2ZO4
Crystal structure of metallo-beta-lactamase family protein TTHA1429 from Thermus thermophilus HB8
Experimental procedure
Experimental method | MAD |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL26B2 |
Synchrotron site | SPring-8 |
Beamline | BL26B2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2005-05-20 |
Detector | RIGAKU JUPITER 210 |
Wavelength(s) | 1.2822, 1.2829, 1.0000 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 55.286, 62.885, 87.425 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 20.000 - 2.100 |
R-factor | 0.2006 |
Rwork | 0.198 |
R-free | 0.25696 |
Structure solution method | MAD |
RMSD bond length | 0.006 |
RMSD bond angle | 1.034 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | SOLVE |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.120 |
High resolution limit [Å] | 2.050 | 2.050 |
Number of reflections | 19700 | |
Completeness [%] | 99.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8 | 293 | 100mM Bicine-NaOH, 25% (w/v) PEG 4000, 5% (v/v) 2-propanol, 5mM zinc acetate, pH 8.0, VAPOR DIFFUSION, SITTING DROP, temperature 293K |