9TP5
Crystal structure of the N-terminal Kelch domain of the Kelch phosphatase BSU1 from Arabidopsis thaliana
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | SLS BEAMLINE X06DA |
| Synchrotron site | SLS |
| Beamline | X06DA |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2019-03-02 |
| Detector | DECTRIS PILATUS 2M |
| Wavelength(s) | 0.999874 |
| Spacegroup name | P 43 21 2 |
| Unit cell lengths | 77.313, 77.313, 134.324 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 42.400 - 2.250 |
| R-factor | 0.2227 |
| Rwork | 0.222 |
| R-free | 0.24590 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.002 |
| RMSD bond angle | 0.488 |
| Data reduction software | XDS |
| Data scaling software | XSCALE |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.21.1_5286) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 42.400 | 2.390 |
| High resolution limit [Å] | 2.250 | 2.250 |
| Rmeas | 0.225 | 3.000 |
| Number of reflections | 36873 | 5942 |
| <I/σ(I)> | 12.72 | 1 |
| Completeness [%] | 100.0 | 100 |
| Redundancy | 13.9 | |
| CC(1/2) | 1.000 | 0.300 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 298 | 18 % [w/v] PEG 8,000, 5% [v/v] PEG 550 MME, 0.2 M sodium acetate trihydrate, 0.1 M sodium cacodylate trihydrate [pH 6.5] |






