6LXR
TvCyP2 in apo form 4
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSRRC BEAMLINE BL13C1 |
Synchrotron site | NSRRC |
Beamline | BL13C1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2018-05-28 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.97622 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 52.079, 54.539, 59.671 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 26.170 - 2.560 |
R-factor | 0.1741 |
Rwork | 0.168 |
R-free | 0.23080 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5yba |
RMSD bond length | 0.008 |
RMSD bond angle | 0.874 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.13_2998) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 26.170 | 2.653 |
High resolution limit [Å] | 2.560 | 2.561 |
Number of reflections | 5340 | 293 |
<I/σ(I)> | 18.5 | 3.2 |
Completeness [%] | 99.9 | 100 |
Redundancy | 6.6 | |
CC(1/2) | 0.978 | 0.918 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7 | 283 | 1.0 M Sodium citrate, 0.2 M Sodium chloride, 0.1 M Tris pH 7.0 |