5KUT
hMiro2 C-terminal GTPase domain, GDP-bound
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-D |
Synchrotron site | APS |
Beamline | 21-ID-D |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-03-26 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 0.978720 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 80.610, 122.760, 103.890 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 37.576 - 1.693 |
R-factor | 0.219 |
Rwork | 0.218 |
R-free | 0.23850 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4c0l |
RMSD bond length | 0.005 |
RMSD bond angle | 0.640 |
Data reduction software | MOSFLM |
Data scaling software | Aimless |
Phasing software | PHENIX |
Refinement software | PHENIX ((1.10_2155: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 52.800 | |
High resolution limit [Å] | 1.690 | 1.690 |
Rmerge | 0.085 | |
Number of reflections | 57061 | |
<I/σ(I)> | 10.1 | |
Completeness [%] | 99.2 | |
Redundancy | 6.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 294 | 14 mg/mL protein, 0.2 M magnesium formate, 20% w/v PEG3350 |