+
Open data
-
Basic information
| Entry | Database: PDB / ID: 9dyg | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Title | iSAT-PNA-RA20, RA20-B-c class | |||||||||
Components |
| |||||||||
Keywords | RIBOSOME / 50S subunit / assembly intermediate / RNA-protein complex | |||||||||
| Function / homology | Function and homology informationtranscriptional attenuation / endoribonuclease inhibitor activity / RNA-binding transcription regulator activity / negative regulation of cytoplasmic translation / translation repressor activity / assembly of large subunit precursor of preribosome / cytosolic ribosome assembly / ribosome assembly / DNA-templated transcription termination / mRNA 5'-UTR binding ...transcriptional attenuation / endoribonuclease inhibitor activity / RNA-binding transcription regulator activity / negative regulation of cytoplasmic translation / translation repressor activity / assembly of large subunit precursor of preribosome / cytosolic ribosome assembly / ribosome assembly / DNA-templated transcription termination / mRNA 5'-UTR binding / large ribosomal subunit / ribosomal large subunit assembly / large ribosomal subunit rRNA binding / cytosolic large ribosomal subunit / cytoplasmic translation / negative regulation of translation / rRNA binding / structural constituent of ribosome / ribosome / translation / ribonucleoprotein complex / response to antibiotic / negative regulation of DNA-templated transcription / mRNA binding / DNA binding / cytosol / cytoplasm Similarity search - Function | |||||||||
| Biological species | ![]() | |||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 5.27 Å | |||||||||
Authors | Sheng, K. / Dong, X. / Lee, J. | |||||||||
| Funding support | United States, 2items
| |||||||||
Citation | Journal: To Be PublishedTitle: Domain consolidation in bacterial 50S assembly revealed by anti-sense oligonucleotide probing Authors: Sheng, K. / Dong, X. / Aiyer, S. / Lee, J. / Djordjevic-Marquardt, S. / Lyumkis, D. / Williamson, J.R. | |||||||||
| History |
|
-
Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
|---|
-
Downloads & links
-
Download
| PDBx/mmCIF format | 9dyg.cif.gz | 1.1 MB | Display | PDBx/mmCIF format |
|---|---|---|---|---|
| PDB format | pdb9dyg.ent.gz | Display | PDB format | |
| PDBx/mmJSON format | 9dyg.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 9dyg_validation.pdf.gz | 1016.1 KB | Display | wwPDB validaton report |
|---|---|---|---|---|
| Full document | 9dyg_full_validation.pdf.gz | 1 MB | Display | |
| Data in XML | 9dyg_validation.xml.gz | 69.3 KB | Display | |
| Data in CIF | 9dyg_validation.cif.gz | 114.7 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/dy/9dyg ftp://data.pdbj.org/pub/pdb/validation_reports/dy/9dyg | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 47303MC M: map data used to model this data C: citing same article ( |
|---|---|
| Similar structure data | Similarity search - Function & homology F&H Search |
-
Links
-
Assembly
| Deposited unit | ![]()
|
|---|---|
| 1 |
|
-
Components
-RNA chain , 1 types, 1 molecules CA
| #1: RNA chain | Mass: 565405.812 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
|---|
-Large ribosomal subunit protein ... , 13 types, 13 molecules 2DEJKNPQRSTUY
| #2: Protein/peptide | Mass: 4290.116 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
|---|---|
| #3: Protein | Mass: 21763.840 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
| #4: Protein | Mass: 22121.566 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
| #5: Protein | Mass: 16050.606 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
| #6: Protein | Mass: 12080.289 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
| #7: Protein | Mass: 13721.938 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
| #8: Protein | Mass: 12941.005 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
| #9: Protein | Mass: 13396.828 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
| #10: Protein | Mass: 11586.374 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
| #11: Protein | Mass: 12253.359 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
| #12: Protein | Mass: 10546.472 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
| #13: Protein | Mass: 11078.874 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
| #14: Protein | Mass: 7286.464 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Source: (natural) ![]() |
-Details
| Has ligand of interest | N |
|---|---|
| Has protein modification | N |
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
|---|---|
| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
-
Sample preparation
| Component | Name: iSAT-PNA-RA20 50S ribosomal subunit assembly intermediate Type: RIBOSOME / Entity ID: all / Source: NATURAL | ||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Molecular weight | Experimental value: NO | ||||||||||||||||||||||||||||||
| Source (natural) | Organism: ![]() | ||||||||||||||||||||||||||||||
| Buffer solution | pH: 7.5 Details: Most of the sucrose was removed by spin concentration. | ||||||||||||||||||||||||||||||
| Buffer component |
| ||||||||||||||||||||||||||||||
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES | ||||||||||||||||||||||||||||||
| Specimen support | Grid material: GOLD / Grid type: Au-flat 1.2/1.3 | ||||||||||||||||||||||||||||||
| Vitrification | Instrument: FEI VITROBOT MARK IV / Cryogen name: ETHANE / Humidity: 90 % / Chamber temperature: 298 K / Details: 3 microliter of the sample was added. |
-
Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
|---|---|
| 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: 2000 nm / Nominal defocus min: 1000 nm |
| Specimen holder | Cryogen: NITROGEN |
| Image recording | Average exposure time: 2 sec. / Electron dose: 25.4 e/Å2 / Detector mode: COUNTING / Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Num. of grids imaged: 1 |
-
Processing
| EM software |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| CTF correction | Details: CTF correction were performed by Patch CTF Estimation of cryoSPARC Type: NONE | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 3D reconstruction | Resolution: 5.27 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 9000 / Symmetry type: POINT | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Atomic model building | B value: 120.42 / Protocol: OTHER / Space: REAL / Target criteria: Comprehensive validation (cryo-EM) Details: The atomic model was fitted into a low resolution (5 Angstrom) EM map; therefore the coordinates should only serve as a general visual representation and should not be looked into detail. ...Details: The atomic model was fitted into a low resolution (5 Angstrom) EM map; therefore the coordinates should only serve as a general visual representation and should not be looked into detail. Initial docking of the atomic model was done in ChimeraX. Coot and Phenix were used for real-space refinements. Geometry minimization in Phenix was used to improve the RNA atomic model. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Atomic model building | 3D fitting-ID: 1 / Source name: PDB / Type: experimental model
|
Movie
Controller
About Yorodumi






United States, 2items
Citation
PDBj































FIELD EMISSION GUN

