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Open data
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Basic information
| Entry | Database: PDB / ID: 7vku | ||||||||||||||||||||||||||||||||||||
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| Title | Cryo-EM structure of SAM-Tom40 intermediate complex | ||||||||||||||||||||||||||||||||||||
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Keywords | TRANSLOCASE / Mitochondrial protein assembly gate | ||||||||||||||||||||||||||||||||||||
| Function / homology | Function and homology informationmembrane insertase activity / mitochondrial outer membrane translocase complex assembly / SAM complex / mitochondrial outer membrane translocase complex / protein insertion into mitochondrial outer membrane / phospholipid transport / porin activity / pore complex / protein import into mitochondrial matrix / protein transmembrane transporter activity ...membrane insertase activity / mitochondrial outer membrane translocase complex assembly / SAM complex / mitochondrial outer membrane translocase complex / protein insertion into mitochondrial outer membrane / phospholipid transport / porin activity / pore complex / protein import into mitochondrial matrix / protein transmembrane transporter activity / monoatomic ion transport / mitochondrion organization / mitochondrial intermembrane space / protein-containing complex assembly / mitochondrial outer membrane / mitochondrion / cytosol / cytoplasm Similarity search - Function | ||||||||||||||||||||||||||||||||||||
| Biological species | ![]() | ||||||||||||||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.2 Å | ||||||||||||||||||||||||||||||||||||
Authors | Takeda, H. / Tsutsumi, A. / Kikkawa, M. / Endo, T. | ||||||||||||||||||||||||||||||||||||
| Funding support | Japan, 3items
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Citation | Journal: Nat Struct Mol Biol / Year: 2023Title: Author Correction: A multipoint guidance mechanism for β-barrel folding on the SAM complex. Authors: Hironori Takeda / Jon V Busto / Caroline Lindau / Akihisa Tsutsumi / Kentaro Tomii / Kenichiro Imai / Yu Yamamori / Takatsugu Hirokawa / Chie Motono / Iniyan Ganesan / Lena-Sophie Wenz / ...Authors: Hironori Takeda / Jon V Busto / Caroline Lindau / Akihisa Tsutsumi / Kentaro Tomii / Kenichiro Imai / Yu Yamamori / Takatsugu Hirokawa / Chie Motono / Iniyan Ganesan / Lena-Sophie Wenz / Thomas Becker / Masahide Kikkawa / Nikolaus Pfanner / Nils Wiedemann / Toshiya Endo / ![]() | ||||||||||||||||||||||||||||||||||||
| History |
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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 | 7vku.cif.gz | 221 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb7vku.ent.gz | 170.9 KB | Display | PDB format |
| PDBx/mmJSON format | 7vku.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/vk/7vku ftp://data.pdbj.org/pub/pdb/validation_reports/vk/7vku | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 32019MC 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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| 1 |
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Components
| #1: Protein | Mass: 54473.840 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() |
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| #2: Protein | Mass: 37446.070 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() |
| #3: Protein | Mass: 37537.797 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() |
| #4: Protein | Mass: 42071.141 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() |
| Has protein modification | N |
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: CELL / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: SAM-Tom40 / Type: COMPLEX / Entity ID: all / Source: RECOMBINANT |
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| Source (natural) | Organism: ![]() |
| Source (recombinant) | Organism: ![]() |
| Buffer solution | pH: 7.5 |
| 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: FEI TITAN KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 1800 nm / Nominal defocus min: 800 nm / Cs: 2.7 mm / C2 aperture diameter: 50 µm |
| Image recording | Electron dose: 48 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
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Processing
| Software | Name: PHENIX / Version: 1.14_3260: / Classification: refinement |
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| EM software | Name: PHENIX / Category: model refinement |
| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
| Symmetry | Point symmetry: C1 (asymmetric) |
| 3D reconstruction | Resolution: 3.2 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 23542 / Symmetry type: POINT |
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About Yorodumi






Japan, 3items
Citation

PDBj

FIELD EMISSION GUN