+Open data
-Basic information
Entry | Database: PDB / ID: 2otu | ||||||
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Title | Crystal structure of Fv polyglutamine complex | ||||||
Components |
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Keywords | IMMUNE SYSTEM / Antibody Fv polyglutamine complex | ||||||
Function / homology | Function and homology information IgG immunoglobulin complex / immunoglobulin mediated immune response / antigen binding / blood microparticle Similarity search - Function | ||||||
Biological species | Mus musculus (house mouse) | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.68 Å | ||||||
Authors | Li, P. | ||||||
Citation | Journal: To be Published Title: Implications of the structure of a poly-Gln/anti-poly-Gln complex for disease progression and therapy Authors: Li, P. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 2otu.cif.gz | 216.4 KB | Display | PDBx/mmCIF format |
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PDB format | pdb2otu.ent.gz | 173.7 KB | Display | PDB format |
PDBx/mmJSON format | 2otu.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 2otu_validation.pdf.gz | 512.1 KB | Display | wwPDB validaton report |
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Full document | 2otu_full_validation.pdf.gz | 528.1 KB | Display | |
Data in XML | 2otu_validation.xml.gz | 46.8 KB | Display | |
Data in CIF | 2otu_validation.cif.gz | 67.9 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ot/2otu ftp://data.pdbj.org/pub/pdb/validation_reports/ot/2otu | HTTPS FTP |
-Related structure data
Related structure data | 2otwC 2gsgS S: Starting model for refinement 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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2 |
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3 |
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4 |
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Unit cell |
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-Components
#1: Antibody | Mass: 12460.883 Da / Num. of mol.: 4 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Mus musculus (house mouse) / Gene: VL / Plasmid: pET22b(+) / Species (production host): Escherichia coli / Production host: Escherichia coli BL21(DE3) (bacteria) / Strain (production host): BL21(DE3) #2: Antibody | Mass: 13330.936 Da / Num. of mol.: 4 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Mus musculus (house mouse) / Gene: VH / Plasmid: pET22b(+) / Production host: Spodoptera frugiperda (fall armyworm) / Strain (production host): BL21 (DE3) / References: UniProt: A2NN81 #3: Protein/peptide | Mass: 1356.355 Da / Num. of mol.: 4 / Source method: obtained synthetically / Details: synthetic peptide #4: 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: 2.48 Å3/Da / Density % sol: 50.33 % |
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Crystal grow | Temperature: 298 K / Method: evaporation / pH: 6 Details: 0.1 M sodium citrate, 0.2 M NH4Ac, 27.5% PEG 4000, pH 6.0, EVAPORATION, temperature 298K |
-Data collection
Diffraction | Mean temperature: 173 K |
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Diffraction source | Source: SYNCHROTRON / Site: ALS / Beamline: 8.2.2 / Wavelength: 1 |
Detector | Type: ADSC QUANTUM 315 / Detector: CCD / Date: Jan 1, 2006 / Details: Si(111) |
Radiation | Monochromator: Si (111) / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 1 Å / Relative weight: 1 |
Reflection | Resolution: 1.68→41 Å / Num. all: 119617 / Num. obs: 116627 / % possible obs: 97.5 % / Redundancy: 4.4 % / Rmerge(I) obs: 0.046 / Rsym value: 4.3 / Net I/σ(I): 34.3 |
Reflection shell | Resolution: 1.68→1.74 Å / Redundancy: 3.5 % / Rmerge(I) obs: 0.258 / Mean I/σ(I) obs: 3.4 / Num. unique all: 10848 / Rsym value: 25.8 / % possible all: 91.1 |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT Starting model: PDB entry 2GSG Resolution: 1.68→41 Å / Isotropic thermal model: isotropic / Cross valid method: THROUGHOUT / σ(F): 0 / σ(I): 0 / Stereochemistry target values: Engh & Huber
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Refinement step | Cycle: LAST / Resolution: 1.68→41 Å
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Refine LS restraints |
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LS refinement shell | Highest resolution: 1.68 Å
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