6A71
Crystal Structure of Human ATP7B and TM Complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2017-12-08 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 1.37906 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 46.267, 87.740, 78.440 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 43.870 - 1.600 |
R-factor | 0.16676 |
Rwork | 0.165 |
R-free | 0.19537 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3cjk |
RMSD bond length | 0.016 |
RMSD bond angle | 1.622 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0103) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.660 |
High resolution limit [Å] | 1.600 | 1.600 |
Rmerge | 0.064 | 0.292 |
Number of reflections | 20975 | 3284 |
<I/σ(I)> | 24.4 | |
Completeness [%] | 97.8 | |
Redundancy | 8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 286 | 20%PEG8000,0.1M MES pH6.0,0.2M Ca(OAc)2 |