5Y18
Crystal structure of DAXX helical bundle domain in complex with ATRX
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 | 2015-01-27 |
| Detector | DECTRIS PILATUS3 S 6M |
| Wavelength(s) | 0.9785 |
| Spacegroup name | C 2 2 21 |
| Unit cell lengths | 69.485, 107.904, 30.887 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 26.976 - 2.202 |
| R-factor | 0.188 |
| Rwork | 0.186 |
| R-free | 0.21920 |
| Structure solution method | SAD |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.530 |
| Data reduction software | HKL-3000 |
| Data scaling software | HKL-3000 |
| Phasing software | SHARP |
| Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 50.000 | 50.000 | 2.280 |
| High resolution limit [Å] | 2.200 | 4.740 | 2.200 |
| Rmerge | 0.077 | 0.053 | 0.413 |
| Rmeas | 0.084 | 0.058 | 0.457 |
| Rpim | 0.033 | 0.024 | 0.192 |
| Total number of observations | 38355 | ||
| Number of reflections | 6179 | 677 | 594 |
| <I/σ(I)> | 6.6 | ||
| Completeness [%] | 99.6 | 98.8 | 99.8 |
| Redundancy | 6.2 | 5.8 | 5.4 |
| CC(1/2) | 0.995 | 0.901 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 289 | 0.1M sodium citrate, pH6.5, 0.2M ammonium acetate, 30% PEG4000 |






