6JG5
Crystal structure of AimR
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U1 |
Synchrotron site | SSRF |
Beamline | BL17U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-10-28 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.9792 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 115.302, 219.429, 33.494 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 49.537 - 2.221 |
R-factor | 0.1983 |
Rwork | 0.196 |
R-free | 0.23940 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5xyb |
RMSD bond length | 0.009 |
RMSD bond angle | 0.956 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX ((1.14rc3_3206: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.290 |
High resolution limit [Å] | 2.220 | 2.220 |
Number of reflections | 42901 | |
<I/σ(I)> | 10.9 | |
Completeness [%] | 99.1 | |
Redundancy | 6.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 291.15 | Sodium cacodylate, PEG 8000, sodium chloride |