8I00
Crystal structure of A97S transthyretin
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSRRC BEAMLINE BL15A1 |
Synchrotron site | NSRRC |
Beamline | BL15A1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2022-10-21 |
Detector | RAYONIX MX300HE |
Wavelength(s) | 1 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 85.630, 43.092, 64.058 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 26.070 - 1.800 |
R-factor | 0.1824 |
Rwork | 0.180 |
R-free | 0.20870 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.006 |
RMSD bond angle | 0.746 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | PHENIX |
Refinement software | PHENIX (1.19.2-4158) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.860 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmeas | 0.038 | 0.074 |
Rpim | 0.015 | 0.028 |
Number of reflections | 22653 | 2197 |
<I/σ(I)> | 41.77 | |
Completeness [%] | 97.5 | |
Redundancy | 6.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 1.6 M Sodium citrate tribasic dihydrate |