7C7C
Crystal structure of human TRAP1 with SJT104
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PAL/PLS BEAMLINE 5C (4A) |
Synchrotron site | PAL/PLS |
Beamline | 5C (4A) |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2019-03-22 |
Detector | DECTRIS EIGER X 9M |
Wavelength(s) | 0.9795 |
Spacegroup name | P 41 21 2 |
Unit cell lengths | 69.543, 69.543, 251.327 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 24.980 - 3.000 |
R-factor | 0.2356 |
Rwork | 0.232 |
R-free | 0.30300 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5y3n |
RMSD bond length | 0.002 |
RMSD bond angle | 0.403 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Refinement software | PHENIX (1.14_3260) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.050 |
High resolution limit [Å] | 3.000 | 3.000 |
Rmerge | 0.107 | 0.520 |
Number of reflections | 13023 | 13023 |
<I/σ(I)> | 17.7 | |
Completeness [%] | 98.8 | |
Redundancy | 9.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.76 | 293 | 0.1M Cacodylate pH 6.76, 0.1M Calcium acetate, 18% PEG 5000 MME |