8CYK
Crystal structure of hallucinated protein HALC1_878
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 8.2.1 |
Synchrotron site | ALS |
Beamline | 8.2.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2022-04-07 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1.00003 |
Spacegroup name | I 1 2 1 |
Unit cell lengths | 64.174, 55.453, 82.807 |
Unit cell angles | 90.00, 94.00, 90.00 |
Refinement procedure
Resolution | 48.980 - 1.650 |
R-factor | 0.1864 |
Rwork | 0.185 |
R-free | 0.21680 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | Design model |
RMSD bond length | 0.011 |
RMSD bond angle | 1.124 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 48.980 | 1.709 |
High resolution limit [Å] | 1.650 | 1.650 |
Number of reflections | 34565 | 3322 |
<I/σ(I)> | 15.91 | 3.96 |
Completeness [%] | 97.2 | 95.7 |
Redundancy | 2 | 2 |
CC(1/2) | 0.999 | 0.942 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 3.5 | 293 | 0.1 M citric acid 3M NaCl |