7Q6C
complement C6 FIM1-2 bound to CP010 antibody
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | MAX IV BEAMLINE BioMAX |
| Synchrotron site | MAX IV |
| Beamline | BioMAX |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2020-02-20 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.9762 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 161.057, 63.527, 128.589 |
| Unit cell angles | 90.00, 128.36, 90.00 |
Refinement procedure
| Resolution | 44.450 - 2.293 |
| R-factor | 0.2092 |
| Rwork | 0.208 |
| R-free | 0.23290 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 6and |
| RMSD bond length | 0.005 |
| RMSD bond angle | 0.876 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.16_3549) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 100.826 | 2.430 |
| High resolution limit [Å] | 2.293 | 2.293 |
| Rmerge | 0.063 | |
| Rmeas | 0.075 | |
| Number of reflections | 45105 | 6899 |
| <I/σ(I)> | 12.08 | |
| Completeness [%] | 97.2 | |
| Redundancy | 3.46 | |
| CC(1/2) | 0.999 | 0.399 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION | 6.4 | 291 | 112 mM calcium acetate, 56 mM sodium cacodylate pH 6.4, 8.5% PEG8000 and 16% glycerol |






