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6OM8

Caenorhabditis Elegans UDP-Glucose Dehydrogenase in complex with UDP-Xylose

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 22-ID
Synchrotron siteAPS
Beamline22-ID
Temperature [K]80
Detector technologyCCD
Collection date2017-06-21
DetectorRAYONIX MX300HE
Wavelength(s)1.0
Spacegroup nameP 2 21 21
Unit cell lengths157.710, 168.170, 279.560
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution52.698 - 2.449
R-factor0.1937
Rwork0.194
R-free0.22040
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2o3j
RMSD bond length0.008
RMSD bond angle0.911
Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwarePHENIX
Refinement softwarePHENIX ((1.12_2829))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]52.6982.510
High resolution limit [Å]2.4492.449
Number of reflections26679119914
<I/σ(I)>9.1
Completeness [%]98.1
Redundancy6.295
CC(1/2)0.9960.455
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP29310 mg/mL C. Elegans UDP-Glucose Dehydrogenase Citric acid buffer pH 5.0 200mM Lithium Chloride 4% PEG 8000

217705

数据于2024-03-27公开中

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