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1BEH

HUMAN PHOSPHATIDYLETHANOLAMINE BINDING PROTEIN IN COMPLEX WITH CACODYLATE

Experimental procedure
Source typeSYNCHROTRON
Source detailsSRS BEAMLINE PX7.2
Synchrotron siteSRS
BeamlinePX7.2
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1997-04-15
DetectorMARRESEARCH
Spacegroup nameP 1 21 1
Unit cell lengths45.430, 61.630, 67.920
Unit cell angles90.00, 101.09, 90.00
Refinement procedure
Resolution20.000 - 1.750
R-factor0.235

*

Rwork0.235
R-free0.28600
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1bd9
RMSD bond length0.009
RMSD bond angle0.025
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.760
High resolution limit [Å]1.7001.700
Rmerge0.0550.280
Number of reflections38803
<I/σ(I)>16.22.6
Completeness [%]95.694.9
Redundancy2.42.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1unknown

*

6.5PROTEIN WAS CRYSTALLIZED FROM 28-32% PEG 4000/6000/8000, 200-300 MM SODIUM ACETATE, 100MM SODIUM CACODYLATE., pH 6.5
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
111protein5 (mg/ml)can be replaced by 10mg/ml
211Bis-Tris5 (mM)
311sodium azide0.01 (%)
412PEG400028-32 (%)can be replaced by PEG6000 or PEG8000
512sodium acetate200-300 (mM)
612sodium azide0.01 (%)
712sodium cacodylate100 (mM)

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