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 |






