2X30
Crystal structure of the r139n mutant of a bifunctional enzyme pria
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE BM16 |
Synchrotron site | ESRF |
Beamline | BM16 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2007-09-24 |
Detector | ADSC CCD |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 63.600, 63.600, 102.900 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 27.520 - 1.950 |
R-factor | 0.21816 |
Rwork | 0.216 |
R-free | 0.27270 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2vep |
RMSD bond length | 0.016 |
RMSD bond angle | 1.389 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 28.000 | 2.020 |
High resolution limit [Å] | 1.950 | 1.950 |
Rmerge | 0.090 | 0.650 |
Number of reflections | 18061 | |
<I/σ(I)> | 23 | 2.4 |
Completeness [%] | 99.8 | 100 |
Redundancy | 10.1 | 9.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 4.8 | 1.50 M AMMONIUM SULFATE AND 100 MM SODIUM CITRATE PH 4.8 |