6K01
Crystal structure of xH2A-H2B
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-06-04 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.9793 |
Spacegroup name | P 31 |
Unit cell lengths | 46.923, 46.923, 67.129 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 40.637 - 2.839 |
R-factor | 0.2286 |
Rwork | 0.223 |
R-free | 0.27820 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1aoi |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | PHENIX ((1.14_3260: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.640 | 2.940 |
High resolution limit [Å] | 2.839 | 2.840 |
Rmerge | 0.831 | |
Number of reflections | 3756 | 3756 |
<I/σ(I)> | 12.7 | |
Completeness [%] | 99.6 | |
Redundancy | 4.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 291 | 0.2M Ammonium sulfate, 0.1M HEPES pH=7.5, 25% PEG 3350 |