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7MMB

Crystal structure of HCV NS3/4A D168A protease in complex with NR01-127

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU MICROMAX-007 HF
Temperature [K]100
Detector technologyCCD
Collection date2010-07-11
DetectorRIGAKU SATURN 944
Wavelength(s)1.54178
Spacegroup nameP 21 21 21
Unit cell lengths54.316, 59.492, 58.731
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution23.840 - 1.990
R-factor0.1847
Rwork0.183
R-free0.22270
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)5voj
RMSD bond length0.007
RMSD bond angle1.050
Data scaling softwareHKL-3000 (703x)
Phasing softwarePHASER
Refinement softwarePHENIX (1.18.2_3874)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]23.8402.060
High resolution limit [Å]1.9901.990
Number of reflections135961309
<I/σ(I)>21.3
Completeness [%]99.8
Redundancy6.8
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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