5O91
Crystal structure of human Mps1 (TTK) C604W mutant in complex with Cpd-5
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE MASSIF-1 |
Synchrotron site | ESRF |
Beamline | MASSIF-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2017-05-15 |
Detector | DECTRIS PILATUS3 2M |
Wavelength(s) | 0.966 |
Spacegroup name | I 2 2 2 |
Unit cell lengths | 70.670, 111.889, 116.800 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 41.760 - 3.200 |
R-factor | 0.2144 |
Rwork | 0.212 |
R-free | 0.25440 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5mrb |
RMSD bond length | 0.008 |
RMSD bond angle | 1.189 |
Data reduction software | XDS |
Data scaling software | Aimless (0.5.32) |
Phasing software | PHASER (2.7.17) |
Refinement software | REFMAC (refmac_5.8.0173) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 41.760 | 41.760 | 3.420 |
High resolution limit [Å] | 3.200 | 9.050 | 3.200 |
Rmerge | 0.282 | 0.065 | 1.784 |
Rmeas | 0.307 | 0.071 | 1.947 |
Rpim | 0.120 | 0.028 | 0.772 |
Total number of observations | 51034 | ||
Number of reflections | 7947 | ||
<I/σ(I)> | 6 | ||
Completeness [%] | 100.0 | 99.3 | 100 |
Redundancy | 6.4 | 6.2 | 6.3 |
CC(1/2) | 0.985 | 0.996 | 0.538 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.8 | 291 | 12.3% (w/v) PEG 350 MME. 1 mM MgCl2, and 100 mM Tris/HCl |