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5KJF

V222I horse liver alcohol dehydrogenase complexed with NAD+ and trifluoroethanol

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsALS BEAMLINE 4.2.2
Synchrotron siteALS
Beamline4.2.2
Temperature [K]100
Detector technologyCCD
Collection date2008-12-04
DetectorNOIR-1
Wavelength(s)0.827
Spacegroup nameP 1
Unit cell lengths44.200, 51.330, 92.530
Unit cell angles91.88, 103.06, 109.84
Refinement procedure
Resolution20.000 - 1.200
R-factor0.13302
Rwork0.133
R-free0.15312
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)5kjc
RMSD bond length0.014
RMSD bond angle1.792
Data reduction softwared*TREK
Data scaling softwared*TREK
Phasing softwareREFMAC
Refinement softwareREFMAC (5.8.0131)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]20.0001.240
High resolution limit [Å]1.2001.200
Rmerge0.0510.404
Number of reflections204334
<I/σ(I)>11.11.9
Completeness [%]88.364.6
Redundancy3.633.57
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1MICRODIALYSIS727850 MM AMMONIUM N-[TRIS(HYDROXYMETHYL) METHYL]-2-AMINOETHANE SULFONATE, PH 6.7 (AT 25 C), 0.25 MM EDTA, 10 MG/ML PROTEIN, 1 MM NAD+, 100 MM 2,2,2-TRIFLUOROETHANOL, 12 TO 25 % 2-METHYL-2,4-PENTANEDIOL

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