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Open data
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Basic information
| Entry | Database: EMDB / ID: EMD-20647 | |||||||||||||||
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| Title | CryoEM Structure of Pyocin R2 - postcontracted - collar | |||||||||||||||
Map data | Structure of Pyocin R2 - postcontracted - collar | |||||||||||||||
Sample |
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Keywords | bacteriocin / pyocin / ANTIMICROBIAL PROTEIN | |||||||||||||||
| Function / homology | : / 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 / Probable bacteriophage protein / Phage protein Function and homology information | |||||||||||||||
| Biological species | Pseudomonas aeruginosa PAO1 (bacteria) / Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) (bacteria) | |||||||||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.5 Å | |||||||||||||||
Authors | Ge P / Avaylon J | |||||||||||||||
| Funding support | United States, Switzerland, 4 items
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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 | EM map: SurfView Molmil Jmol/JSmol |
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_20647.map.gz | 261.8 MB | EMDB map data format | |
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| Header (meta data) | emd-20647-v30.xml emd-20647.xml | 16.2 KB 16.2 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_20647_fsc.xml | 14.9 KB | Display | FSC data file |
| Images | emd_20647.png | 226.1 KB | ||
| Filedesc metadata | emd-20647.cif.gz | 6 KB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-20647 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-20647 | HTTPS FTP |
-Validation report
| Summary document | emd_20647_validation.pdf.gz | 749.2 KB | Display | EMDB validaton report |
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| Full document | emd_20647_full_validation.pdf.gz | 748.8 KB | Display | |
| Data in XML | emd_20647_validation.xml.gz | 14.5 KB | Display | |
| Data in CIF | emd_20647_validation.cif.gz | 19.6 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-20647 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-20647 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 6u5jMC ![]() 5cesC ![]() 6pytC ![]() 6u5bC ![]() 6u5fC ![]() 6u5hC ![]() 6u5kC C: citing same article ( M: atomic model generated by this map |
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| Similar structure data |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_20647.map.gz / Format: CCP4 / Size: 282.6 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | Structure of Pyocin R2 - postcontracted - collar | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.041 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
CCP4 map header:
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-Supplemental data
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Sample components
-Entire : Pyocin R2 - Postcontracted
| Entire | Name: Pyocin R2 - Postcontracted |
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| Components |
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-Supramolecule #1: Pyocin R2 - Postcontracted
| Supramolecule | Name: Pyocin R2 - Postcontracted / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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| Source (natural) | Organism: Pseudomonas aeruginosa PAO1 (bacteria) |
-Macromolecule #1: Collar PA0615
| Macromolecule | Name: Collar PA0615 / type: protein_or_peptide / ID: 1 / Number of copies: 6 / Enantiomer: LEVO |
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| Source (natural) | Organism: 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 |
| Molecular weight | Theoretical: 18.965461 KDa |
| Sequence | String: MPEQAVTLEA LYAAIEQVLR ERLPEAQLIG FWPGVPENTP AVSLEIAELL PERDPGTGES ALLCRLQARI MVPPGADRQA VSIACGIVR TLREQTWNLS LQPARFVRSA VDGSREELKS LRVWLVEWTQ SLRLGDPEWA WEDQPPGSLM LGFDPQTGPG H EPDYFAPE ALA UniProtKB: Phage protein |
-Macromolecule #2: Sheath PA0622
| Macromolecule | Name: Sheath PA0622 / type: protein_or_peptide / ID: 2 / Number of copies: 18 / Enantiomer: LEVO |
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| Source (natural) | Organism: 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 |
| Molecular weight | Theoretical: 41.247332 KDa |
| Sequence | String: MSFFHGVTVT NVDIGARTIA LPASSVIGLC DVFTPGAQAS AKPNVPVLLT SKKDAAAAFG IGSSIYLACE AIYNRAQAVI VAVGVETAE TPEAQASAVI GGISAAGERT GLQALLDGKS RFNAQPRLLV APGHSAQQAV ATAMDGLAEK LRAIAILDGP N STDEAAVA ...String: MSFFHGVTVT NVDIGARTIA LPASSVIGLC DVFTPGAQAS AKPNVPVLLT SKKDAAAAFG IGSSIYLACE AIYNRAQAVI VAVGVETAE TPEAQASAVI GGISAAGERT GLQALLDGKS RFNAQPRLLV APGHSAQQAV ATAMDGLAEK LRAIAILDGP N STDEAAVA YAKNFGSKRL FMVDPGVQVW DSATNAARNA PASAYAAGLF AWTDAEYGFW SSPSNKEIKG VTGTSRPVEF LD GDETCRA NLLNNANIAT IIRDDGYRLW GNRTLSSDSK WAFVTRVRTM DLVMDAILAG HKWAVDRGIT KTYVKDVTEG LRA FMRDLK NQGAVINFEV YADPDLNSAS QLAQGKVYWN IRFTDVPPAE NPNFRVEVTD QWLTEVLDVA UniProtKB: Probable bacteriophage protein |
-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 Component:
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| Grid | Support film - Material: CARBON / Support film - topology: HOLEY ARRAY / Details: unspecified | |||||||||
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 295 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | FEI TITAN KRIOS |
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| Temperature | Min: 80.0 K / Max: 81.0 K |
| Specialist optics | Energy filter - Name: GIF Quantum LS / Energy filter - Lower energy threshold: -10 eV / Energy filter - Upper energy threshold: 10 eV |
| Image recording | Film or detector model: GATAN K2 QUANTUM (4k x 4k) / Detector mode: COUNTING / Digitization - Frames/image: 3-20 / Number grids imaged: 1 / Number real images: 7331 / Average exposure time: 10.0 sec. / Average electron dose: 80.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 70.0 µm / Calibrated defocus max: 3.4 µm / Calibrated defocus min: 1.1 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.16 µm / Nominal defocus min: 2.16 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
| Refinement | Space: REAL / Protocol: AB INITIO MODEL |
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| Output model | ![]() PDB-6u5j: |
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About Yorodumi



Keywords
Pseudomonas aeruginosa PAO1 (bacteria)
Authors
United States,
Switzerland, 4 items
Citation

UCSF Chimera















Z (Sec.)
Y (Row.)
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