3L5H
Crystal structure of the full ectodomain of human gp130: New insights into the molecular assembly of receptor complexes
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
Synchrotron site | Australian Synchrotron |
Beamline | MX2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-10-28 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.95369 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 89.001, 51.821, 167.157 |
Unit cell angles | 90.00, 102.17, 90.00 |
Refinement procedure
Resolution | 44.430 - 3.600 |
R-factor | 0.2667 |
Rwork | 0.263 |
R-free | 0.33469 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.018 |
RMSD bond angle | 2.236 |
Data scaling software | SCALA (3.3.9) |
Phasing software | PHASER |
Refinement software | REFMAC (5.5.0066) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 163.400 | 3.790 |
High resolution limit [Å] | 3.600 | 3.600 |
Rmerge | 0.134 | |
Number of reflections | 17748 | |
<I/σ(I)> | 1.1 | |
Completeness [%] | 99.8 | |
Redundancy | 4 | 4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 6 | 298 | 1.5-2.0M (NH4)2SO4, 0.1M imidazole-malonate buffer, pH 6.0, EVAPORATION, temperature 298K |