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1MTB

Viability of a drug-resistant HIV-1 protease mutant: structural insights for better antiviral therapy

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU
Temperature [K]298
Detector technologyIMAGE PLATE
Collection date2001-08-08
DetectorRIGAKU RAXIS IV
Wavelength(s)1.5418
Spacegroup nameP 21 21 21
Unit cell lengths51.439, 60.039, 62.021
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution26.560 - 2.500
R-factor0.191
Rwork0.191
R-free0.25700
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)1f7a
RMSD bond length0.008
RMSD bond angle26.500

*

Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]26.6002.590
High resolution limit [Å]2.5002.500
Rmerge0.080

*

0.360

*

Total number of observations28072

*

Number of reflections6743496

*

<I/σ(I)>7
Completeness [%]93.471
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.2298sodium phosphate, sodium citrate, ammonium sulphate, pH 6.2, VAPOR DIFFUSION, HANGING DROP at 298K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein2.5 (mg/ml)
21reservoirphosphate126 (mM)pH6.2
31reservoirsodium citrate63 (mM)
41reservoirammonium sulfate28-31 (%)

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