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7MMD

Crystal structure of HCV NS3/4A D168A protease in complex with JZ01-19

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU MICROMAX-007 HF
Temperature [K]100
Detector technologyCCD
Collection date2019-07-11
DetectorRIGAKU SATURN 944
Wavelength(s)1.54178
Spacegroup nameP 21 21 21
Unit cell lengths55.151, 58.700, 59.858
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution23.780 - 1.890
R-factor0.1614
Rwork0.160
R-free0.19820
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)5voj
RMSD bond length0.006
RMSD bond angle1.250
Data scaling softwareHKL-3000 (703x)
Phasing softwarePHASER
Refinement softwarePHENIX (1.19.1_4122)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]23.7801.958
High resolution limit [Å]1.8901.890
Number of reflections138361414
<I/σ(I)>12.13
Completeness [%]85.9
Redundancy4
CC(1/2)0.9970.917
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.5298100 mM MES Buffer pH 6.5, 4% (W/V) Ammonium Sulfate, 20-26% PEG 3350 The cryogenic condition is 100 mM MES Buffer pH 6.5, 4% (W/V) Ammonium Sulfate, 20-26% PEG 3350, 15% Ethylene glycol

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