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1NFW

CRYSTAL STRUCTURE OF HUMAN COAGULATION FACTOR XA COMPLEXED WITH RPR209685

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-3
Synchrotron siteESRF
BeamlineID14-3
Temperature [K]100
Detector technologyCCD
Collection date1999-08-01
DetectorMARRESEARCH
Wavelength(s)0.933
Spacegroup nameP 21 21 21
Unit cell lengths55.950, 71.730, 78.960
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution20.000 - 2.100
R-factor0.2
Rwork0.200
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1ezq
RMSD bond length0.006
RMSD bond angle1.270
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareX-PLOR (98.0)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.000
High resolution limit [Å]2.100
Rmerge0.0580.147

*

Number of reflections18587
Completeness [%]96.998.4

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Redundancy2.3

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Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6

*

19

*

18-20% PEG 600, 50MM MES-NAOH,1MM RPR209685, pH 5.70 , VAPOR DIFFUSION, HANGING DROP, temperature 292 K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein8 (mg/ml)
21dropMES/NaOH5 (mM)pH6.0
31drop5 (mM)
41dropcompound 51000 (nM)
51reservoirPEG60018-20 (%)
61reservoirMES/NaOH50 (mM)pH5.7

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