2VBL
Molecular basis of human XPC gene recognition and cleavage by engineered homing endonuclease heterodimers
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | CCD |
Detector | MARRESEARCH |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 44.612, 69.209, 88.671 |
Unit cell angles | 90.00, 95.46, 90.00 |
Refinement procedure
Resolution | 32.920 - 1.800 |
R-factor | 0.149 |
Rwork | 0.147 |
R-free | 0.19700 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1g9z |
RMSD bond length | 0.012 |
RMSD bond angle | 1.975 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | MOLREP |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 32.920 |
High resolution limit [Å] | 1.800 |
Rmerge | 0.050 |
Number of reflections | 45123 |
Completeness [%] | 95.5 |
Redundancy | 3.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 6.5 | 4 MG/ML PROTEIN, 35% METHANOL, 0.1M NACACODYLATE PH 6.5 |