2UX1
Identification of two zinc-binding sites in the Streptococcus suis Dpr protein
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | MAX II BEAMLINE I711 |
Synchrotron site | MAX II |
Beamline | I711 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2005-04-02 |
Detector | MARRESEARCH |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 104.520, 137.690, 142.060 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 19.970 - 1.800 |
R-factor | 0.208 |
Rwork | 0.206 |
R-free | 0.24800 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1umn |
RMSD bond length | 0.011 |
RMSD bond angle | 1.175 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | AMoRE |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.970 | 1.900 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.090 | 0.440 |
Number of reflections | 180247 | |
<I/σ(I)> | 17.98 | 3.6 |
Completeness [%] | 99.9 | 99.4 |
Redundancy | 12.004 | 4.78 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.3 | PROTEIN WAS CRYSTALLIZED FROM 30% PEG 400, 0.2 M CACL2, 0.1 M HEPES-NA, PH 7.4 AND 1 MM ZNCL2. |