3LC8
Crystal structure of the cytoplasmic tail of (pro)renin receptor as a MBP fusion (Maltose-free form)
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-G |
Synchrotron site | APS |
Beamline | 21-ID-G |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2007-01-01 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 0.98 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 47.780, 112.700, 175.110 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 29.745 - 2.000 |
R-factor | 0.19732 |
Rwork | 0.195 |
R-free | 0.25741 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1jw4 |
RMSD bond length | 0.023 |
RMSD bond angle | 1.813 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | AMoRE |
Refinement software | REFMAC (5.5.0102) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 29.745 | 2.070 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.086 | 0.529 |
Number of reflections | 63627 | |
<I/σ(I)> | 15.15 | 4 |
Completeness [%] | 97.8 | 98.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 8.5 | 293 | 20% PEG 4000, 0.2M Magnesium Chloride, 0.1M Tris, pH 8.5, EVAPORATION, temperature 293K |