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1V7N

Human Thrombopoietin Functional Domain Complexed To Neutralizing Antibody TN1 Fab

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsPHOTON FACTORY BEAMLINE BL-6B
Synchrotron sitePhoton Factory
BeamlineBL-6B
Temperature [K]100
Detector technologyDIFFRACTOMETER
Collection date1998-12-01
DetectorWEISSENBERG
Wavelength(s)1.0
Spacegroup nameP 1 21 1
Unit cell lengths133.038, 46.582, 191.359
Unit cell angles90.00, 90.28, 90.00
Refinement procedure
Resolution15.000

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- 3.300
R-factor0.17405
Rwork0.167
R-free0.29200

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Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1iai
RMSD bond length0.028
RMSD bond angle2.800

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareREFMAC (5.1.19)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]60.0003.420
High resolution limit [Å]3.3003.300
Rmerge0.098

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0.214

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Total number of observations74809

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Number of reflections35598
<I/σ(I)>31.1
Completeness [%]98.097
Redundancy1.61.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP7

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295

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Kuroki, R., (2002) Acta Crystallogr.,Sect.D, 58, 856.

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Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein18-20 (mg/ml)
21dropimidazole20 (mM)pH7.0
31reservoirPEG335019-21 (%(w/v))
41reservoirpotassium phosphate100 (mM)pH6.0

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PDB entries from 2024-05-15

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