4KYR
Structure of a product bound plant phosphatase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-ID |
Synchrotron site | APS |
Beamline | 22-ID |
Temperature [K] | 110 |
Detector technology | CCD |
Collection date | 2012-03-19 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 1.0 |
Spacegroup name | P 65 2 2 |
Unit cell lengths | 92.776, 92.776, 144.942 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 19.530 - 2.300 |
R-factor | 0.17634 |
Rwork | 0.174 |
R-free | 0.22858 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.014 |
RMSD bond angle | 2.078 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.7.0029) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 2.380 |
High resolution limit [Å] | 2.300 | 2.300 |
Rmerge | 0.391 | |
Number of reflections | 16172 | |
<I/σ(I)> | 2.17 | |
Completeness [%] | 94.8 | 87.3 |
Redundancy | 2.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.7 | 291 | 25mM maltohexaose, 0.1M di-ammonium hydrogen phosphate, 17% 2-propanol, 31% PEG 4000, pH 5.7, VAPOR DIFFUSION, HANGING DROP, temperature 291K |