7PB8
Crystal structure of the CENP-OPQUR complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I24 |
Synchrotron site | Diamond |
Beamline | I24 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2021-06-20 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.9795 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 199.614, 51.299, 109.999 |
Unit cell angles | 90.00, 117.49, 90.00 |
Refinement procedure
Resolution | 25.650 - 3.680 |
R-factor | 0.2608 |
Rwork | 0.256 |
R-free | 0.35210 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6qlf |
RMSD bond length | 0.004 |
RMSD bond angle | 0.754 |
Data reduction software | MOSFLM |
Data scaling software | STARANISO |
Phasing software | PHASER |
Refinement software | REFMAC (1.17.1_3660) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 46.300 | 3.900 |
High resolution limit [Å] | 3.680 | 3.680 |
Rmerge | 0.084 | 0.350 |
Number of reflections | 6104 | 6104 |
<I/σ(I)> | 7.6 | |
Completeness [%] | 77.5 | |
Redundancy | 2.5 | |
CC(1/2) | 0.980 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 291 | 15% PEG2kmme, 40 mM NaFormate, 200 mM bis-tris propane pH 6.9 |