4XB7
Crystal structure of Dscam1 isoform 4.4, 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 41 21 2 |
Unit cell lengths | 100.212, 100.212, 351.761 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 50.106 - 4.004 |
R-factor | 0.2252 |
Rwork | 0.224 |
R-free | 0.25610 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2v5m |
RMSD bond length | 0.004 |
RMSD bond angle | 0.867 |
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] | 50.106 |
High resolution limit [Å] | 4.000 |
Number of reflections | 15793 |
<I/σ(I)> | 7.6 |
Completeness [%] | 99.9 |
Redundancy | 9.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 289 | 0.1M HEPES pH7.5, 0.5M Magnesium Chloride, 20% (w/v) PEG 3350 |