8T51
Crystal structure of Fab 3.10C2 bound to TREM2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 24-ID-C |
Synchrotron site | APS |
Beamline | 24-ID-C |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2021-03-23 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 1.000 |
Spacegroup name | P 2 21 21 |
Unit cell lengths | 66.380, 96.029, 144.316 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 1.968 - 1.900 |
Rwork | 0.193 |
R-free | 0.24040 |
Structure solution method | MOLECULAR REPLACEMENT |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (v1.2) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 38.900 | 1.968 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.122 | |
Number of reflections | 73396 | 7234 |
<I/σ(I)> | 12.9 | |
Completeness [%] | 99.9 | |
Redundancy | 6.7 | |
CC(1/2) | 0.998 | 0.626 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.1 M MES pH6.5, 0.01 M ZnSO4, 25% PEG MME 550, 0.01 M Praseodymium acetate hydrate |