6WZA
Ni-bound structure of an engineered metal-dependent protein trimer, TriCyt1
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ALS BEAMLINE 5.0.2 |
| Synchrotron site | ALS |
| Beamline | 5.0.2 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2018-11-08 |
| Detector | DECTRIS PILATUS3 6M |
| Wavelength(s) | 1.239840 |
| Spacegroup name | P 31 2 1 |
| Unit cell lengths | 82.115, 82.115, 137.517 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 39.346 - 2.500 |
| R-factor | 0.2473 |
| Rwork | 0.241 |
| R-free | 0.30590 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 2bc5 |
| RMSD bond length | 0.009 |
| RMSD bond angle | 1.058 |
| Data reduction software | XDS |
| Data scaling software | Aimless |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.14_3260: ???)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 39.346 | 2.589 |
| High resolution limit [Å] | 2.500 | 2.500 |
| Rmerge | 0.142 | 0.688 |
| Rmeas | 0.145 | 0.706 |
| Rpim | 0.033 | 0.159 |
| Number of reflections | 19138 | 1865 |
| <I/σ(I)> | 18.23 | |
| Completeness [%] | 99.7 | |
| Redundancy | 19.2 | |
| CC(1/2) | 0.999 | 0.979 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 298 | 22.5% PEG 400, 0.2 M NaCl, 0.1 M HEPES (pH 7.5) |






