5B3H
The crystal structure of the JACKDAW/IDD10 bound to the heterodimeric SHR-SCR complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SPRING-8 BEAMLINE BL41XU |
Synchrotron site | SPring-8 |
Beamline | BL41XU |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-07-04 |
Detector | RAYONIX MX225HE |
Wavelength(s) | 1.0000 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 57.668, 203.389, 88.451 |
Unit cell angles | 90.00, 90.46, 90.00 |
Refinement procedure
Resolution | 39.438 - 2.700 |
R-factor | 0.2096 |
Rwork | 0.208 |
R-free | 0.24620 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5b3g |
RMSD bond length | 0.008 |
RMSD bond angle | 0.968 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.750 |
High resolution limit [Å] | 2.700 | 2.700 |
Number of reflections | 54886 | |
<I/σ(I)> | 14.2 | |
Completeness [%] | 98.9 | |
Redundancy | 3.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8 | 293 | tris-HCl (pH 8.0) buffer, 8% w/v PEG 3350 |