7B3Z
Crystal structure of c-MET bound by compound 5
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I03 |
Synchrotron site | Diamond |
Beamline | I03 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-07-18 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 0.97625 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 109.880, 42.450, 85.600 |
Unit cell angles | 90.00, 120.86, 90.00 |
Refinement procedure
Resolution | 21.340 - 1.800 |
R-factor | 0.194 |
Rwork | 0.193 |
R-free | 0.21500 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | internal |
RMSD bond length | 0.010 |
RMSD bond angle | 0.940 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | BUSTER (2.11.6) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 21.340 | 1.830 |
High resolution limit [Å] | 1.800 | 1.800 |
Number of reflections | 31317 | 1480 |
<I/σ(I)> | 10.9 | |
Completeness [%] | 98.7 | |
Redundancy | 3 | |
CC(1/2) | 0.998 | 0.548 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 20 % PEG10000, 0.1 M Na-HEPES pH 7.5 |