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1HWU

STRUCTURE OF PII PROTEIN FROM HERBASPIRILLUM SEROPEDICAE

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsLNLS BEAMLINE D03B-MX1
Synchrotron siteLNLS
BeamlineD03B-MX1
Temperature [K]120
Detector technologyIMAGE PLATE
Collection date1998-06-18
DetectorMARRESEARCH
Wavelength(s)1.38
Spacegroup nameP 21 21 21
Unit cell lengths78.410, 82.320, 100.950
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution13.000 - 2.100
Rwork0.203
R-free0.27200
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2pii
RMSD bond length0.018
RMSD bond angle0.044
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]13.0002.150
High resolution limit [Å]2.1002.100
Rmerge0.0570.322
Number of reflections365232415

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Completeness [%]94.0

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95

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Redundancy3.

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Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP8

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291Sodium Cacodylate, Magnesium Acetate, Methylpentadiol, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 291K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein13 (mg/ml)
21dropTris-HCl10 (mM)pH8.0
31drop50 (mM)
41dropglycerol20 (%)
51dropEDTA0.1 (mM)
61reservoirMPD30 (%)
71reservoirsodium cacodylate0.1 (mM)pH6.5
81reservoirmagnesium acetate0.2 (mM)

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