3LUZ
Crystal structure of extragenic suppressor protein suhB from Bartonella henselae, via combined iodide SAD molecular replacement
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU FR-E+ SUPERBRIGHT |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-01-13 |
Detector | RIGAKU SATURN 944+ |
Wavelength(s) | 1.5418 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 48.540, 81.280, 58.760 |
Unit cell angles | 90.00, 98.78, 90.00 |
Refinement procedure
Resolution | 29.040 - 2.050 |
R-factor | 0.219 |
Rwork | 0.217 |
R-free | 0.26200 |
Structure solution method | SAD, MOLECULAR REPLACEMENT |
Starting model (for MR) | 2qfl |
RMSD bond length | 0.014 |
RMSD bond angle | 1.472 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | REFMAC |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 2.100 |
High resolution limit [Å] | 2.050 | 2.050 |
Rmerge | 0.066 | 0.439 |
Number of reflections | 27477 | 1738 |
<I/σ(I)> | 18.26 | 4.2 |
Completeness [%] | 96.7 | 82.1 |
Redundancy | 7.3 | 5.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 289 | 24 mg/mL protein in 0.2 M MgCl2, 0.1 M Hepes pH 7.5, 30% PEG 400 soaked into 0.2 M MgCl2, 0.75 M KI, 0.1 M Hepes pH 8.2, 35% PEG 400; crystal tracking ID for growth 206523d2 and 206575a1 for iodide soak, VAPOR DIFFUSION, SITTING DROP, temperature 289K |