6QW2
The Transcriptional Regulator PrfA-A218G mutant from Listeria Monocytogenes
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE MASSIF-3 |
| Synchrotron site | ESRF |
| Beamline | MASSIF-3 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2018-02-19 |
| Detector | DECTRIS EIGER X 4M |
| Wavelength(s) | 0.9680 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 47.837, 88.021, 116.386 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 48.543 - 2.600 |
| R-factor | 0.1817 |
| Rwork | 0.178 |
| R-free | 0.25440 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5f1r |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.445 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.12_2829: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 48.600 | 2.700 |
| High resolution limit [Å] | 2.600 | 2.600 |
| Rmerge | 0.231 | 1.860 |
| Rpim | 0.093 | 0.742 |
| Number of reflections | 15707 | |
| <I/σ(I)> | 10.3 | 1.8 |
| Completeness [%] | 99.9 | 99.9 |
| Redundancy | 13.4 | 13.9 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 5.5 | 291 | Droplets of 2 to 4 microl protein solution in 50 mM sodium phosphate pH 6.5 and 200 mM NaCl at 3 mg per ml were mixed with 2 microl reservoir solution consisting of 22-25% PEG 4000, 100 mM sodium citrate pH 5.5, and 17% |






