6JBI
Structure of Tps1 apo structure
Experimental procedure
| Experimental method | SINGLE WAVELENGTH | 
| Source type | SYNCHROTRON | 
| Source details | SSRF BEAMLINE BL17U1 | 
| Synchrotron site | SSRF | 
| Beamline | BL17U1 | 
| Temperature [K] | 100 | 
| Detector technology | CCD | 
| Collection date | 2017-11-26 | 
| Detector | MARRESEARCH | 
| Wavelength(s) | 0.9791 | 
| Spacegroup name | P 21 21 2 | 
| Unit cell lengths | 99.130, 121.480, 93.030 | 
| Unit cell angles | 90.00, 90.00, 90.00 | 
Refinement procedure
| Resolution | 29.716 - 2.500 | 
| R-factor | 0.2291 | 
| Rwork | 0.226 | 
| R-free | 0.28380 | 
| Structure solution method | MOLECULAR REPLACEMENT | 
| Starting model (for MR) | 1uqt | 
| RMSD bond length | 0.007 | 
| RMSD bond angle | 1.150 | 
| Data reduction software | XDS | 
| Data scaling software | XDS | 
| Phasing software | PHASER | 
| Refinement software | PHENIX ((1.10.1_2155: ???)) | 
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 46.510 | 2.589 | 
| High resolution limit [Å] | 2.500 | 2.500 | 
| Rmerge | 0.071 | |
| Rpim | 0.020 | |
| Number of reflections | 38668 | 3843 | 
| <I/σ(I)> | 23.6 | |
| Completeness [%] | 97.7 | |
| Redundancy | 13.7 | |
| CC(1/2) | 1.000 | 0.859 | 
Crystallization Conditions
| crystal ID | method | pH | temperature | details | 
| 1 | VAPOR DIFFUSION, SITTING DROP | 8.9 | 289 | 0.2 M Ammonium sulfate, 0.1 M Tris-HCl, pH 8.9, 20% PEG 3350 | 











