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1F4E

CRYSTAL STRUCTURE OF E. COLI THYMIDYLATE SYNTHASE COMPLEXED WITH TOSYL-D-PROLINE

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RUH3R
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1999-06-10
DetectorRIGAKU RAXIS IV
Spacegroup nameI 21 3
Unit cell lengths131.880, 131.880, 131.880
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution10.000 - 1.900
R-factor0.192

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Rwork0.192
R-free0.23800
RMSD bond length0.011
RMSD bond angle0.031
Data scaling softwared*TREK
Phasing softwareAMoRE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]10.0001.970
High resolution limit [Å]1.9001.900
Rmerge0.0740.282

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Total number of observations202300

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Number of reflections31422
<I/σ(I)>19.73.8
Completeness [%]100.0

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100

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Redundancy6.42.8
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

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7293Perry, K.M., (1990) Proteins: Struct.,Funct., Genet., 8, 315.

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Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropthymidylate synthases2.5 (mg/ml)
21dropEDTA0.2 (mM)
31dropdithiothreitol1 (mM)
41droppotassium phosphate20 (mM)
51dropammonium sulfate1.15 (mM)
61reservoirammonium sulfate2.3 (M)
71reservoirEDTA0.2 (mM)
81reservoirdithiothreitol1 (mM)
91reservoirpotassium phisphate20 (mM)

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