4E59
Crystal structure of GCCGCCGC duplex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.2 |
Synchrotron site | BESSY |
Beamline | 14.2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-10-05 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.9184 |
Spacegroup name | H 3 |
Unit cell lengths | 40.580, 40.580, 56.144 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 18.715 - 1.540 |
R-factor | 0.2553 |
Rwork | 0.255 |
R-free | 0.30350 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4e58 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.290 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine: 1.7_650)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 1.570 |
High resolution limit [Å] | 1.540 | 1.540 |
Number of reflections | 5101 | |
<I/σ(I)> | 26.14 | 2.06 |
Completeness [%] | 99.9 | 100 |
Redundancy | 4.3 | 3.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.6 | 303 | magnesium acetate, MES and ammonium sulphate, pH 5.6, VAPOR DIFFUSION, HANGING DROP, temperature 303K |