7V62
Crystal structure of human OSBP ORD in complex with cholesterol
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PHOTON FACTORY BEAMLINE BL-17A |
Synchrotron site | Photon Factory |
Beamline | BL-17A |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-10-26 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 1.9 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 111.880, 111.880, 367.880 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 49.580 - 3.250 |
R-factor | 0.2146 |
Rwork | 0.213 |
R-free | 0.25240 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5zm8 |
RMSD bond length | 0.003 |
RMSD bond angle | 0.714 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | CRANK2 |
Refinement software | PHENIX (1.18.2_3874) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 49.600 | 3.340 |
High resolution limit [Å] | 3.250 | 3.250 |
Number of reflections | 37700 | 6043 |
<I/σ(I)> | 14.99 | |
Completeness [%] | 99.7 | |
Redundancy | 28.4 | |
CC(1/2) | 0.998 | 0.837 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | citrate, PEG4000, sodium acetate, GSH/GSSG |