1NXM
The high resolution structures of RmlC from Streptococcus suis
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-1 |
Synchrotron site | ESRF |
Beamline | ID14-1 |
Temperature [K] | 110 |
Detector technology | CCD |
Collection date | 2001-11-03 |
Detector | ADSC QUANTUM 4 |
Wavelength(s) | 0.933 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 45.671, 81.624, 52.098 |
Unit cell angles | 90.00, 108.80, 90.00 |
Refinement procedure
Resolution | 49.390 - 1.300 |
R-factor | 0.14465 |
Rwork | 0.143 |
R-free | 0.17400 * |
Structure solution method | SAD |
RMSD bond length | 0.013 |
RMSD bond angle | 1.480 * |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | MLPHARE |
Refinement software | REFMAC (5.1.19) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 28.300 | 1.330 |
High resolution limit [Å] | 1.300 | 1.300 |
Rmerge | 0.039 * | 0.241 * |
Total number of observations | 1012876 * | |
Number of reflections | 85539 * | |
<I/σ(I)> | 11.7 | 3.1 |
Completeness [%] | 95.2 | 84 * |
Redundancy | 5.9 | 2.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 20 * | 25% PEG 2000, 0.2 M MgCl2, 0.1 M Tris , 4 mM NiCl2, pH 8.5, VAPOR DIFFUSION, SITTING DROP, temperature 293K |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 7 (mg/ml) | |
2 | 1 | reservoir | 0.2 (M) | ||
3 | 1 | reservoir | Tris-HCl | 0.1 (M) | pH8.5 |
4 | 1 | reservoir | PEG2000 | 25 (%) |