2H6N
Histone H3 recognition and presentation by the WDR5 module of the MLL1 complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 5.0.2 |
Synchrotron site | ALS |
Beamline | 5.0.2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2006-01-15 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.98710 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 134.745, 46.131, 112.694 |
Unit cell angles | 90.00, 117.17, 90.00 |
Refinement procedure
Resolution | 43.400 - 1.500 |
R-factor | 0.17964 |
Rwork | 0.179 |
R-free | 0.19766 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1erj |
RMSD bond length | 0.009 |
RMSD bond angle | 1.292 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | REFMAC (5.2.0005) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 43.400 | 1.550 |
High resolution limit [Å] | 1.500 | 1.500 |
Rmerge | 0.148 | 0.464 |
Number of reflections | 90444 | |
<I/σ(I)> | 9.2 | 2.86 |
Completeness [%] | 99.9 | 99.6 |
Redundancy | 4.3 | 3.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Crystals were grown by hanging drop vapour equilibration in Nextal plates as follows: 1 ul of 10 15 mg ml-1 protein solution (10 mM Tris HCl (pH 7.4), 50 mM NaCl, and 10 mM 2-mercaptoethanol) were mixed with 1 ul of well solution composed of 50 mM HEPES (pH 7.5), 100 mM potassium formate, and 10-20% (w/v) polyethylene glycol 3350 and equilibrated at room temperature overnight against 1 ml of well solution. |