9C4T
menin mutant M327I 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 | 49.075, 80.456, 124.946 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 31.131 - 1.461 |
Rwork | 0.156 |
R-free | 0.18440 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.012 |
RMSD bond angle | 1.995 |
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 | 1.490 |
High resolution limit [Å] | 1.460 | 1.460 |
Rmerge | 0.082 | 0.726 |
Number of reflections | 86122 | 4168 |
<I/σ(I)> | 28.13 | 2.27 |
Completeness [%] | 99.5 | 97.1 |
Redundancy | 7 |
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 |