4E0A
Crystal Structure of the mutant F44R BH1408 protein from Bacillus halodurans, Northeast Structural Genomics Consortium (NESG) Target BhR182
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X4A |
Synchrotron site | NSLS |
Beamline | X4A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2011-08-24 |
Detector | ADSC QUANTUM 4 |
Wavelength(s) | 0.979 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 39.384, 99.414, 39.398 |
Unit cell angles | 90.00, 92.70, 90.00 |
Refinement procedure
Resolution | 28.500 - 1.801 |
R-factor | 0.1943 |
Rwork | 0.192 |
R-free | 0.22470 |
Structure solution method | SAD |
RMSD bond length | 0.008 |
RMSD bond angle | 1.106 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | AutoSol |
Refinement software | PHENIX (dev_988) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 28.500 | 1.860 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.056 | |
Number of reflections | 48794 | |
<I/σ(I)> | 11.3 | 1.1 |
Completeness [%] | 88.3 | 39.7 |
Redundancy | 2.6 | 1.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 5.5 | 293 | Protein solution: 100mM NaCl, 5mM DTT, 0.02% NaN3, 10mM Tris-HCl (pH 7.5) . Reservoir solution: 0.2M NH4-Acetate, 0.1M Bis Tris, 25% PEG 3350, MICROBATCH UNDER OIL, TEMPERATURE 293 |