3G9D
Crystal structure glycohydrolase
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 | 2007-11-29 |
Detector | PSI PILATUS 6M |
Wavelength(s) | 1.0 |
Spacegroup name | P 65 |
Unit cell lengths | 163.866, 163.866, 46.274 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 25.000 - 2.500 |
R-factor | 0.20207 |
Rwork | 0.199 |
R-free | 0.26638 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2cwc |
RMSD bond length | 0.009 |
RMSD bond angle | 1.193 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASES |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 25.000 | 2.600 |
High resolution limit [Å] | 2.500 | 2.500 |
Rmerge | 0.076 | 0.200 |
Number of reflections | 24409 | |
<I/σ(I)> | 14.3 | 4.8 |
Completeness [%] | 94.8 | 91.9 |
Redundancy | 7.9 | 6.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 293 | 0.1M Hepes, pH7.5, 15% PEG 20000, VAPOR DIFFUSION, SITTING DROP, temperature 293K |