6F8F
Co-crystal structure of SPOP MATH domain and human Pdx1 fragment
Experimental procedure
Experimental method | MAD |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID30B |
Synchrotron site | ESRF |
Beamline | ID30B |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-12-16 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.82655 |
Spacegroup name | P 65 2 2 |
Unit cell lengths | 53.925, 53.925, 207.410 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 19.940 - 2.000 |
R-factor | 0.21841 |
Rwork | 0.215 |
R-free | 0.27433 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3ivv |
RMSD bond length | 0.017 |
RMSD bond angle | 1.830 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | MOLREP |
Refinement software | REFMAC (5.8.0189) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 100.000 | 2.051 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.039 | |
Number of reflections | 13193 | |
<I/σ(I)> | 26.23 | |
Completeness [%] | 99.0 | |
Redundancy | 8.96 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7 | 277 | 0.1 M HEPES pH 6.5, 10% (w/v) PEG6000 (final pH 7.0) |