5SVH
Crystal structure of the KIX domain of CBP in complex with a MLL/c-Myb chimera
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 23-ID-B |
| Synchrotron site | APS |
| Beamline | 23-ID-B |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2014-08-14 |
| Detector | MAR CCD 165 mm |
| Wavelength(s) | 1.0332 |
| Spacegroup name | P 63 2 2 |
| Unit cell lengths | 119.820, 119.820, 50.430 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 59.900 - 2.050 |
| R-factor | 0.2082 |
| Rwork | 0.206 |
| R-free | 0.24200 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2agh |
| RMSD bond length | 0.007 |
| RMSD bond angle | 0.970 |
| Data reduction software | iMOSFLM |
| Data scaling software | SCALA |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 59.900 | 2.123 |
| High resolution limit [Å] | 2.050 | 2.050 |
| Rmerge | 0.066 | 0.959 |
| Number of reflections | 13648 | |
| <I/σ(I)> | 31 | 3.8 |
| Completeness [%] | 98.7 | 96.5 |
| Redundancy | 27.1 | 24.7 |
| CC(1/2) | 0.871 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 295 | 0.1 M potassium sulfate 2.3M Ammonium sulphate |






