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Open data
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Basic information
| Entry | Database: PDB / ID: 1c7y | ||||||
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| Title | E.COLI RUVA-HOLLIDAY JUNCTION COMPLEX | ||||||
Components |
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Keywords | RECOMBINATION/DNA / helix-hairpin-helix / protein-DNA complex / homologous recombination / Holliday junction / RECOMBINATION-DNA COMPLEX | ||||||
| Function / homology | Function and homology informationHolliday junction helicase complex / Holliday junction resolvase complex / four-way junction helicase activity / SOS response / recombinational repair / four-way junction DNA binding / response to radiation / ATP binding / identical protein binding / cytoplasm Similarity search - Function | ||||||
| Biological species | ![]() | ||||||
| Method | X-RAY DIFFRACTION / SYNCHROTRON / Resolution: 3.1 Å | ||||||
Authors | Ariyoshi, M. / Nishino, T. / Iwasaki, H. / Shinagawa, H. / Morikawa, K. | ||||||
Citation | Journal: Proc.Natl.Acad.Sci.USA / Year: 2000Title: Crystal structure of the holliday junction DNA in complex with a single RuvA tetramer. Authors: Ariyoshi, M. / Nishino, T. / Iwasaki, H. / Shinagawa, H. / Morikawa, K. | ||||||
| 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 | 1c7y.cif.gz | 90.2 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb1c7y.ent.gz | 70.6 KB | Display | PDB format |
| PDBx/mmJSON format | 1c7y.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 1c7y_validation.pdf.gz | 462 KB | Display | wwPDB validaton report |
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| Full document | 1c7y_full_validation.pdf.gz | 482.5 KB | Display | |
| Data in XML | 1c7y_validation.xml.gz | 14.9 KB | Display | |
| Data in CIF | 1c7y_validation.cif.gz | 20.4 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/c7/1c7y ftp://data.pdbj.org/pub/pdb/validation_reports/c7/1c7y | HTTPS FTP |
-Related structure data
| Related structure data | |
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| Similar 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
-DNA chain , 8 types, 8 molecules BCDEFGHI
| #1: DNA chain | Mass: 4061.655 Da / Num. of mol.: 1 / Source method: obtained synthetically |
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| #2: DNA chain | Mass: 3693.414 Da / Num. of mol.: 1 / Source method: obtained synthetically |
| #3: DNA chain | Mass: 3944.601 Da / Num. of mol.: 1 / Source method: obtained synthetically |
| #4: DNA chain | Mass: 3782.476 Da / Num. of mol.: 1 / Source method: obtained synthetically |
| #5: DNA chain | Mass: 3855.539 Da / Num. of mol.: 1 / Source method: obtained synthetically |
| #6: DNA chain | Mass: 3631.394 Da / Num. of mol.: 1 / Source method: obtained synthetically |
| #7: DNA chain | Mass: 3997.607 Da / Num. of mol.: 1 / Source method: obtained synthetically |
| #8: DNA chain | Mass: 3566.357 Da / Num. of mol.: 1 / Source method: obtained synthetically |
-Protein , 1 types, 1 molecules A
| #9: Protein | Mass: 22111.668 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() |
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-Experimental details
-Experiment
| Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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Sample preparation
| Crystal grow | Temperature: 293 K / Method: vapor diffusion, hanging drop / pH: 6 Details: ammonium sulfate, sodium chloride, glycerol, MES, pH 6.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K | ||||||||||||||||||||||||||||||||||||||||
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| Components of the solutions |
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| Crystal grow | *PLUS Temperature: 20 ℃ / pH: 7.5 | ||||||||||||||||||||||||||||||||||||||||
| 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: Photon Factory / Beamline: BL-6B / Wavelength: 1 |
| Detector | Detector: IMAGE PLATE / Date: Dec 15, 1998 |
| Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
| Radiation wavelength | Wavelength: 1 Å / Relative weight: 1 |
| Reflection | Resolution: 3→80 Å / Num. all: 7136 / Num. obs: 7136 / % possible obs: 99.9 % / Observed criterion σ(I): 0 / Redundancy: 13.4 % / Biso Wilson estimate: 34.9 Å2 / Rmerge(I) obs: 0.054 / Net I/σ(I): 47 |
| Reflection shell | Resolution: 3→3.11 Å / Rmerge(I) obs: 0.275 / Num. unique all: 691 / % possible all: 100 |
| Reflection | *PLUS Num. measured all: 143269 |
| Reflection shell | *PLUS % possible obs: 100 % |
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Processing
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| Refinement | Resolution: 3.1→45.8 Å / Rfactor Rfree error: 0.011 / Data cutoff high absF: 3475770.71 / Data cutoff low absF: 0 / Cross valid method: THROUGHOUT / σ(F): 0
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| Solvent computation | Bsol: 88.2948 Å2 / ksol: 0.425315 e/Å3 | |||||||||||||||||||||||||
| Refine analyze |
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| Refinement step | Cycle: LAST / Resolution: 3.1→45.8 Å
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| Refine LS restraints |
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| LS refinement shell | Resolution: 3.1→3.24 Å / Rfactor Rfree error: 0.039 / Total num. of bins used: 8
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| Software | *PLUS Name: CNS / Version: 0.9 / Classification: refinement | |||||||||||||||||||||||||
| Refine LS restraints | *PLUS
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