2X3X
structure of mouse syndapin I (crystal form 1)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.1 |
Synchrotron site | BESSY |
Beamline | 14.1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-08-15 |
Detector | MARMOSAIC 225 mm CCD |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 83.077, 154.545, 255.808 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 73.130 - 3.350 |
R-factor | 0.2234 |
Rwork | 0.221 |
R-free | 0.27701 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.007 |
RMSD bond angle | 0.972 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | REFMAC (5.3.0040) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 73.170 | 3.450 |
High resolution limit [Å] | 3.350 | 3.350 |
Rmerge | 0.120 | 0.860 |
Number of reflections | 23772 | |
<I/σ(I)> | 14.97 | 2.62 |
Completeness [%] | 98.3 | 99.1 |
Redundancy | 6.11 | 6.16 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 5.3 | 2.5UL SYNDAPIN (5MG/ML IN 50MM HEPES, 50MM NACL) MIXED WITH 0.5UL 0.3M GLYCYL-GLYCYL-GLYCINE AND 2UL WELL SOLUTION 0.1M NAAC/HAC PH5.3, 3%(W/V) PEG4000. |