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7VAH

The crystal structure of COVID-19 main protease in H41A mutation

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSSRF BEAMLINE BL19U1
Synchrotron siteSSRF
BeamlineBL19U1
Temperature [K]100
Detector technologyPIXEL
Collection date2020-05-04
DetectorDECTRIS PILATUS3 6M
Wavelength(s)0.978530
Spacegroup nameC 1 2 1
Unit cell lengths98.201, 83.048, 51.597
Unit cell angles90.00, 115.58, 90.00
Refinement procedure
Resolution42.542 - 1.491
R-factor0.1944
Rwork0.193
R-free0.21660
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)6lu7
Data reduction softwareXDS
Data scaling softwareXSCALE
Phasing softwarePHASER
Refinement softwarePHENIX (1.14_3260)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]42.54242.5421.530
High resolution limit [Å]1.4906.6701.490
Rmerge0.0370.0220.915
Rmeas0.0410.0240.994
Total number of observations396268
Number of reflections601337024053
<I/σ(I)>21.6264.742.09
Completeness [%]98.897.890.3
Redundancy6.596.7156.46
CC(1/2)1.0000.9990.800
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1EVAPORATION62932% polyethylene glycol (PEG) 6000, 3% DMSO, 1mM DTT, 0.1M MES buffer (pH 6.0), protein concentration 5mg/ml

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