8V9Y
X-ray crystal structure of nanobody JGFN4
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 24-ID-E |
| Synchrotron site | APS |
| Beamline | 24-ID-E |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2022-06-10 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.9792 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 91.243, 26.858, 36.962 |
| Unit cell angles | 90.00, 106.99, 90.00 |
Refinement procedure
| Resolution | 43.630 - 1.760 |
| R-factor | 0.193 |
| Rwork | 0.191 |
| R-free | 0.23210 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.599 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 43.630 | 1.810 |
| High resolution limit [Å] | 1.760 | 1.760 |
| Rmerge | 0.061 | 0.278 |
| Rmeas | 0.070 | 0.226 |
| Rpim | 0.035 | 0.359 |
| Number of reflections | 7992 | 400 |
| <I/σ(I)> | 10.4 | |
| Completeness [%] | 91.4 | |
| Redundancy | 3.6 | 2.2 |
| CC(1/2) | 0.998 | 0.901 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 295 | RD22EH53, G4.1 20 w/v polyethylene glycol monomethyl ether 2000, 0.1 M Tris pH8.5, 0.2 M Trimethylamine N-oxide |






