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1C3K

CRYSTAL STRUCTURE OF HELIANTHUS TUBEROSUS LECTIN

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsEMBL/DESY, HAMBURG BEAMLINE BW7A
Synchrotron siteEMBL/DESY, HAMBURG
BeamlineBW7A
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1998-11-11
DetectorMARRESEARCH
Spacegroup nameI 4 2 2
Unit cell lengths104.927, 104.927, 63.751
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution15.000 - 2.000
R-factor0.2
Rwork0.200
R-free0.25500
RMSD bond length0.012
RMSD bond angle26.900

*

Data reduction softwareDENZO
Data scaling softwareCCP4 ((SCALA))
Phasing softwareAMoRE
Refinement softwareCNS
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0002.100
High resolution limit [Å]2.0002.000
Rmerge0.0770.233
Total number of observations86459

*

Number of reflections11028
<I/σ(I)>8.7
Completeness [%]90.792.3

*

Redundancy32.9
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION720

*

26-28% PEG MONOMETHYL ESTER 550, 0.2 M MAGNESIUM ACETATE, pH 7.0, VAPOR DIFFUSION, temperature 298K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein2.5 (mg/ml)
21dropHEPES10 (mM)
31drop150 (mM)
41dropEDTA3 (mM)
51dropP200.005 (%)
61reservoirmPEG55026-28 (%)
71reservoircalcium acetate0.2 (M)or magnesium acetate
81reservoirHEPES0.1 (M)

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