5D4S
Crystal Structure of AraR(DBD) in complex with operator ORX1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE BM14 |
Synchrotron site | ESRF |
Beamline | BM14 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2012-03-09 |
Detector | MAR CCD 165 mm |
Wavelength(s) | 1 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 138.228, 42.454, 67.211 |
Unit cell angles | 90.00, 114.99, 90.00 |
Refinement procedure
Resolution | 35.868 - 1.972 |
R-factor | 0.1972 |
Rwork | 0.195 |
R-free | 0.24140 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4h0e |
RMSD bond length | 0.009 |
RMSD bond angle | 1.233 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Refinement software | PHENIX (1.8.4_1496) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 36.000 |
High resolution limit [Å] | 1.970 |
Number of reflections | 25149 |
<I/σ(I)> | 10.6 |
Completeness [%] | 99.8 |
Redundancy | 3.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 295 | sodium acetate, PEG 8000, potassium chloride |