10PW
Crystal structure of Glutathione Transferase from Shrimp Litopenaeus vannamei in complex with silver ions and a molecules of Glutathione binding in G-site and H-site
Replaces: 7SO8Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | APS BEAMLINE 19-BM |
| Synchrotron site | APS |
| Beamline | 19-BM |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2018-01-26 |
| Detector | ADSC QUANTUM 210r |
| Wavelength(s) | 0.9793 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 57.390, 93.020, 169.110 |
| Unit cell angles | 90.00, 90.75, 90.00 |
Refinement procedure
| Resolution | 56.370 - 2.200 |
| R-factor | 0.195 |
| Rwork | 0.192 |
| R-free | 0.24300 |
| Structure solution method | MOLECULAR REPLACEMENT |
| RMSD bond length | 0.010 |
| RMSD bond angle | 1.139 |
| Data reduction software | XDS |
| Data scaling software | SCALEPACK |
| Phasing software | PHASER |
| Refinement software | PHENIX ((1.18.2_3874)) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 56.370 | 2.280 |
| High resolution limit [Å] | 2.200 | 2.200 |
| Rmerge | 0.160 | 0.610 |
| Rmeas | 0.200 | 0.750 |
| Rpim | 0.110 | 0.420 |
| Number of reflections | 88718 | 8800 |
| <I/σ(I)> | 6.6 | 1.98 |
| Completeness [%] | 98.2 | 97.52 |
| Redundancy | 3.1 | 3.1 |
| CC(1/2) | 0.980 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | MICROBATCH | 6.5 | 277.15 | 100 MM AMMONIUM SULPHATE, 100 BIS-TRIS, PH 6.5, 30% PEG 3350, 300 UM SILVER NITRATE |






