3MI8
The structure of TL1A-DCR3 COMPLEX
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X29A |
Synchrotron site | NSLS |
Beamline | X29A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-08-15 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.9791 |
Spacegroup name | P 43 3 2 |
Unit cell lengths | 161.080, 161.080, 161.080 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 25.160 - 2.951 |
R-factor | 0.23367 |
Rwork | 0.232 |
R-free | 0.26096 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3k51 |
RMSD bond length | 0.007 |
RMSD bond angle | 1.126 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.5.0109) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.000 |
High resolution limit [Å] | 2.950 | 2.950 |
Rmerge | 0.092 | 0.898 |
Number of reflections | 15595 | |
<I/σ(I)> | 36.6 | 3.9 |
Redundancy | 20.9 | 21.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 290 | 0.4M K/Na tartrate, pH 6.5, VAPOR DIFFUSION, SITTING DROP, temperature 290.0K |