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2WDW

The Native Crystal Structure of the Primary Hexose Oxidase (Dbv29) in Antibiotic A40926 Biosynthesis

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSRRC BEAMLINE BL13C1
Synchrotron siteNSRRC
BeamlineBL13C1
Temperature [K]100
Detector technologyCCD
Collection date2007-10-25
DetectorADSC QUANTUM 210
Spacegroup nameP 61 2 2
Unit cell lengths66.092, 66.092, 790.462
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution29.540 - 3.210
R-factor0.24
Rwork0.237
R-free0.29100
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2ipi
RMSD bond length0.005
RMSD bond angle0.837
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwareMOLREP
Refinement softwareREFMAC (5.2.0019)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]30.0003.320
High resolution limit [Å]3.2103.210
Rmerge0.0800.160
Number of reflections17824
<I/σ(I)>24.817
Completeness [%]95.792
Redundancy9.79.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
16.5PROTEIN WAS CRYSTALLIZED FROM 30% PEG 550 MME, 0.05M CALCIUM CHLORIDE, 0.1M BIS TRIS, PH 6.5

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