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9MI2

Crystal structure of Purine nucleoside phosphorylase from Trichomonas vaginalis (C2 form)

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsNSLS-II BEAMLINE 19-ID
Synchrotron siteNSLS-II
Beamline19-ID
Temperature [K]100
Detector technologyPIXEL
Collection date2024-10-26
DetectorDECTRIS EIGER2 XE 9M
Wavelength(s)0.9786
Spacegroup nameC 1 2 1
Unit cell lengths170.269, 50.364, 175.485
Unit cell angles90.00, 98.82, 90.00
Refinement procedure
Resolution48.250 - 1.800
R-factor0.1654
Rwork0.164
R-free0.19740
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.009
RMSD bond angle0.999
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwarePHASER
Refinement softwarePHENIX (dev_5533)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]48.2501.830
High resolution limit [Å]1.8001.800
Rmerge0.1020.872
Rmeas0.1130.968
Rpim0.0500.416
Total number of observations70587835407
Number of reflections1368836707
<I/σ(I)>91.8
Completeness [%]99.9
Redundancy5.25.3
CC(1/2)0.9960.740
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP4.2291Berkeley C8: 20% (w/v) PEG 3350, 100 mM magnesium chloride, 100 mM NaCl, TrvaA.01033.d.B1.PW39308 at 17.4 mg/mL. plate 14462 well C8 drop 1, Puck: PSL1411. Cryo: 20% Glycerol + 80% crystallant

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