6Q3V
Crystal structure of Human N4BP1 KH domains
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.1 |
Synchrotron site | BESSY |
Beamline | 14.1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2016-12-05 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.91841 |
Spacegroup name | P 62 |
Unit cell lengths | 108.690, 108.690, 27.727 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 35.577 - 1.882 |
R-factor | 0.1831 |
Rwork | 0.181 |
R-free | 0.23100 |
Structure solution method | SAD |
RMSD bond length | 0.006 |
RMSD bond angle | 0.951 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.060 | 1.950 |
High resolution limit [Å] | 1.882 | 1.882 |
Rmeas | 0.063 | |
Number of reflections | 15568 | |
<I/σ(I)> | 19.78 | |
Completeness [%] | 99.7 | |
Redundancy | 6.51 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 277 | Sodium malonate |