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- PDB-6g6f: Crystal structure of a parallel eight-helix coiled coil CC-Type2-LF -
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Open data
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Basic information
Entry | Database: PDB / ID: 6g6f | |||||||||
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Title | Crystal structure of a parallel eight-helix coiled coil CC-Type2-LF | |||||||||
![]() | CC-Type2-LF | |||||||||
![]() | DE NOVO PROTEIN / de novo / coiled coil / alpha-helical bundle / synthetic construct | |||||||||
Biological species | synthetic construct (others) | |||||||||
Method | ![]() ![]() ![]() ![]() | |||||||||
![]() | Rhys, G.G. / Brady, R.L. / Woolfson, D.N. | |||||||||
Funding support | ![]()
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![]() | ![]() Title: Maintaining and breaking symmetry in homomeric coiled-coil assemblies. Authors: Rhys, G.G. / Wood, C.W. / Lang, E.J.M. / Mulholland, A.J. / Brady, R.L. / Thomson, A.R. / Woolfson, D.N. | |||||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 62 KB | Display | ![]() |
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PDB format | ![]() | 50.4 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 479 KB | Display | ![]() |
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Full document | ![]() | 479.6 KB | Display | |
Data in XML | ![]() | 12.8 KB | Display | |
Data in CIF | ![]() | 18.9 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 6g65C ![]() 6g66C ![]() 6g67C ![]() 6g68C ![]() 6g69C ![]() 6g6aC ![]() 6g6bC ![]() 6g6cC ![]() 6g6dC ![]() 6g6eC ![]() 6g6gC ![]() 6g6hC C: citing same article ( |
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Similar structure data |
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Links
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Assembly
Deposited unit | ![]()
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Unit cell |
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Components
#1: Protein/peptide | Mass: 3370.935 Da / Num. of mol.: 8 / Source method: obtained synthetically Details: solid-phase peptide synthesis using the fmoc-based strategy Source: (synth.) synthetic construct (others) #2: Chemical | ChemComp-TRS / | #3: Water | ChemComp-HOH / | |
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-Experimental details
-Experiment
Experiment | Method: ![]() |
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Sample preparation
Crystal | Density Matthews: 2.04 Å3/Da / Density % sol: 39.76 % / Mosaicity: 0.26 ° |
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Crystal grow | Temperature: 293 K / Method: vapor diffusion, sitting drop / pH: 8.5 / Details: 50 mM Tris and 10 % w/v PEG 6000 |
-Data collection
Diffraction | Mean temperature: 80 K | ||||||||||||||||||||||||
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Diffraction source | Source: ![]() ![]() ![]() | ||||||||||||||||||||||||
Detector | Type: DECTRIS PILATUS 6M-F / Detector: PIXEL / Date: Jul 31, 2015 | ||||||||||||||||||||||||
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray | ||||||||||||||||||||||||
Radiation wavelength | Wavelength: 0.97949 Å / Relative weight: 1 | ||||||||||||||||||||||||
Reflection | Resolution: 1.7→58.99 Å / Num. obs: 22185 / % possible obs: 92.6 % / Redundancy: 5.7 % / CC1/2: 1 / Rmerge(I) obs: 0.028 / Rpim(I) all: 0.012 / Rrim(I) all: 0.031 / Net I/σ(I): 36.7 / Num. measured all: 125674 / Scaling rejects: 215 | ||||||||||||||||||||||||
Reflection shell | Diffraction-ID: 1
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-Phasing
Phasing | Method: ![]() | |||||||||
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Phasing MR | Model details: Phaser MODE: MR_AUTO
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Processing
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Refinement | Method to determine structure: ![]()
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Solvent computation | Shrinkage radii: 0.9 Å / VDW probe radii: 1.11 Å | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso max: 60.78 Å2 / Biso mean: 18.19 Å2 / Biso min: 4.37 Å2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Refinement step | Cycle: final / Resolution: 1.7→44.452 Å
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Refine LS restraints |
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LS refinement shell | Refine-ID: X-RAY DIFFRACTION / Rfactor Rfree error: 0 / Total num. of bins used: 8
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