8CE6
Crystal structure of human Cd11b I domain in P212121 space group
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I03 |
Synchrotron site | Diamond |
Beamline | I03 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2022-04-08 |
Detector | DECTRIS EIGER2 XE 16M |
Wavelength(s) | 0.9763 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 39.482, 50.906, 101.399 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 50.700 - 1.582 |
Rwork | 0.175 |
R-free | 0.20840 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.011 |
RMSD bond angle | 1.685 |
Data reduction software | autoPROC |
Data scaling software | autoPROC |
Phasing software | REFMAC |
Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.700 | 1.696 |
High resolution limit [Å] | 1.575 | 1.575 |
Number of reflections | 26352 | 1133 |
<I/σ(I)> | 16.5 | |
Completeness [%] | 91.5 | |
Redundancy | 11.7 | |
CC(1/2) | 0.999 | 0.711 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.15M ammonium sulfate 25% PEG4000 15% glycerol |