6TX2
Human HPF1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I03 |
Synchrotron site | Diamond |
Beamline | I03 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-02-18 |
Detector | DECTRIS EIGER2 XE 16M |
Wavelength(s) | 0.9787 |
Spacegroup name | P 65 |
Unit cell lengths | 115.099, 115.099, 90.388 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 57.550 - 2.090 |
R-factor | 0.1894 |
Rwork | 0.189 |
R-free | 0.20730 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | HPF1 from Nematostella vectensis |
Data reduction software | xia2 |
Data scaling software | xia2 |
Phasing software | PHASER |
Refinement software | PHENIX (dev_3126) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 99.680 | 2.170 |
High resolution limit [Å] | 2.090 | 2.090 |
Rmerge | 0.170 | 2.670 |
Number of reflections | 80356 | 7931 |
<I/σ(I)> | 11.5 | 1.2 |
Completeness [%] | 99.7 | 98.94 |
Redundancy | 19.66 | 18.68 |
CC(1/2) | 1.000 | 0.790 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 33% glycerol ethoxylate, 0.23 M lithium citrate tribasic tetrahydrate |