2I1N
Crystal structure of the 1st PDZ domain of Human DLG3
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2006-07-12 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.9791 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 81.817, 80.545, 67.693 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 29.160 - 1.850 |
R-factor | 0.18746 |
Rwork | 0.186 |
R-free | 0.21775 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | PDB ID = 2FE5 |
RMSD bond length | 0.013 |
RMSD bond angle | 1.416 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.920 |
High resolution limit [Å] | 1.850 | 1.850 |
Number of reflections | 19545 | |
Completeness [%] | 99.6 | 96.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 1.0M LiSO4; 0.5M TMAO, VAPOR DIFFUSION, SITTING DROP, temperature 293K |