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1F4D

CRYSTAL STRUCTURE OF E. COLI THYMIDYLATE SYNTHASE C146S, L143C COVALENTLY MODIFIED AT C143 WITH N-[TOSYL-D-PROLINYL]AMINO-ETHANETHIOL

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeROTATING ANODE
Source detailsRIGAKU RUH3R
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1999-04-17
DetectorRIGAKU RAXIS IV
Spacegroup nameP 63
Unit cell lengths126.330, 126.330, 67.120
Unit cell angles90.00, 90.00, 120.00
Refinement procedure
Resolution10.000 - 2.150
R-factor0.196

*

Rwork0.196
R-free0.26700
RMSD bond length0.014
RMSD bond angle0.040
Data scaling softwared*TREK
Phasing softwareAMoRE
Refinement softwareREFMAC
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]10.0002.220
High resolution limit [Å]2.1502.150
Rmerge0.0810.286
Total number of observations78793

*

Number of reflections32045
<I/σ(I)>12.84.5
Completeness [%]96.792.1
Redundancy2.432.26
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

*

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

*

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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PDB entries from 2024-11-06

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