4Y1S
Structural basis for Ca2+-mediated interaction of the perforin C2 domain with lipid membranes
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 | 2014-12-18 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 0.953697 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 37.700, 43.211, 68.077 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 36.482 - 1.611 |
| R-factor | 0.1671 |
| Rwork | 0.166 |
| R-free | 0.18520 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3nsj |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.286 |
| Data reduction software | XDS |
| Data scaling software | SCALA |
| Phasing software | PHASER |
| Refinement software | PHENIX ((phenix.refine: 1.9_1692)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 36.482 | 1.669 |
| High resolution limit [Å] | 1.611 | 1.611 |
| Rmerge | 0.216 | 0.547 |
| Number of reflections | 14926 | |
| <I/σ(I)> | 30.06 | 4.83 |
| Completeness [%] | 99.9 | 98.9 |
| Redundancy | 7.1 | 6.8 |
| CC(1/2) | 0.979 | 0.860 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 6 | 293 | 0.1M MES pH 6.0, 0.2 M NaCl and 20% (w/v) polyethylene glycol 2000 monomethyl ether |






