6AVY
Crystal structure of Zea mays acyl-protein thioesterase 2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 8.2.1 |
Synchrotron site | ALS |
Beamline | 8.2.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2016-02-03 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1.000 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 48.880, 89.570, 105.210 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 42.907 - 2.240 |
R-factor | 0.1842 |
Rwork | 0.182 |
R-free | 0.22410 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1fj2 |
RMSD bond length | 0.003 |
RMSD bond angle | 0.687 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 42.910 | 2.320 |
High resolution limit [Å] | 2.240 | 2.240 |
Rmerge | 0.057 | 0.215 |
Number of reflections | 21370 | 1636 |
<I/σ(I)> | 14.6 | 3.92 |
Completeness [%] | 93.0 | 72 |
Redundancy | 3.1 | 1.9 |
CC(1/2) | 0.997 | 0.849 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.5 | 298 | 0.1 M Bis-Tris pH 5.5, 1% (v/v) PEG 3350, 1 M Ammonium sulfate |