6IHU
Crystal structure of bacterial serine phosphatase bearing R161A mutation
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL19U1 |
| Synchrotron site | SSRF |
| Beamline | BL19U1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2017-11-30 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 0.9735 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 46.998, 37.745, 65.575 |
| Unit cell angles | 90.00, 102.87, 90.00 |
Refinement procedure
| Resolution | 29.475 - 1.840 |
| R-factor | 0.1705 |
| Rwork | 0.169 |
| R-free | 0.20040 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5f1m |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.593 |
| Data reduction software | HKL-3000 |
| Data scaling software | HKL-3000 |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.10.1_2155: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 30.000 | 1.920 |
| High resolution limit [Å] | 1.840 | 1.840 |
| Rmerge | 0.100 | 0.272 |
| Number of reflections | 18646 | 1702 |
| <I/σ(I)> | 12.3 | |
| Completeness [%] | 95.4 | |
| Redundancy | 3.8 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 289 | 0.2 M NaCl, 0.1 M HEPES (pH=7.5), 25% PEG 3350. |
