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4MAP

Crystal structure of Ara h 8 purified with heating

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-BM
Synchrotron siteAPS
Beamline19-BM
Temperature [K]100
Detector technologyCCD
Collection date2012-11-09
DetectorADSC QUANTUM 210r
Wavelength(s)0.98
Spacegroup nameP 1 21 1
Unit cell lengths40.922, 87.113, 42.863
Unit cell angles90.00, 96.74, 90.00
Refinement procedure
Resolution30.460 - 1.900
R-factor0.20001
Rwork0.197
R-free0.25226
Structure solution methodFOURIER SYNTHESIS
Starting model (for MR)4m9b
RMSD bond length0.017
RMSD bond angle1.891
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareHKL-3000
Refinement softwareREFMAC (5.7.0029)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0001.930
High resolution limit [Å]1.9001.900
Rmerge0.0480.360
Number of reflections23735
<I/σ(I)>29.42.75
Completeness [%]99.699.8
Redundancy3.13
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP82930.1 M Tris (8.0), 0.2 M Lithium sulfate, 34% (w/v) PEG 4000, VAPOR DIFFUSION, HANGING DROP, temperature 293K

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