1AX9
ACETYLCHOLINESTERASE COMPLEXED WITH EDROPHONIUM, LAUE DATA
Experimental procedure
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID09 |
| Synchrotron site | ESRF |
| Beamline | ID09 |
| Temperature [K] | 273 |
| Detector technology | CCD |
| Collection date | 1995-04-30 |
| Spacegroup name | P 31 2 1 |
| Unit cell lengths | 113.000, 113.000, 136.900 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 20.000 - 2.800 |
| R-factor | 0.207 |
| R-free | 0.26800 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2ace |
| Data reduction software | LaueView |
| Data scaling software | LaueView |
| Refinement software | REFMAC |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 20.200 | 3.000 |
| High resolution limit [Å] | 2.800 | 2.800 |
| Rmerge | 0.148 * | |
| Total number of observations | 83171 * | |
| Number of reflections | 21492 | |
| Completeness [%] | 84.5 | 61.3 |
| Redundancy | 4.2 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | Vapor diffusion, hanging drop * | 5.8 | 4 * | Raves, M.L., (1997) Nature Struct.Biol., 4, 57. * |
Crystallization Reagents in Literatures
| ID | crystal ID | solution | reagent name | concentration (unit) | details |
| 1 | 1 | reservoir | PEG200 | 38 (%) | |
| 2 | 1 | reservoir | MES | 0.1 (M) | |
| 3 | 1 | drop | protein | 12 (mg/ml) |






