2XOV
Crystal Structure of E.coli rhomboid protease GlpG, native enzyme
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2008-11-19 |
Detector | DECTRIS PILATUS 6M |
Spacegroup name | H 3 2 |
Unit cell lengths | 110.400, 110.400, 127.860 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 34.775 - 1.650 |
R-factor | 0.1935 |
Rwork | 0.192 |
R-free | 0.21840 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3b45 |
RMSD bond length | 0.006 |
RMSD bond angle | 1.000 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 55.200 | 1.740 |
High resolution limit [Å] | 1.650 | 1.650 |
Rmerge | 0.060 | 0.580 |
Number of reflections | 36099 | |
<I/σ(I)> | 12.4 | 2.4 |
Completeness [%] | 99.8 | 100 |
Redundancy | 4.5 | 4.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7 | 298 | 3M AMMONIUM CHLORIDE, 0.1M BIS-TRIS PH7.0, 298K |