7N86
Crystal Structure of Human Protocadherin-24 EC1-2 Form II
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 24-ID-E |
Synchrotron site | APS |
Beamline | 24-ID-E |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2020-12-01 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.97918 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 63.899, 86.641, 104.892 |
Unit cell angles | 90.00, 103.46, 90.00 |
Refinement procedure
Resolution | 49.147 - 3.175 |
Rwork | 0.213 |
R-free | 0.28960 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5czr |
RMSD bond length | 0.017 |
RMSD bond angle | 2.020 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.230 |
High resolution limit [Å] | 3.175 | 3.175 |
Number of reflections | 18809 | 810 |
<I/σ(I)> | 5.6 | 2.63 |
Completeness [%] | 96.3 | 89.1 |
Redundancy | 3.5 | 2.5 |
CC(1/2) | 0.987 | 0.277 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8 | 277 | 0.2 MM NaI 20% PEG3350 CDHR5 EC1-2 |