9FHC
Crystallographic structure of AcrB V612F with bound minocycline
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2007-04-30 |
Detector | MARRESEARCH |
Wavelength(s) | 1.0 |
Spacegroup name | I 2 3 |
Unit cell lengths | 227.460, 227.460, 227.460 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 29.870 - 2.200 |
Rwork | 0.208 |
R-free | 0.23800 |
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] | 29.870 | 2.279 |
High resolution limit [Å] | 2.200 | 2.200 |
Number of reflections | 93149 | 6554 |
<I/σ(I)> | 27.16 | |
Completeness [%] | 94.5 | |
Redundancy | 24.9 | |
CC(1/2) | 0.999 | 0.822 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 4.5 | 291 | 0.1M sodium acetate pH 4.5, 3-7% PEG200, 15-25% PEG400, 0.15M MgCl2, 0.15M NaCl |