6JGM
Crystal structure of CDK2 IN complex with Inhibitor NU-6140
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2018-10-17 |
| Detector | Nonius Kappa CCD |
| Wavelength(s) | 1.0 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 53.491, 72.010, 72.330 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 51.030 - 2.300 |
| R-factor | 0.2179 |
| Rwork | 0.214 |
| R-free | 0.29036 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3qxp |
| RMSD bond length | 0.013 |
| RMSD bond angle | 1.728 |
| Data reduction software | XDS |
| Data scaling software | SCALEPACK |
| Phasing software | MOLREP |
| Refinement software | REFMAC (5.8.0158) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 53.010 | 2.380 |
| High resolution limit [Å] | 2.300 | 2.300 |
| Rmerge | 0.098 | 0.570 |
| Number of reflections | 12976 | 1194 |
| <I/σ(I)> | 9.6 | 2.2 |
| Completeness [%] | 99.5 | 95.6 |
| Redundancy | 6.6 | 6.6 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 8 | 293 | 0.1M Tris pH 8.0, 0.1M NaCl, 20% PEG monomethyl ether 550 |
