4N6W
X-Ray Crystal Structure of Citrate-bound PhnZ
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-G |
Synchrotron site | APS |
Beamline | 21-ID-G |
Temperature [K] | 120 |
Detector technology | CCD |
Collection date | 2013-04-23 |
Detector | MARRESEARCH |
Wavelength(s) | 0.98 |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 68.871, 68.871, 98.842 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 32.947 - 1.850 |
R-factor | 0.1896 |
Rwork | 0.188 |
R-free | 0.21180 |
Structure solution method | SAD |
RMSD bond length | 0.009 |
RMSD bond angle | 0.940 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | SHARP |
Refinement software | PHENIX (1.8.2_1309) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 32.947 | 1.880 |
High resolution limit [Å] | 1.850 | 1.850 |
Rmerge | 0.063 | 0.817 |
Number of reflections | 23752 | |
<I/σ(I)> | 49.6 | 3.1 |
Completeness [%] | 99.9 | 99.4 |
Redundancy | 10.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 294 | trisodium citrate, HEPES, pH 7.5, Vapor diffusion, sitting drop, temperature 294K |