8A9X
Crystal structure of PulM C-ter domain
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SOLEIL BEAMLINE PROXIMA 1 |
| Synchrotron site | SOLEIL |
| Beamline | PROXIMA 1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2021-05-29 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.9793 |
| Spacegroup name | C 2 2 21 |
| Unit cell lengths | 80.850, 135.529, 109.408 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 67.760 - 1.523 |
| R-factor | 0.2174 |
| Rwork | 0.217 |
| R-free | 0.23050 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | NMR structure |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.040 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | BUSTER (2.10.4 (8-JUN-2022)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 67.760 | 1.549 |
| High resolution limit [Å] | 1.520 | 1.520 |
| Rmerge | 0.070 | 0.951 |
| Rmeas | 0.073 | 0.987 |
| Rpim | 0.020 | 0.264 |
| Number of reflections | 91712 | 4530 |
| <I/σ(I)> | 17.6 | 2.2 |
| Completeness [%] | 100.0 | 100 |
| Redundancy | 13.5 | 13.7 |
| CC(1/2) | 0.999 | 0.900 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION | 291 | 0.1 M HEPES pH 7.5, 0.2 M CaCl2 |






