6ZTB
Crystal Structure of human P-Cadherin EC1_EC2
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SLS BEAMLINE X10SA |
| Synchrotron site | SLS |
| Beamline | X10SA |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2012-06-22 |
| Detector | PSI PILATUS 6M |
| Wavelength(s) | 0.99999 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 120.889, 76.522, 46.208 |
| Unit cell angles | 90.00, 107.79, 90.00 |
Refinement procedure
| Resolution | 57.550 - 1.400 |
| R-factor | 0.1989 |
| Rwork | 0.198 |
| R-free | 0.21350 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1l3w |
| RMSD bond length | 0.010 |
| RMSD bond angle | 1.130 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHASER (2.3.0) |
| Refinement software | BUSTER |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 57.550 | 57.550 | 1.440 |
| High resolution limit [Å] | 1.400 | 6.260 | 1.400 |
| Rmerge | 0.022 | 0.018 | 0.523 |
| Rmeas | 0.026 | 0.021 | 0.620 |
| Number of reflections | 78188 | 915 | 5758 |
| <I/σ(I)> | 23.72 | 67.59 | 2.06 |
| Completeness [%] | 99.2 | 98.4 | 99.6 |
| Redundancy | 3.328 | 3.502 | 3.409 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 293 | 3.655M NaCl, 85mM HEPES, 15.0% GLYCEROL |
