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4R1B

Crystal Structure of 3D7 strain Plasmodium falciparum AMA1

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAUSTRALIAN SYNCHROTRON BEAMLINE MX2
Synchrotron siteAustralian Synchrotron
BeamlineMX2
Temperature [K]100
Detector technologyCCD
Collection date2013-11-30
DetectorADSC QUANTUM 315r
Wavelength(s)0.9537
Spacegroup nameC 1 2 1
Unit cell lengths74.920, 51.416, 87.567
Unit cell angles90.00, 114.30, 90.00
Refinement procedure
Resolution37.454 - 1.600
R-factor0.1833
Rwork0.182
R-free0.20880
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)PDB ID: 1Z40
RMSD bond length0.006
RMSD bond angle0.986
Data reduction softwareMOSFLM
Data scaling softwareSCALA
Phasing softwarePHASES
Refinement softwarePHENIX ((phenix.refine: 1.8.4_1496))
Data quality characteristics
 Overall
Low resolution limit [Å]41.070
High resolution limit [Å]1.600
Number of reflections40241
Completeness [%]100.0
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP629812-15% (v/v) polyethylene glycol 3350, 0.02 M MES and 10 mM manganese chloride. Crystals were dehydrated overnight in reservoir solution with increased (35%) (v/v) polyethylene glycol 3350 before cryo-stabilisation in 38% (v/v) polyethylene glycol 3350, 0.088 M MES (pH 6.0) and 44 mM manganese chloride for 6-8 h prior to data collection. MilliQ water was added to the stabilisation solution, VAPOR DIFFUSION, HANGING DROP, temperature 298K

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