4X9H
Crystal structure of Dscam1 isoform 8.4, 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 | 2014-07-12 |
Detector | DECTRIS PILATUS 2M |
Wavelength(s) | 1 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 95.222, 60.950, 92.351 |
Unit cell angles | 90.00, 93.56, 90.00 |
Refinement procedure
Resolution | 47.519 - 2.950 |
R-factor | 0.2744 |
Rwork | 0.272 |
R-free | 0.32350 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2v5m |
RMSD bond length | 0.004 |
RMSD bond angle | 1.007 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
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] | 2.950 |
Number of reflections | 22498 |
<I/σ(I)> | 14.1 |
Completeness [%] | 97.2 |
Redundancy | 2.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 289 | 0.1 M MES pH6.5, 20% (w/v) PEG 3350 |