6AP0
Crystal structure of human FLASH N-terminal domain C54S/C83A (Crystal form 2)
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 24-ID-E |
| Synchrotron site | APS |
| Beamline | 24-ID-E |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2016-03-10 |
| Detector | ADSC QUANTUM 315 |
| Wavelength(s) | 0.9792 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 63.478, 44.346, 68.433 |
| Unit cell angles | 90.00, 98.65, 90.00 |
Refinement procedure
| Resolution | 36.216 - 2.581 |
| R-factor | 0.2156 |
| Rwork | 0.214 |
| R-free | 0.24870 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 6ano |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.534 |
| Data reduction software | XDS |
| Data scaling software | XDS |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 36.216 | 2.740 |
| High resolution limit [Å] | 2.580 | 2.580 |
| Rmerge | 0.079 | 0.467 |
| Number of reflections | 11542 | 1848 |
| <I/σ(I)> | 13.42 | 3.82 |
| Completeness [%] | 99.6 | 99.2 |
| Redundancy | 3.8 | 3.7 |
| CC(1/2) | 0.998 | 0.898 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 293 | 100 mM sodium formate, 15% (w/v) PEG 3350, 3% (v/v) 1,6-hexanediol |






