7AT5
Structure of protein kinase ck2 catalytic subunit (csnk2a1 gene product) in complex with the bivalent inhibitor KN2
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | PETRA III, EMBL c/o DESY BEAMLINE P13 (MX1) |
| Synchrotron site | PETRA III, EMBL c/o DESY |
| Beamline | P13 (MX1) |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2019-09-15 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 0.920200 |
| Spacegroup name | P 43 21 2 |
| Unit cell lengths | 127.591, 127.591, 124.520 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 73.060 - 1.770 |
| R-factor | 0.1743 |
| Rwork | 0.174 |
| R-free | 0.19470 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 6tei |
| RMSD bond length | 0.005 |
| RMSD bond angle | 0.713 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHENIX |
| Refinement software | PHENIX (1.18.2_3874) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 89.115 | 1.921 |
| High resolution limit [Å] | 1.763 | 1.763 |
| Rmerge | 0.111 | 2.229 |
| Rmeas | 0.113 | 2.270 |
| Rpim | 0.022 | 0.428 |
| Number of reflections | 74986 | 3749 |
| <I/σ(I)> | 20.4 | |
| Completeness [%] | 74.0 | 16.4 |
| Redundancy | 26.5 | 27.9 |
| CC(1/2) | 0.998 | 0.697 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 293 | reservoir composition: 30 % (w/v) PEG8000, 0.2 M ammonium sulfate, 0.1 M sodium cacodylate, pH 6.5; crystallization drop composition before equilibration: 0.01 ml reservoir solution plus 0.02 ml enzyme stock solution (6 mg/ml enzyme, 0.5 M NaCl, 25 mM Tris/HCl, pH 8.5); the bivalent inhibitor KN2 was introduced by extensive soaking |






