4N6L
Crystal structure of human cystatin E/M
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID29 |
Synchrotron site | ESRF |
Beamline | ID29 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2012-07-24 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.9763 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 42.730, 68.600, 40.280 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 36.269 - 1.952 |
R-factor | 0.211 |
Rwork | 0.211 |
R-free | 0.23960 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3gax |
RMSD bond length | 0.005 |
RMSD bond angle | 0.941 |
Data reduction software | iMOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine: 1.8.1_1168)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 68.600 | 2.060 |
High resolution limit [Å] | 1.950 | 1.950 |
Number of reflections | 8955 | |
Completeness [%] | 98.9 | 98.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 4.6 | 293 | 30 % PEG 4000, 100 mM sodium acetate pH 4.6, 200 mM ammonium sulfate, VAPOR DIFFUSION, SITTING DROP, temperature 293K |