8SXC
Crystal Structure of Fluorescent Protein Fusion Red 2
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 22-BM |
| Synchrotron site | APS |
| Beamline | 22-BM |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2019-11-08 |
| Detector | MARMOSAIC 300 mm CCD |
| Wavelength(s) | 1.0 |
| Spacegroup name | P 21 21 2 |
| Unit cell lengths | 71.155, 81.442, 42.539 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 27.310 - 1.500 |
| R-factor | 0.16253 |
| Rwork | 0.161 |
| R-free | 0.21927 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.017 |
| RMSD bond angle | 1.937 |
| Data reduction software | HKL-2000 |
| Data scaling software | SCALEPACK |
| Phasing software | MOLREP |
| Refinement software | REFMAC (5.8.0222) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 30.000 | 30.000 | 1.550 |
| High resolution limit [Å] | 1.500 | 3.230 | 1.500 |
| Rmerge | 0.085 | 0.074 | 0.907 |
| Rmeas | 0.092 | 0.080 | 1.011 |
| Rpim | 0.035 | 0.031 | 0.433 |
| Total number of observations | 267152 | ||
| Number of reflections | 39722 | 4218 | 3641 |
| <I/σ(I)> | 9.7 | ||
| Completeness [%] | 99.2 | 99.1 | 93 |
| Redundancy | 6.7 | 6.8 | 4.3 |
| CC(1/2) | 0.993 | 0.992 | 0.699 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 293 | 20% w/v PEG 6000, 1.0M LiCl, 0.1M HEPES, pH 7.0 |






