5BWA
Crystal structure of ODC-PLP-AZ1 ternary complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2014-03-13 |
Detector | PSI PILATUS 6M |
Wavelength(s) | 1.000 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 53.154, 74.084, 157.083 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 42.759 - 3.200 |
R-factor | 0.232 |
Rwork | 0.229 |
R-free | 0.28950 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1d7k 1zo0 |
RMSD bond length | 0.006 |
RMSD bond angle | 1.254 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine: 1.8.2_1309)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 78.540 | 3.270 |
High resolution limit [Å] | 3.200 | 3.200 |
Rmerge | 0.084 | 0.667 |
Number of reflections | 10195 | |
<I/σ(I)> | 15.7 | 3.4 |
Completeness [%] | 94.7 | 94.4 |
Redundancy | 10 | 10.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 8.5 | 288 | 0.2 M di-Ammonium tartrate, 20% PEG 3350 |