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7MMK

Crystal structure of HCV NS3/4A D168A protease in complex with NR01-149

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU MICROMAX-007 HF
Temperature [K]100
Detector technologyCCD
Collection date2019-06-27
DetectorRIGAKU SATURN 944
Wavelength(s)1.54178
Spacegroup nameP 21 21 21
Unit cell lengths54.365, 58.604, 59.629
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution23.870 - 1.890
R-factor0.1645
Rwork0.162
R-free0.20820
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)5voj
RMSD bond length0.006
RMSD bond angle1.497
Data scaling softwareHKL-3000 (703x)
Phasing softwarePHASER
Refinement softwarePHENIX (1.18.2_3874)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]23.8702.010
High resolution limit [Å]1.8901.890
Rmerge0.354
Number of reflections15843659
<I/σ(I)>27.5
Completeness [%]99.6
Redundancy6.8
CC(1/2)0.919
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.5298100 mM MES Buffer pH 6.5, 4% (W/V) Ammonium Sulfate, 20-26% PEG 3350 cryogenic conditions is 100 mM MES Buffer pH 6.5, 4% (W/V) Ammonium Sulfate, 20-26% PEG 3350, 15% Ethylene glycol

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