1M3H
Crystal Structure of Hogg1 D268E Mutant with Product Oligonucleotide
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | CHESS BEAMLINE A1 |
Synchrotron site | CHESS |
Beamline | A1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2001-12-15 |
Detector | ADSC QUANTUM 210 |
Wavelength(s) | 0.9500 |
Spacegroup name | P 65 2 2 |
Unit cell lengths | 92.345, 92.345, 211.345 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 26.660 - 2.050 |
R-factor | 0.239 |
Rwork | 0.239 |
R-free | 0.28200 |
Structure solution method | FOURIER SYNTHESIS |
Starting model (for MR) | 1ebm |
RMSD bond length | 0.006 |
RMSD bond angle | 1.200 |
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 | 2.120 |
High resolution limit [Å] | 2.050 | 2.050 |
Rmerge | 0.070 | 0.612 |
Number of reflections | 33658 | |
<I/σ(I)> | 23.1 | 2.1 |
Completeness [%] | 88.4 | |
Redundancy | 5.2 | 4.53 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 277 | PEG 8000, cacodylate, Calcium Acetate, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 277K |
Crystallization Reagents
ID | crystal ID | solution ID | reagent name | concentration | details |
1 | 1 | 1 | PEG 8000 | ||
2 | 1 | 1 | cacodylate | ||
3 | 1 | 1 | Calcium Acetate |