5J1I
Structure of the spectrin repeats 7, 8, and 9 of the plakin domain of plectin
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | ESRF BEAMLINE ID14-2 |
| Synchrotron site | ESRF |
| Beamline | ID14-2 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2009-12-10 |
| Detector | ADSC QUANTUM 4 |
| Wavelength(s) | 0.9330 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 75.240, 90.700, 154.540 |
| Unit cell angles | 90.00, 99.13, 90.00 |
Refinement procedure
| Resolution | 48.878 - 2.801 |
| R-factor | 0.2971 |
| Rwork | 0.296 |
| R-free | 0.32150 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 5j1g |
| RMSD bond length | 0.005 |
| RMSD bond angle | 0.761 |
| Data reduction software | XDS (November 3, 2014) |
| Data scaling software | XSCALE (November 3, 2014) |
| Phasing software | PHASER (2.3.0) |
| Refinement software | PHENIX (dev_2299) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 48.878 | 2.870 |
| High resolution limit [Å] | 2.800 | 2.800 |
| Rpim | 0.083 | 1.380 |
| Number of reflections | 14129 | |
| <I/σ(I)> | 17.2 | 1.7 |
| Completeness [%] | 55.7 | 11.4 |
| Redundancy | 7.5 | 6.2 |
| CC(1/2) | 1.000 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 8 | 298 | Protein solution at 12 mg/ml in 10 mM Tris-HCl (pH 7.5), 50 mM NaCl, 1 mM DTT was mixed with crystallization solution 0.1 M Bis-Tris-propane (pH 8.0), 16% PEG 3350, 0.3 M Na/K tartrate |






