4X9G
Crystal structure of Dscam1 isoform 6.44, N-terminal four Ig domains
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BSRF BEAMLINE 3W1A |
Synchrotron site | BSRF |
Beamline | 3W1A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2014-07-12 |
Detector | MARRESEARCH |
Wavelength(s) | 1 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 193.639, 63.416, 90.073 |
Unit cell angles | 90.00, 99.94, 90.00 |
Refinement procedure
Resolution | 48.587 - 3.403 |
R-factor | 0.2518 |
Rwork | 0.248 |
R-free | 0.31720 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2v5m |
RMSD bond length | 0.004 |
RMSD bond angle | 0.812 |
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] | 3.400 |
Number of reflections | 14910 |
<I/σ(I)> | 8.3 |
Completeness [%] | 98.9 |
Redundancy | 3.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 289 | 0.1 M HEPES pH 7.5, 15% (w/v)PEG 3350 |