8VV5
The crystal structure of Brucella abortus FtrA
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 22-ID |
| Synchrotron site | APS |
| Beamline | 22-ID |
| Temperature [K] | 93 |
| Detector technology | PIXEL |
| Collection date | 2021-07-21 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 1.0 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 142.759, 58.161, 100.907 |
| Unit cell angles | 90.00, 130.06, 90.00 |
Refinement procedure
| Resolution | 38.620 - 1.840 |
| R-factor | 0.1924 |
| Rwork | 0.191 |
| R-free | 0.22550 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5i0v |
| RMSD bond length | 0.004 |
| RMSD bond angle | 0.656 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 38.620 | 38.620 | 1.920 |
| High resolution limit [Å] | 1.840 | 3.990 | 1.840 |
| Rmeas | 0.113 | 0.062 | 0.718 |
| Rpim | 0.058 | 0.032 | 0.369 |
| Number of reflections | 53016 | 5121 | 5344 |
| <I/σ(I)> | 13 | 16.1 | 1.8 |
| Completeness [%] | 97.1 | ||
| Redundancy | 3.6 | ||
| CC(1/2) | 0.992 | 0.992 | 0.778 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 293 | 0.2 M ammonium acetate, 0.1 M Bis-Tris, pH 6.5, 25% PEG3350 |






