7E5T
Crystal structure of Fsa2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL32XU |
Synchrotron site | SPring-8 |
Beamline | BL32XU |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-02-09 |
Detector | DECTRIS EIGER X 9M |
Wavelength(s) | 0.979400 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 133.929, 80.229, 135.159 |
Unit cell angles | 90.00, 108.53, 90.00 |
Refinement procedure
Resolution | 45.044 - 2.170 |
R-factor | 0.182641334888 |
Rwork | 0.180 |
R-free | 0.23522 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | Phm7 |
RMSD bond length | 0.004 |
RMSD bond angle | 0.700 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER (2.7.17) |
Refinement software | PHENIX (1.11.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 45.044 | 2.248 |
High resolution limit [Å] | 2.170 | 2.170 |
Rmerge | 0.109 | |
Number of reflections | 141327 | 13856 |
<I/σ(I)> | 8.48 | |
Completeness [%] | 97.6 | |
Redundancy | 3.5 | |
CC(1/2) | 0.998 | 0.780 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7 | 293 | 26-29% (v/v) polyethylene glycol 3350, 0.10M Bis-Tris HCl |