3BEP
Structure of a sliding clamp on DNA
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X4A |
Synchrotron site | NSLS |
Beamline | X4A |
Temperature [K] | 100 |
Detector technology | CCD |
Detector | ADSC QUANTUM 4 |
Wavelength(s) | 0.959 |
Spacegroup name | P 1 |
Unit cell lengths | 40.203, 70.080, 73.872 |
Unit cell angles | 113.28, 92.07, 99.36 |
Refinement procedure
Resolution | 36.560 - 1.920 |
Rwork | 0.210 |
R-free | 0.26800 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2pol |
RMSD bond length | 0.006 |
RMSD bond angle | 1.303 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | CNS |
Refinement software | CNS |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.990 |
High resolution limit [Å] | 1.920 | 1.920 |
Rmerge | 0.069 | 0.395 |
Number of reflections | 53902 | |
<I/σ(I)> | 10.9 | |
Completeness [%] | 95.7 | 79.2 |
Redundancy | 2.9 | 2.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 5.9 | 298 | 26% PEG 400, 75mM MES (pH 5.9), 75mM CaCl2, 5% glycerol, 0.5% DMSO, VAPOR DIFFUSION, temperature 298K |
Crystallization Reagents
ID | crystal ID | solution ID | reagent name | concentration | details |
1 | 1 | 1 | PEG 400 | ||
10 | 1 | 2 | DMSO | ||
2 | 1 | 1 | MES | ||
3 | 1 | 1 | CaCl2, | ||
4 | 1 | 1 | glycerol | ||
5 | 1 | 1 | DMSO | ||
6 | 1 | 2 | PEG 400 | ||
7 | 1 | 2 | MES | ||
8 | 1 | 2 | CaCl2, | ||
9 | 1 | 2 | glycerol |