1KFX
Crystal Structure of Human m-Calpain Form I
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | MPG/DESY, HAMBURG BEAMLINE BW6 |
Synchrotron site | MPG/DESY, HAMBURG |
Beamline | BW6 |
Temperature [K] | 100 |
Detector technology | CCD |
Detector | MARRESEARCH |
Wavelength(s) | 1.100 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 64.780, 133.250, 77.530 |
Unit cell angles | 90.00, 102.07, 90.00 |
Refinement procedure
Resolution | 30.000 - 3.150 |
Rwork | 0.243 |
R-free | 0.31800 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1kfu |
RMSD bond length | 0.011 |
RMSD bond angle | 1.620 |
Data reduction software | DENZO |
Data scaling software | CCP4 ((SCALA)) |
Phasing software | MAIN |
Refinement software | CNS |
Data quality characteristics
Overall | |
High resolution limit [Å] | 3.000 |
Rmerge | 0.056 |
Number of reflections | 25010 |
Completeness [%] | 96.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 291 | PEG 10000, isopropanol, guanidinium chloride, pH 7.5, VAPOR DIFFUSION, SITTING DROP at 291K, VAPOR DIFFUSION, SITTING DROP |