1U9C
Crystallographic structure of APC35852
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-ID |
Synchrotron site | APS |
Beamline | 19-ID |
Temperature [K] | 110 |
Detector technology | CCD |
Collection date | 2004-04-12 |
Detector | CUSTOM-MADE |
Wavelength(s) | 0.97970 |
Spacegroup name | P 43 |
Unit cell lengths | 66.183, 66.183, 53.905 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 15.000 - 1.350 |
R-factor | 0.1734 |
Rwork | 0.172 |
R-free | 0.19729 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1RW7 |
RMSD bond length | 0.018 |
RMSD bond angle | 1.849 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | MOLREP |
Refinement software | REFMAC (5.2.0005) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.400 |
High resolution limit [Å] | 1.350 | 1.350 |
Rmerge | 0.236 | 0.368 |
Number of reflections | 49550 | |
<I/σ(I)> | 53.7 | 4.1 |
Completeness [%] | 96.2 | 72.8 |
Redundancy | 8.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.9 | 293 | 0.2M magnesium sulfate heptahydrate, 20% w/v PEG 3350, pH 5.9, VAPOR DIFFUSION, HANGING DROP, temperature 293K |