8Y2K
The crystal structure of QX006N-Fab
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL18U1 |
Synchrotron site | SSRF |
Beamline | BL18U1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2021-10-03 |
Detector | MAR CCD 130 mm |
Wavelength(s) | 0.979 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 47.748, 137.496, 73.723 |
Unit cell angles | 90.00, 93.96, 90.00 |
Refinement procedure
Resolution | 47.630 - 2.870 |
R-factor | 0.2174 |
Rwork | 0.215 |
R-free | 0.26840 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.004 |
RMSD bond angle | 0.707 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((1.18.2_3874: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.950 |
High resolution limit [Å] | 2.850 | 2.850 |
Number of reflections | 21423 | 2170 |
<I/σ(I)> | 13.9 | |
Completeness [%] | 98.0 | |
Redundancy | 3.3 | |
CC(1/2) | 1.000 | 1.000 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION, RECRYSTALLIZATION | 289 | 0.2 M potassium sodium tartrate tetrahydrate pH 4.5, 20%(w/v) PEG 3350 |