5TEW
Crystal structure of a tryptophanyl-tRNA synthetase from Neisseria gonorrhoeae bound to tryptophan
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 21-ID-F |
| Synchrotron site | APS |
| Beamline | 21-ID-F |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2016-08-23 |
| Detector | MARMOSAIC 300 mm CCD |
| Wavelength(s) | 0.97872 |
| Spacegroup name | P 32 2 1 |
| Unit cell lengths | 59.940, 59.940, 162.930 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 43.777 - 2.500 |
| R-factor | 0.1901 |
| Rwork | 0.181 |
| R-free | 0.26340 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3tzl |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.811 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | MOLREP |
| Refinement software | PHENIX ((dev_2499: ???)) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 50.000 | 2.570 | |
| High resolution limit [Å] | 2.500 | 11.180 | 2.500 |
| Rmerge | 0.051 | 0.017 | 0.534 |
| Number of reflections | 12305 | ||
| <I/σ(I)> | 28.73 | 76.31 | 3.69 |
| Completeness [%] | 99.5 | 95.6 | 100 |
| Redundancy | 7.2 | ||
| CC(1/2) | 1.000 | 1.000 | 0.889 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 289 | NegoA.00743.a.B1.PS37949 at 19.2 mg/mL with 2 mM MgCl2, 2 mM tryptophan against morpheus screen condition C5 10% PEG 20000, 20% PEG 550 MME, 0.1 M MOPS/Hepes pH 7.5, 0.03M sodium nitrate, disodium hydrogen phosphate, ammonium sulfate |






