3ZLV
Crystal structure of mouse acetylcholinesterase in complex with tabun and HI-6
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | MAX II BEAMLINE I911-3 |
Synchrotron site | MAX II |
Beamline | I911-3 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-06-26 |
Detector | MARREASERCH |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 79.570, 112.380, 226.990 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 29.193 - 2.500 |
R-factor | 0.177 |
Rwork | 0.176 |
R-free | 0.22550 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1j06 |
RMSD bond length | 0.009 |
RMSD bond angle | 1.013 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | REFMAC |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 29.210 | 2.640 |
High resolution limit [Å] | 2.500 | 2.500 |
Rmerge | 0.090 | 0.500 |
Number of reflections | 71276 | |
<I/σ(I)> | 17 | 4.9 |
Completeness [%] | 99.9 | 100 |
Redundancy | 7.4 | 7.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7 | pH 7 |