6ISC
complex structure of mCD226-ecto and hCD155-D1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U1 |
Synchrotron site | SSRF |
Beamline | BL17U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2014-05-13 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 0.97923 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 50.220, 78.303, 184.600 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 42.273 - 2.200 |
R-factor | 0.2347 |
Rwork | 0.233 |
R-free | 0.26510 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6isa 3EOW |
RMSD bond length | 0.002 |
RMSD bond angle | 0.489 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((1.13_2998: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.280 |
High resolution limit [Å] | 2.200 | 2.200 |
Rmerge | 0.099 | |
Rpim | 0.036 | 0.378 |
Number of reflections | 18895 | 1772 |
<I/σ(I)> | 23.456 | |
Completeness [%] | 99.5 | 96.2 |
Redundancy | 8.6 | 6 |
CC(1/2) | 0.999 | 0.798 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 291 | 0.1 M Tris (pH 8.0), 0.15 M ammonium sulfate, and 15% (w/v) PEG4000 |