6NWD
X-ray Crystallographic structure of Gloeobacter rhodopsin
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 23-ID-D |
| Synchrotron site | APS |
| Beamline | 23-ID-D |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2016-03-11 |
| Detector | DECTRIS PILATUS3 S 6M |
| Wavelength(s) | 1.0332 |
| Spacegroup name | C 2 2 21 |
| Unit cell lengths | 54.250, 129.250, 82.650 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 42.790 - 2.000 |
| Rwork | 0.230 |
| R-free | 0.24440 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3ddl |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | BALBES |
| Refinement software | PHENIX ((1.15.2_3472)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 42.790 | 2.072 |
| High resolution limit [Å] | 2.000 | 2.000 |
| Rmerge | 0.044 | 0.215 |
| Rmeas | 0.063 | 0.305 |
| Rpim | 0.044 | 0.215 |
| Number of reflections | 19500 | 19313 |
| <I/σ(I)> | 6.6 | |
| Completeness [%] | 96.4 | |
| Redundancy | 1.8 | |
| CC(1/2) | 0.997 | 0.891 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 3.4 | 307 | 2.6-2.8 M NaH2PO4, 1,6-hexanediol, triethylene glycol, zinc acetate, n-Octyl-beta-D-Glucoside |






