8YP1
Crystal structure of HARS WHEP domain fused with Fc
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL17U1 |
| Synchrotron site | SSRF |
| Beamline | BL17U1 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2019-07-04 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.97918 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 59.943, 112.984, 110.211 |
| Unit cell angles | 90.00, 90.37, 90.00 |
Refinement procedure
| Resolution | 49.580 - 2.790 |
| R-factor | 0.21869 |
| Rwork | 0.217 |
| R-free | 0.25634 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5vh5 |
| RMSD bond length | 0.007 |
| RMSD bond angle | 1.442 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | REFMAC (5.8.0253) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 50.000 | 50.000 | 2.850 |
| High resolution limit [Å] | 2.790 | 7.590 | 2.800 |
| Rmerge | 0.165 | 0.057 | 1.785 |
| Rmeas | 0.181 | 0.064 | 1.954 |
| Rpim | 0.073 | 0.027 | 0.788 |
| Number of reflections | 36360 | 1863 | 1842 |
| <I/σ(I)> | 6 | ||
| Completeness [%] | 99.9 | 99.4 | 100 |
| Redundancy | 6 | 5.2 | 5.8 |
| CC(1/2) | 0.990 | 0.996 | 0.639 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | EVAPORATION | 5.5 | 289 | 100mM BIS-TRIS pH 5.5, 25% PEG 3350 |






