6MAJ
HBO1 is required for the maintenance of leukaemia stem cells
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2017-10-06 |
| Detector | ADSC QUANTUM 315 |
| Wavelength(s) | 0.95365 |
| Spacegroup name | H 3 |
| Unit cell lengths | 111.543, 111.543, 73.702 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 58.595 - 2.139 |
| R-factor | 0.1967 |
| Rwork | 0.195 |
| R-free | 0.23740 |
| RMSD bond length | 0.004 |
| RMSD bond angle | 0.733 |
| Data reduction software | DIALS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.12_2829: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 58.600 | 2.200 |
| High resolution limit [Å] | 2.140 | 2.140 |
| Rmerge | 0.198 | 1.292 |
| Rpim | 0.095 | 0.614 |
| Number of reflections | 18887 | 1486 |
| <I/σ(I)> | 5.7 | 1.9 |
| Completeness [%] | 100.0 | 100 |
| Redundancy | 5.3 | 5.3 |
| CC(1/2) | 0.987 | 0.583 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 293 | Crystals were grown at 20 C in sitting drop plates in drops of 200 nL crystallant and 200 nL protein. The protein was at 2.5 mg/mL and the reservoir was 20% PEG 3350 with 244 mM diammonium tartrate. |






