2HF2
Domain shifting confirms monomeric structure of Escherichia sugar phosphatase SUPH
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU RU200 |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2006-05-03 |
Detector | RIGAKU RAXIS IV |
Wavelength(s) | 1.5418 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 38.774, 111.295, 68.802 |
Unit cell angles | 90.00, 106.23, 90.00 |
Refinement procedure
Resolution | 20.000 - 1.900 |
R-factor | 0.2058 |
Rwork | 0.204 |
R-free | 0.25188 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1rlm |
RMSD bond length | 0.023 |
RMSD bond angle | 1.410 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | MOLREP |
Refinement software | REFMAC (5.2.0005) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.970 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.056 | 0.323 |
Number of reflections | 42397 | |
<I/σ(I)> | 13.4 | 3.6 |
Completeness [%] | 95.6 | 73.6 |
Redundancy | 7 | 4.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 4.5 | 290 | 20% PEG8000, 0.1 M SODIUM PHOSPHATE-CITRATE, 10% GLYCEROL, pH 4.50, VAPOR DIFFUSION, SITTING DROP, temperature 290K |