8G6B
Crystal structure of PfAMA1-RON2L chimera
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | CLSI BEAMLINE 08ID-1 |
Synchrotron site | CLSI |
Beamline | 08ID-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-01-30 |
Detector | DECTRIS EIGER X 9M |
Wavelength(s) | 0.984 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 92.499, 92.499, 173.681 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 57.894 - 1.550 |
R-factor | 0.1826 |
Rwork | 0.181 |
R-free | 0.21120 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.008 |
RMSD bond angle | 1.139 |
Data reduction software | iMOSFLM |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.8.3) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 58.880 | 1.580 |
High resolution limit [Å] | 1.550 | 1.550 |
Rmerge | 0.075 | 0.624 |
Number of reflections | 124774 | 6114 |
<I/σ(I)> | 11.4 | |
Completeness [%] | 99.7 | 100 |
Redundancy | 6.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7 | 291 | 0.1 M Tris-HCl pH 7.0, 1.5 M lithium sulfate |