5WMB
Structure of the 10S (-)-cis-BP-dG modified Rev1 ternary complex (the BP residue is disordered)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X25 |
Synchrotron site | NSLS |
Beamline | X25 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2013-10-24 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 1.10 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 63.307, 65.476, 131.657 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 65.830 - 2.250 |
R-factor | 0.17223 |
Rwork | 0.170 |
R-free | 0.21710 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2aq4 |
RMSD bond length | 0.011 |
RMSD bond angle | 1.474 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHENIX |
Refinement software | REFMAC (5.8.0158) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 65.830 |
High resolution limit [Å] | 2.250 |
Number of reflections | 26824 |
<I/σ(I)> | 18.6 |
Completeness [%] | 100.0 |
Redundancy | 7.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6 | 293 | 0.25 M sodium citrate pH 6.0 buffer 15-20% PEG3350 |