7YJC
Crystal structure of Human HPSE1 in complex with inhibitor
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2017-12-11 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.99998 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 44.610, 71.200, 78.719 |
Unit cell angles | 90.00, 98.01, 90.00 |
Refinement procedure
Resolution | 77.950 - 2.300 |
R-factor | 0.27633 |
Rwork | 0.273 |
R-free | 0.33932 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5e8m |
RMSD bond length | 0.012 |
RMSD bond angle | 1.559 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | MOLREP |
Refinement software | REFMAC (5.8.0218) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 77.950 | 2.420 |
High resolution limit [Å] | 2.300 | 2.300 |
Number of reflections | 21509 | 3121 |
<I/σ(I)> | 8.7 | |
Completeness [%] | 98.7 | |
Redundancy | 5.6 | |
CC(1/2) | 0.993 | 0.500 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 6.3 | 293 | 20% w/v Polyethylene glycol 3,350, 200 mM Ammonium chloride; pH 6.3 |