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1AAX

CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B COMPLEXED WITH TWO BIS(PARA-PHOSPHOPHENYL)METHANE (BPPM) MOLECULES

Experimental procedure
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X9B
Synchrotron siteNSLS
BeamlineX9B
Temperature [K]140
Detector technologyIMAGE PLATE
Collection date1996-02
DetectorFUJI
Spacegroup nameP 31 2 1
Unit cell lengths88.369, 88.369, 104.532
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution22.000 - 1.900
R-factor0.182
Rwork0.182
Structure solution methodDIFFERENCE FOURIER
Starting model (for MR)2hnq
RMSD bond length0.009
RMSD bond angle1.850
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR (3.1)
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]22.0001.970
High resolution limit [Å]1.9001.900
Rmerge0.0520.267
Total number of observations138889

*

Number of reflections311972558

*

<I/σ(I)>24.72.9
Completeness [%]82.169.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

7.54

*

pH 7.5
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein5 (mg/ml)
101reservoirHEPES0.1 (mM)
111reservoirmagnesium acetate0.2 (M)
121reservoirPEG800012-14 (%(w/v))
21dropTris-HCl5 (mM)
31drop12.5 (mM)
41dropEDTA0.1 (mM)
51dropdithiothreitol1.5 (mM)
61dropBPPM1.7 (mM)
71dropHEPES0.05 (mM)
81dropmagnesium acetate0.1 (M)
91dropPEG80006-7 (%(w/v))

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PDB entries from 2024-05-15

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