5HME
Crystal structure of Triazine Hydrolase variant (P214T/Y215H)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
Synchrotron site | Australian Synchrotron |
Beamline | MX2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-09-26 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.9537 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 56.551, 100.718, 78.851 |
Unit cell angles | 90.00, 102.30, 90.00 |
Refinement procedure
Resolution | 35.979 - 2.151 |
R-factor | 0.2045 |
Rwork | 0.203 |
R-free | 0.22660 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4lh8 |
RMSD bond length | 0.015 |
RMSD bond angle | 1.486 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | REFMAC |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 35.980 | 2.230 |
High resolution limit [Å] | 2.150 | 2.150 |
Number of reflections | 46881 | |
<I/σ(I)> | 7.3 | 2.3 |
Completeness [%] | 99.7 | 98.5 |
Redundancy | 6.4 | 6.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 277.15 | 0.1 M Bis Tris, 0.1M Ammonium Acetate, 16% PEG3350 |