8CE9
Crystal structure of human Cd11b I domain in C121 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 | 2022-01-29 |
Detector | DECTRIS EIGER2 XE 16M |
Wavelength(s) | 0.9763 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 128.495, 51.494, 90.172 |
Unit cell angles | 90.00, 132.96, 90.00 |
Refinement procedure
Resolution | 65.989 - 2.110 |
Rwork | 0.188 |
R-free | 0.23890 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.009 |
RMSD bond angle | 1.609 |
Data reduction software | xia2 |
Data scaling software | xia2 |
Phasing software | REFMAC |
Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 65.990 | 2.150 |
High resolution limit [Å] | 2.110 | 2.110 |
Number of reflections | 23208 | 728 |
<I/σ(I)> | 7.5 | |
Completeness [%] | 92.5 | |
Redundancy | 6.4 | |
CC(1/2) | 0.981 | 0.298 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293.15 | 25% PEG Smear Medium 0.1M cacodylate pH 5.5 0.2M ammonium sulfate |