6K09
Crystal structure B of ceNAP1-H2A-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) | 0.9790 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 68.795, 79.180, 172.340 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 49.723 - 2.248 |
| R-factor | 0.2157 |
| Rwork | 0.214 |
| R-free | 0.24850 |
| 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] | 49.723 | 2.330 |
| High resolution limit [Å] | 2.248 | 2.248 |
| Rmerge | 0.557 | |
| Number of reflections | 45336 | 45336 |
| <I/σ(I)> | 25.14 | |
| Completeness [%] | 99.4 | |
| Redundancy | 11 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 291 | 20% PEG 3350 |






