6AO5
Crystal structure of human MST2 in complex with SAV1 SARAH domain
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 | 2015-10-12 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.97918 |
Spacegroup name | H 3 2 |
Unit cell lengths | 223.678, 223.678, 79.645 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 42.271 - 2.955 |
R-factor | 0.2357 |
Rwork | 0.235 |
R-free | 0.25640 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4lgd |
RMSD bond length | 0.009 |
RMSD bond angle | 0.600 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.12_2829) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.000 | 50.000 | 3.000 |
High resolution limit [Å] | 2.950 | 8.000 | 2.950 |
Rmerge | 0.124 | 0.051 | 1.715 |
Rmeas | 0.128 | 0.053 | 1.788 |
Rpim | 0.029 | 0.012 | 0.483 |
Total number of observations | 303392 | ||
Number of reflections | 15976 | 839 | 763 |
<I/σ(I)> | 7 | ||
Completeness [%] | 99.9 | 99.3 | 98.5 |
Redundancy | 19 | 18.4 | 12 |
CC(1/2) | 0.999 | 0.841 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 0.05 M NaCl, 0.1 M Hepes, 0.19 mM CYMAL-7, 1 mM TCEP, 40% PEG 400 |