1ISA
STRUCTURE-FUNCTION IN E. COLI IRON SUPEROXIDE DISMUTASE: COMPARISONS WITH THE MANGANESE ENZYME FROM T. THERMOPHILUS
Experimental procedure
Spacegroup name | P 21 21 21 |
Unit cell lengths | 81.550, 75.080, 71.530 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 40.000 - 1.800 |
R-factor | 0.188 |
Rwork | 0.188 |
RMSD bond length | 0.013 |
RMSD bond angle | 2.739 |
Phasing software | X-PLOR |
Refinement software | X-PLOR |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 40.000 * |
High resolution limit [Å] | 1.800 * |
Rmerge | 0.059 * |
Number of reflections | 37923 * |
Completeness [%] | 92.0 * |
Redundancy | 4.2 * |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, hanging drop * | 7.5 * | 4 * | taken from Stallings, W.C.(1983). Proc. Natl. Acad. Sci. U.S.A., 80, 3884-3888. * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 5-10 (mg/ml) | 0.01ml |
2 | 1 | drop | phosphate | 5 (mM) | |
3 | 1 | drop | ammonium sulfate | 0.005ml | |
4 | 1 | reservoir | ammonium sulfate | 40 (%sat) | |
5 | 1 | reservoir | potassium acid | 0.5 (M) |