8PMU
Crystal structure of the HC7 apo form
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALBA BEAMLINE XALOC |
Synchrotron site | ALBA |
Beamline | XALOC |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2022-01-30 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 0.9793 |
Spacegroup name | P 41 21 2 |
Unit cell lengths | 93.854, 93.854, 87.287 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 66.360 - 1.750 |
R-factor | 0.19293 |
Rwork | 0.191 |
R-free | 0.23117 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.019 |
RMSD bond angle | 1.932 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0135) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 93.850 | 1.840 |
High resolution limit [Å] | 1.750 | 1.750 |
Rmerge | 0.034 | 1.209 |
Number of reflections | 36731 | 5728 |
<I/σ(I)> | 11.5 | |
Completeness [%] | 91.9 | |
Redundancy | 8.7 | |
CC(1/2) | 0.644 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 291 | Lithium chloride Tris PEG 8000 |