4X9B
Crystal structure of Dscam1 isoform 4.44, N-terminal four Ig domains
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2014-09-21 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.979 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 88.902, 59.815, 89.560 |
Unit cell angles | 90.00, 109.06, 90.00 |
Refinement procedure
Resolution | 48.850 - 2.200 |
R-factor | 0.2087 |
Rwork | 0.207 |
R-free | 0.26120 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2v5m |
RMSD bond length | 0.005 |
RMSD bond angle | 1.025 |
Data reduction software | XDS |
Data scaling software | XSCALE |
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] | 2.200 |
Number of reflections | 45397 |
<I/σ(I)> | 11.3 |
Completeness [%] | 99.7 |
Redundancy | 4.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 289 | 0.1M HEPES pH 7.5, 0.1M Calcium Chloride, 30%(w/v) PEG 400 |