9FE2
Crystallographic structure of AcrB V612W with bound minocycline
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PETRA III, EMBL c/o DESY BEAMLINE P13 (MX1) |
Synchrotron site | PETRA III, EMBL c/o DESY |
Beamline | P13 (MX1) |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2022-11-04 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.99182 |
Spacegroup name | I 2 3 |
Unit cell lengths | 227.497, 227.497, 227.497 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 46.440 - 1.890 |
Rwork | 0.222 |
R-free | 0.24360 |
Structure solution method | MOLECULAR REPLACEMENT |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | PHENIX (1.20.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 46.440 | 1.958 |
High resolution limit [Å] | 1.890 | 1.890 |
Number of reflections | 155079 | 15464 |
<I/σ(I)> | 21.91 | |
Completeness [%] | 97.0 | |
Redundancy | 2 | |
CC(1/2) | 0.999 | 0.297 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 291 | 0.1M MES pH 6.5, 5.5-20.5% PEG400 |