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Open data
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Basic information
| Entry | Database: PDB / ID: 1rfr | ||||||
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| Title | NMR structure of the 30mer stemloop-D of coxsackieviral RNA | ||||||
Components | stemloop-D RNA of the 5'-cloverleaf of coxsackievirus B3 | ||||||
Keywords | RNA / loop with conformation similar to stable UNCG-tetraloops and U:G closing base pair / base-paired U:U-C:U-U:U mismatch / A-form helix stems | ||||||
| Function / homology | RNA / RNA (> 10) Function and homology information | ||||||
| Biological species | ![]() Human coxsackievirus B3 | ||||||
| Method | SOLUTION NMR / distance geometry, simulated annealing, energy minimisation | ||||||
Authors | Ohlenschlager, O. / Wohnert, J. / Bucci, E. / Seitz, S. / Hafner, S. / Ramachandran, R. / Zell, R. / Gorlach, M. | ||||||
Citation | Journal: STRUCTURE / Year: 2004Title: The structure of the stemloop D subdomain of coxsackievirus B3 cloverleaf RNA and its interaction with the proteinase 3C. Authors: Ohlenschlager, O. / Wohnert, J. / Bucci, E. / Seitz, S. / Hafner, S. / Ramachandran, R. / Zell, R. / Gorlach, M. | ||||||
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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 | 1rfr.cif.gz | 367.4 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb1rfr.ent.gz | 308.8 KB | Display | PDB format |
| PDBx/mmJSON format | 1rfr.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 1rfr_validation.pdf.gz | 327.7 KB | Display | wwPDB validaton report |
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| Full document | 1rfr_full_validation.pdf.gz | 441 KB | Display | |
| Data in XML | 1rfr_validation.xml.gz | 8.2 KB | Display | |
| Data in CIF | 1rfr_validation.cif.gz | 15.8 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/rf/1rfr ftp://data.pdbj.org/pub/pdb/validation_reports/rf/1rfr | HTTPS FTP |
-Related structure data
| Similar structure data |
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Links
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Assembly
| Deposited unit | ![]()
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| NMR ensembles |
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Components
| #1: RNA chain | Mass: 9536.624 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Details: PROTEINASE 3C BINDING DOMAIN / Source: (gene. exp.) ![]() Human coxsackievirus B3 / Genus: Enterovirus / Species: Human enterovirus BDescription: two nucleotides (GG) at 5'-end and two nucleotides (UC) at the 3'-end were added for in vitro production Gene: 5'-nontranslated region / Plasmid: pUC-19 / Production host: in vitro (unknown) |
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-Experimental details
-Experiment
| Experiment | Method: SOLUTION NMR |
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| NMR experiment | Type: see below |
| NMR details | Text: the structure was determined using heteronuclear 2D and 3D NMR experiments, e.g. 3D HCCH-COSY, RELAY-COSY, TOCSY, H6/H5(C4N)H, C6/C5(C4N)H, H(CCN)H-TOCSY, HCCH-TOCSY, 2D H(N)CO, 2D CPMG-HSQC- ...Text: the structure was determined using heteronuclear 2D and 3D NMR experiments, e.g. 3D HCCH-COSY, RELAY-COSY, TOCSY, H6/H5(C4N)H, C6/C5(C4N)H, H(CCN)H-TOCSY, HCCH-TOCSY, 2D H(N)CO, 2D CPMG-HSQC-NOESY, 2D NOESY, 3D 1H,1H,15N-NOESY-HSQC, 3D 1H,1H,13C-NOESY-HSQC, CLEAN-TOCSY, 31P-SPINECHO-DIFFERENCE-CT-HMQC, HNN-COSY, 2D 1H,13C-HSQC, 2D 1H,15N-HSQC, HCN, H5(C5C4N)H, H8(C8C2)H2, 3D 13C-F1-FILTERED,13C-F3-EDITED-NOESY-HSQC |
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Sample preparation
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| Crystal grow | *PLUS Method: other / Details: NMR |
-NMR measurement
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M | |||||||||||||||
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| Radiation wavelength | Relative weight: 1 | |||||||||||||||
| NMR spectrometer |
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Processing
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| Refinement | Method: distance geometry, simulated annealing, energy minimisation Software ordinal: 1 Details: 1001 experimental distances derived from NOE cross peaks, 280 torsion angle constraints describing 258 torsion angles, 52 hydrogen bond constraints | ||||||||||||||||||||||||||||
| NMR representative | Selection criteria: closest to the average | ||||||||||||||||||||||||||||
| NMR ensemble | Conformer selection criteria: structures with the lowest energy,target function Conformers calculated total number: 100 / Conformers submitted total number: 20 |
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