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Open data
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Basic information
| Entry | Database: PDB / ID: 6u5f | |||||||||||||||
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| Title | CryoEM Structure of Pyocin R2 - precontracted - collar | |||||||||||||||
 Components | 
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 Keywords | ANTIMICROBIAL PROTEIN / bacteriocin / pyocin | |||||||||||||||
| Function / homology |  Function and homology informationTail tube protein / Phage tail tube protein FII / :  / Tail sheath protein Gp18 domain III N-terminal region / :  / Tail sheath protein, subtilisin-like domain / Phage tail sheath protein subtilisin-like domain / Tail sheath protein, C-terminal domain / Phage tail sheath C-terminal domain Similarity search - Domain/homology  | |||||||||||||||
| Biological species | ![]()  | |||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.8 Å | |||||||||||||||
 Authors | Ge, P. / Avaylon, J. / Scholl, D. / Shneider, M.M. / Browning, C. / Buth, S.A. / Plattner, M. / Ding, K. / Leiman, P.G. / Miller, J.F. / Zhou, Z.H. | |||||||||||||||
| Funding support |   United States,   Switzerland, 4items 
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 Citation |  Journal: Nature / Year: 2020Title: Action of a minimal contractile bactericidal nanomachine. Authors: Peng Ge / Dean Scholl / Nikolai S Prokhorov / Jaycob Avaylon / Mikhail M Shneider / Christopher Browning / Sergey A Buth / Michel Plattner / Urmi Chakraborty / Ke Ding / Petr G Leiman / Jeff ...Authors: Peng Ge / Dean Scholl / Nikolai S Prokhorov / Jaycob Avaylon / Mikhail M Shneider / Christopher Browning / Sergey A Buth / Michel Plattner / Urmi Chakraborty / Ke Ding / Petr G Leiman / Jeff F Miller / Z Hong Zhou /     ![]() Abstract: R-type bacteriocins are minimal contractile nanomachines that hold promise as precision antibiotics. Each bactericidal complex uses a collar to bridge a hollow tube with a contractile sheath loaded ...R-type bacteriocins are minimal contractile nanomachines that hold promise as precision antibiotics. Each bactericidal complex uses a collar to bridge a hollow tube with a contractile sheath loaded in a metastable state by a baseplate scaffold. Fine-tuning of such nucleic acid-free protein machines for precision medicine calls for an atomic description of the entire complex and contraction mechanism, which is not available from baseplate structures of the (DNA-containing) T4 bacteriophage. Here we report the atomic model of the complete R2 pyocin in its pre-contraction and post-contraction states, each containing 384 subunits of 11 unique atomic models of 10 gene products. Comparison of these structures suggests the following sequence of events during pyocin contraction: tail fibres trigger lateral dissociation of baseplate triplexes; the dissociation then initiates a cascade of events leading to sheath contraction; and this contraction converts chemical energy into mechanical force to drive the iron-tipped tube across the bacterial cell surface, killing the bacterium.  | |||||||||||||||
| History | 
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Structure visualization
| Movie | 
 
 
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| Structure viewer | Molecule:  Molmil Jmol/JSmol | 
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Downloads & links
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Download
| PDBx/mmCIF format |  6u5f.cif.gz | 2.2 MB | Display |  PDBx/mmCIF format | 
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| PDB format |  pdb6u5f.ent.gz | Display |  PDB format | |
| PDBx/mmJSON format |  6u5f.json.gz | Tree view |  PDBx/mmJSON format | |
| Others |  Other downloads | 
-Validation report
| Summary document |  6u5f_validation.pdf.gz | 1.3 MB | Display |  wwPDB validaton report | 
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| Full document |  6u5f_full_validation.pdf.gz | 1.3 MB | Display | |
| Data in XML |  6u5f_validation.xml.gz | 305.3 KB | Display | |
| Data in CIF |  6u5f_validation.cif.gz | 473.7 KB | Display | |
| Arichive directory |  https://data.pdbj.org/pub/pdb/validation_reports/u5/6u5f ftp://data.pdbj.org/pub/pdb/validation_reports/u5/6u5f | HTTPS FTP  | 
-Related structure data
| Related structure data | ![]() 20644MC ![]() 5cesC ![]() 6pytC ![]() 6u5bC ![]() 6u5hC ![]() 6u5jC ![]() 6u5kC C: citing same article ( M: map data used to model this data  | 
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| Similar structure data | 
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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: 18965.461 Da / Num. of mol.: 6 / Source method: isolated from a natural source Source: (natural)  Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) (bacteria)Strain: ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1 References: UniProt: G3XD82 #2: Protein | Mass: 41247.332 Da / Num. of mol.: 24 / Source method: isolated from a natural source Source: (natural)  Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) (bacteria)Strain: ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1 References: UniProt: G3XD39 #3: Protein | Mass: 17957.352 Da / Num. of mol.: 24 / Source method: isolated from a natural source Source: (natural)  Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) (bacteria)Strain: ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1 References: UniProt: Q9I5S9  | 
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-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY | 
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction | 
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Sample preparation
| Component | Name: Pyocin R2 / Type: COMPLEX / Entity ID: all / Source: NATURAL | |||||||||||||||
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| Molecular weight | Experimental value: NO | |||||||||||||||
| Source (natural) | Organism:  Pseudomonas aeruginosa PAO1 (bacteria) | |||||||||||||||
| Buffer solution | pH: 7.4 | |||||||||||||||
| Buffer component | 
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| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES | |||||||||||||||
| Specimen support | Details: unspecified | |||||||||||||||
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 100 % / Chamber temperature: 295 K | 
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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 magnification: 130000 X / Nominal defocus max: 2160 nm / Nominal defocus min: 2160 nm / Calibrated defocus min: 1100 nm / Calibrated defocus max: 3400 nm / Cs: 2.7 mm / C2 aperture diameter: 70 µm / Alignment procedure: COMA FREE | 
| Specimen holder | Cryogen: NITROGEN / Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Temperature (max): 81 K / Temperature (min): 80 K | 
| Image recording | Average exposure time: 10 sec. / Electron dose: 80 e/Å2 / Detector mode: COUNTING / Film or detector model: GATAN K2 QUANTUM (4k x 4k) / Num. of grids imaged: 1 / Num. of real images: 7331 | 
| EM imaging optics | Energyfilter name: GIF Quantum LS / Energyfilter upper: 10 eV / Energyfilter lower: -10 eV | 
| Image scans | Movie frames/image: 50 / Used frames/image: 3-20 | 
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Processing
| Software | Name: PHENIX / Version: 1.13_2998: / Classification: refinement | ||||||||||||||||||||||||||||
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| EM software | 
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||||||
| Particle selection | Num. of particles selected: 43934 | ||||||||||||||||||||||||||||
| Symmetry | Point symmetry: C6 (6 fold cyclic) | ||||||||||||||||||||||||||||
| 3D reconstruction | Resolution: 3.8 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 4110 / Symmetry type: POINT | ||||||||||||||||||||||||||||
| Atomic model building | Protocol: AB INITIO MODEL / Space: REAL | 
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About Yorodumi






United States,  
Switzerland, 4items 
Citation
 
UCSF Chimera

















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