8JBA
Discovery and Crystallography Study of Novel Oxadiazole Analogs as Small Molecule PD-1/PD-L1 inhibitors
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2023-04-13 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.979 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 83.170, 98.400, 32.650 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 25.860 - 2.600 |
R-factor | 0.219 |
Rwork | 0.214 |
R-free | 0.25680 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.002 |
RMSD bond angle | 0.596 |
Data reduction software | HKL-2000 |
Data scaling software | SCALA |
Phasing software | PHENIX |
Refinement software | PHENIX ((1.20.1_4487: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 25.860 | 2.693 |
High resolution limit [Å] | 2.600 | 2.601 |
Rmerge | 0.031 | 0.163 |
Number of reflections | 8760 | 863 |
<I/σ(I)> | 13 | 3.94 |
Completeness [%] | 99.8 | |
Redundancy | 2 | |
CC(1/2) | 0.998 | 0.939 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 289.15 | Tris, Potassium sodium tartrate tetrahydrate |