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Yorodumi- PDB-4ydu: Crystal structure of E. coli YgjD-YeaZ heterodimer in complex with ADP -
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Open data
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Basic information
| Entry | Database: PDB / ID: 4ydu | |||||||||
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| Title | Crystal structure of E. coli YgjD-YeaZ heterodimer in complex with ADP | |||||||||
Components |
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Keywords | TRANSFERASE / YgjD-YeaZ complex / t6A transferase | |||||||||
| Function / homology | Function and homology informationglycosylation-dependent protein binding / N6-L-threonylcarbamoyladenine synthase / tRNA N(6)-L-threonylcarbamoyladenine synthase activity / EKC/KEOPS complex / tRNA threonylcarbamoyladenosine modification / maintenance of translational fidelity / metallopeptidase activity / iron ion binding / magnesium ion binding / identical protein binding / cytosol Similarity search - Function | |||||||||
| Biological species | ![]() | |||||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.33 Å | |||||||||
Authors | Zhang, W. / Collinet, B. / Perrochia, L. / Durand, D. / Van Tilbeurgh, H. | |||||||||
Citation | Journal: Nucleic Acids Res. / Year: 2015Title: The ATP-mediated formation of the YgjD-YeaZ-YjeE complex is required for the biosynthesis of tRNA t6A in Escherichia coli. Authors: Zhang, W. / Collinet, B. / Perrochia, L. / Durand, D. / Van Tilbeurgh, H. | |||||||||
| 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 | 4ydu.cif.gz | 441.1 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb4ydu.ent.gz | 360.3 KB | Display | PDB format |
| PDBx/mmJSON format | 4ydu.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 4ydu_validation.pdf.gz | 1.7 MB | Display | wwPDB validaton report |
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| Full document | 4ydu_full_validation.pdf.gz | 1.7 MB | Display | |
| Data in XML | 4ydu_validation.xml.gz | 46.8 KB | Display | |
| Data in CIF | 4ydu_validation.cif.gz | 66.4 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/yd/4ydu ftp://data.pdbj.org/pub/pdb/validation_reports/yd/4ydu | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 4wq4C ![]() 4wq5C ![]() 2ivpS S: Starting model for refinement 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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| Unit cell |
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| Noncrystallographic symmetry (NCS) | NCS domain:
NCS domain segments: Component-ID: 1 / Beg auth comp-ID: ARG / Beg label comp-ID: ARG / Refine code: 4
NCS ensembles :
NCS oper:
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Components
-Protein , 2 types, 4 molecules ABCD
| #1: Protein | Mass: 36879.238 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() #2: Protein | Mass: 26033.635 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Production host: ![]() References: UniProt: P76256 |
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-Non-polymers , 5 types, 459 molecules 








| #3: Chemical | ChemComp-ADP / #4: Chemical | #5: Chemical | #6: Chemical | ChemComp-ACT / #7: Water | ChemComp-HOH / | |
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-Details
| Has protein modification | Y |
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-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION |
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Sample preparation
| Crystal | Density Matthews: 2.48 Å3/Da / Density % sol: 50.46 % / Description: thin plate |
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| Crystal grow | Temperature: 293 K / Method: vapor diffusion, hanging drop / pH: 7.4 Details: 30% PEG4000, 0.3M Lithium Sulfate, 0.1 M Sodium Acetate and 0.1 M HEPES PH range: 7.2 - 7.6 |
-Data collection
| Diffraction | Mean temperature: 100 K |
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| Diffraction source | Source: SYNCHROTRON / Site: SOLEIL / Beamline: PROXIMA 1 / Wavelength: 0.9801 Å |
| Detector | Type: PSI PILATUS 6M / Detector: PIXEL / Date: Oct 2, 2012 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 0.9801 Å / Relative weight: 1 |
| Reflection | Resolution: 2.25→49.38 Å / Num. obs: 55653 / % possible obs: 97.9 % / Redundancy: 3.97 % / Rsym value: 0.121 / Net I/σ(I): 11 |
| Reflection shell | Resolution: 2.25→2.33 Å / Rmerge(I) obs: 0.57 / Mean I/σ(I) obs: 2.46 / Rsym value: 0.483 / % possible all: 95.69 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENTStarting model: 2IVP Resolution: 2.33→49.38 Å / Cor.coef. Fo:Fc: 0.96 / Cor.coef. Fo:Fc free: 0.935 / SU B: 12.862 / SU ML: 0.171 / Cross valid method: THROUGHOUT / ESU R: 0.281 / ESU R Free: 0.209 / Stereochemistry target values: MAXIMUM LIKELIHOOD / 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 / Solvent model: MASK | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Displacement parameters | Biso mean: 35.999 Å2
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| Refinement step | Cycle: 1 / Resolution: 2.33→49.38 Å
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| Refine LS restraints |
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