5UCJ
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 | 2016-06-27 |
Detector | DECTRIS PILATUS3 X 6M |
Wavelength(s) | 0.97921 |
Spacegroup name | P 65 |
Unit cell lengths | 129.464, 129.464, 106.357 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 42.377 - 1.693 |
R-factor | 0.1749 |
Rwork | 0.174 |
R-free | 0.19660 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1uym |
RMSD bond length | 0.008 |
RMSD bond angle | 1.004 |
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 | 1.760 |
High resolution limit [Å] | 1.690 | 1.700 |
Number of reflections | 112035 | |
<I/σ(I)> | 23 | 1.9 |
Completeness [%] | 100.0 | 100 |
Redundancy | 5.7 | 5.9 |
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 |