2VN2
Crystal structure of the N-terminal domain of DnaD protein from Geobacillus kaustophilus HTA426
Experimental procedure
Experimental method | MAD |
Source type | SYNCHROTRON |
Source details | NSRRC BEAMLINE BL13B1 |
Synchrotron site | NSRRC |
Beamline | BL13B1 |
Temperature [K] | 100 |
Detector technology | CCD |
Detector | ADSC CCD |
Wavelength(s) | 0.9794, 0.9795, 0.9643 |
Spacegroup name | F 2 2 2 |
Unit cell lengths | 116.514, 124.707, 157.230 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 27.490 - 2.300 |
R-factor | 0.217 |
Rwork | 0.217 |
R-free | 0.22300 |
Structure solution method | MAD |
Starting model (for MR) | NONE |
RMSD bond length | 0.034 |
RMSD bond angle | 2.600 |
Data reduction software | Blu-Ice (CONTROL SOFTWARE) |
Data scaling software | HKL-2000 |
Phasing software | SOLVE |
Refinement software | CNS (1.2) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 27.490 | 2.380 |
High resolution limit [Å] | 2.300 | 2.300 |
Rmerge | 0.110 | 0.370 |
Number of reflections | 46920 | |
<I/σ(I)> | 22.59 | 9.2 |
Completeness [%] | 95.4 | 100 |
Redundancy | 12.3 | 12.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 |