7EOE
Crystal structure of CCDC25 homodimer
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL18U1 |
Synchrotron site | SSRF |
Beamline | BL18U1 |
Temperature [K] | 193 |
Detector technology | PIXEL |
Collection date | 2020-10-25 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.979 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 124.192, 47.730, 83.024 |
Unit cell angles | 90.00, 118.84, 90.00 |
Refinement procedure
Resolution | 27.197 - 2.900 |
R-factor | 0.2526 |
Rwork | 0.251 |
R-free | 0.28700 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | de novo prediction |
RMSD bond length | 0.004 |
RMSD bond angle | 0.634 |
Data reduction software | HKL-3000 |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX (1.10-2155) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.000 |
High resolution limit [Å] | 2.900 | 2.900 |
Rmerge | 0.138 | 0.333 |
Number of reflections | 9735 | 820 |
<I/σ(I)> | 11.5 | |
Completeness [%] | 97.0 | |
Redundancy | 5.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 291 | 0.1M CHES 9.5, 50% PEG 200 |