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1A71

TERNARY COMPLEX OF AN ACTIVE SITE DOUBLE MUTANT OF HORSE LIVER ALCOHOL DEHYDROGENASE, PHE93=>TRP, VAL203=>ALA WITH NAD AND TRIFLUOROETHANOL

Experimental procedure
Source typeROTATING ANODE
Source detailsRIGAKU RUH2R
Temperature [K]100
Detector technologyIMAGE PLATE
Collection date1996-05
DetectorRIGAKU RAXIS II
Spacegroup nameP 1
Unit cell lengths50.600, 44.100, 92.600
Unit cell angles103.00, 87.90, 70.70
Refinement procedure
Resolution10.000 - 2.000
R-factor0.199
Rwork0.199
R-free0.28800
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)2ohx
RMSD bond length0.008
RMSD bond angle24.000

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Data reduction softwareDENZO
Data scaling softwareSCALEPACK
Phasing softwareX-PLOR (3.1)
Refinement softwareX-PLOR (3.1)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]50.0002.030
High resolution limit [Å]2.0002.000
Rmerge0.0710.340
Total number of observations77199

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Number of reflections38046
<I/σ(I)>7.52
Completeness [%]77.142.3
Redundancy1.71.7
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1Vapor diffusion

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8.44

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4MICROLITER HANGING DROPS TRIS PH 8.4 AT 4C, 5MM TRIFLUROETHANOL, 4% PEG400 EQUILIBRATED AGAINST WELLS CONTAINING 5MM TFE AND 18%PEG 400, vapor diffusion - hanging drop
Crystallization Reagents in Literatures
IDcrystal IDsolutionreagent nameconcentration (unit)details
11dropprotein13 (mg/ml)
21dropTris-HCl50 (mM)
31dropPEG4004 (%(v/v))
41dropNAD5 (mM)
51reservoirTris-HCl50 (mM)
61reservoirPEG40018 (%(v/v))

218196

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