3K6F
Crystal structure of mouse T-cadherin EC1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X4C |
Synchrotron site | NSLS |
Beamline | X4C |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Detector | MAR scanner 345 mm plate |
Wavelength(s) | 0.9791 |
Spacegroup name | P 62 |
Unit cell lengths | 50.355, 50.355, 122.460 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 19.447 - 1.813 |
R-factor | 0.168 |
Rwork | 0.168 |
R-free | 0.22600 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | PRB entry 3K6D |
RMSD bond length | 0.009 |
RMSD bond angle | 1.361 |
Data reduction software | DENZO |
Data scaling software | HKL-3000 |
Phasing software | PHASER |
Refinement software | PHENIX |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 1.900 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.048 | 0.125 |
Number of reflections | 16137 | |
Completeness [%] | 99.3 | 99.9 |
Redundancy | 10.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6 | 277 | 0.2M Ammonium sulfate, 20% PEG 3350, pH 6.0, VAPOR DIFFUSION, HANGING DROP, temperature 277K |