8E9L
Crystal structure of E. coli aspartate aminotransferase mutant VFIT in the ligand-free form at 278 K
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ALS BEAMLINE 8.3.1 |
| Synchrotron site | ALS |
| Beamline | 8.3.1 |
| Temperature [K] | 278 |
| Detector technology | PIXEL |
| Collection date | 2021-06-01 |
| Detector | DECTRIS PILATUS3 S 6M |
| Wavelength(s) | 1.1158 |
| Spacegroup name | P 63 |
| Unit cell lengths | 143.830, 143.830, 81.570 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 124.380 - 2.310 |
| R-factor | 0.1868 |
| Rwork | 0.183 |
| R-free | 0.22180 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1x28 |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.500 |
| Data reduction software | xia2 |
| Data scaling software | DIALS |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.17.1_3660) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 124.380 | 2.350 |
| High resolution limit [Å] | 2.310 | 2.310 |
| Rmerge | 0.200 | |
| Number of reflections | 42181 | 2069 |
| <I/σ(I)> | 3.3 | |
| Completeness [%] | 100.0 | |
| Redundancy | 10.3 | |
| CC(1/2) | 0.982 | 0.295 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 293 | HEPES, maleate, PEG 400, ammonium sulfate |






