5IFO
X-ray structure of HSA-Myr-KP1019
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-1 |
Synchrotron site | ESRF |
Beamline | ID23-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-07-03 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.973 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 181.110, 38.060, 94.950 |
Unit cell angles | 90.00, 105.06, 90.00 |
Refinement procedure
Resolution | 45.844 - 3.200 |
R-factor | 0.245 |
Rwork | 0.244 |
R-free | 0.26150 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3b9m |
RMSD bond length | 0.016 |
RMSD bond angle | 0.413 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHENIX ((1.10_2155)) |
Refinement software | PHENIX ((1.10_2155: ???)) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 45.844 |
High resolution limit [Å] | 3.200 |
Number of reflections | 10508 |
<I/σ(I)> | 17.89 |
Completeness [%] | 98.0 |
Redundancy | 3.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.4 | 293 | 75-120 mg/ml protein, 50 mM potassium phosphate, 25-30% PEG4000, 150 mM KCl, 5 mM sodium azide |