6XAU
Structure of the PR domain from PRDM3
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-ID |
Synchrotron site | APS |
Beamline | 19-ID |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-02-12 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.979 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 44.421, 44.421, 147.317 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 42.530 - 1.890 |
Rwork | 0.204 |
R-free | 0.23840 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2n1i |
RMSD bond length | 0.009 |
RMSD bond angle | 0.940 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.17) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 42.530 | 1.960 |
High resolution limit [Å] | 1.890 | 1.890 |
Number of reflections | 12329 | 1108 |
<I/σ(I)> | 34 | 1.6 |
Completeness [%] | 98.4 | 90.9 |
Redundancy | 12.1 | 4 |
CC(1/2) | 0.998 | 0.998 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 277 | 0.25M calcium acetate, 20% PEG 3350 |