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2X0J

2.8 A RESOLUTION STRUCTURE OF MALATE DEHYDROGENASE FROM ARCHAEOGLOBUS FULGIDUS IN COMPLEX WITH ETHENO-NAD

Replaces:  1OJU
Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID14-2
Synchrotron siteESRF
BeamlineID14-2
Temperature [K]100
Detector technologyCCD
DetectorMARRESEARCH
Spacegroup nameP 41 21 2
Unit cell lengths112.990, 112.990, 70.600
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution35.731 - 2.786
R-factor0.167
Rwork0.164
R-free0.21650
Structure solution methodOTHER
RMSD bond length0.009
RMSD bond angle1.249
Data reduction softwareXDS
Data scaling softwareBIOMOL
Refinement softwarePHENIX ((PHENIX.REFINE))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]35.8002.890
High resolution limit [Å]2.7902.790
Rmerge0.0500.150
Number of reflections10861
<I/σ(I)>43.512.7
Completeness [%]90.971
Redundancy15.510.3
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
14INITIAL PROTEIN DROPLET: 22 MG/ML PROTEIN, 10 MM ETHENO-NAD RESERVOIR: 1.6 % (W/V) POLYETHYLENE GLYCOL 8000, 0.8 M LISO4 DROPLET: EQUAL VOLUMES OF INITIAL PROTEIN DROPLET AND RESERVOIR, pH 4.0

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