6K9X
Crystal Structure Analysis of Protein
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 80 |
Detector technology | CCD |
Collection date | 2018-11-07 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1.0 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 48.597, 58.268, 70.239 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 39.964 - 1.200 |
R-factor | 0.1304 |
Rwork | 0.130 |
R-free | 0.14120 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2dfc |
RMSD bond length | 0.009 |
RMSD bond angle | 1.110 |
Data reduction software | XDS |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | PHENIX (1.11.1_2575) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 39.964 | 1.243 |
High resolution limit [Å] | 1.200 | 1.200 |
Number of reflections | 62650 | 6177 |
<I/σ(I)> | 18.32 | |
Completeness [%] | 99.2 | |
Redundancy | 5.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 6 | 291 | PEG 8000, NaI, MES |