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Yorodumi- PDB-8bys: Outer membrane attachment porin OmpM1 from Veillonella parvula, native -
+Open data
-Basic information
Entry | Database: PDB / ID: 8bys | ||||||
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Title | Outer membrane attachment porin OmpM1 from Veillonella parvula, native | ||||||
Components | S-layer homology domain-containing protein | ||||||
Keywords | MEMBRANE PROTEIN / Outer membrane attachment / porin / peptidoglycan-binding / nutrient transport | ||||||
Function / homology | S-layer / S-layer homology domain / S-layer homology domain / S-layer homology (SLH) domain profile. / S-layer homology domain-containing protein Function and homology information | ||||||
Biological species | Veillonella parvula (bacteria) | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.28 Å | ||||||
Authors | Silale, A. / van den Berg, B. | ||||||
Funding support | United Kingdom, 1items
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Citation | Journal: Nat Commun / Year: 2023 Title: Dual function of OmpM as outer membrane tether and nutrient uptake channel in diderm Firmicutes. Authors: Augustinas Silale / Yiling Zhu / Jerzy Witwinowski / Robert E Smith / Kahlan E Newman / Satya P Bhamidimarri / Arnaud Baslé / Syma Khalid / Christophe Beloin / Simonetta Gribaldo / Bert van den Berg / Abstract: The outer membrane (OM) in diderm, or Gram-negative, bacteria must be tethered to peptidoglycan for mechanical stability and to maintain cell morphology. Most diderm phyla from the Terrabacteria ...The outer membrane (OM) in diderm, or Gram-negative, bacteria must be tethered to peptidoglycan for mechanical stability and to maintain cell morphology. Most diderm phyla from the Terrabacteria group have recently been shown to lack well-characterised OM attachment systems, but instead have OmpM, which could represent an ancestral tethering system in bacteria. Here, we have determined the structure of the most abundant OmpM protein from Veillonella parvula (diderm Firmicutes) by single particle cryogenic electron microscopy. We also characterised the channel properties of the transmembrane β-barrel of OmpM and investigated the structure and PG-binding properties of its periplasmic stalk region. Our results show that OM tethering and nutrient acquisition are genetically linked in V. parvula, and probably other diderm Terrabacteria. This dual function of OmpM may have played a role in the loss of the OM in ancestral bacteria and the emergence of monoderm bacterial lineages. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 8bys.cif.gz | 206.7 KB | Display | PDBx/mmCIF format |
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PDB format | pdb8bys.ent.gz | 150.9 KB | Display | PDB format |
PDBx/mmJSON format | 8bys.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 8bys_validation.pdf.gz | 1.2 MB | Display | wwPDB validaton report |
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Full document | 8bys_full_validation.pdf.gz | 1.2 MB | Display | |
Data in XML | 8bys_validation.xml.gz | 42.4 KB | Display | |
Data in CIF | 8bys_validation.cif.gz | 61.1 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/by/8bys ftp://data.pdbj.org/pub/pdb/validation_reports/by/8bys | HTTPS FTP |
-Related structure data
Related structure data | 16332MC 8bymC 8bytC 8bz2C C: citing same article (ref.) M: map data used to model this data |
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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: 46547.863 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Veillonella parvula (bacteria) / Strain: SKV38 Gene: D3219_09385, DWV36_08570, FNLLGLLA_01389, GL281_07935, HMPREF1865_01844 Production host: Veillonella parvula (bacteria) / Strain (production host): SKV38 / Variant (production host): ompM1-3 deletion strain / References: UniProt: A0A100YN03 |
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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: Outer membrane attachment porin OmpM1 trimer / Type: COMPLEX / Entity ID: all / Source: RECOMBINANT |
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Molecular weight | Value: 0.13 MDa / Experimental value: NO |
Source (natural) | Organism: Veillonella parvula (bacteria) / Strain: SKV38 |
Source (recombinant) | Organism: Veillonella parvula (bacteria) / Strain: SKV38 |
Buffer solution | pH: 7.5 Details: 10 mM HEPES-NaOH, 100 mM NaCl, 0.12% decyl maltoside |
Specimen | Conc.: 8 mg/ml / Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
Specimen support | Grid material: COPPER / Grid mesh size: 200 divisions/in. / Grid type: Quantifoil R1.2/1.3 |
Vitrification | Cryogen name: ETHANE / Humidity: 100 % / Chamber temperature: 277 K |
-Electron microscopy imaging
Microscopy | Model: TFS GLACIOS |
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Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 200 kV / Illumination mode: FLOOD BEAM |
Electron lens | Mode: BRIGHT FIELD / Nominal magnification: 240000 X / Nominal defocus max: 2000 nm / Nominal defocus min: 1000 nm |
Image recording | Electron dose: 50 e/Å2 / Film or detector model: FEI FALCON IV (4k x 4k) / Num. of grids imaged: 1 / Num. of real images: 6505 |
-Processing
Software |
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EM software |
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CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||||||||||||||
Symmetry | Point symmetry: C1 (asymmetric) | ||||||||||||||||||||||||||||||||||||
3D reconstruction | Resolution: 3.28 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 144245 / Symmetry type: POINT | ||||||||||||||||||||||||||||||||||||
Atomic model building | Protocol: AB INITIO MODEL / Space: REAL | ||||||||||||||||||||||||||||||||||||
Refinement | Cross valid method: NONE |