4X8X
Crystal structure of Dscam1 isoform 1.9, N-terminal four Ig domains
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 19-ID |
Synchrotron site | APS |
Beamline | 19-ID |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2014-07-03 |
Detector | DECTRIS PILATUS 2M |
Wavelength(s) | 1 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 92.858, 59.806, 93.604 |
Unit cell angles | 90.00, 92.84, 90.00 |
Refinement procedure
Resolution | 46.744 - 2.500 |
R-factor | 0.212 |
Rwork | 0.211 |
R-free | 0.23720 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2v5m |
RMSD bond length | 0.004 |
RMSD bond angle | 0.792 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine: 1.8.4_1496)) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 50.000 |
High resolution limit [Å] | 2.500 |
Number of reflections | 35836 |
<I/σ(I)> | 18.5 |
Completeness [%] | 99.4 |
Redundancy | 4.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 289 | 0.1M Bistris pH 5.5, 0.1M Ammonium Acetate, 20% (w/v) PEG 10000 |