3CO1
Crystal structure of microtubule binding domain of human EB3
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2007-11-25 |
Detector | PSI PILATUS 6M |
Wavelength(s) | 1.0090 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 47.188, 85.365, 32.161 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 42.680 - 1.400 |
R-factor | 0.20161 |
Rwork | 0.200 |
R-free | 0.23355 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1pa7 |
RMSD bond length | 0.008 |
RMSD bond angle | 1.067 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.450 |
High resolution limit [Å] | 1.400 | 1.400 |
Number of reflections | 25525 | |
<I/σ(I)> | 10.85 | |
Completeness [%] | 96.9 | 92.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.4 | 298 | 0.04M potassium phosphate, 16% PEG 8000, 20% glycerol anhydrous, pH 7.4, VAPOR DIFFUSION, SITTING DROP, temperature 298K |