5E52
Crystal structure of human CNTN5 FN1-FN3 domains
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-ID |
Synchrotron site | APS |
Beamline | 22-ID |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-08-08 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 1.00 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 83.770, 154.518, 90.417 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 38.630 - 2.685 |
R-factor | 0.198 |
Rwork | 0.194 |
R-free | 0.23140 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5eq4 |
RMSD bond length | 0.009 |
RMSD bond angle | 1.134 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER (2.5.3) |
Refinement software | PHENIX |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.000 | 50.000 | 2.800 |
High resolution limit [Å] | 2.685 | 5.810 | 2.685 |
Rmerge | 0.112 | 0.086 | 0.418 |
Total number of observations | 171135 | ||
Number of reflections | 14285 | ||
<I/σ(I)> | 14 | ||
Completeness [%] | 85.7 | 99.2 | 56.3 |
Redundancy | 12 | 13.4 | 5.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5 | 293 | 1M NH4H2PO4, 10% (v/v) Tacsimate pH 5.0 |