5LZ1
Crystal structure of human ACBD3 GOLD domain
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | BESSY BEAMLINE 14.1 |
| Synchrotron site | BESSY |
| Beamline | 14.1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2014-07-25 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 1.282724 |
| Spacegroup name | P 43 21 2 |
| Unit cell lengths | 56.210, 56.210, 163.920 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 39.746 - 2.000 |
| R-factor | 0.2195 |
| Rwork | 0.218 |
| R-free | 0.24750 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1olm |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.896 |
| Data reduction software | XDS (version Oct 15, 2015) |
| Data scaling software | XDS (version Oct 15, 2015) |
| Phasing software | PHASER (2.5.6) |
| Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 39.750 | 2.071 |
| High resolution limit [Å] | 2.000 | 2.000 |
| Rmerge | 0.059 | 1.349 |
| Number of reflections | 18582 | |
| <I/σ(I)> | 18.66 | 1.43 |
| Completeness [%] | 99.8 | 99.45 |
| Redundancy | 7.7 | 7.9 |
| CC(1/2) | 0.999 | 0.631 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 291 | 100mM Tris pH 8.8, 25% w/v PEG 3.350, 20% glycerol, 20mM 2-propanol/1,2 -propanediol/1,3-propanediol/1-butanol/1,4-butanediol/1,6-hexanediol |






