5UCH
Hsp90b N-terminal domain with inhibitors
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-ID |
Synchrotron site | APS |
Beamline | 19-ID |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-12-02 |
Detector | DECTRIS PILATUS3 X 6M |
Wavelength(s) | 0.97922 |
Spacegroup name | P 65 |
Unit cell lengths | 128.942, 128.942, 106.727 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 30.971 - 2.654 |
R-factor | 0.1762 |
Rwork | 0.172 |
R-free | 0.22580 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1uym |
RMSD bond length | 0.008 |
RMSD bond angle | 0.995 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | PHENIX ((1.10.1_2155: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.740 |
High resolution limit [Å] | 2.650 | 2.650 |
Number of reflections | 29177 | 2911 |
<I/σ(I)> | 26.5 | 4.7 |
Completeness [%] | 99.8 | 99.9 |
Redundancy | 11.2 | 11.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 293 | 30% PEG 8,000, 0.2 M sodium acetate, 0.1 sodium cacodylate pH 6.5 |