3W8J
Crystal structure of P5 a0 in a complex with Prx4 c-term
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PHOTON FACTORY BEAMLINE BL-5A |
Synchrotron site | Photon Factory |
Beamline | BL-5A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-01-25 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1.0 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 39.045, 53.375, 133.353 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 41.669 - 2.100 |
R-factor | 0.1854 |
Rwork | 0.182 |
R-free | 0.24510 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.007 |
RMSD bond angle | 1.036 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine: 1.8.1_1168)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 41.670 | 2.140 |
High resolution limit [Å] | 2.100 | 2.100 |
Number of reflections | 16851 | |
Completeness [%] | 98.9 | 100 |
Redundancy | 6.7 | 6.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.3 | 293 | 22% PEG 2000 MME, 0.1M potassium thiocyanate, 0.1M Tris-HCl (pH 7.3), VAPOR DIFFUSION, HANGING DROP, temperature 293K |