2HP5
Crystal Structure of the OXA-10 W154G mutant at pH 7.0
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE BM30A |
Synchrotron site | ESRF |
Beamline | BM30A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2006-02-26 |
Detector | MAR CCD 165 mm |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 47.110, 125.400, 92.360 |
Unit cell angles | 90.00, 99.80, 90.00 |
Refinement procedure
Resolution | 46.470 - 2.700 |
R-factor | 0.213 |
Rwork | 0.210 |
R-free | 0.26700 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1k4f |
RMSD bond length | 0.007 |
RMSD bond angle | 1.075 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | AMoRE |
Refinement software | REFMAC (5.2.0005) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 46.470 | 2.850 |
High resolution limit [Å] | 2.700 | 2.700 |
Rmerge | 0.122 | 0.452 |
Number of reflections | 28824 | |
<I/σ(I)> | 11 | 3.1 |
Completeness [%] | 99.2 | 99.3 |
Redundancy | 3.3 | 3.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7 | 293 | Ammonium Sulfate 2.2 M, HEPES, pH 7, VAPOR DIFFUSION, HANGING DROP, temperature 293K, pH 7.00 |