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6T9D

Crystal structure of a bispecific DutaFab in complex with human VEGF121

This is a non-PDB format compatible entry.
Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsMAX II BEAMLINE I911-3
Synchrotron siteMAX II
BeamlineI911-3
Temperature [K]100
Detector technologyCCD
Collection date2014-11-11
DetectorMARMOSAIC 225 mm CCD
Wavelength(s)1.0000
Spacegroup nameP 1 21 1
Unit cell lengths70.080, 107.875, 87.369
Unit cell angles90.00, 95.34, 90.00
Refinement procedure
Resolution29.294 - 2.905
Rwork0.212
R-free0.28010
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1bj1 1jps
RMSD bond length0.007
RMSD bond angle1.525
Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwarePHASER
Refinement softwareREFMAC (5.8.0257)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0003.100
High resolution limit [Å]2.9002.900
Rmerge0.2120.842
Number of reflections283184494
<I/σ(I)>6.71.5
Completeness [%]98.998.2
Redundancy33
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP6.5293VEGFA-121 from Peprotech, catalogue number 100-20A, was mixed at a 1:1 molar ratio to VEGF monomer. The complex was concentrated to 11 mg/ml. Crystallization involved hanging drop vapour diffusion against 0.1 M MES pH 6.5 and 1.6 M magnesium sulphate. Crystals grew in about 120 days and were frozen in liquid nitrogen with 20 % glycerol as cryoprotectant.

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