8HC0
Crystal structure of the extracellular domains of GPR110
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRF BEAMLINE BL10U2 |
| Synchrotron site | SSRF |
| Beamline | BL10U2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2022-03-10 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.9792 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 134.825, 47.993, 87.023 |
| Unit cell angles | 90.00, 127.35, 90.00 |
Refinement procedure
| Resolution | 19.800 - 2.900 |
| R-factor | 0.2355 |
| Rwork | 0.233 |
| R-free | 0.29180 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | predicted by AlphaFold2 |
| RMSD bond length | 0.005 |
| RMSD bond angle | 0.579 |
| Data reduction software | XDS |
| Data scaling software | XDS |
| Phasing software | PHASER |
| Refinement software | PHENIX (phenix-1.19.2-4158) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 43.800 | 43.800 | 3.070 |
| High resolution limit [Å] | 2.900 | 8.540 | 2.900 |
| Rmerge | 0.124 | 0.049 | 0.579 |
| Rmeas | 0.149 | 0.060 | 0.701 |
| Number of reflections | 18390 | 409 | 1555 |
| <I/σ(I)> | 9.68 | ||
| Completeness [%] | 98.0 | ||
| Redundancy | 3.18 | ||
| CC(1/2) | 0.989 | 0.995 | 0.732 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION | 289 | 0.2 M ammonium sulfate, 0.1 M sodium acetate trihydrate pH 4.6, 30% PEG-MME 2,000, 15% glycerol |






