6FBD
KlenTaq DNA polymerase processing a modified primer - bearing the modification upstream at the second 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 | 2015-08-22 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 1.000000 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 109.964, 109.964, 91.165 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 47.082 - 2.099 |
R-factor | 0.2001 |
Rwork | 0.198 |
R-free | 0.23310 |
RMSD bond length | 0.007 |
RMSD bond angle | 0.575 |
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] | 47.616 | 2.110 |
High resolution limit [Å] | 2.099 | 2.099 |
Rmeas | 0.073 | 0.873 |
Number of reflections | 72040 | 11669 |
<I/σ(I)> | 13.91 | 1.94 |
Completeness [%] | 99.9 | 99.8 |
Redundancy | 5.18 | 5.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 7 | 291 | 16 % PEG 4000, 0.1 M HEPES, 25 mM manganese(II) chloride, 0.1 M sodium acetate |