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Yorodumi- EMDB-50211: Subtomogram average of the Chlamydomonas reinhardtii mitochondria... -
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Basic information
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| Title | Subtomogram average of the Chlamydomonas reinhardtii mitochondrial respirasome - C2 expanded | |||||||||
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Keywords | respirasome / alga / respiration / mitochondria / MEMBRANE PROTEIN | |||||||||
| Biological species | ![]() | |||||||||
| Method | subtomogram averaging / cryo EM / Resolution: 6.18 Å | |||||||||
Authors | Waltz F / Righetto R / Kotecha A / Engel BD | |||||||||
| Funding support | Germany, Switzerland, 2 items
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Citation | Journal: Science / Year: 2025Title: In-cell architecture of the mitochondrial respiratory chain. Authors: Florent Waltz / Ricardo D Righetto / Lorenz Lamm / Thalia Salinas-Giegé / Ron Kelley / Xianjun Zhang / Martin Obr / Sagar Khavnekar / Abhay Kotecha / Benjamin D Engel / ![]() Abstract: Mitochondria regenerate adenosine triphosphate (ATP) through oxidative phosphorylation. This process is carried out by five membrane-bound complexes collectively known as the respiratory chain, ...Mitochondria regenerate adenosine triphosphate (ATP) through oxidative phosphorylation. This process is carried out by five membrane-bound complexes collectively known as the respiratory chain, working in concert to transfer electrons and pump protons. The precise organization of these complexes in native cells is debated. We used in situ cryo-electron tomography to visualize the native structures and organization of several major mitochondrial complexes in cells. ATP synthases and respiratory complexes segregate into curved and flat crista membrane domains, respectively. Respiratory complexes I, III, and IV assemble into a respirasome supercomplex, from which we determined a native 5-angstrom (Å) resolution structure showing binding of electron carrier cytochrome . Combined with single-particle cryo-electron microscopy at 2.4-Å resolution, we model how the respiratory complexes organize inside native mitochondria. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_50211.map.gz | 8.9 MB | EMDB map data format | |
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| Header (meta data) | emd-50211-v30.xml emd-50211.xml | 17.5 KB 17.5 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_50211_fsc.xml | 10.2 KB | Display | FSC data file |
| Images | emd_50211.png | 81.2 KB | ||
| Masks | emd_50211_msk_1.map | 91.1 MB | Mask map | |
| Filedesc metadata | emd-50211.cif.gz | 4.7 KB | ||
| Others | emd_50211_half_map_1.map.gz emd_50211_half_map_2.map.gz | 71.2 MB 71.2 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-50211 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-50211 | HTTPS FTP |
-Validation report
| Summary document | emd_50211_validation.pdf.gz | 942.1 KB | Display | EMDB validaton report |
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| Full document | emd_50211_full_validation.pdf.gz | 941.7 KB | Display | |
| Data in XML | emd_50211_validation.xml.gz | 17.1 KB | Display | |
| Data in CIF | emd_50211_validation.cif.gz | 22.5 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-50211 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-50211 | HTTPS FTP |
-Related structure data
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_50211.map.gz / Format: CCP4 / Size: 91.1 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.91 Å | ||||||||||||||||||||||||||||||||||||
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_50211_msk_1.map | ||||||||||||
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-Half map: #1
| File | emd_50211_half_map_1.map | ||||||||||||
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-Half map: #2
| File | emd_50211_half_map_2.map | ||||||||||||
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Sample components
-Entire : Chlamydomonas reinhardtii
| Entire | Name: ![]() |
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-Supramolecule #1: Chlamydomonas reinhardtii
| Supramolecule | Name: Chlamydomonas reinhardtii / type: cell / ID: 1 / Parent: 0 |
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| Source (natural) | Organism: ![]() |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | subtomogram averaging |
| Aggregation state | cell |
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Sample preparation
| Buffer | pH: 7 |
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| Grid | Model: Quantifoil R2/1 / Material: COPPER / Support film - Material: CARBON / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 20 sec. / Pretreatment - Atmosphere: AIR |
| Vitrification | Cryogen name: ETHANE-PROPANE / Chamber humidity: 100 % / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Specialist optics | Energy filter - Name: TFS Selectris X |
| Image recording | Film or detector model: TFS FALCON 4i (4k x 4k) / Digitization - Dimensions - Width: 4096 pixel / Digitization - Dimensions - Height: 4096 pixel / Average electron dose: 3.5 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 3.5 µm / Nominal defocus min: 0.8 µm / Nominal magnification: 64000 |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi



Keywords
Authors
Germany,
Switzerland, 2 items
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Processing
FIELD EMISSION GUN

