6K0C
Crystal structure of ceNAP1-H2A.Z-H2B complex
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 | 2018-10-15 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.9789 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 67.728, 79.313, 174.329 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 49.394 - 2.281 |
R-factor | 0.2187 |
Rwork | 0.217 |
R-free | 0.26230 |
Structure solution method | MOLECULAR REPLACEMENT |
Data reduction software | HKL-2000 |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((1.14_3260: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 49.394 | 2.360 |
High resolution limit [Å] | 2.280 | 2.280 |
Rmerge | 0.642 | |
Number of reflections | 43537 | 43537 |
<I/σ(I)> | 14.43 | |
Completeness [%] | 99.9 | |
Redundancy | 6.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 291 | 20% PEG 3350 |