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5C1C

Crystal Structure of the Pectin Methylesterase from Aspergillus niger in Deglycosylated Form

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU MICROMAX-007
Temperature [K]123
Detector technologyIMAGE PLATE
Collection date2013-10-23
DetectorRIGAKU RAXIS IV++
Wavelength(s)1.5418
Spacegroup nameC 2 2 21
Unit cell lengths75.249, 113.843, 88.741
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution36.230 - 1.800
R-factor0.172
Rwork0.170
R-free0.20330
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1xg2
RMSD bond length0.007
RMSD bond angle1.258
Data reduction softwareCrystalClear
Data scaling softwared*TREK
Phasing softwareMrBUMP
Refinement softwareREFMAC (5.8.0073)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]36.2301.860
High resolution limit [Å]1.8001.800
Rmerge0.0750.313
Number of reflections34221
<I/σ(I)>5.23.7
Completeness [%]95.791.4
Redundancy3.793.75
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP4.1294Protein (6.5 mg/mL) in 50-100 mM acetate buffer mixed 1:1 with 1.8 M ammonium sulfate, 100 mM sodium acetate, pH 4.1

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