6GLK
Crystal structure of hMTH1 N33A in the presence of acetate
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SLS BEAMLINE X06DA |
| Synchrotron site | SLS |
| Beamline | X06DA |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2017-10-27 |
| Detector | DECTRIS PILATUS 2M-F |
| Wavelength(s) | 1 |
| Spacegroup name | P 2 21 21 |
| Unit cell lengths | 36.150, 60.242, 65.944 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 44.477 - 1.500 |
| R-factor | 0.1882 |
| Rwork | 0.185 |
| R-free | 0.22370 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4c9x |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.792 |
| Data reduction software | XDS |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.12-2829) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 50.000 | 1.590 |
| High resolution limit [Å] | 1.500 | 1.500 |
| Rmeas | 0.021 | 0.193 |
| Number of reflections | 42667 | 6943 |
| <I/σ(I)> | 27.3 | 5.11 |
| Completeness [%] | 95.7 | 96.7 |
| Redundancy | 1.96 | 1.92 |
| CC(1/2) | 1.000 | 0.950 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 4.5 | 293 | 23-27% PEG3350, 0.2 M LiSO4, 0.1 M sodium acetate pH 4.5 |
