1HUF
CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF THE TYROSINE PHOSPHATASE YOPH FROM YERSINIA PESTIS.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2000-11-05 |
Detector | MARRESEARCH |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 48.063, 120.651, 49.036 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 100.000 - 2.000 |
R-factor | 0.1921 |
Rwork | 0.189 |
R-free | 0.26000 |
Structure solution method | MIR |
RMSD bond length | 0.007 |
RMSD bond angle | 5.200 * |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | SOLVE |
Refinement software | CNS |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 100.000 | 2.080 |
High resolution limit [Å] | 2.000 | 2.010 |
Rmerge | 0.072 | 0.340 |
Number of reflections | 8860 | |
<I/σ(I)> | 15.3 | 3.6 |
Completeness [%] | 83.3 | 55 * |
Redundancy | 4.01 | 3.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion * | 8 * | 293 | PEG4000, bicine, pH 9, VAPOR DIFFUSION, HANGING DROP, temperature 293K |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | reservoir | PEG6000 | 12 (%) | |
2 | 1 | reservoir | Tris-acetate | 100 (mM) | or sodium-bicine |