7BSO
Crystal structure of the human NLRP9 pyrin domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PAL/PLS BEAMLINE 5C (4A) |
Synchrotron site | PAL/PLS |
Beamline | 5C (4A) |
Temperature [K] | 125 |
Detector technology | PIXEL |
Collection date | 2019-12-08 |
Detector | DECTRIS EIGER2 X 9M |
Wavelength(s) | 1.000 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 51.970, 33.685, 49.667 |
Unit cell angles | 90.00, 102.40, 90.00 |
Refinement procedure
Resolution | 28.080 - 2.080 |
Rwork | 0.213 |
R-free | 0.28250 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4ewi |
RMSD bond length | 0.015 |
RMSD bond angle | 1.754 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0257) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 28.080 | 2.150 |
High resolution limit [Å] | 2.080 | 2.100 |
Number of reflections | 5035 | 306 |
<I/σ(I)> | 22.28 | |
Completeness [%] | 98.9 | |
Redundancy | 6.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 295 | 20%(w/v) PEG MME 2,000 0.1M Tris pH 8.5 0.2M Trimethylamine n-oxide |