3TJE
Crystal structure of Fas receptor extracellular domain in complex with Fab E09
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 90 |
Detector technology | PIXEL |
Collection date | 2007-09-30 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.9000 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 89.490, 166.400, 110.720 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 46.090 - 1.930 |
R-factor | 0.2058 |
Rwork | 0.204 |
R-free | 0.23170 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | PDB ENTRIES 2H9G 1gig |
RMSD bond length | 0.009 |
RMSD bond angle | 1.089 |
Data scaling software | XSCALE |
Phasing software | PHASER (1.3.3) |
Refinement software | PHENIX (1.7.1_743) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 50.848 | 1.980 | |
High resolution limit [Å] | 1.930 | 8.630 | 1.930 |
Rmerge | 0.045 | 0.032 | 0.439 |
Number of reflections | 61296 | 766 | 4548 |
<I/σ(I)> | 22.51 | 51.81 | 4.73 |
Completeness [%] | 98.3 | 97.5 | 99.6 |
Redundancy | 6.5 | 6.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8.5 | 277 | 20% PEG4000, 5 mM CdCl2, 100 mM Tris/HOAc, pH 8.5, vapor diffusion, sitting drop, temperature 277K |