1HTD
STRUCTURAL INTERACTION OF NATURAL AND SYNTHETIC INHIBITORS WITH THE VENOM METALLOPROTEINASE, ATROLYSIN C (HT-D)
Experimental procedure
| Spacegroup name | P 65 |
| Unit cell lengths | 97.320, 97.320, 87.760 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 25.000 - 2.100 |
| R-factor | 0.18 |
| Rwork | 0.180 |
| RMSD bond length | 0.012 |
| RMSD bond angle | 2.260 |
| Phasing software | X-PLOR |
| Refinement software | X-PLOR |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | Vapor diffusion * | 6.8 * |
Crystallization Reagents in Literatures
| ID | crystal ID | solution | reagent name | concentration (unit) | details |
| 1 | 1 | drop | Ht-d | 10 (mg/ml) | |
| 2 | 1 | drop | imidazole | 0.1 (M) | |
| 3 | 1 | reservoir | 20 (mM) | ||
| 4 | 1 | reservoir | ammonium sulfate | 2.4 (M) |
