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Open data
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Basic information
| Entry | ![]() | |||||||||
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| Title | Drosophila melanogaster complex I in the Cracked state (Dm3) | |||||||||
Map data | Globally sharpened consensus map generated using RELION Postprocess | |||||||||
Sample |
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| Biological species | ![]() | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.96 Å | |||||||||
Authors | Agip AA / Chung I / Sanchez-Martinez A / Whitworth AJ / Hirst J | |||||||||
| Funding support | United Kingdom, 2 items
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Citation | Journal: Elife / Year: 2023Title: Cryo-EM structures of mitochondrial respiratory complex I from . Authors: Ahmed-Noor A Agip / Injae Chung / Alvaro Sanchez-Martinez / Alexander J Whitworth / Judy Hirst / ![]() Abstract: Respiratory complex I powers ATP synthesis by oxidative phosphorylation, exploiting the energy from NADH oxidation by ubiquinone to drive protons across an energy-transducing membrane. is a ...Respiratory complex I powers ATP synthesis by oxidative phosphorylation, exploiting the energy from NADH oxidation by ubiquinone to drive protons across an energy-transducing membrane. is a candidate model organism for complex I due to its high evolutionary conservation with the mammalian enzyme, well-developed genetic toolkit, and complex physiology for studies in specific cell types and tissues. Here, we isolate complex I from and determine its structure, revealing a 43-subunit assembly with high structural homology to its 45-subunit mammalian counterpart, including a hitherto unknown homologue to subunit NDUFA3. The major conformational state of the enzyme is the mammalian-type 'ready-to-go' active resting state, with a fully ordered and enclosed ubiquinone-binding site, but a subtly altered global conformation related to changes in subunit ND6. The mammalian-type 'deactive' pronounced resting state is not observed: in two minor states, the ubiquinone-binding site is unchanged, but a deactive-type π-bulge is present in ND6-TMH3. Our detailed structural knowledge of complex I provides a foundation for new approaches to disentangle mechanisms of complex I catalysis and regulation in bioenergetics and physiology. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_15938.map.gz | 317.9 MB | EMDB map data format | |
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| Header (meta data) | emd-15938-v30.xml emd-15938.xml | 24.5 KB 24.5 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_15938_fsc.xml | 15.9 KB | Display | FSC data file |
| Images | emd_15938.png | 84 KB | ||
| Masks | emd_15938_msk_1.map | 347.6 MB | Mask map | |
| Others | emd_15938_additional_1.map.gz emd_15938_half_map_1.map.gz emd_15938_half_map_2.map.gz | 287.4 MB 279.6 MB 279.6 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-15938 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-15938 | HTTPS FTP |
-Validation report
| Summary document | emd_15938_validation.pdf.gz | 1003 KB | Display | EMDB validaton report |
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| Full document | emd_15938_full_validation.pdf.gz | 1002.6 KB | Display | |
| Data in XML | emd_15938_validation.xml.gz | 23.3 KB | Display | |
| Data in CIF | emd_15938_validation.cif.gz | 31 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-15938 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-15938 | 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_15938.map.gz / Format: CCP4 / Size: 347.6 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | Globally sharpened consensus map generated using RELION Postprocess | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.048 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Mask #1
| File | emd_15938_msk_1.map | ||||||||||||
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-Additional map: Unsharpened and unfiltered consensus map generated using RELION...
| File | emd_15938_additional_1.map | ||||||||||||
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| Annotation | Unsharpened and unfiltered consensus map generated using RELION Postprocess | ||||||||||||
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| Density Histograms |
-Half map: Half map 2 generated using RELION Postprocess (unsharpened...
| File | emd_15938_half_map_1.map | ||||||||||||
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| Annotation | Half map 2 generated using RELION Postprocess (unsharpened and unfiltered) | ||||||||||||
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| Density Histograms |
-Half map: Half map 1 generated using RELION Postprocess (unsharpened...
| File | emd_15938_half_map_2.map | ||||||||||||
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| Annotation | Half map 1 generated using RELION Postprocess (unsharpened and unfiltered) | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : Mitochondrial respiratory complex I
| Entire | Name: Mitochondrial respiratory complex I |
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| Components |
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-Supramolecule #1: Mitochondrial respiratory complex I
| Supramolecule | Name: Mitochondrial respiratory complex I / type: complex / ID: 1 / Chimera: Yes / Parent: 0 / Macromolecule list: #1-#43 Details: Native purification of mitochondrial complex I from Drosophila melanogaster (fruit fly) W1118. |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 1 MDa |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 3.4 mg/mL | ||||||||||||
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| Buffer | pH: 7.8 Component:
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| Grid | Model: UltrAuFoil / Material: GOLD / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 90 sec. Details: Following glow discharge for 90 s at 20 mA, the grid was treated for 7 days in an anaerobic glovebox in ethanol containing 5 mM 11-mercaptoundecyl hexaethyleneglycol, washed three times in ...Details: Following glow discharge for 90 s at 20 mA, the grid was treated for 7 days in an anaerobic glovebox in ethanol containing 5 mM 11-mercaptoundecyl hexaethyleneglycol, washed three times in ethanol and dried prior to blotting | ||||||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV / Details: blot for 10 seconds before plunging. |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Image recording | Film or detector model: GATAN K2 QUANTUM (4k x 4k) / Detector mode: COUNTING / Number grids imaged: 1 / Number real images: 3082 / Average exposure time: 10.0 sec. / Average electron dose: 41.88 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 70.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.0 µm / Nominal defocus min: 1.0 µm / Nominal magnification: 130000 |
| 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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Image processing
-Atomic model buiding 1
| Initial model | PDB ID: |
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| Refinement | Space: REAL |
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About Yorodumi





Authors
United Kingdom, 2 items
Citation



Z (Sec.)
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FIELD EMISSION GUN



