4R33
X-ray structure of the tryptophan lyase NosL with Tryptophan and S-adenosyl-L-homocysteine bound
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID23-2 |
| Synchrotron site | ESRF |
| Beamline | ID23-2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2014-05-15 |
| Detector | PSI PILATUS 6M |
| Wavelength(s) | 0.8726 |
| Spacegroup name | P 1 2 1 |
| Unit cell lengths | 94.720, 47.230, 114.360 |
| Unit cell angles | 90.00, 108.71, 90.00 |
Refinement procedure
| Resolution | 47.230 - 1.780 |
| R-factor | 0.1597 |
| Rwork | 0.159 |
| R-free | 0.18130 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.010 |
| RMSD bond angle | 1.156 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHASER |
| Refinement software | PHENIX ((phenix.refine: 1.9_1692)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 47.230 | 1.890 |
| High resolution limit [Å] | 1.780 | 1.780 |
| Number of reflections | 179387 | |
| Completeness [%] | 1.0 | 0.983 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 8 | 298 | 14-20% PEG 3350; 200 mM KBr; 1 mM Tryptophan; 15 mg/mL protein, pH 8, VAPOR DIFFUSION, HANGING DROP, temperature 298K |






