1AHO
THE AB INITIO STRUCTURE DETERMINATION AND REFINEMENT OF A SCORPION PROTEIN TOXIN
Experimental procedure
| Source type | SYNCHROTRON |
| Source details | EMBL/DESY, HAMBURG BEAMLINE X31 |
| Synchrotron site | EMBL/DESY, HAMBURG |
| Beamline | X31 |
| Temperature [K] | 287 |
| Detector technology | IMAGE PLATE |
| Collection date | 1994-06 |
| Detector | MARRESEARCH |
| Wavelength(s) | 0.72, 0.92 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 45.900, 40.700, 30.100 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 8.000 - 0.960 |
| R-factor | 0.158 * |
| Rwork | 0.158 |
| Structure solution method | DIRECT METHODS |
| RMSD bond length | 0.014 |
| RMSD bond angle | 0.030 |
| Data reduction software | ROTAVATA |
| Data scaling software | CCP4 ((AGROVATA) |
| Phasing software | SHAKE-N-BAKE |
| Refinement software | PROFFT |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 16.000 | 0.990 |
| High resolution limit [Å] | 0.964 | 0.960 |
| Rmerge | 0.073 | 0.543 |
| Number of reflections | 31001 | |
| <I/σ(I)> | 6.7 | 1.3 |
| Completeness [%] | 91.0 | 75.6 * |
| Redundancy | 6 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | other * | 6.8 | none * |






