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2TNF

1.4 A RESOLUTION STRUCTURE OF MOUSE TUMOR NECROSIS FACTOR, TOWARDS MODULATION OF ITS SELECTIVITY AND TRIMERISATION

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE BW7B
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineBW7B
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1997-06-15
DetectorMARRESEARCH
Spacegroup nameP 1
Unit cell lengths48.214, 48.300, 51.095
Unit cell angles114.81, 103.65, 91.05
Refinement procedure
Resolution8.000 - 1.400
R-factor0.201
Rwork0.201
R-free0.23500
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1tnf
RMSD bond length0.010
RMSD bond angle1.600
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR
Refinement softwareX-PLOR (3.843)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.500
High resolution limit [Å]1.4001.400
Rmerge0.0290.148
Total number of observations128698

*

Number of reflections72552
<I/σ(I)>195.7
Completeness [%]90.985.5
Redundancy1.81.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, sitting drop

*

6.8

*

277

*

EQUAL VOLUMES OF RESERVOIR SOLUTION, CONTAINING 7 % ISOPROP, pH 8.5
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoir2-propanol7 (%)
21reservoirPEGME200030 (%)
31reservoirTris-HCl0.1 (M)
41drop0.5 (%)
51dropprotain11 (mg/ml)
61dropHEPES10 (mM)

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