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2AXM

HEPARIN-LINKED BIOLOGICALLY-ACTIVE DIMER OF FIBROBLAST GROWTH FACTOR

Experimental procedure
Source typeSYNCHROTRON
Source detailsNSLS BEAMLINE X4A
Synchrotron siteNSLS
BeamlineX4A
Temperature [K]110
Detector technologyIMAGE PLATE
Collection date1994-08-08
DetectorFUJI
Spacegroup nameP 61 2 2
Unit cell lengths91.100, 91.100, 193.900
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution13.000 - 3.000
R-factor0.218
Rwork0.218
R-free0.30700
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1axm
RMSD bond length0.013
RMSD bond angle27.100

*

Data reduction softwareDENZO
Data scaling softwareCCP4 ((AGROVATA)
Phasing softwareX-PLOR (3.1)
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0003.120
High resolution limit [Å]3.0003.000
Rmerge0.1830.487
Number of reflections9682
<I/σ(I)>3.31.5
Completeness [%]99.799.7
Redundancy10.79.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

720

*

PROTEIN/HEPARIN COMPLEX WAS CRYSTALLIZED FROM 25% PEG 8000, 200 MM MGSO4, 100 MM HEPES, PH 7.0; CRYSTAL WAS SOAKED IN 22% XYLITOL PRIOR TO DATA COLLECTION.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein20 (mg/ml)
21reservoirPEG800020 (%)
31reservoir200 (mM)
41reservoirHEPES100 (mM)pH7.0

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