5IVH
The alpha-esterase-7 carboxylesterase, E3, from the blowfly Lucilia cuprina: apo-enzyme ensemble refinement
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID14-4 |
| Synchrotron site | ESRF |
| Beamline | ID14-4 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2010-11-20 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 0.9393 |
| Spacegroup name | C 2 2 21 |
| Unit cell lengths | 48.574, 100.472, 221.715 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 45.757 - 1.710 |
| R-factor | 0.1695 |
| Rwork | 0.167 |
| R-free | 0.20790 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 4fng |
| RMSD bond length | 0.013 |
| RMSD bond angle | 1.355 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 45.800 | 1.740 |
| High resolution limit [Å] | 1.710 | 1.710 |
| Rmerge | 0.145 | 3.800 |
| Number of reflections | 59125 | |
| <I/σ(I)> | 19.5 | 1.1 |
| Completeness [%] | 99.9 | 98.6 |
| Redundancy | 29 | 28.3 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 298 | 100mM sodium acetate pH 4.5, PEG 2K MME |
