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- EMDB-16560: Structure of the yeast delta mtg1 mitochondrial ribosome assembly... -

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Basic information

Entry
Database: EMDB / ID: EMD-16560
TitleStructure of the yeast delta mtg1 mitochondrial ribosome assembly intermediate - State 2
Map dataState 2, mt-monosome, consensus
Sample
  • Complex: yeast mitochondrial ribosome- State2
KeywordsYeast mitochondrial ribosome / monosome / RIBOSOME
Biological speciesSaccharomyces cerevisiae W303 (yeast)
Methodsingle particle reconstruction / cryo EM / Resolution: 6.0 Å
AuthorsConrad J / Rathore S / Barrientos A
Funding support United States, Sweden, Germany, 4 items
OrganizationGrant numberCountry
National Institutes of Health/National Institute of General Medical Sciences (NIH/NIGMS)GM118141 United States
Swedish Research Council201803694 Sweden
Knut and Alice Wallenberg Foundation2017009 Sweden
German Research Foundation (DFG)SFB860 Germany
CitationJournal: To Be Published
Title: The late stages of yeast mitoribosome large subunit biogenesis
Authors: Rathore S / Conrad J / De Silva D / Ferrari A / Bouquio D / Kim H-J / Urlaub H / Ott M / Barrientos A
History
DepositionJan 27, 2023-
Header (metadata) releaseFeb 7, 2024-
Map releaseFeb 7, 2024-
UpdateFeb 7, 2024-
Current statusFeb 7, 2024Processing site: PDBe / Status: Released

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Structure visualization

Supplemental images

Downloads & links

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Map

FileDownload / File: emd_16560.map.gz / Format: CCP4 / Size: 178 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
AnnotationState 2, mt-monosome, consensus
Voxel sizeX=Y=Z: 1.37 Å
Density
Contour LevelBy AUTHOR: 1.8
Minimum - Maximum-18.885147 - 9.550606999999999
Average (Standard dev.)0.000000000003877 (±1.0)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderZYX
Origin000
Dimensions360360360
Spacing360360360
CellA=B=C: 493.2 Å
α=β=γ: 90.0 °

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Supplemental data

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Additional map: State 2, mt-monosome, LSU body

Fileemd_16560_additional_1.map
AnnotationState 2, mt-monosome, LSU body
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

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Additional map: State 2, mt-monosome, SSU body

Fileemd_16560_additional_2.map
AnnotationState 2, mt-monosome, SSU body
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

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Additional map: State 2, mt-monosome, SSU head

Fileemd_16560_additional_3.map
AnnotationState 2, mt-monosome, SSU head
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

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Additional map: State 2, mt-monosome, CP

Fileemd_16560_additional_4.map
AnnotationState 2, mt-monosome, CP
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

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Half map: State 2, mt-monosome, halfmap 1

Fileemd_16560_half_map_1.map
AnnotationState 2, mt-monosome, halfmap 1
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

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Half map: State 2, mt-monosome, halfmap 2

Fileemd_16560_half_map_2.map
AnnotationState 2, mt-monosome, halfmap 2
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

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Sample components

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Entire : yeast mitochondrial ribosome- State2

EntireName: yeast mitochondrial ribosome- State2
Components
  • Complex: yeast mitochondrial ribosome- State2

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Supramolecule #1: yeast mitochondrial ribosome- State2

SupramoleculeName: yeast mitochondrial ribosome- State2 / type: complex / ID: 1 / Parent: 0
Details: Mitoribosomal particles from an mtg1-deletion strain were purified by sucrose cushion sedimentation of mitochondrial extracts prepared in the presence of 20% Mg2+ and 1% Triton X-100. This ...Details: Mitoribosomal particles from an mtg1-deletion strain were purified by sucrose cushion sedimentation of mitochondrial extracts prepared in the presence of 20% Mg2+ and 1% Triton X-100. This approach revealed the structures of novel mitoribosome assembly intermediates at resolutions 3.2 A. After processing, the structural characterization of the mtg1-deletion mitoribosome particles allowed us to define three major states: state 1, state 2, and state 3.
Source (natural)Organism: Saccharomyces cerevisiae W303 (yeast) / Strain: delta mtg1 / Organelle: Mitochondria

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Experimental details

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Structure determination

Methodcryo EM
Processingsingle particle reconstruction
Aggregation stateparticle

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Sample preparation

BufferpH: 7.4
GridModel: Quantifoil R2/2 / Material: COPPER / Support film - Material: CARBON / Support film - topology: CONTINUOUS / Pretreatment - Type: GLOW DISCHARGE
VitrificationCryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277.15 K / Instrument: FEI VITROBOT MARK IV

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Electron microscopy

MicroscopeFEI TITAN KRIOS
Image recordingFilm or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: COUNTING / Average electron dose: 39.7 e/Å2
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsC2 aperture diameter: 50.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 3.0 µm / Nominal defocus min: 1.2 µm
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

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Image processing

Startup modelType of model: EMDB MAP
EMDB ID:
Final reconstructionResolution.type: BY AUTHOR / Resolution: 6.0 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 23000
Initial angle assignmentType: MAXIMUM LIKELIHOOD
Final angle assignmentType: MAXIMUM LIKELIHOOD
FSC plot (resolution estimation)

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