3RR5
DNA ligase from the archaeon Thermococcus sp. 1519
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL41XU |
Synchrotron site | SPring-8 |
Beamline | BL41XU |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-12-14 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.8 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 76.950, 85.600, 105.960 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 29.257 - 3.018 |
R-factor | 0.2365 |
Rwork | 0.233 |
R-free | 0.30960 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3gde |
RMSD bond length | 0.009 |
RMSD bond angle | 1.319 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | BALBES |
Refinement software | PHENIX ((phenix.refine: 1.7_650)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 29.257 | 3.200 |
High resolution limit [Å] | 3.000 | 3.020 |
Number of reflections | 14237 | |
<I/σ(I)> | 25.09 | 3.43 |
Completeness [%] | 97.8 | 98.7 |
Redundancy | 4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | LIQUID DIFFUSION | 7.5 | 291 | 0.1 Na Cacodilate, 0.2 M MgCl2, 20% Glicerol, 16% PEG 8000, 100 mM NaCl, 50mM Tris-HCl, Protein 22mg/mL (protein buffer: 50mM Tris-Hcl, 100 mM NaCl, 0.5 DTT), Gel-tube counter-diffusion method, pH 7.5, LIQUID DIFFUSION, temperature 291K |