7ULJ
Hsp90b N-terminal domain in complex with 42C
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-BM |
Synchrotron site | APS |
Beamline | 22-BM |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-08-02 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 1.000 |
Spacegroup name | P 65 |
Unit cell lengths | 129.506, 129.506, 104.454 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 42.391 - 1.820 |
R-factor | 0.1947 |
Rwork | 0.193 |
R-free | 0.21910 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5ucj |
RMSD bond length | 0.005 |
RMSD bond angle | 0.838 |
Data reduction software | XDS |
Data scaling software | Aimless (0.5.32) |
Phasing software | PHASER |
Refinement software | PHENIX (1.18) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 42.391 | 42.391 | 1.890 |
High resolution limit [Å] | 1.820 | 9.800 | 1.820 |
Rmerge | 0.128 | 0.020 | 1.940 |
Rmeas | 0.079 | 0.021 | 1.817 |
Rpim | 0.028 | 0.008 | 1.158 |
Number of reflections | 88988 | 586 | 8854 |
<I/σ(I)> | 10.83 | ||
Completeness [%] | 100.0 | 98.9 | 99.95 |
Redundancy | 7.7 | 7.4 | 5.5 |
CC(1/2) | 1.000 | 1.000 | 0.317 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 291 | 0.1 M Sodium cacodylate pH 6.5, 0.1 M Sodium acetate, 5% MPD and 25% PEG8000 |