6JLI
Crystal structure of CTLD7 domain of human PLA2R
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL18U1 |
Synchrotron site | SSRF |
Beamline | BL18U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2017-12-02 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.98 |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 70.652, 70.652, 64.641 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 35.326 - 1.778 |
R-factor | 0.1641 |
Rwork | 0.162 |
R-free | 0.18720 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5xts |
RMSD bond length | 0.015 |
RMSD bond angle | 1.304 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHENIX |
Refinement software | PHENIX ((1.14_3260: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 35.330 | 1.842 |
High resolution limit [Å] | 1.778 | 1.778 |
Rmerge | 0.090 | 0.280 |
Number of reflections | 18297 | 1775 |
<I/σ(I)> | 30.95 | |
Completeness [%] | 99.8 | |
Redundancy | 16.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 6 | 293 | 20% PEG3350, 0.2M Ammonium sulfate pH6.0 |