6A27
Crystal structure of PprA W183R mutant form 1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL41XU |
Synchrotron site | SPring-8 |
Beamline | BL41XU |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2011-07-12 |
Detector | RAYONIX MX225HE |
Wavelength(s) | 1.00 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 43.459, 99.357, 48.101 |
Unit cell angles | 90.00, 110.05, 90.00 |
Refinement procedure
Resolution | 25.720 - 1.353 |
R-factor | 0.179 |
Rwork | 0.178 |
R-free | 0.20150 |
Structure solution method | FOURIER SYNTHESIS |
Starting model (for MR) | 6a28 |
RMSD bond length | 0.005 |
RMSD bond angle | 1.034 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | PHENIX (1.9_1692) |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 25.720 | 1.400 |
High resolution limit [Å] | 1.350 | 1.350 |
Rmerge | 0.051 | 0.380 |
Number of reflections | 76916 | 7671 |
<I/σ(I)> | 33.8 | 2.3 |
Completeness [%] | 92.4 | 92.6 |
Redundancy | 3 | 2.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8.5 | 293 | 0.1 M Tris buffer (pH 8.5) containing 0.2 M LiSO4 and 30% PEG4000 |