9CXM
Crystal structure of Human FN3K bound with ATP and DMF
This is a non-PDB format compatible entry.
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 | 2021-11-10 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.97918 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 52.932, 112.275, 132.796 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 66.400 - 1.760 |
R-factor | 0.1779 |
Rwork | 0.176 |
R-free | 0.20840 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.018 |
RMSD bond angle | 1.986 |
Data reduction software | RAPD |
Data scaling software | RAPD |
Phasing software | PHASER |
Refinement software | PHENIX ((1.20.1_4487:0000)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 132.800 | 1.820 |
High resolution limit [Å] | 1.760 | 1.760 |
Rmerge | 0.043 | |
Number of reflections | 79306 | 7822 |
<I/σ(I)> | 23.2 | |
Completeness [%] | 99.8 | |
Redundancy | 5.6 | |
CC(1/2) | 0.990 | 0.890 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 0.5 M ammonium sulfate, 0.1 M tri-sodium citrate, and 1 M lithium sulfate |