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1J3I

Wild-type Plasmodium falciparum dihydrofolate reductase-thymidylate synthase (PfDHFR-TS) complexed with WR99210, NADPH, and dUMP

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-1
Synchrotron siteESRF
BeamlineID14-1
Temperature [K]100
Detector technologyCCD
DetectorADSC
Wavelength(s)0.934
Spacegroup nameP 21 21 21
Unit cell lengths59.117, 157.249, 165.443
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution29.400 - 2.330
R-factor0.187
Rwork0.185
R-free0.23600
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.013
RMSD bond angle23.400

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareAMoRE
Refinement softwareCNS (1.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]33.0002.430
High resolution limit [Å]2.3302.330
Rmerge0.057

*

0.313

*

Total number of observations653647

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Number of reflections64441
<I/σ(I)>10.4
Completeness [%]97.989
Redundancy10.1
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Batch method

*

4.6298PEG 4000, ammonium acetate, sodium acetate, pH 4.6, microbatch under oil, temperature 298K
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
111enzyme10 (mg/ml)
211sodium acetate0.1 (mM)pH4.6
311PEG400025 (%(w/v))
411ammonium acetate0.2 (M)

219869

PDB entries from 2024-05-15

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