23TM
Structure of the 328-692 fragment of FlhA (A489E) form 2
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SPRING-8 BEAMLINE BL45XU |
| Synchrotron site | SPring-8 |
| Beamline | BL45XU |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2019-10-13 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 1.00 |
| Spacegroup name | I 41 |
| Unit cell lengths | 215.970, 215.970, 64.460 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 53.990 - 3.280 |
| R-factor | 0.2185 |
| Rwork | 0.216 |
| R-free | 0.23980 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3a5i |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.645 |
| Data reduction software | MOSFLM |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.21.2_5419) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 53.990 | 3.540 |
| High resolution limit [Å] | 3.280 | 3.280 |
| Rmerge | 0.075 | 0.458 |
| Number of reflections | 23119 | 4751 |
| <I/σ(I)> | 12 | 3.3 |
| Completeness [%] | 99.8 | |
| Redundancy | 3.9 | |
| CC(1/2) | 0.998 | 0.816 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 293 | 20% PEG3000, 0.1 M HEPES-NaOH, 0.2 M NaCl. Protein conc.: 10 mg/mL |






