7R8U
LOX-1 - Structural and Functional Studies of a Receptor Implicated in Atherosclerosis
This is a non-PDB format compatible entry.
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SSRL BEAMLINE BL14-1 |
| Synchrotron site | SSRL |
| Beamline | BL14-1 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2019-01-28 |
| Detector | MARMOSAIC 325 mm CCD |
| Wavelength(s) | 1.19499 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 71.908, 89.901, 110.925 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 39.492 - 1.901 |
| Rwork | 0.186 |
| R-free | 0.21810 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1ypu |
| RMSD bond length | 0.009 |
| RMSD bond angle | 1.611 |
| Data reduction software | XDS |
| Data scaling software | XDS |
| Phasing software | MOLREP |
| Refinement software | REFMAC (5.8.0258) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 39.492 | 1.940 |
| High resolution limit [Å] | 1.900 | 1.900 |
| Number of reflections | 57364 | 3538 |
| <I/σ(I)> | 1.6 | |
| Completeness [%] | 96.9 | |
| Redundancy | 6.5 | |
| CC(1/2) | 0.995 | 0.650 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION | 293 | 0.2 M 1,6-hexanediol, 0.2 M 1-butanol, 0.2 M 1,2-propanediol, 0.2 M 2-propanol, 0.2 M 1,4-butanediol, 0.2 M 1,3-propanediol, 1 M Tris base, BICINE, pH 8.5, 50% v/v precipitant mix (25% v/v MPD, 25% PEG1000, 25% w/v PEG3350) |






