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8H82

Crystal structure of SARS-CoV-2 main protease (Mpro) Mutant (E166V) in complex with protease inhibitor Nirmatrelvir

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I04
Synchrotron siteDiamond
BeamlineI04
Temperature [K]100
Detector technologyPIXEL
Collection date2022-08-10
DetectorDECTRIS EIGER2 X 16M
Wavelength(s)0.953740
Spacegroup nameP 21 21 2
Unit cell lengths45.951, 64.037, 105.284
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution27.890 - 1.930
R-factor0.1738
Rwork0.170
R-free0.21560
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)7vh8
Data reduction softwareautoPROC
Data scaling softwareXSCALE
Phasing softwarePHENIX
Refinement softwarePHENIX (1.19.2_4158)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]27.89027.8902.050
High resolution limit [Å]1.9305.6901.930
Rmerge0.1060.0420.654
Rmeas0.1110.0440.682
Total number of observations320663
Number of reflections2402510523773
<I/σ(I)>17.6551.143.48
Completeness [%]99.898.699.3
Redundancy13.34712.45312.579
CC(1/2)0.9990.9990.904
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1EVAPORATION2930.1 M Tris pH 7.6, 14% v/v ethylene glycol, 7% w/v PEG 8,000

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