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Yorodumi- EMDB-19964: III2IV respiratory supercomplex from Saccharomyces cerevisiae (co... -
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Open data
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Basic information
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| Title | III2IV respiratory supercomplex from Saccharomyces cerevisiae (consensus map) | ||||||||||||
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Keywords | Respiration / supercomplex / MEMBRANE PROTEIN | ||||||||||||
| Biological species | ![]() | ||||||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.4 Å | ||||||||||||
Authors | Wu F / Di Trani JM / Rubinstein JL / Brzezinski P / Moe A | ||||||||||||
| Funding support | Sweden, Canada, 3 items
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Citation | Journal: Nat Commun / Year: 2024Title: Electron transfer in the respiratory chain at low salinity. Authors: Ana Paula Lobez / Fei Wu / Justin M Di Trani / John L Rubinstein / Mikael Oliveberg / Peter Brzezinski / Agnes Moe / ![]() Abstract: Recent studies have established that cellular electrostatic interactions are more influential than assumed previously. Here, we use cryo-EM and perform steady-state kinetic studies to investigate ...Recent studies have established that cellular electrostatic interactions are more influential than assumed previously. Here, we use cryo-EM and perform steady-state kinetic studies to investigate electrostatic interactions between cytochrome (cyt.) c and the complex (C) III-IV supercomplex from Saccharomyces cerevisiae at low salinity. The kinetic studies show a sharp transition with a Hill coefficient ≥2, which together with the cryo-EM data at 2.4 Å resolution indicate multiple cyt. c molecules bound along the supercomplex surface. Negatively charged loops of CIII subunits Qcr6 and Qcr9 become structured to interact with cyt. c. In addition, the higher resolution allows us to identify water molecules in proton pathways of CIV and, to the best of our knowledge, previously unresolved cardiolipin molecules. In conclusion, the lowered electrostatic screening renders engagement of multiple cyt. c molecules that are directed by electrostatically structured CIII loops to conduct electron transfer between CIII and CIV. | ||||||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_19964.map.gz | 290.7 MB | EMDB map data format | |
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| Header (meta data) | emd-19964-v30.xml emd-19964.xml | 17.6 KB 17.6 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_19964_fsc.xml | 14.7 KB | Display | FSC data file |
| Images | emd_19964.png | 76.8 KB | ||
| Filedesc metadata | emd-19964.cif.gz | 4.1 KB | ||
| Others | emd_19964_additional_1.map.gz emd_19964_additional_2.map.gz emd_19964_additional_3.map.gz | 4.1 MB 4.1 MB 4.1 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-19964 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-19964 | 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_19964.map.gz / Format: CCP4 / Size: 307.5 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: 0.8464 Å | ||||||||||||||||||||||||||||||||||||
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Additional map: 3D classification class 2
| File | emd_19964_additional_1.map | ||||||||||||
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| Annotation | 3D classification class 2 | ||||||||||||
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-Additional map: 3D classification class 3
| File | emd_19964_additional_2.map | ||||||||||||
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| Annotation | 3D classification class 3 | ||||||||||||
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-Additional map: 3D classification class 1
| File | emd_19964_additional_3.map | ||||||||||||
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| Annotation | 3D classification class 1 | ||||||||||||
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Sample components
-Entire : III2-IV respiratory supercomplex
| Entire | Name: III2-IV respiratory supercomplex |
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| Components |
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-Supramolecule #1: III2-IV respiratory supercomplex
| Supramolecule | Name: III2-IV respiratory supercomplex / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#22 |
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| Source (natural) | Organism: ![]() |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 7.4 |
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| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 40.0 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: 2.0 µm / Nominal defocus min: 0.6 µm / Nominal magnification: 105000 |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi



Keywords
Authors
Sweden,
Canada, 3 items
Citation




Z (Sec.)
Y (Row.)
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Processing
FIELD EMISSION GUN


