4N1J
Crystal structures of NLRP14 pyrin domain reveal a conformational switch mechanism, regulating its molecular interactions
Experimental procedure
Experimental method | MAD |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.1 |
Synchrotron site | BESSY |
Beamline | 14.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2011-10-04 |
Detector | RAYONIX MX-225 |
Wavelength(s) | 0.97973, 0.97626, 1.00801, 0.97985 |
Spacegroup name | P 63 |
Unit cell lengths | 89.610, 89.610, 107.871 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 44.790 - 2.600 |
R-factor | 0.2116 |
Rwork | 0.209 |
R-free | 0.25460 |
Structure solution method | MAD |
RMSD bond length | 0.004 |
RMSD bond angle | 0.802 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | Auto-Rickshaw |
Refinement software | PHENIX ((phenix.refine: 1.8.3_1479)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 44.790 | 2.490 |
High resolution limit [Å] | 2.360 | 2.360 |
Number of reflections | 19457 | |
Completeness [%] | 95.9 | 99.9 |
Redundancy | 7.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 293 | 0.1 M HEPES pH 7.5, 2.6 M Ammonium sulfate and 2% PEG400, VAPOR DIFFUSION, SITTING DROP, temperature 293K |