5UC4
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 | CCD |
Collection date | 2015-12-02 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.97922 |
Spacegroup name | P 65 |
Unit cell lengths | 129.251, 129.251, 106.724 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 29.809 - 2.050 |
R-factor | 0.1671 |
Rwork | 0.166 |
R-free | 0.20680 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1uym |
RMSD bond length | 0.008 |
RMSD bond angle | 0.919 |
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 | 2.120 |
High resolution limit [Å] | 2.050 | 2.050 |
Number of reflections | 63537 | 6332 |
<I/σ(I)> | 26 | 3.8 |
Completeness [%] | 99.9 | 100 |
Redundancy | 10.9 | 10.1 |
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 |