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Open data
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Basic information
| Entry | Database: PDB / ID: 4k4x | ||||||
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| Title | Coxsackievirus B3 polymerase elongation complex (r2_form), rna | ||||||
Components |
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Keywords | Transferase/rna / polymerase / RNA-dependent RNA polymerase / protein-RNA complex / Transferase-rna complex | ||||||
| Function / homology | Function and homology informationsymbiont-mediated suppression of host cytoplasmic pattern recognition receptor signaling pathway via inhibition of RIG-I activity / picornain 2A / symbiont-mediated suppression of host mRNA export from nucleus / symbiont genome entry into host cell via pore formation in plasma membrane / picornain 3C / T=pseudo3 icosahedral viral capsid / host cell cytoplasmic vesicle membrane / nucleoside-triphosphate phosphatase / channel activity / monoatomic ion transmembrane transport ...symbiont-mediated suppression of host cytoplasmic pattern recognition receptor signaling pathway via inhibition of RIG-I activity / picornain 2A / symbiont-mediated suppression of host mRNA export from nucleus / symbiont genome entry into host cell via pore formation in plasma membrane / picornain 3C / T=pseudo3 icosahedral viral capsid / host cell cytoplasmic vesicle membrane / nucleoside-triphosphate phosphatase / channel activity / monoatomic ion transmembrane transport / DNA replication / RNA helicase activity / endocytosis involved in viral entry into host cell / symbiont-mediated activation of host autophagy / RNA-directed RNA polymerase / cysteine-type endopeptidase activity / viral RNA genome replication / RNA-directed RNA polymerase activity / DNA-templated transcription / virion attachment to host cell / host cell nucleus / structural molecule activity / ATP hydrolysis activity / proteolysis / RNA binding / zinc ion binding / ATP binding / membrane Similarity search - Function | ||||||
| Biological species | ![]() Human coxsackievirus B3 | ||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.37 Å | ||||||
Authors | Gong, P. / Peersen, O.B. | ||||||
Citation | Journal: Plos One / Year: 2013Title: Structures of coxsackievirus, rhinovirus, and poliovirus polymerase elongation complexes solved by engineering RNA mediated crystal contacts. Authors: Gong, P. / Kortus, M.G. / Nix, J.C. / Davis, R.E. / Peersen, O.B. | ||||||
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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 | 4k4x.cif.gz | 455.7 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb4k4x.ent.gz | 366.7 KB | Display | PDB format |
| PDBx/mmJSON format | 4k4x.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 4k4x_validation.pdf.gz | 555.3 KB | Display | wwPDB validaton report |
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| Full document | 4k4x_full_validation.pdf.gz | 582.1 KB | Display | |
| Data in XML | 4k4x_validation.xml.gz | 76.1 KB | Display | |
| Data in CIF | 4k4x_validation.cif.gz | 109.1 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/k4/4k4x ftp://data.pdbj.org/pub/pdb/validation_reports/k4/4k4x | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 4k4sC ![]() 4k4tC ![]() 4k4uC ![]() 4k4vC ![]() 4k4wC ![]() 4k4yC ![]() 4k4zC ![]() 4k50C C: citing same article ( |
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| Similar structure data |
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Links
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Assembly
| Deposited unit | ![]()
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| 1 | ![]()
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| 2 | ![]()
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| 3 | ![]()
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| 4 | ![]()
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| Unit cell |
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Components
-Protein , 1 types, 4 molecules AEIM
| #1: Protein | Mass: 53624.203 Da / Num. of mol.: 4 / Fragment: UNP RESIDUES 1724-2185 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Human coxsackievirus B3 / Production host: ![]() References: UniProt: Q66338, UniProt: Q5UEA2*PLUS, RNA-directed RNA polymerase |
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-RNA chain , 3 types, 12 molecules BFJNCGKODHLP
| #2: RNA chain | Mass: 7629.574 Da / Num. of mol.: 4 / Source method: obtained synthetically #3: RNA chain | Mass: 4526.756 Da / Num. of mol.: 4 / Source method: obtained synthetically #4: RNA chain | Mass: 2974.854 Da / Num. of mol.: 4 / Source method: obtained synthetically |
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-Non-polymers , 3 types, 737 molecules 




| #5: Chemical | ChemComp-GOL / #6: Chemical | ChemComp-MG / #7: Water | ChemComp-HOH / | |
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-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 2.59 Å3/Da / Density % sol: 52.44 % |
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| Crystal grow | Temperature: 289 K / pH: 8.5 Details: 0.17 M sodium acetate, 0.085 M Tris, 25.5% PEG 4000, and 15% glycerol and directly frozen, pH 8.5, VAPOR DIFFUSION, SITTING DROP, temperature 289K |
-Data collection
| Diffraction | Mean temperature: 100 K |
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| Diffraction source | Source: SYNCHROTRON / Site: ALS / Beamline: 4.2.2 / Wavelength: 1 |
| Detector | Type: NOIR-1 / Detector: CCD |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1 Å / Relative weight: 1 |
| Reflection | Resolution: 2.37→48.78 Å / Num. obs: 109647 / % possible obs: 98 % / Observed criterion σ(I): 2 / Redundancy: 1.99 % / Biso Wilson estimate: 41.68 Å2 / Rmerge(I) obs: 0.064 / Net I/σ(I): 6.8 |
| Reflection shell | Resolution: 2.37→2.45 Å / Redundancy: 1.94 % / Rmerge(I) obs: 0.302 / Mean I/σ(I) obs: 1.5 / % possible all: 96.6 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENT / Resolution: 2.37→44.01 Å / Occupancy max: 1 / Occupancy min: 1 / SU ML: 0.31 / σ(F): 1.96 / Phase error: 29.85 / Stereochemistry target values: ML
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| Solvent computation | Shrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å / Solvent model: FLAT BULK SOLVENT MODEL | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso mean: 47.46 Å2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Refinement step | Cycle: LAST / Resolution: 2.37→44.01 Å
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| Refine LS restraints |
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| LS refinement shell |
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Human coxsackievirus B3
X-RAY DIFFRACTION
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