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Yorodumi- PDB-5htx: Putative sugar kinases from Arabidopsis thaliana in complex with ADP -
+Open data
-Basic information
Entry | Database: PDB / ID: 5htx | ||||||
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Title | Putative sugar kinases from Arabidopsis thaliana in complex with ADP | ||||||
Components | Putative xylulose kinase | ||||||
Keywords | TRANSFERASE / putative sugar kinases / Arabidopsis thaliana / ADP | ||||||
Function / homology | Function and homology information D-ribulokinase / D-ribulokinase activity / plastid / chloroplast / ATP binding / cytosol / cytoplasm Similarity search - Function | ||||||
Biological species | Arabidopsis thaliana (thale cress) | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.492 Å | ||||||
Authors | Xie, Y. / Li, M. / Chang, W. | ||||||
Citation | Journal: Plos One / Year: 2016 Title: Crystal Structures of Putative Sugar Kinases from Synechococcus Elongatus PCC 7942 and Arabidopsis Thaliana Authors: Xie, Y. / Li, M. / Chang, W. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 5htx.cif.gz | 181.9 KB | Display | PDBx/mmCIF format |
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PDB format | pdb5htx.ent.gz | 141.4 KB | Display | PDB format |
PDBx/mmJSON format | 5htx.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 5htx_validation.pdf.gz | 731.7 KB | Display | wwPDB validaton report |
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Full document | 5htx_full_validation.pdf.gz | 732.7 KB | Display | |
Data in XML | 5htx_validation.xml.gz | 19.2 KB | Display | |
Data in CIF | 5htx_validation.cif.gz | 28.8 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ht/5htx ftp://data.pdbj.org/pub/pdb/validation_reports/ht/5htx | HTTPS FTP |
-Related structure data
Related structure data | 5htjC 5htnC 5htpC 5htrC 5htvC 5htyC 5hu2C 5huxC 5hv7C C: citing same article (ref.) |
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Similar structure data |
-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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-Components
#1: Protein | Mass: 47756.930 Da / Num. of mol.: 1 / Fragment: UNP residues 43-478 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Arabidopsis thaliana (thale cress) / Gene: XK-1, At2g21370 / Plasmid: pMCSG7 / Production host: Escherichia coli (E. coli) / References: UniProt: Q8L794 |
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#2: Chemical | ChemComp-ADP / |
#3: Water | ChemComp-HOH / |
-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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-Sample preparation
Crystal | Density Matthews: 2.41 Å3/Da / Density % sol: 49.07 % |
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Crystal grow | Temperature: 281 K / Method: vapor diffusion, sitting drop / pH: 6.5 Details: 0.1M BIS-TRIS pH 6.5, 20% w/v Polyethylene glycol monomethyl ether 5000 |
-Data collection
Diffraction | Mean temperature: 100 K |
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Diffraction source | Source: SYNCHROTRON / Site: SSRF / Beamline: BL17U / Wavelength: 0.97917 Å |
Detector | Type: ADSC QUANTUM 315 / Detector: CCD / Date: May 5, 2015 |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.97917 Å / Relative weight: 1 |
Reflection | Resolution: 1.49→50 Å / Num. obs: 73256 / % possible obs: 96.3 % / Redundancy: 4.2 % / Rmerge(I) obs: 0.044 / Net I/σ(I): 27.37 |
Reflection shell | Resolution: 1.49→1.51 Å / Redundancy: 4.1 % / Rmerge(I) obs: 0.301 / Mean I/σ(I) obs: 5.26 / % possible all: 90 |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT / Resolution: 1.492→42.835 Å / SU ML: 0.12 / Cross valid method: FREE R-VALUE / σ(F): 1.35 / Phase error: 15.65
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Solvent computation | Shrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 1.492→42.835 Å
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Refine LS restraints |
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LS refinement shell |
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