5H0X
Crystal structure of H88S mutated human transthyretin
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SPRING-8 BEAMLINE BL38B1 |
| Synchrotron site | SPring-8 |
| Beamline | BL38B1 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2013-06-06 |
| Detector | ADSC QUANTUM 315 |
| Wavelength(s) | 1 |
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 42.330, 85.480, 64.060 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 37.934 - 1.573 |
| R-factor | 0.2403 |
| Rwork | 0.240 |
| R-free | 0.25310 |
| RMSD bond length | 0.006 |
| RMSD bond angle | 0.851 |
| Data reduction software | MOSFLM |
| Data scaling software | SCALA |
| Phasing software | MOLREP |
| Refinement software | PHENIX ((1.10.1-2155_1069: ???)) |
Data quality characteristics
| Overall | |
| Low resolution limit [Å] | 38.900 |
| High resolution limit [Å] | 1.570 |
| Number of reflections | 32905 |
| <I/σ(I)> | 20.6 |
| Completeness [%] | 99.7 |
| Redundancy | 6 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 4.8 | 293 | 1.8 M ammonium sulfate, 25% glycerol, 0.1 M sodium acetate |






