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1A94

STRUCTURAL BASIS FOR SPECIFICITY OF RETROVIRAL PROTEASES

Experimental procedure
Source typeROTATING ANODE
Source detailsRIGAKU RUH2R
Temperature [K]293
Detector technologyIMAGE PLATE
Collection date1996-11
DetectorRIGAKU
Spacegroup nameP 1 1 21
Unit cell lengths59.610, 51.940, 61.700
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution8.000 - 2.000
R-factor0.182
Rwork0.182
R-free0.28100
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.014
RMSD bond angle27.070

*

Data reduction softwareR-AXIS
Data scaling softwareR-AXIS
Phasing softwareAMoRE
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]8.0002.250
High resolution limit [Å]2.0002.000
Rmerge0.0830.083
Number of reflections20944
<I/σ(I)>2
Completeness [%]86.176.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

4.7pH 4.7
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropHIV-1 protease5.8 (mg/ml)
21dropsodium acetate20 (mM)
31dropdithiothreitol5 (mM)
41dropinhibitor5-fold molar excess
51reservoirsodium citrate66 (mM)
61reservoirsodium phosphate132 (mM)
71reservoirdithiothreitol10 (mM)
81reservoirDMSO10 (%)
91reservoirammonium sulfate45 (%sat)

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