7KX2
Spermidine N-acetyltransferase SpeG F149A mutant from Vibrio cholerae
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX1 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2018-10-24 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.9537 |
| Spacegroup name | I 2 2 2 |
| Unit cell lengths | 73.435, 135.942, 139.519 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 47.400 - 2.600 |
| R-factor | 0.253 |
| Rwork | 0.250 |
| R-free | 0.30790 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4jjx |
| RMSD bond length | 0.001 |
| RMSD bond angle | 0.358 |
| Data reduction software | HKL-2000 |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.18.2_3874) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 48.680 | 2.693 |
| High resolution limit [Å] | 2.600 | 2.600 |
| Number of reflections | 21877 | 2623 |
| <I/σ(I)> | 16.7 | 2.1 |
| Completeness [%] | 100.0 | |
| Redundancy | 12.9 | |
| CC(1/2) | 0.998 | 0.484 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 295 | 0.2M potassium chloride pH 7.0, 20% PEG3350 |






