4C48
Crystal structure of AcrB-AcrZ complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I24 |
Synchrotron site | Diamond |
Beamline | I24 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Detector | DECTRIS PILATUS |
Spacegroup name | H 3 2 |
Unit cell lengths | 145.010, 145.010, 538.340 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 29.670 - 3.300 |
R-factor | 0.28343 |
Rwork | 0.281 |
R-free | 0.32200 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4dx5 |
RMSD bond length | 0.011 |
RMSD bond angle | 1.389 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.7.0029) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 3.460 |
High resolution limit [Å] | 3.300 | 3.300 |
Rmerge | 0.130 | 0.990 |
Number of reflections | 33271 | |
<I/σ(I)> | 11 | 1.6 |
Completeness [%] | 99.8 | 100 |
Redundancy | 5 | 5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.5 | CRYSTALLISATION SOLUTION 100 MM HEPES, PH 7.5, 10 MM MGCL2 AND 12% (W/V) PEG 3350. SAMPLE BUFFER 10 MM HEPES PH: 7.5, 50 MM SODIUM CHLORIDE, 0.03% DDM N-DODECYL BETA-D-MALTOPYRANOSIDE |