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Crystal structure of SARS-CoV-2 main protease L50F/E166V mutant in complex with leritrelvir

This is a non-PDB format compatible entry.
Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRF BEAMLINE BL19U1
Synchrotron siteSSRF
BeamlineBL19U1
Temperature [K]100
Detector technologyPIXEL
Collection date2024-09-08
DetectorDECTRIS PILATUS3 6M
Wavelength(s)0.97923
Spacegroup nameP 1 21 1
Unit cell lengths48.464, 106.553, 54.133
Unit cell angles90.00, 103.02, 90.00
Refinement procedure
Resolution53.277 - 2.500
Rwork0.178
R-free0.24630
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.005
RMSD bond angle1.397
Data reduction softwareXDS (BUILT 20240630)
Data scaling softwareAimless (0.7.7)
Phasing softwarePHASER (2.8.3)
Refinement softwareREFMAC (5.8.0430)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]53.2802.600
High resolution limit [Å]2.5002.500
Rmerge0.1480.932
Number of reflections183731955
<I/σ(I)>10.91.7
Completeness [%]98.8
Redundancy6
CC(1/2)0.9950.390
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP2890.2 M Lithium sulfate monohydrate, 0.1 M TRIS hydrochloride pH 8.5, 30% w/v Polyethylene glycol 4,000

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