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Yorodumi- PDB-2a6i: Crystal structure analysis of the anti-arsonate germline antibody... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 2a6i | ||||||
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| Title | Crystal structure analysis of the anti-arsonate germline antibody 36-65 in complex with a phage display derived dodecapeptide KLASIPTHTSPL | ||||||
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Keywords | IMMUNE SYSTEM / Immunoglobulin fold / Fab-peptide complex | ||||||
| Function / homology | Immunoglobulins / Immunoglobulin-like / Sandwich / Mainly Beta Function and homology information | ||||||
| Biological species | ![]() | ||||||
| Method | X-RAY DIFFRACTION / MOLECULAR REPLACEMENT / Resolution: 2.5 Å | ||||||
Authors | Sethi, D.K. / Agarwal, A. / Manivel, V. / Rao, K.V. / Salunke, D.M. | ||||||
Citation | Journal: Immunity / Year: 2006Title: Differential epitope positioning within the germline antibody paratope enhances promiscuity in the primary immune response. Authors: Sethi, D.K. / Agarwal, A. / Manivel, V. / Rao, K.V. / Salunke, D.M. | ||||||
| History |
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| Remark 999 | SEQUENCE THE SEQUENCE IS NOT DEPOSITED IN ANY SEQUENCE DATABASE EXCEPT RESIDUES 1 TO 120 OF CHAINS ...SEQUENCE THE SEQUENCE IS NOT DEPOSITED IN ANY SEQUENCE DATABASE EXCEPT RESIDUES 1 TO 120 OF CHAINS B,H WHICH CORRESPOND TO DEPOSITED SEQUENCE OF THE HEAVY CHAIN VARIABLE REGION OF ANTI-ARSONATE ANTIBODY 36-65 |
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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 | 2a6i.cif.gz | 96.6 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb2a6i.ent.gz | 73.9 KB | Display | PDB format |
| PDBx/mmJSON format | 2a6i.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 2a6i_validation.pdf.gz | 446 KB | Display | wwPDB validaton report |
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| Full document | 2a6i_full_validation.pdf.gz | 471 KB | Display | |
| Data in XML | 2a6i_validation.xml.gz | 21.1 KB | Display | |
| Data in CIF | 2a6i_validation.cif.gz | 28.3 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/a6/2a6i ftp://data.pdbj.org/pub/pdb/validation_reports/a6/2a6i | HTTPS FTP |
-Related structure data
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Links
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Assembly
| Deposited unit | ![]()
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| 1 |
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| Unit cell |
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Components
| #1: Antibody | Mass: 23707.049 Da / Num. of mol.: 1 / Fragment: Fab / Source method: isolated from a natural source / Details: Mouse monoclonal / Source: (natural) ![]() |
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| #2: Antibody | Mass: 23942.768 Da / Num. of mol.: 1 / Source method: isolated from a natural source / Details: Mouse monoclonal / Source: (natural) ![]() |
| #3: Protein/peptide | Mass: 1266.486 Da / Num. of mol.: 1 / Source method: obtained synthetically Details: Chemically synthesized (Phage display derived peptide) |
| #4: Water | ChemComp-HOH / |
| Has protein modification | Y |
-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal | Density Matthews: 2.47 Å3/Da / Density % sol: 50.11 % |
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| Crystal grow | Temperature: 298 K / Method: vapor diffusion, hanging drop / pH: 6.7 Details: 16% PEG 8000, cacodylate, 0.05% azide , pH 6.7, VAPOR DIFFUSION, HANGING DROP, temperature 298.0K |
-Data collection
| Diffraction | Mean temperature: 120 K |
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| Diffraction source | Source: ROTATING ANODE / Type: RIGAKU RU300 / Wavelength: 1.5418 Å |
| Detector | Type: MARRESEARCH / Detector: IMAGE PLATE / Date: Jan 24, 2004 / Details: mirrors |
| Radiation | Monochromator: Osmic mirrors / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1.5418 Å / Relative weight: 1 |
| Reflection | Resolution: 2.5→50 Å / Num. all: 15724 / Num. obs: 15724 / % possible obs: 94.2 % / Observed criterion σ(F): 0 / Observed criterion σ(I): 0 / Redundancy: 2.9 % / Rmerge(I) obs: 0.104 / Net I/σ(I): 5.1 |
| Reflection shell | Resolution: 2.5→2.59 Å / Redundancy: 2.84 % / Mean I/σ(I) obs: 1.7 / % possible all: 96.3 |
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Processing
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| Refinement | Method to determine structure: MOLECULAR REPLACEMENT / Resolution: 2.5→50 Å / σ(F): 0 / Stereochemistry target values: Engh & Huber
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| Refinement step | Cycle: LAST / Resolution: 2.5→50 Å
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| Refine LS restraints |
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X-RAY DIFFRACTION
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