3Q29
Cyrstal structure of human alpha-synuclein (1-19) fused to maltose binding protein (MBP)
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 24-ID-C |
| Synchrotron site | APS |
| Beamline | 24-ID-C |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2010-04-26 |
| Detector | ADSC QUANTUM 315 |
| Wavelength(s) | 0.97938 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 68.390, 117.470, 146.490 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 34.532 - 2.300 |
| R-factor | 0.1945 |
| Rwork | 0.193 |
| R-free | 0.23180 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1anf |
| RMSD bond length | 0.004 |
| RMSD bond angle | 0.837 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHASER (2.1.4) |
| Refinement software | PHENIX (1.6.4_486) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 34.532 | 2.360 | |
| High resolution limit [Å] | 2.300 | 10.290 | 2.300 |
| Rmerge | 0.059 | 0.031 | 0.461 |
| Number of reflections | 53017 | 604 | 3883 |
| <I/σ(I)> | 16.32 | 33.2 | 3.3 |
| Completeness [%] | 99.6 | 87 | 100 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, HANGING DROP | 8 | 290 | 0.1M TRIS pH 8.0, 2.4 M AMMONIUM SULFATE, vapor diffusion, hanging drop, temperature 290K |






