2JLL
Crystal structure of NCAM2 IgIV-FN3II
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID29 |
| Synchrotron site | ESRF |
| Beamline | ID29 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2008-04-05 |
| Detector | ADSC CCD |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 151.740, 33.800, 97.670 |
| Unit cell angles | 90.00, 98.36, 90.00 |
Refinement procedure
| Resolution | 19.791 - 2.300 |
| R-factor | 0.2183 |
| Rwork | 0.216 |
| R-free | 0.26850 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.000 |
| RMSD bond angle | 0.920 |
| Data reduction software | MOSFLM |
| Data scaling software | SCALEPACK |
| Phasing software | PHASER |
| Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 19.790 | 2.420 |
| High resolution limit [Å] | 2.300 | 2.300 |
| Rmerge | 0.042 | 0.272 |
| Number of reflections | 38513 | |
| <I/σ(I)> | 8.6 | 2.3 |
| Completeness [%] | 90.4 | 99.9 |
| Redundancy | 3.7 | 3.8 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | 6.5 | 0.1M HEPES PH6.5, 14% PEG10000, 0.2M CALCIUM ACETATE |
