7RY1
human Hsp90_MC domain structure
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 | 2019-12-04 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.97951 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 159.850, 311.964, 88.150 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 47.421 - 3.523 |
R-factor | 0.2204 |
Rwork | 0.216 |
R-free | 0.27200 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3q6m |
RMSD bond length | 0.004 |
RMSD bond angle | 0.806 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-2000 |
Phasing software | PHENIX |
Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.000 | 50.000 | 3.630 |
High resolution limit [Å] | 3.500 | 7.530 | 3.500 |
Rmerge | 0.148 | 0.055 | 1.366 |
Rmeas | 0.161 | 0.060 | 1.487 |
Rpim | 0.063 | 0.023 | 0.581 |
Total number of observations | 176259 | ||
Number of reflections | 27438 | 2902 | 2708 |
<I/σ(I)> | 3.9 | ||
Completeness [%] | 99.9 | 99.8 | 100 |
Redundancy | 6.4 | 6.1 | 6.4 |
CC(1/2) | 0.998 | 0.536 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 0.1M Succinic acid PH 6.5, 12% PEG3350, 20mM CaCl2 |