9G3C
Crystal Structure of the artificial protein METP in complex with cadmium ion at different temperatures. 200 K data collection
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ELETTRA BEAMLINE 11.2C |
Synchrotron site | ELETTRA |
Beamline | 11.2C |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2000-01-01 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.534 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 37.830, 56.655, 19.349 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 31.460 - 1.900 |
R-factor | 0.132 |
Rwork | 0.130 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.015 |
RMSD bond angle | 1.506 |
Data reduction software | XDS |
Phasing software | PHENIX |
Refinement software | PHENIX (1.21_5207) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 31.460 | 1.610 |
High resolution limit [Å] | 1.510 | 1.510 |
Rmerge | 0.077 | 0.367 |
Number of reflections | 13763 | 367 |
<I/σ(I)> | 8.21 | |
Completeness [%] | 96.3 | |
Redundancy | 1.9 | |
CC(1/2) | 0.991 | 0.806 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 298 | drop containing 2.0 μL of 1:1 (v/v) mixture of protein solution (10 mg/mL, 7 mM DTT, 4 mM CdCl2) and 2.0 μL of precipitant buffer (0.1 M HEPES at pH 7.5, 1.4 M sodium citrate tribasic dihydrate) was equilibrated against 0.5 mL reservoir of precipitant buffer |