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7KZ4

Crystal structure of Plasmodium falciparum dihydroorotate dehydrogenase bound with Inhibitor DSM705 (N-(1-(1H-1,2,4-triazol-3-yl)ethyl)-3-methyl-4-(1-(6-(trifluoromethyl)pyridin-3-yl)cyclopropyl)-1H-pyrrole-2-carboxamide)

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAPS BEAMLINE 19-ID
Synchrotron siteAPS
Beamline19-ID
Temperature [K]100
Detector technologyCCD
Collection date2018-08-08
DetectorADSC QUANTUM 315r
Wavelength(s)0.9724
Spacegroup nameP 1 21 1
Unit cell lengths51.914, 157.990, 63.152
Unit cell angles90.00, 107.01, 90.00
Refinement procedure
Resolution43.650 - 1.750
R-factor0.1727
Rwork0.172
R-free0.20650
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)3i65
RMSD bond length0.009
RMSD bond angle0.936
Data reduction softwareHKL-2000
Data scaling softwareHKL-2000
Phasing softwarePHASER
Refinement softwarePHENIX (1.18_3855)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]43.6501.780
High resolution limit [Å]1.7501.750
Rpim0.0390.565
Number of reflections908514351
<I/σ(I)>17.41.1
Completeness [%]93.589.1
Redundancy4.43.8
CC(1/2)0.700
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP8.829350 mM MgCl2, PEG4000 v/v 28%, 100 mM Tris-HCl, pH 8.8

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