5FHB
Crystal Structure of Protective Ebola Virus Antibody 100
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 19-ID |
| Synchrotron site | APS |
| Beamline | 19-ID |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2015-07-23 |
| Detector | ADSC QUANTUM 315r |
| Wavelength(s) | 0.9793 |
| Spacegroup name | P 32 2 1 |
| Unit cell lengths | 71.540, 71.540, 199.012 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 33.487 - 1.973 |
| R-factor | 0.1602 |
| Rwork | 0.159 |
| R-free | 0.19370 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | PDB ID: 4QHK |
| RMSD bond length | 0.018 |
| RMSD bond angle | 1.623 |
| Data reduction software | MOSFLM |
| Data scaling software | Aimless (0.5.15) |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.10_2155) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 33.487 | 38.790 | 2.020 |
| High resolution limit [Å] | 1.970 | 9.040 | 1.970 |
| Rmerge | 0.134 | 0.043 | 0.751 |
| Rpim | 0.044 | 0.015 | 0.261 |
| Total number of observations | 443933 | 4398 | 26792 |
| Number of reflections | 42605 | ||
| <I/σ(I)> | 11.3 | 18.5 | 3.1 |
| Completeness [%] | 100.0 | 97.8 | 100 |
| Redundancy | 10.4 | 8.5 | 9.1 |
| CC(1/2) | 0.997 | 0.998 | 0.860 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 5.5 | 293 | 3.4mg/ml 100 Fab, 38% PEG 400, 4.75% PEG 3350, 0.1M sodium acetate pH 5.5 |






