7YTE
crystal structure of human FcmR-D1 bound to IgM C4-domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2021-05-27 |
Detector | RAYONIX MX-225 |
Wavelength(s) | 1.00895 |
Spacegroup name | P 3 |
Unit cell lengths | 85.718, 85.718, 60.676 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 28.080 - 3.000 |
R-factor | 0.232 |
Rwork | 0.230 |
R-free | 0.26880 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6kxs |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.19.2_4158) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.050 |
High resolution limit [Å] | 3.000 | 3.000 |
Rmerge | 0.171 | 0.363 |
Number of reflections | 9518 | 2435 |
<I/σ(I)> | 7.9 | |
Completeness [%] | 95.3 | |
Redundancy | 2.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 291 | 1:1 ratio of protein:reservoir solution containing 0.1 M Ammonium citrate tribasic (pH 7.0) and 12% (w/v) PEG 3,350 |