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Yorodumi- PDB-8q85: Outer kinetochore Dam1 protomer monomer Ndc80-Nuf2 coiled-coil complex -
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Open data
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Basic information
| Entry | Database: PDB / ID: 8q85 | |||||||||
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| Title | Outer kinetochore Dam1 protomer monomer Ndc80-Nuf2 coiled-coil complex | |||||||||
Components |
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Keywords | CELL CYCLE / Kinetochore / microtubule / error correction / chromosome segregation | |||||||||
| Function / homology | Function and homology informationmitotic spindle polar microtubule / centromere clustering / Ndc80 complex / DASH complex / protein transport along microtubule to mitotic spindle pole body / mitotic sister chromatid biorientation / kinetochore organization / meiotic chromosome segregation / mitotic spindle midzone / mitotic spindle pole body ...mitotic spindle polar microtubule / centromere clustering / Ndc80 complex / DASH complex / protein transport along microtubule to mitotic spindle pole body / mitotic sister chromatid biorientation / kinetochore organization / meiotic chromosome segregation / mitotic spindle midzone / mitotic spindle pole body / positive regulation of attachment of spindle microtubules to kinetochore / attachment of spindle microtubules to kinetochore / protein localization to chromosome, centromeric region / outer kinetochore / attachment of mitotic spindle microtubules to kinetochore / condensed chromosome, centromeric region / protein localization to kinetochore / spindle pole body / positive regulation of microtubule polymerization / mitotic spindle organization / spindle microtubule / chromosome segregation / kinetochore / spindle pole / mitotic spindle / microtubule binding / microtubule / cell division / protein-containing complex binding / identical protein binding / nucleus / cytoplasm Similarity search - Function | |||||||||
| Biological species | ![]() | |||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.97 Å | |||||||||
Authors | Muir, K.W. / Barford, D. | |||||||||
| Funding support | United Kingdom, 2items
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Citation | Journal: Science / Year: 2023Title: Structural mechanism of outer kinetochore Dam1-Ndc80 complex assembly on microtubules. Authors: Kyle W Muir / Christopher Batters / Tom Dendooven / Jing Yang / Ziguo Zhang / Alister Burt / David Barford / ![]() Abstract: Kinetochores couple chromosomes to the mitotic spindle to segregate the genome during cell division. An error correction mechanism drives the turnover of kinetochore-microtubule attachments until ...Kinetochores couple chromosomes to the mitotic spindle to segregate the genome during cell division. An error correction mechanism drives the turnover of kinetochore-microtubule attachments until biorientation is achieved. The structural basis for how kinetochore-mediated chromosome segregation is accomplished and regulated remains an outstanding question. In this work, we describe the cryo-electron microscopy structure of the budding yeast outer kinetochore Ndc80 and Dam1 ring complexes assembled onto microtubules. Complex assembly occurs through multiple interfaces, and a staple within Dam1 aids ring assembly. Perturbation of key interfaces suppresses yeast viability. Force-rupture assays indicated that this is a consequence of impaired kinetochore-microtubule attachment. The presence of error correction phosphorylation sites at Ndc80-Dam1 ring complex interfaces and the Dam1 staple explains how kinetochore-microtubule attachments are destabilized and reset. | |||||||||
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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 | 8q85.cif.gz | 281.6 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb8q85.ent.gz | 200.4 KB | Display | PDB format |
| PDBx/mmJSON format | 8q85.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 8q85_validation.pdf.gz | 1.3 MB | Display | wwPDB validaton report |
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| Full document | 8q85_full_validation.pdf.gz | 1.3 MB | Display | |
| Data in XML | 8q85_validation.xml.gz | 45.9 KB | Display | |
| Data in CIF | 8q85_validation.cif.gz | 70.4 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/q8/8q85 ftp://data.pdbj.org/pub/pdb/validation_reports/q8/8q85 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 18247MC ![]() 8q84C M: map data used to model this data C: citing same article ( |
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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 protein ... , 2 types, 2 molecules FG
| #1: Protein | Mass: 80609.375 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: NDC80 / Production host: Trichoplusia ni (cabbage looper) / References: UniProt: P40460 |
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| #2: Protein | Mass: 53025.949 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: NUF2 / Production host: Trichoplusia ni (cabbage looper) / References: UniProt: P33895 |
-DASH complex subunit ... , 10 types, 10 molecules UVWXYZabcd
| #3: Protein | Mass: 38477.871 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: DAM1 / Production host: Trichoplusia ni (cabbage looper) / References: UniProt: P53267 |
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| #4: Protein | Mass: 27515.008 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: DUO1 / Production host: Trichoplusia ni (cabbage looper) / References: UniProt: P53168 |
| #5: Protein | Mass: 15084.501 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: DAD2 / Production host: Trichoplusia ni (cabbage looper) / References: UniProt: P36162 |
| #6: Protein | Mass: 10522.616 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: DAD1 / Production host: Trichoplusia ni (cabbage looper) / References: UniProt: Q12248 |
| #7: Protein | Mass: 8164.255 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: DAD4 / Production host: Trichoplusia ni (cabbage looper) / References: UniProt: P69851 |
| #8: Protein | Mass: 10862.234 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: DAD3 / Production host: Trichoplusia ni (cabbage looper) / References: UniProt: P69850 |
| #9: Protein | Mass: 34131.812 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: SPC34 / Production host: Trichoplusia ni (cabbage looper) / References: UniProt: P36131 |
| #10: Protein | Mass: 32106.631 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: ASK1 / Production host: Trichoplusia ni (cabbage looper) / References: UniProt: P35734 |
| #11: Protein | Mass: 8097.205 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: HSK3 / Production host: Trichoplusia ni (cabbage looper) / References: UniProt: P69852 |
| #12: Protein | Mass: 18935.559 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: SPC19 / Production host: Trichoplusia ni (cabbage looper) / References: UniProt: Q03954 |
-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
| Component | Name: Outer kinetochore Dam1 protomer monomer with staple and Ndc80-Nuf2 coiled-coils Type: COMPLEX / Entity ID: all / Source: RECOMBINANT |
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| Molecular weight | Value: 673772.36 ° / Experimental value: NO |
| Source (natural) | Organism: ![]() |
| Source (recombinant) | Organism: Trichoplusia ni (cabbage looper) |
| Buffer solution | pH: 6.8 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | 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 defocus max: 3000 nm / Nominal defocus min: 1200 nm |
| Image recording | Electron dose: 50 e/Å2 / Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||||||
| 3D reconstruction | Resolution: 3.97 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 77272 / Symmetry type: POINT | ||||||||||||||||||||||||||||
| Atomic model building | B value: 540.98 / Protocol: OTHER / Space: REAL Details: Initial rigid body fitting was performed in chimera, with manual correction in coot and real-space refinement in PHENIX | ||||||||||||||||||||||||||||
| Atomic model building | Source name: AlphaFold / Type: in silico model | ||||||||||||||||||||||||||||
| Refinement | Cross valid method: NONE Stereochemistry target values: GeoStd + Monomer Library + CDL v1.2 | ||||||||||||||||||||||||||||
| Displacement parameters | Biso mean: 524.1 Å2 | ||||||||||||||||||||||||||||
| Refine LS restraints |
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About Yorodumi





United Kingdom, 2items
Citation



PDBj


Trichoplusia ni (cabbage looper)
FIELD EMISSION GUN