-terminal truncation of residues 1-444 / Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: P53148 |
-Kinetochore protein ... , 2 types, 2 molecules 2425
| #6: Protein | Mass: 24639.814 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: Q04477 |
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| #7: Protein | Mass: 25280.326 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Trichoplusia ni (cabbage looper) / References: UniProt: P40014 |
-Details
| Has protein modification | N |
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-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
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| Source (natural) |
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| Buffer solution | pH: 7.5 | |||||||||||||||||||||||||||||||||||
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| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES | |||||||||||||||||||||||||||||||||||
| Specimen support | Details: Edwards S150B glow discharger / Grid material: GOLD / Grid mesh size: 300 divisions/in. / Grid type: UltrAuFoil R1.2/1.3 | |||||||||||||||||||||||||||||||||||
| Vitrification | Instrument: FEI VITROBOT MARK III / Cryogen name: ETHANE |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: TFS KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal magnification: 105000 X / Nominal defocus max: 3000 nm / Nominal defocus min: 1400 nm |
| Specimen holder | Cryogen: NITROGEN / Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER |
| Image recording | Electron dose: 40 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
| EM imaging optics | Energyfilter slit width: 20 eV |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||||||||||
| Particle selection | Num. of particles selected: 2592458 Details: Selected using Topaz particle picker trained on manually picked micrographs | ||||||||||||||||||||||||||||||||
| 3D reconstruction | Resolution: 4.9 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 113688 / Algorithm: BACK PROJECTION Details: Composite cryo-EM of two multibody refinement-derived map refined to the consensus map. Num. of class averages: 1 / Symmetry type: POINT | ||||||||||||||||||||||||||||||||
| Atomic model building | Protocol: FLEXIBLE FIT / Space: REAL Details: Flexible fitting using Isolde, real-space refinement using Phenix | ||||||||||||||||||||||||||||||||
| Atomic model building | Source name: AlphaFold / Type: in silico model | ||||||||||||||||||||||||||||||||
| Refine LS restraints |
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About Yorodumi





United Kingdom, 3items
Citation







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Trichoplusia ni (cabbage looper)
FIELD EMISSION GUN