7VA8
Crystal structure of MiCGT
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2020-11-15 |
Detector | PSI PILATUS 6M |
Wavelength(s) | 1.0 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 92.390, 104.680, 109.730 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 75.742 - 2.850 |
R-factor | 0.263633226401 |
Rwork | 0.262 |
R-free | 0.28641 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2vce |
RMSD bond length | 0.004 |
RMSD bond angle | 0.885 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692+SVN) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 75.750 | 2.920 |
High resolution limit [Å] | 2.850 | 2.850 |
Number of reflections | 25435 | 25435 |
<I/σ(I)> | 6.6 | |
Completeness [%] | 99.7 | |
Redundancy | 6.2 | |
CC(1/2) | 0.986 | 0.765 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 20% (v/v) PEG3350, 0.1 M Bis-Tris pH 6.5, 200 mM calcium acetate and 4% (v/v) formamide were |