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Yorodumi- PDB-1r11: Structure Determination of the Dimeric Endonuclease in a Pseudo-f... -
+Open data
-Basic information
Entry | Database: PDB / ID: 1r11 | ||||||
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Title | Structure Determination of the Dimeric Endonuclease in a Pseudo-face-centerd P21 space group | ||||||
Components | tRNA-intron endonuclease | ||||||
Keywords | TRANSLATION / HYDROLASE / RNA splicing / endonuclease / x-ray crystallography | ||||||
Function / homology | Function and homology information tRNA-intron lyase / tRNA-intron endonuclease activity / tRNA splicing, via endonucleolytic cleavage and ligation / nucleic acid binding / lyase activity Similarity search - Function | ||||||
Biological species | Archaeoglobus fulgidus (archaea) | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.7 Å | ||||||
Authors | Li, H. / Zhang, Y. | ||||||
Citation | Journal: Acta Crystallogr.,Sect.D / Year: 2004 Title: Structure determination of a truncated dimeric splicing endonuclease in pseudo-face-centered space group P2(1)2(1)2. Authors: Zhang, Y. / Li, H. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 1r11.cif.gz | 128.9 KB | Display | PDBx/mmCIF format |
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PDB format | pdb1r11.ent.gz | 101.2 KB | Display | PDB format |
PDBx/mmJSON format | 1r11.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 1r11_validation.pdf.gz | 445.9 KB | Display | wwPDB validaton report |
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Full document | 1r11_full_validation.pdf.gz | 489.8 KB | Display | |
Data in XML | 1r11_validation.xml.gz | 26.5 KB | Display | |
Data in CIF | 1r11_validation.cif.gz | 35.3 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/r1/1r11 ftp://data.pdbj.org/pub/pdb/validation_reports/r1/1r11 | HTTPS FTP |
-Related 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: 36000.234 Da / Num. of mol.: 2 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Archaeoglobus fulgidus (archaea) / Strain: DSM 4304 / Gene: ENDA / Production host: Escherichia coli (E. coli) / References: UniProt: O29362, EC: 3.1.27.9 |
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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: 2.24 Å3/Da / Density % sol: 44.8 % | ||||||||||||||||||||||||||||||
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Crystal grow | pH: 6.6 Details: 100 mM Na-cacodylic acid pH 6.5 - 6.8, 20 mM (NH4)2SO4, 300-400 mM NaCH2COOH, pH 6.6 | ||||||||||||||||||||||||||||||
Crystal grow | *PLUS Method: vapor diffusion, hanging drop / PH range low: 6.8 / PH range high: 6.5 | ||||||||||||||||||||||||||||||
Components of the solutions | *PLUS
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-Data collection
Diffraction | Mean temperature: 100 K |
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Diffraction source | Source: SYNCHROTRON / Site: SSRL / Beamline: BL9-3 / Wavelength: 1 Å |
Detector | Type: ADSC QUANTUM 4 / Detector: CCD / Date: Nov 6, 1998 |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1 Å / Relative weight: 1 |
Reflection | Resolution: 2.7→500 Å / Num. all: 17717 / Num. obs: 17292 / % possible obs: 97.6 % / Observed criterion σ(F): 2 / Observed criterion σ(I): 1 / Biso Wilson estimate: 22 Å2 |
Reflection | *PLUS Highest resolution: 2 Å / Lowest resolution: 20 Å / Num. obs: 77465 / % possible obs: 90.8 % / Redundancy: 3.89 % / Rmerge(I) obs: 0.088 |
Reflection shell | *PLUS Highest resolution: 2 Å / Lowest resolution: 2.05 Å / % possible obs: 76.5 % / Redundancy: 2.46 % / Rmerge(I) obs: 0.352 / Mean I/σ(I) obs: 4.3 |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT / Resolution: 2.7→26.66 Å / Rfactor Rfree error: 0.01 / Isotropic thermal model: RESTRAINED / Cross valid method: THROUGHOUT / σ(F): 2 / Stereochemistry target values: Engh & Huber
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Solvent computation | Solvent model: FLAT MODEL / Bsol: 20.1469 Å2 / ksol: 0.382405 e/Å3 | |||||||||||||||||||||||||
Displacement parameters | Biso mean: 27.1 Å2
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Refine analyze | Luzzati coordinate error free: 0.4 Å / Luzzati sigma a free: 0.38 Å | |||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 2.7→26.66 Å
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Refine LS restraints |
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LS refinement shell | Highest resolution: 2.7 Å / Total num. of bins used: 6 /
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Xplor file |
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Refinement | *PLUS Highest resolution: 2 Å / Lowest resolution: 20 Å / % reflection Rfree: 5 % / Rfactor Rfree: 0.229 / Rfactor Rwork: 0.1856 | |||||||||||||||||||||||||
Solvent computation | *PLUS | |||||||||||||||||||||||||
Displacement parameters | *PLUS | |||||||||||||||||||||||||
Refine LS restraints | *PLUS
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LS refinement shell | *PLUS Highest resolution: 2 Å / Lowest resolution: 2.05 Å / Rfactor Rfree: 0.307 / Rfactor Rwork: 0.233 |