3I3N
Crystal structure of the BTB-BACK domains of human KLHL11
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-11-11 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.99590 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 41.093, 68.879, 136.834 |
Unit cell angles | 90.00, 97.44, 90.00 |
Refinement procedure
Resolution | 26.330 - 2.600 |
Rwork | 0.260 |
R-free | 0.28600 |
Structure solution method | SAD |
RMSD bond length | 0.008 |
RMSD bond angle | 1.250 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | SHARP |
Refinement software | CNS (1.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 45.000 | 2.740 |
High resolution limit [Å] | 2.600 | 2.600 |
Rmerge | 0.115 | 0.492 |
Number of reflections | 23589 | |
<I/σ(I)> | 13.3 | 3.1 |
Completeness [%] | 99.6 | 98.2 |
Redundancy | 6.2 | 4.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 277 | 0.25M K thiocyanate, 25w/v PEG 3350, 5v/v ethylene glycol, bis tris propane, pH 7.5, VAPOR DIFFUSION, SITTING DROP, temperature 277K |