5DWD
Crystal structure of esterase PE8
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-05-05 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.9785 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 41.772, 73.398, 66.403 |
Unit cell angles | 90.00, 102.37, 90.00 |
Refinement procedure
Resolution | 64.860 - 1.660 |
R-factor | 0.15813 |
Rwork | 0.156 |
R-free | 0.20010 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.020 |
RMSD bond angle | 2.063 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0131) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 64.860 |
High resolution limit [Å] | 1.660 |
Number of reflections | 45616 |
<I/σ(I)> | 22.54 |
Completeness [%] | 99.1 |
Redundancy | 6.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 0.05M Calcium chloride dehydrate;0.1M BIS-TRIS pH 6.5;30%(v/v) Polyethylene glycol monomethyl ether 550 |