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1AXM

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 date1995-02-04
DetectorFUJI
Spacegroup nameC 2 2 21
Unit cell lengths87.690, 158.050, 190.580
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution14.000 - 3.000
R-factor0.217
Rwork0.217
R-free0.30400
Structure solution methodMAD
Starting model (for MR)PDB ENTRIES 1AFC 1hpn
RMSD bond length0.014
RMSD bond angle26.700

*

Data reduction softwareDENZO
Data scaling softwareCCP4 ((AGROVATA)
Phasing softwareMADSYS
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0003.080
High resolution limit [Å]3.0003.000
Rmerge0.0950.337
Number of reflections25115
<I/σ(I)>5.22.2
Completeness [%]94.186.9
Redundancy3.92.9
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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