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2DOR

DIHYDROOROTATE DEHYDROGENASE A FROM LACTOCOCCUS LACTIS COMPLEXED WITH OROTATE

Experimental procedure
Source typeROTATING ANODE
Source detailsRIGAKU RUH2R
Temperature [K]288
Detector technologyIMAGE PLATE
Collection date1995-11
DetectorRIGAKU RAXIS II
Spacegroup nameP 1 21 1
Unit cell lengths53.910, 109.030, 67.070
Unit cell angles90.00, 104.43, 90.00
Refinement procedure
Resolution25.000 - 2.000
R-factor0.161
Rwork0.161
R-free0.18700
Structure solution methodDIFFERENCE MAP
RMSD bond length0.011
RMSD bond angle23.813

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR (3.1)
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]25.0002.030
High resolution limit [Å]2.0002.000
Rmerge0.061

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0.250

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Total number of observations179226

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Number of reflections50309
<I/σ(I)>18.73.6
Completeness [%]99.390.5
Redundancy3.52.6
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

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8.5PROTEIN WAS CRYSTALLISED FROM A SOLUTION CONTAINING 30% PEG 6000, 0.2M SODIUM ACETATE AND 0.1M TRIS-HCL, PH 8.5.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirPEG600030 (%)
21reservoirsodium acetate0.2 (M)
31reservoirTris-HCl0.1 (M)pH8.5
41dropprotein18 (mg/ml)

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PDB entries from 2024-07-17

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