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1A1Q

HEPATITIS C VIRUS NS3 PROTEINASE

Experimental procedure
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-3
Synchrotron siteESRF
BeamlineID14-3
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1995-11
DetectorMARRESEARCH
Spacegroup nameH 3 2
Unit cell lengths133.000, 133.000, 223.000
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution8.000 - 2.400
R-factor0.225
Rwork0.225
R-free0.32000
Structure solution methodHEAVY ATOMS: ISOMORPHOUS + ANOMALOUS SIGNALS
RMSD bond length0.020
RMSD bond angle28.000

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwarePHASES
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.500
High resolution limit [Å]2.4002.400
Rmerge0.079

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Total number of observations96285

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Number of reflections30000
<I/σ(I)>104
Completeness [%]98.098
Redundancy33
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

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6.54

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VAPOR DIFFUSION. PROTEIN MIXED WITH WELL SOLUTION OF: 3.5M NACL, 150MM TRIS-HCL (PH 6.0), 5% PEG400., pH 6.5
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein5 (mg/ml)
21dropsodium acetate25 (mM)
31dropdithiothreitol5 (mM)
41drop1.9 (M)
51dropPEG4002.5 (%)
61dropTris-HCl75 (mM)
71reservoirPEG4005 (%)
81reservoir3.5 (M)
91reservoirTris-HCl150 (mM)

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