7KXW
Crystal structure of DCLK1-KD in complex with DCLK1-IN-1
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 | PIXEL |
| Collection date | 2018-03-21 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.9537 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 143.950, 61.714, 65.312 |
| Unit cell angles | 90.00, 103.04, 90.00 |
Refinement procedure
| Resolution | 44.288 - 3.002 |
| R-factor | 0.2031 |
| Rwork | 0.200 |
| R-free | 0.25970 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5jzj |
| Data scaling software | Aimless (0.5.32) |
| Refinement software | PHENIX (1.13_2998) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 44.290 | 44.290 | 3.180 |
| High resolution limit [Å] | 3.000 | 9.010 | 3.000 |
| Rmerge | 0.156 | 0.057 | 0.775 |
| Rmeas | 0.169 | 0.062 | 0.839 |
| Rpim | 0.064 | 0.023 | 0.316 |
| Total number of observations | 76277 | 2942 | 11337 |
| Number of reflections | 11200 | 439 | 1669 |
| <I/σ(I)> | 11.4 | 25.6 | 3.6 |
| Completeness [%] | 98.8 | 99.2 | 93 |
| Redundancy | 6.8 | 6.7 | 6.8 |
| CC(1/2) | 0.996 | 0.997 | 0.819 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | EVAPORATION | 7.25 | 298 | PEG400, ammonium sulfphate, Hepes |






