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2OAT

ORNITHINE AMINOTRANSFERASE COMPLEXED WITH 5-FLUOROMETHYLORNITHINE

Experimental procedure
Source typeSYNCHROTRON
Source detailsMPG/DESY, HAMBURG BEAMLINE BW6
Synchrotron siteMPG/DESY, HAMBURG
BeamlineBW6
Temperature [K]90
Detector technologyIMAGE PLATE
Collection date1996-11
DetectorMARRESEARCH
Spacegroup nameP 32 2 1
Unit cell lengths115.280, 115.280, 186.810
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution19.500

*

- 1.950
R-factor0.206
Rwork0.204
R-free0.23200
Structure solution methodDIFFERENCE FOURIER TECHNIQUES
Starting model (for MR)1oat
RMSD bond length0.013
RMSD bond angle1.950

*

Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]19.9001.980
High resolution limit [Å]1.9501.950
Rmerge0.076

*

0.297

*

Number of reflections101836
<I/σ(I)>12.53.4
Completeness [%]97.094
Redundancy3.2
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion, hanging drop

*

7.9(2S,5S)5FMORN-OAT WAS CO-CRYSTALLIZED FROM 6-10% PEG 6000, 1MM DTT, 120-160 MM NACL, 10-20% GLYCEROL, 50 MM TRICIN, PH 7.9.
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11reservoirPEG60006-10 (%(v/v))
21reservoir1,4-dithiothreitol1 (mM)
31reservoir120-160 (mM)
41reservoirTricin50 (mM)
51reservoirglycerol15-20 (%(v/v))

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