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Yorodumi- PDB-5xaq: Crystal structure of Animalia-specific tRNA deacylase from Mus mu... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 5xaq | ||||||
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| Title | Crystal structure of Animalia-specific tRNA deacylase from Mus musculus | ||||||
Components | Probable D-tyrosyl-tRNA(Tyr) deacylase 2 | ||||||
Keywords | HYDROLASE / tRNA / deacylase | ||||||
| Function / homology | Function and homology informationAla-tRNA(Thr) deacylase activity / aminoacyl-tRNA metabolism involved in translational fidelity / D-tyrosyl-tRNA(Tyr) deacylase activity / D-aminoacyl-tRNA deacylase / tRNA metabolic process / tRNA binding / cytoplasm Similarity search - Function | ||||||
| Biological species | ![]() | ||||||
| Method | X-RAY DIFFRACTION / MOLECULAR REPLACEMENT / Resolution: 1.86 Å | ||||||
Authors | Kuncha, K.S. / Kattula, B. / Sankarnarayanan, R. | ||||||
| Funding support | India, 1items
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Citation | Journal: Nat Commun / Year: 2018Title: A chiral selectivity relaxed paralog of DTD for proofreading tRNA mischarging in Animalia Authors: Kuncha, S.K. / Mazeed, M. / Singh, R. / Kattula, B. / Routh, S.B. / Sankaranarayanan, R. | ||||||
| History |
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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 | 5xaq.cif.gz | 80.7 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb5xaq.ent.gz | 58.9 KB | Display | PDB format |
| PDBx/mmJSON format | 5xaq.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 5xaq_validation.pdf.gz | 434.7 KB | Display | wwPDB validaton report |
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| Full document | 5xaq_full_validation.pdf.gz | 436.3 KB | Display | |
| Data in XML | 5xaq_validation.xml.gz | 15.8 KB | Display | |
| Data in CIF | 5xaq_validation.cif.gz | 22.8 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/xa/5xaq ftp://data.pdbj.org/pub/pdb/validation_reports/xa/5xaq | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 4nbiS S: Starting model for refinement |
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| Similar structure data |
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Links
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Assembly
| Deposited unit | ![]()
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| Unit cell |
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Components
| #1: Protein | Mass: 18258.836 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() References: UniProt: Q8BHA3, Hydrolases; Acting on ester bonds #2: 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: 2.32 Å3/Da / Density % sol: 46.95 % |
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| Crystal grow | Temperature: 277 K / Method: vapor diffusion, sitting drop / pH: 8 / Details: BICINE (pH 8.0), PEG1500 |
-Data collection
| Diffraction | Mean temperature: 100 K |
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| Diffraction source | Source: ROTATING ANODE / Type: RIGAKU MICROMAX-007 HF / Wavelength: 1.54179 Å |
| Detector | Type: MAR scanner 345 mm plate / Detector: IMAGE PLATE / Date: Jul 1, 2016 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1.54179 Å / Relative weight: 1 |
| Reflection | Resolution: 1.86→60.94 Å / Num. obs: 29268 / % possible obs: 89.5 % / Redundancy: 6.4 % / Rmerge(I) obs: 0.076 / Net I/σ(I): 21.8 |
| Reflection shell | Resolution: 1.86→1.93 Å / Redundancy: 3.7 % / Rmerge(I) obs: 0.38 / Mean I/σ(I) obs: 2.4 / % possible all: 51.2 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 4NBI Resolution: 1.86→60.94 Å / Cor.coef. Fo:Fc: 0.952 / Cor.coef. Fo:Fc free: 0.931 / SU B: 3.778 / SU ML: 0.11 / Cross valid method: FREE R-VALUE / ESU R: 0.175 / ESU R Free: 0.162 / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
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| Solvent computation | Ion probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso mean: 31.403 Å2
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| Refinement step | Cycle: 1 / Resolution: 1.86→60.94 Å
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| Refine LS restraints |
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X-RAY DIFFRACTION
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