9FE4
Crystallographic structure of AcrB V612F
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 | 2006-08-22 |
Detector | MARRESEARCH |
Wavelength(s) | 1.0 |
Spacegroup name | P 3 2 1 |
Unit cell lengths | 134.410, 134.410, 190.970 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 49.700 - 2.800 |
Rwork | 0.259 |
R-free | 0.30040 |
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] | 49.700 | 2.900 |
High resolution limit [Å] | 2.800 | 2.800 |
Number of reflections | 49616 | 4859 |
<I/σ(I)> | 20.19 | |
Completeness [%] | 99.7 | |
Redundancy | 11 | |
CC(1/2) | 0.999 | 0.335 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 4.6 | 291 | 0.1M citrate pH 4.6, 5% PEG400, 16-21% PEG300, 8-11% glycerol |