8G5U
Crystal structure of TnmK2 complexed with TNM B
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 | 2019-11-15 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.979 |
Spacegroup name | H 3 |
Unit cell lengths | 134.110, 134.110, 355.757 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 29.646 - 1.804 |
R-factor | 0.1904 |
Rwork | 0.189 |
R-free | 0.21580 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.005 |
RMSD bond angle | 0.823 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((dev_2689: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 1.840 |
High resolution limit [Å] | 1.800 | 1.800 |
Number of reflections | 217453 | 10962 |
<I/σ(I)> | 27.9 | |
Completeness [%] | 99.9 | |
Redundancy | 6.3 | |
CC(1/2) | 0.997 | 0.658 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 298 | 0.2 M calcium acetate, 0.1 M imidazole/HCl, pH 8.0, 20% w/v PEG 1000 |