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4MNS

Crystal structure of the major pollen allergen Bet v 1-A in complex with P303

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsSOLEIL BEAMLINE PROXIMA 1
Synchrotron siteSOLEIL
BeamlinePROXIMA 1
Temperature [K]100
Wavelength(s)0.9334
Spacegroup nameP 21 21 21
Unit cell lengths39.928, 58.577, 58.767
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution30.000 - 1.200
R-factor0.13275
Rwork0.131
R-free0.15969
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1fsk
RMSD bond length0.010
RMSD bond angle1.473
Data reduction softwareXDS
Data scaling softwareSCALA
Phasing softwareAMoRE
Refinement softwareREFMAC (5.7.0032)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]40.0001.260
High resolution limit [Å]1.2001.200
Rmerge0.0370.297
Number of reflections41699
<I/σ(I)>20.32.6
Completeness [%]100.0100
Redundancy3.51.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP4.629328% PEG MME 2000, 20mM ammonium sulfate, 0.1M sodium acetate, pH 4.6, VAPOR DIFFUSION, HANGING DROP, temperature 293K

220113

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