+Open data
-Basic information
Entry | Database: PDB / ID: 9bgn | |||||||||
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Title | Pseudomonas phage DEV 5-fold vertex (major coat protein) | |||||||||
Components | gp77 major coat protein | |||||||||
Keywords | STRUCTURAL PROTEIN / virion coat / complex / gp77 | |||||||||
Function / homology | Major coat protein Function and homology information | |||||||||
Biological species | Pseudomonas phage vB_PaeP_DEV (virus) | |||||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.3 Å | |||||||||
Authors | Iglesias, S.M. / Hou, C.F.D. / Li, F. / Cingolani, G. | |||||||||
Funding support | United States, 2items
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Citation | Journal: Nat Commun / Year: 2024 Title: Integrative structural analysis of Pseudomonas phage DEV reveals a genome ejection motor. Authors: Ravi K Lokareddy / Chun-Feng David Hou / Francesca Forti / Stephano M Iglesias / Fenglin Li / Mikhail Pavlenok / David S Horner / Michael Niederweis / Federica Briani / Gino Cingolani / Abstract: DEV is an obligatory lytic Pseudomonas phage of the N4-like genus, recently reclassified as Schitoviridae. The DEV genome encodes 91 ORFs, including a 3398 amino acid virion-associated RNA polymerase ...DEV is an obligatory lytic Pseudomonas phage of the N4-like genus, recently reclassified as Schitoviridae. The DEV genome encodes 91 ORFs, including a 3398 amino acid virion-associated RNA polymerase (vRNAP). Here, we describe the complete architecture of DEV, determined using a combination of cryo-electron microscopy localized reconstruction, biochemical methods, and genetic knockouts. We built de novo structures of all capsid factors and tail components involved in host attachment. We demonstrate that DEV long tail fibers are essential for infection of Pseudomonas aeruginosa but dispensable for infecting mutants with a truncated lipopolysaccharide devoid of the O-antigen. We determine that DEV vRNAP is part of a three-gene operon conserved in 191 Schitoviridae genomes. We propose these three proteins are ejected into the host to form a genome ejection motor spanning the cell envelope. We posit that the design principles of the DEV ejection apparatus are conserved in all Schitoviridae. | |||||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 9bgn.cif.gz | 592.5 KB | Display | PDBx/mmCIF format |
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PDB format | pdb9bgn.ent.gz | 499.9 KB | Display | PDB format |
PDBx/mmJSON format | 9bgn.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 9bgn_validation.pdf.gz | 1.6 MB | Display | wwPDB validaton report |
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Full document | 9bgn_full_validation.pdf.gz | 1.6 MB | Display | |
Data in XML | 9bgn_validation.xml.gz | 107.6 KB | Display | |
Data in CIF | 9bgn_validation.cif.gz | 163.6 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/bg/9bgn ftp://data.pdbj.org/pub/pdb/validation_reports/bg/9bgn | HTTPS FTP |
-Related structure data
Related structure data | 44518MC 8vxqC 9bgmC 9bgoC 9codC M: map data used to model this data C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
-Assembly
Deposited unit |
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1 |
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-Components
#1: Protein | Mass: 44114.113 Da / Num. of mol.: 9 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Pseudomonas phage vB_PaeP_DEV (virus) / Gene: vBPaePDEV_00077 / Production host: Pseudomonas (RNA similarity group I) / References: UniProt: A0A2K8HRH4 Has protein modification | N | |
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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 |
-Sample preparation
Component | Name: Major coat protein of Pseudomonas phage DEV / Type: COMPLEX / Entity ID: all / Source: NATURAL |
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Molecular weight | Experimental value: NO |
Source (natural) | Organism: Pseudomonas phage vB_PaeP_DEV (virus) |
Source (recombinant) | Organism: Pseudomonas aeruginosa (bacteria) |
Buffer solution | pH: 7.5 |
Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
Vitrification | Cryogen name: ETHANE |
-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: 1600 nm / Nominal defocus min: 800 nm |
Image recording | Electron dose: 50 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
-Processing
CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
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Symmetry | Point symmetry: C5 (5 fold cyclic) |
3D reconstruction | Resolution: 3.3 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 18913 / Symmetry type: POINT |
Refinement | Highest resolution: 3.3 Å |