8VYT
Crystal Structure of the ER-alpha Ligand-binding Domain (L372S, L536S) in complex with k-411
This is a non-PDB format compatible entry.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-ID |
Synchrotron site | APS |
Beamline | 22-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2020-02-12 |
Detector | RAYONIX MX300-HS |
Wavelength(s) | 1.0 |
Spacegroup name | P 1 |
Unit cell lengths | 53.394, 58.696, 93.356 |
Unit cell angles | 86.88, 74.94, 63.05 |
Refinement procedure
Resolution | 37.100 - 1.610 |
R-factor | 0.1812 |
Rwork | 0.180 |
R-free | 0.21180 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.020 |
RMSD bond angle | 2.043 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.18.2_3874) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 37.550 | 5.234 |
High resolution limit [Å] | 1.610 | 1.930 |
Number of reflections | 77536 | 66646 |
<I/σ(I)> | 12 | |
Completeness [%] | 90.4 | |
Redundancy | 7.1 | |
CC(1/2) | 0.998 | 0.998 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 298 | 20-25% PEG 3350, 200 mM MgCl2, 0.1 M Bis-Tris/Hepes/Tris-HCl |