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1PX7

A folding mutant of human class pi glutathione transferase, created by mutating aspartate 153 of the wild-type protein to glutamate

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RU200
Temperature [K]105
Detector technologyIMAGE PLATE
Collection date2001-04-05
DetectorMARRESEARCH
Wavelength(s)1.54179
Spacegroup nameC 1 2 1
Unit cell lengths77.750, 89.330, 68.790
Unit cell angles90.00, 97.88, 90.00
Refinement procedure
Resolution15.000 - 2.030
R-factor0.177
Rwork0.177
R-free0.21800
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)10gs
RMSD bond length0.011
RMSD bond angle1.500
Data scaling softwareSCALEPACK
Phasing softwareCNS
Refinement softwareCNS (1.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]15.0002.100
High resolution limit [Å]2.0302.030
Rmerge0.0860.377
Number of reflections29306
<I/σ(I)>12.42.2
Completeness [%]97.584.2
Redundancy2.5
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP5.6295MES, PEG 8000, CALCIUM CHLORIDE, DTT(DITHIOTHREITOL), GLUTATHIONE(REDUCED), pH 5.6, VAPOR DIFFUSION, HANGING DROP, temperature 295K

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