6OU3
Crystal Structure of the D478S Variant of the Myocilin Olfactomedin Domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-ID |
Synchrotron site | APS |
Beamline | 22-ID |
Temperature [K] | 80 |
Detector technology | CCD |
Collection date | 2018-07-26 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 1.000 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 45.353, 57.241, 90.474 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 40.544 - 1.796 |
R-factor | 0.1517 |
Rwork | 0.150 |
R-free | 0.17310 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.008 |
RMSD bond angle | 0.811 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHENIX |
Refinement software | PHENIX ((1.13_2998: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.544 | 1.860 |
High resolution limit [Å] | 1.796 | 1.796 |
Rmerge | 0.127 | |
Number of reflections | 22530 | 2139 |
<I/σ(I)> | 15.02 | 2.9 |
Completeness [%] | 99.6 | |
Redundancy | 11.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 277 | 20% PEG 3350, 0.2 M Bis Tris pH 6.0, 0.4 M Magnesium formate |