6FSQ
Structure of A3_bGFPD, an artificial bi-domain protein based on two different alphaRep domains : A3 and a GFP binding domain (bGFPD)
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID29 |
| Synchrotron site | ESRF |
| Beamline | ID29 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2015-12-11 |
| Detector | DECTRIS PILATUS 6M |
| Wavelength(s) | 0.970 |
| Spacegroup name | C 2 2 21 |
| Unit cell lengths | 66.940, 89.030, 143.610 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 44.510 - 2.790 |
| R-factor | 0.2088 |
| Rwork | 0.206 |
| R-free | 0.26980 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 3ltj |
| RMSD bond length | 0.010 |
| RMSD bond angle | 1.339 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | MOLREP |
| Refinement software | REFMAC (5.8.0158) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 47.869 | 47.869 | 2.960 |
| High resolution limit [Å] | 2.790 | 8.250 | 2.790 |
| Rmerge | 0.206 | 0.068 | 1.231 |
| Rmeas | 0.214 | 0.071 | 1.283 |
| Total number of observations | 139553 | ||
| Number of reflections | 10938 | 474 | 1680 |
| <I/σ(I)> | 12.95 | 38.8 | 2.08 |
| Completeness [%] | 99.6 | 99.4 | 98 |
| Redundancy | 12.759 | 11.812 | 12.521 |
| CC(1/2) | 0.997 | 0.999 | 0.897 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 293 | 1.6M Tri-sodium citrate |






