4UFB
Crystal structure of the Angiotensin-1 converting enzyme N-domain in complex with Lys-Pro
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I03 |
Synchrotron site | Diamond |
Beamline | I03 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2014-11-25 |
Detector | DECTRIS PILATUS 6M |
Spacegroup name | P 1 |
Unit cell lengths | 73.480, 101.590, 114.510 |
Unit cell angles | 85.46, 85.90, 81.62 |
Refinement procedure
Resolution | 113.940 - 1.800 |
R-factor | 0.20812 |
Rwork | 0.207 |
R-free | 0.23510 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3nxq |
RMSD bond length | 0.007 |
RMSD bond angle | 1.185 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0073) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.300 | 1.900 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.100 | 0.700 |
Number of reflections | 293868 | |
<I/σ(I)> | 6.2 | 1.5 |
Completeness [%] | 97.2 | 96 |
Redundancy | 3.2 | 3.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8.5 | 0.06 M DIVALENT CATIONS, 0.1 M TRIS/BICINE PH 8.5, 30 % PEG550MME/PEG20000 |