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6C3S

AMYLOID FORMING PEPTIDE YTIAAL FROM TRANSTHYRETIN

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID13
Synchrotron siteESRF
BeamlineID13
Temperature [K]100
Detector technologyCCD
Collection date2007-07-13
DetectorMARRESEARCH
Wavelength(s)0.895432
Spacegroup nameI 2 2 2
Unit cell lengths18.746, 9.578, 44.796
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution22.398 - 1.602
R-factor0.2036
Rwork0.200
R-free0.24400
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)Ideal beta strand
RMSD bond length0.007
RMSD bond angle0.896
Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwarePHASER
Refinement softwarePHENIX (dev_1555)
Data quality characteristics
 OverallInner shellOuter shell
Low resolution limit [Å]90.00090.0001.720
High resolution limit [Å]1.6002.7401.600
Rmerge0.1030.0680.318
Total number of observations3501
Number of reflections625139112
<I/σ(I)>9.6
Completeness [%]98.995.999.1
Redundancy5.65.45.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP5.5298YTIAAL crystals were grown from a solution containing 10mg/mL peptide. The reservoir contained 100mM Bis-Tris pH 5.5 and 3 M sodium chloride. Crystals were soaked on 25% Glycerol, prior to diffraction

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