5CBE
E10 in complex with CXCL13
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 17-ID |
Synchrotron site | APS |
Beamline | 17-ID |
Temperature [K] | 193 |
Detector technology | PIXEL |
Collection date | 2013-04-10 |
Detector | PSI PILATUS 6M |
Wavelength(s) | 1.0 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 125.000, 125.000, 98.000 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 40.920 - 2.400 |
R-factor | 0.2495 |
Rwork | 0.248 |
R-free | 0.27460 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | E10 and 3GV3/2R3Z/4HSV/3IL8 |
RMSD bond length | 0.008 |
RMSD bond angle | 1.060 |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | BUSTER (2.11.5) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.490 |
High resolution limit [Å] | 2.400 | 2.400 |
Rmerge | 0.070 | 0.605 |
Number of reflections | 34874 | |
<I/σ(I)> | 30.4 | 3.6 |
Completeness [%] | 100.0 | 100 |
Redundancy | 11.6 | 9.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6 | 291 | 100 mM KH2PO4, 100 mM NaH2PO4, 100 mM MES pH 6, 2000 mM NaCl |