4OY9
Crystal structure of human P-Cadherin EC1-EC2 in closed conformation
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06DA |
Synchrotron site | SLS |
Beamline | X06DA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2013-10-04 |
Detector | PSI PILATUS 6M |
Wavelength(s) | 1.0 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 75.381, 40.949, 72.409 |
Unit cell angles | 90.00, 98.05, 90.00 |
Refinement procedure
Resolution | 37.320 - 1.620 |
R-factor | 0.16505 |
Rwork | 0.163 |
R-free | 0.20239 |
RMSD bond length | 0.012 |
RMSD bond angle | 1.434 |
Refinement software | REFMAC (5.8.0049) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 37.320 |
High resolution limit [Å] | 1.600 |
Number of reflections | 27755 |
<I/σ(I)> | 13.64 |
Completeness [%] | 98.8 |
Redundancy | 3.68 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.4 | 293 | PEG 8000, calcium chloride, HEPES, dimethylsulfoxyde |