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5IMS

Saccharomyces cerevisiae acetohydroxyacid synthase

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAUSTRALIAN SYNCHROTRON BEAMLINE MX1
Synchrotron siteAustralian Synchrotron
BeamlineMX1
Temperature [K]100
Detector technologyCCD
Collection date2014-03-20
DetectorADSC QUANTUM 210r
Wavelength(s)0.9537
Spacegroup nameP 21 21 21
Unit cell lengths95.683, 110.180, 180.005
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution42.176 - 1.984
R-factor0.166
Rwork0.166
R-free0.19250
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)1jsc
RMSD bond length0.016
RMSD bond angle1.485
Data reduction softwareXDS
Data scaling softwareXDS
Phasing softwarePHENIX
Refinement softwarePHENIX (1.9_1692)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]47.8402.300
High resolution limit [Å]1.9802.000
Rmerge0.0750.645
Number of reflections130638
<I/σ(I)>112.1
Completeness [%]99.396
Redundancy5.4
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP5.827334 mg/ml enzyme incubated with 1.4 mM ThDP, 0.5 mM FAD, 14 mM MgCl2, and 4.5 mM DTT. Crystals were obtained my mixing equal volumes (1 ul) of well solution (14 % PEG 4000, 0.25-0.3 M potassium phosphate, 0.2 M ammonium acetate.) and enzyme solution

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