9C9D
Protein receptor
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
| Synchrotron site | Australian Synchrotron |
| Beamline | MX2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2019-09-19 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.953731000423 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 83.292, 115.530, 92.404 |
| Unit cell angles | 90.00, 114.60, 90.00 |
Refinement procedure
| Resolution | 43.780 - 2.900 |
| R-factor | 0.1911 |
| Rwork | 0.190 |
| R-free | 0.21550 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.490 |
| Data reduction software | XDS |
| Data scaling software | XDS |
| Phasing software | PHENIX |
| Refinement software | PHENIX (1.20.1_4487) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 43.780 | 3.004 |
| High resolution limit [Å] | 2.900 | 2.900 |
| Number of reflections | 35257 | 3482 |
| <I/σ(I)> | 9.55 | |
| Completeness [%] | 99.7 | |
| Redundancy | 3.5 | |
| CC(1/2) | 0.994 | 0.574 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | EVAPORATION | 295 | PEG 8K, (NH4)2SO4, MES |






