5TPH
Crystal structure of a de novo designed protein homodimer with curved beta-sheet
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 8.2.1 |
Synchrotron site | ALS |
Beamline | 8.2.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-07-09 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.97625 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 38.210, 32.790, 86.480 |
Unit cell angles | 90.00, 92.11, 90.00 |
Refinement procedure
Resolution | 43.210 - 2.470 |
R-factor | 0.2262 |
Rwork | 0.223 |
R-free | 0.25730 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.003 |
RMSD bond angle | 0.502 |
Data reduction software | iMOSFLM (7.1.0) |
Data scaling software | Aimless (0.2.8) |
Phasing software | PHASER (2.5.6) |
Refinement software | PHENIX (dev_1616) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 43.210 |
High resolution limit [Å] | 2.470 |
Number of reflections | 7955 |
<I/σ(I)> | 22.1 |
Completeness [%] | 99.9 |
Redundancy | 3.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 298 | 0.1 M potassium thiocyanate, pH 8 and 30% PEG MME 2000 |