3OG3
Crystal structure of an artificial thermostable (BA)8-barrel protein from identical half barrels
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SEALED TUBE |
Source details | OXFORD DIFFRACTION ENHANCE ULTRA |
Temperature [K] | 123 |
Detector technology | CCD |
Collection date | 2009-12-18 |
Detector | OXFORD RUBY CCD |
Wavelength(s) | 1.5418 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 31.374, 82.086, 74.511 |
Unit cell angles | 90.00, 90.11, 90.00 |
Refinement procedure
Resolution | 14.650 - 2.080 |
R-factor | 0.15194 |
Rwork | 0.150 |
R-free | 0.19591 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1THF (Amino acids 99-219) dimer |
RMSD bond length | 0.025 |
RMSD bond angle | 2.006 |
Data reduction software | CrysalisPro |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.5.0088) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 14.700 | 2.140 |
High resolution limit [Å] | 2.080 | 2.040 |
Number of reflections | 11304 | |
<I/σ(I)> | 18.58 | 3.8 |
Completeness [%] | 99.6 | 96.8 |
Redundancy | 2.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 293 | 0.2 M ammonium sulfate, 18% PEG 4000, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K |