1EDD
CRYSTALLOGRAPHIC AND FLUORESCENCE STUDIES OF THE INTERACTION OF HALOALKANE DEHALOGENASE WITH HALIDE IONS: STUDIES WITH HALIDE COMPOUNDS REVEAL A HALIDE BINDING SITE IN THE ACTIVE SITE
Experimental procedure
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 94.400, 72.500, 41.300 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 15.000 - 2.190 |
| R-factor | 0.181 |
| RMSD bond length | 0.013 |
| RMSD bond angle | 3.400 |
| Refinement software | TNT |
Data quality characteristics
| Overall | |
| Low resolution limit [Å] | 9999.000 * |
| High resolution limit [Å] | 2.190 * |
| Rmerge | 0.061 * |
| Total number of observations | 34777 * |
| Number of reflections | 12376 * |
| Completeness [%] | 81.2 * |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | Vapor diffusion, hanging drop * | referred to J.Mol.Biol. 200.611-612 * |
Crystallization Reagents in Literatures
| ID | crystal ID | solution | reagent name | concentration (unit) | details |
| 1 | 1 | drop | protein solution | 0.005ml | |
| 2 | 1 | drop | ammonium sulfate | 60-70 (%sat) | |
| 3 | 1 | drop | bis-Tris-H2SO4 | ||
| 4 | 1 | reservoir | ammonium sulfate | 60-70 (%sat) | |
| 5 | 1 | reservoir | bis-Tris-H2SO4 |






