4CJ1
Crystal structure of CelD in complex with affitin H3
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF |
| Synchrotron site | ESRF |
| Beamline | ID23-2 |
| Temperature [K] | 100 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 74.422, 97.736, 106.580 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 46.830 - 1.630 |
| R-factor | 0.10798 |
| Rwork | 0.106 |
| R-free | 0.14374 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1clc |
| RMSD bond length | 0.020 |
| RMSD bond angle | 1.814 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | REFMAC (5.7.0029) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 46.790 | 1.660 |
| High resolution limit [Å] | 1.630 | 1.630 |
| Rmerge | 0.050 | 0.360 |
| Number of reflections | 96777 | |
| <I/σ(I)> | 15.4 | 3.2 |
| Completeness [%] | 99.7 | 96.9 |
| Redundancy | 4 | 3.9 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 |
