3H8N
Crystal Structure Analysis of KIR2DS4
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL11-1 |
Synchrotron site | SSRL |
Beamline | BL11-1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-01-07 |
Detector | MARMOSAIC 325 mm CCD |
Wavelength(s) | 0.979 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 51.232, 62.851, 65.934 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 40.450 - 2.500 |
R-factor | 0.241 |
Rwork | 0.238 |
R-free | 0.28400 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1im9 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.358 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | PHENIX |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.450 | 2.590 |
High resolution limit [Å] | 2.500 | 2.500 |
Number of reflections | 7795 | |
<I/σ(I)> | 64.4 | 9.7 |
Completeness [%] | 99.8 | 97 |
Redundancy | 13.7 | 10 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8.5 | 283 | 0.22 M Mg-Formate, 100 mM BIS-TRIS, pH 5.5, VAPOR DIFFUSION, HANGING DROP, temperature 283K |