7O5Q
Crystal Structure of a Class D Carbapenemase Complexed with Hydrolyzed Oxacillin
This is a non-PDB format compatible entry.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U1 |
Synchrotron site | SSRF |
Beamline | BL17U1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2020-06-26 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.979150 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 47.053, 126.902, 111.201 |
Unit cell angles | 90.00, 98.29, 90.00 |
Refinement procedure
Resolution | 19.807 - 1.850 |
Rwork | 0.173 |
R-free | 0.21110 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4s2p |
RMSD bond length | 0.010 |
RMSD bond angle | 1.631 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | MOLREP |
Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.810 | 1.880 |
High resolution limit [Å] | 1.850 | 1.850 |
Number of reflections | 109814 | 5493 |
<I/σ(I)> | 10 | 1.2 |
Completeness [%] | 99.9 | |
Redundancy | 6.9 | |
CC(1/2) | 0.997 | 0.725 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 291 | 0.1M HEPES pH 8.0, 10% PEG 8000, 10% 1-BUTANOL mixed with the 10 mg/mL protein stock at 1:1 ratio. |