1P0I
Crystal structure of human butyryl cholinesterase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-2 |
Synchrotron site | ESRF |
Beamline | ID14-2 |
Temperature [K] | 100 |
Detector technology | CCD |
Detector | ADSC QUANTUM 4 |
Wavelength(s) | 0.933 |
Spacegroup name | I 4 2 2 |
Unit cell lengths | 154.660, 154.660, 127.890 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 55.000 * - 2.000 |
R-factor | 0.195 |
Rwork | 0.195 |
R-free | 0.22500 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2ace |
RMSD bond length | 0.014 |
RMSD bond angle | 23.700 * |
Data reduction software | MOSFLM |
Data scaling software | CCP4 ((SCALA)) |
Phasing software | AMoRE |
Refinement software | CNS (0.9) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 55.000 * | 2.110 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.074 * | 0.448 * |
Number of reflections | 51326 * | |
<I/σ(I)> | 6.8 | 1.7 |
Completeness [%] | 98.6 | 99.6 |
Redundancy | 7.3 | 6.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 20 * | Nachon, F., (2002) Eur.J.Biochem., 269, 630. * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 6.6 (mg/ml) | |
2 | 1 | drop | MES | 0.1 (M) | pH6.5 |
3 | 1 | reservoir | ammonium sulfate | 2.05-2.15 (M) |