+Open data
-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 information Holliday junction helicase complex / Holliday junction resolvase complex / four-way junction helicase activity / recombinational repair / SOS response / four-way junction DNA binding / response to radiation / ATP binding / identical protein binding / cytoplasm Similarity search - Function | ||||||
Biological species | Escherichia coli (E. coli) | ||||||
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: 2000 Title: 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: MolmilJmol/JSmol |
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-Downloads & links
-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
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/c7/1c7y ftp://data.pdbj.org/pub/pdb/validation_reports/c7/1c7y | HTTPS FTP |
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-Related structure data
Related structure data | |
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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
-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.) Escherichia coli (E. coli) / Plasmid: PET / Production host: Escherichia coli (E. coli) / References: UniProt: P0A809 |
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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 % |
-Processing
Software |
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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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