8FDO
SARS-CoV-2 fusion peptide epitope scaffold FP15 bound to DH1058
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 22-ID |
| Synchrotron site | APS |
| Beamline | 22-ID |
| Temperature [K] | 80 |
| Detector technology | PIXEL |
| Collection date | 2022-11-29 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 1.000 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 48.390, 50.580, 146.240 |
| Unit cell angles | 90.00, 96.89, 90.00 |
Refinement procedure
| Resolution | 48.390 - 2.200 |
| R-factor | 0.1911 |
| Rwork | 0.189 |
| R-free | 0.22920 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 7tow 5yo4 |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.834 |
| Data reduction software | iMOSFLM |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (dev-3758-000) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 48.390 | 2.279 |
| High resolution limit [Å] | 2.200 | 2.200 |
| Number of reflections | 35552 | 3518 |
| <I/σ(I)> | 23.64 | 2.26 |
| Completeness [%] | 98.2 | |
| Redundancy | 7.5 | |
| CC(1/2) | 0.501 | 0.529 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 277 | 0.1M Bis-Tris, 25% PEG 3350 |






