7OBP
Crystal structure of the human NCOA7-AS TLDc domain
Experimental procedure
| Experimental method | SINGLE WAVELENGTH | 
| Source type | SYNCHROTRON | 
| Source details | ESRF BEAMLINE MASSIF-1 | 
| Synchrotron site | ESRF | 
| Beamline | MASSIF-1 | 
| Temperature [K] | 100 | 
| Detector technology | PIXEL | 
| Collection date | 2021-03-12 | 
| Detector | DECTRIS PILATUS3 2M | 
| Wavelength(s) | 0.965 | 
| Spacegroup name | P 21 21 21 | 
| Unit cell lengths | 68.410, 107.060, 146.440 | 
| Unit cell angles | 90.00, 90.00, 90.00 | 
Refinement procedure
| Resolution | 45.290 - 1.800 | 
| R-factor | 0.1774 | 
| Rwork | 0.177 | 
| R-free | 0.22120 | 
| Structure solution method | MOLECULAR REPLACEMENT | 
| Starting model (for MR) | 4acj | 
| RMSD bond length | 0.005 | 
| RMSD bond angle | 0.786 | 
| Data reduction software | XDS | 
| Data scaling software | XSCALE | 
| Phasing software | PHASER | 
| Refinement software | PHENIX (1.19_4092) | 
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 45.290 | 1.860 | 
| High resolution limit [Å] | 1.800 | 1.800 | 
| Rmeas | 0.147 | 1.140 | 
| Number of reflections | 100055 | 9863 | 
| <I/σ(I)> | 10.1 | |
| Completeness [%] | 99.7 | |
| Redundancy | 5.2 | |
| CC(1/2) | 0.997 | 0.580 | 
Crystallization Conditions
| crystal ID | method | pH | temperature | details | 
| 1 | VAPOR DIFFUSION, SITTING DROP | 4.5 | 291 | 0.1 M sodium acetate pH4.5, 30% PEG 300 | 











