6PNW
X-RAY STRUCTURE OF ERABUTOXIN C, A DIMERIC NEUROTOXIN
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SEALED TUBE |
Source details | OTHER |
Temperature [K] | 290 |
Detector technology | DIFFRACTOMETER |
Collection date | 1983-02-01 |
Detector | SYNTEX |
Wavelength(s) | 1.542 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 55.600, 53.750, 40.990 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 10.000 - 2.000 |
Rwork | 0.161 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3ebx ERABUTOXIN B |
Data reduction software | SORTVA |
Data scaling software | SORTAV |
Phasing software | TFORM |
Refinement software | PROLSQ |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 38.000 | 2.200 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.080 | |
Number of reflections | 7681 | 986 |
<I/σ(I)> | 7.3 | |
Completeness [%] | 85.6 | 70 |
Redundancy | 2.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 6 | 298 | PHOSPHATE BUFFER, AMMONIUM SULFATE PH 6 |