5WAS
Corynebacterium glutamicum Hydrolyzed Homoserine kinase
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 | 2015-10-16 |
| Detector | MARMOSAIC 325 mm CCD |
| Wavelength(s) | 0.97872 |
| Spacegroup name | P 41 21 2 |
| Unit cell lengths | 46.227, 46.227, 267.295 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 34.967 - 1.799 |
| R-factor | 0.2448 |
| Rwork | 0.241 |
| R-free | 0.28710 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5wat |
| RMSD bond length | 0.006 |
| RMSD bond angle | 1.043 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | HKL-2000 |
| Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.000 | |
| High resolution limit [Å] | 1.799 | 1.800 |
| Rmerge | 0.061 | 0.262 |
| Number of reflections | 27709 | 2537 |
| <I/σ(I)> | 43.7 | 6.3 |
| Completeness [%] | 97.8 | 92.8 |
| Redundancy | 23.4 | 19.5 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 293 | The CglThrB protein concentrated to 16.2 mg/mL in 20 mM Tris pH 7.5, 150 mM NaCl, 50 mM KCl and 50 mM MgCl2 was used for crystallization experiments. Drops were equilibrated against a 100 microLitter of well solution containing 0.25 M ammonium sulfate, 25 % PEG 3,350 and 0.1 M HEPES pH 7.5 |






