5V6O
Crystal Structure of the highly open channel-stabilized mutant G-2'I + I9'A of GLIC
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-G |
Synchrotron site | APS |
Beamline | 21-ID-G |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2013-08-04 |
Detector | MAR scanner 300 mm plate |
Wavelength(s) | 0.97857 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 178.388, 133.338, 160.312 |
Unit cell angles | 90.00, 101.77, 90.00 |
Refinement procedure
Resolution | 70.443 - 3.121 |
R-factor | 0.2423 |
Rwork | 0.240 |
R-free | 0.27950 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3ehz |
RMSD bond length | 0.011 |
RMSD bond angle | 1.549 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHENIX (1.9_1692) |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Inner shell | |
Low resolution limit [Å] | 105.979 | 3.132 |
High resolution limit [Å] | 3.121 | 3.121 |
Rmerge | 0.162 | 1.090 |
Rmeas | 0.186 | 1.248 |
Rpim | 0.089 | 0.602 |
Total number of observations | 276516 | |
Number of reflections | 65357 | |
<I/σ(I)> | 8.7 | |
Completeness [%] | 99.9 | 99.5 |
Redundancy | 4.2 | 4.3 |
CC(1/2) | 0.995 | 0.764 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 277 | Sodium Acetate 50 mM pH 3.9-4.2 Ammonium Sulfate 200-250 mM PEG 4000 10-12% |