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Yorodumi- PDB-9qt5: Structure of the 50S ribosomal subunit from the antibiotic-produc... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 9qt5 | ||||||||||||||||||||||||
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| Title | Structure of the 50S ribosomal subunit from the antibiotic-producing bacterium Streptomyces fradiae | ||||||||||||||||||||||||
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Keywords | RIBOSOME / Streptomyces / 50S / ribosome-targeting antibiotics | ||||||||||||||||||||||||
| Function / homology | Function and homology informationlarge ribosomal subunit / transferase activity / 5S rRNA binding / ribosomal large subunit assembly / large ribosomal subunit rRNA binding / cytosolic large ribosomal subunit / cytoplasmic translation / tRNA binding / negative regulation of translation / rRNA binding ...large ribosomal subunit / transferase activity / 5S rRNA binding / ribosomal large subunit assembly / large ribosomal subunit rRNA binding / cytosolic large ribosomal subunit / cytoplasmic translation / tRNA binding / negative regulation of translation / rRNA binding / structural constituent of ribosome / ribosome / translation / ribonucleoprotein complex / mRNA binding / cytoplasm Similarity search - Function | ||||||||||||||||||||||||
| Biological species | Streptomyces fradiae ATCC 10745 = DSM 40063 (bacteria) | ||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.13 Å | ||||||||||||||||||||||||
Authors | Ekemezie, C.L. / Melnikov, S.V. | ||||||||||||||||||||||||
| Funding support | United Kingdom, 2items
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Citation | Journal: Cell Rep / Year: 2025Title: Extensive natural variation in bacterial ribosomal drug-binding sites. Authors: Chinenye L Ekemezie / Lewis I Chan / Charlotte R Brown / Karla Helena-Bueno / Tom A Williams / Sergey V Melnikov / ![]() Abstract: Ribosomes from certain bacteria possess divergent drug-binding sites compared to those of Escherichia coli, leading to natural evasion or hypersensitivity to antibiotics. However, in the absence of ...Ribosomes from certain bacteria possess divergent drug-binding sites compared to those of Escherichia coli, leading to natural evasion or hypersensitivity to antibiotics. However, in the absence of systematic studies, it is unknown whether this divergence is rare or common among bacterial species. Here, we address this by reconstructing the evolutionary history of drug-binding residues in bacterial ribosomes. We find that many rRNA residues that are currently viewed as bacterial-specific features of ribosomal drug-binding sites are in fact conserved only in a subset of bacteria. Conversely, species with divergent drug-binding sites are widespread in nature, arising from ancient rRNA polymorphisms at the direct ribosome-drug interface. Using a few bacterial species harboring divergent drug-binding sites, we identify their intrinsic resistance to corresponding ribosome-targeting antibiotics. Overall, we reveal the extensive lineage-specific diversity of ribosomal drug-binding sites, offering a resource for developing more targeted antibiotics and enabling personalized drug selection for specific pathogens. | ||||||||||||||||||||||||
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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 | 9qt5.cif.gz | 2 MB | Display | PDBx/mmCIF format |
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| PDB format | pdb9qt5.ent.gz | 1.5 MB | Display | PDB format |
| PDBx/mmJSON format | 9qt5.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/qt/9qt5 ftp://data.pdbj.org/pub/pdb/validation_reports/qt/9qt5 | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 53347MC 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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Components
+Large ribosomal subunit protein ... , 28 types, 28 molecules MBCDEFGJKOLPQRSTUVWXYZ34567N
-RNA chain , 2 types, 2 molecules 21
| #2: RNA chain | Mass: 37883.551 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) Streptomyces fradiae ATCC 10745 = DSM 40063 (bacteria)References: GenBank: 1751465408 |
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| #30: RNA chain | Mass: 1012266.625 Da / Num. of mol.: 1 / Source method: isolated from a natural source Source: (natural) Streptomyces fradiae ATCC 10745 = DSM 40063 (bacteria)References: GenBank: 1751465408 |
-Details
| 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 |
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Sample preparation
| Component | Name: Streptomyces fradiae ribosome / Type: RIBOSOME / Entity ID: all / Source: NATURAL | ||||||||||||||||||||
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| Molecular weight | Value: 2.5 MDa / Experimental value: NO | ||||||||||||||||||||
| Source (natural) | Organism: Streptomyces fradiae ATCC 10745 = DSM 40063 (bacteria) | ||||||||||||||||||||
| Buffer solution | pH: 7.5 | ||||||||||||||||||||
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| Specimen | 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 | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 100 % / Chamber temperature: 277.15 K |
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Electron microscopy imaging
| Microscopy | Model: TFS GLACIOS |
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| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 200 kV / Illumination mode: SPOT SCAN |
| Electron lens | Mode: BRIGHT FIELD / Nominal magnification: 150000 X / Nominal defocus max: 2000 nm / Nominal defocus min: 600 nm / Cs: 2.7 mm / C2 aperture diameter: 50 µm / Alignment procedure: COMA FREE |
| Specimen holder | Cryogen: NITROGEN / Temperature (max): 77 K |
| Image recording | Average exposure time: 7.94 sec. / Electron dose: 50 e/Å2 / Film or detector model: FEI FALCON IV (4k x 4k) / Num. of grids imaged: 1 / Num. of real images: 4219 |
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Processing
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||||||||||||||||||
| Particle selection | Num. of particles selected: 966178 | ||||||||||||||||||||||||||||||||||||||||
| Symmetry | Point symmetry: C1 (asymmetric) | ||||||||||||||||||||||||||||||||||||||||
| 3D reconstruction | Resolution: 3.13 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 250126 / Algorithm: FOURIER SPACE / Symmetry type: POINT | ||||||||||||||||||||||||||||||||||||||||
| Atomic model building | Protocol: RIGID BODY FIT / Space: REAL | ||||||||||||||||||||||||||||||||||||||||
| Atomic model building | Source name: AlphaFold / Type: in silico model | ||||||||||||||||||||||||||||||||||||||||
| Refinement | Cross valid method: NONE |
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Streptomyces fradiae ATCC 10745 = DSM 40063 (bacteria)
United Kingdom, 2items
Citation
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FIELD EMISSION GUN