6FBH
KlenTaq DNA polymerase processing a modified primer - bearing the modification upstream at the sixth primer nucleotide.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-06-10 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 1.00002 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 109.706, 109.706, 91.292 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 47.504 - 1.800 |
R-factor | 0.1975 |
Rwork | 0.196 |
R-free | 0.22300 |
RMSD bond length | 0.009 |
RMSD bond angle | 0.841 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHENIX |
Refinement software | PHENIX ((1.12rc1_2815: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.504 | 1.809 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmeas | 0.099 | 1.862 |
Number of reflections | 113900 | 18357 |
<I/σ(I)> | 8.68 | 0.67 |
Completeness [%] | 99.8 | 99.7 |
Redundancy | 5.14 | 5.02 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 7 | 291 | 29 % PEG 4000, 0.05 M TRIS, 20 mM manganese(II) chloride, 0.2 M ammonium chloride |