8G5S
Crystal structure of apo TnmJ
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 19-ID |
| Synchrotron site | APS |
| Beamline | 19-ID |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2020-12-09 |
| Detector | DECTRIS PILATUS3 6M |
| Wavelength(s) | 0.979 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 58.784, 100.908, 58.836 |
| Unit cell angles | 90.00, 102.86, 90.00 |
Refinement procedure
| Resolution | 29.020 - 1.500 |
| R-factor | 0.1678 |
| Rwork | 0.166 |
| R-free | 0.19520 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5f8c |
| RMSD bond length | 0.009 |
| RMSD bond angle | 1.009 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.20.1_4487: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 29.020 | 1.556 |
| High resolution limit [Å] | 1.500 | 1.500 |
| Rmerge | 0.057 | 0.090 |
| Number of reflections | 98178 | 7779 |
| <I/σ(I)> | 9.96 | |
| Completeness [%] | 93.5 | |
| Redundancy | 1.54 | |
| CC(1/2) | 0.986 | 0.927 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 298 | 0.2 M magnesium chloride, 0.1 M Tris-HCl pH 8.5, and 25% (v/v) PEG 3350 |






