4U7I
Structure of the complex of Spartin MIT and IST1 MIM
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-F |
Synchrotron site | APS |
Beamline | 21-ID-F |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-08-09 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.97828 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 46.257, 46.257, 115.620 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 29.610 - 1.794 |
R-factor | 0.1916 |
Rwork | 0.190 |
R-free | 0.22040 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2dl1 |
RMSD bond length | 0.006 |
RMSD bond angle | 0.942 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine: dev_1593)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 29.610 | |
High resolution limit [Å] | 1.790 | |
Rmerge | 0.081 | 0.584 |
Number of reflections | 12400 | |
<I/σ(I)> | 43 | 4 |
Completeness [%] | 99.6 | 100 |
Redundancy | 8.1 | 8.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.3 | 277 | 2.9 M Na-malonate |