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 |