7BJU
Crystal structure of the ligand-binding domains of the heterodimer EcR/USP bound to the synthetic agonist BYI08346
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-3 |
Synchrotron site | ESRF |
Beamline | ID14-3 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2003-10-13 |
Detector | MAR CCD 165 mm |
Wavelength(s) | 0.931 |
Spacegroup name | P 3 2 1 |
Unit cell lengths | 147.875, 147.875, 59.776 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 48.400 - 2.850 |
R-factor | 0.1849 |
Rwork | 0.183 |
R-free | 0.23050 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1r20 |
Data reduction software | HKL-2000 |
Data scaling software | SCALA |
Phasing software | AMoRE |
Refinement software | PHENIX (dev 3951) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 48.400 | 2.952 |
High resolution limit [Å] | 2.850 | 2.850 |
Rmerge | 0.054 | 0.338 |
Number of reflections | 17798 | 1738 |
<I/σ(I)> | 39.8 | 7 |
Completeness [%] | 99.9 | 99.94 |
Redundancy | 7.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 297 | 10% PEG 1000, 10% PEG 8000, 0.3M MgCl2, 0.1M HEPES pH 7.5 |