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CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF THE TYROSINE PHOSPHATASE YOPH FROM YERSINIA PESTIS.

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date2000-11-05
DetectorMARRESEARCH
Spacegroup nameC 2 2 21
Unit cell lengths48.063, 120.651, 49.036
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution100.000 - 2.000
R-factor0.1921
Rwork0.189
R-free0.26000
Structure solution methodMIR
RMSD bond length0.007
RMSD bond angle5.200

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareSOLVE
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]100.0002.080
High resolution limit [Å]2.0002.010
Rmerge0.0720.340
Number of reflections8860
<I/σ(I)>15.33.6
Completeness [%]83.355

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Redundancy4.013.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

8

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293PEG4000, bicine, pH 9, VAPOR DIFFUSION, HANGING DROP, temperature 293K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirPEG600012 (%)
21reservoirTris-acetate100 (mM)or sodium-bicine

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