3IX7
Crystal structure of a domain of functionally unknown protein from Thermus thermophilus HB8
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-BM |
Synchrotron site | APS |
Beamline | 19-BM |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-07-01 |
Detector | ADSC QUANTUM 210r |
Wavelength(s) | 0.97937 |
Spacegroup name | P 61 |
Unit cell lengths | 110.152, 110.152, 39.205 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 50.000 - 2.150 |
R-factor | 0.21167 |
Rwork | 0.209 |
R-free | 0.25609 |
Structure solution method | SAD |
RMSD bond length | 0.015 |
RMSD bond angle | 1.431 |
Data reduction software | HKL-3000 |
Data scaling software | HKL-3000 |
Phasing software | HKL-3000 |
Refinement software | REFMAC (5.5.0102) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.170 |
High resolution limit [Å] | 2.150 | 2.150 |
Rmerge | 0.049 | 0.427 |
Number of reflections | 15031 | |
<I/σ(I)> | 58.18 | 6.22 |
Completeness [%] | 99.8 | 100 |
Redundancy | 10.2 | 9.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8 | 289 | 0.2M Calcium acetate, 0.1M imidazol, 10% PEG8000, pH 8.0, VAPOR DIFFUSION, SITTING DROP, temperature 289K |