8DYP
Crystal structure of human cystine transporter cystinosin
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 23-ID-B |
| Synchrotron site | APS |
| Beamline | 23-ID-B |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2018-08-19 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.9794 |
| Spacegroup name | P 2 21 21 |
| Unit cell lengths | 49.510, 71.270, 194.640 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 40.190 - 3.400 |
| R-factor | 0.2721 |
| Rwork | 0.270 |
| R-free | 0.30200 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3p0g 4x5n |
| RMSD bond length | 0.003 |
| RMSD bond angle | 0.724 |
| Data reduction software | HKL-2000 |
| Data scaling software | HKL-2000 |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.19.2_4158) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 40.190 | 3.520 |
| High resolution limit [Å] | 3.400 | 3.400 |
| Number of reflections | 9815 | 886 |
| <I/σ(I)> | 15.2 | 1.69 |
| Completeness [%] | 97.3 | 88.9 |
| Redundancy | 14.9 | 8.3 |
| CC(1/2) | 0.967 | 0.722 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | LIPIDIC CUBIC PHASE | 6.5 | 293.15 | 12% PEG400, 80mM Li2SO4, and 50mM MES pH6.0 |
| 1 | LIPIDIC CUBIC PHASE | 6.5 | 293.15 | 12% PEG400, 80mM Li2SO4, and 50mM MES pH6.0 |
| 1 | LIPIDIC CUBIC PHASE | 6.5 | 293.15 | 12% PEG400, 80mM Li2SO4, and 50mM MES pH6.0 |






