5WPR
Crystal structure HpiC1 in C2 space group
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 23-ID-B |
Synchrotron site | APS |
Beamline | 23-ID-B |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2017-03-07 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 1.03 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 113.846, 49.522, 53.135 |
Unit cell angles | 90.00, 110.51, 90.00 |
Refinement procedure
Resolution | 45.108 - 1.490 |
R-factor | 0.1644 |
Rwork | 0.163 |
R-free | 0.18280 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5wpp |
RMSD bond length | 0.005 |
RMSD bond angle | 0.831 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Refinement software | PHENIX (1.11.1_2575) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 45.110 |
High resolution limit [Å] | 1.490 |
Number of reflections | 45278 |
<I/σ(I)> | 19.41 |
Completeness [%] | 99.7 |
Redundancy | 6.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 293 | 22% PEG 4000, 150 mM CaCl2, 100 mM Tris pH 8.5, 5% ethylene glycol |