9C4U
Menin mutant T349M in complex with MLL peptide
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-G |
Synchrotron site | APS |
Beamline | 21-ID-G |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2023-04-08 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 0.97857 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 49.045, 80.235, 125.085 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 29.153 - 1.569 |
Rwork | 0.160 |
R-free | 0.19710 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.010 |
RMSD bond angle | 1.852 |
Data reduction software | HKL-2000 (722) |
Data scaling software | HKL-2000 (722) |
Phasing software | MOLREP (11.0 / 22.07.2010) |
Refinement software | REFMAC (5.8.0425) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.600 |
High resolution limit [Å] | 1.569 | 1.569 |
Rmerge | 0.150 | 0.963 |
Number of reflections | 69845 | 3438 |
<I/σ(I)> | 20.952 | 2.03 |
Completeness [%] | 100.0 | |
Redundancy | 7 | 5.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 285 | 0.2 M lithium sulfate, 0.1 M HEPES, pH 7.5, 25% (w/v) PEG-3,350 |