Lack of Evidence for a Role of Cys-138 as a Base Catalyst in the Skeletal Muscle 6-Phosphofructo-2-kinase Reaction

The role of Cys-138 in the catalysis of the skeletal muscle 6-phosphofructo-2-kinase reaction was investigated by mutating this residue to serine, glutamine and alanine, expressing the mutants in E. coli with a T7 RNA polymerase-based expression system, and analyzing their kinetic properties. The Cy...

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Veröffentlicht in:Biochemical and biophysical research communications 1993-08, Vol.195 (1), p.229-236
Hauptverfasser: Kurland, I.J., Elmaghrabi, M.R., Pilkis, S.J.
Format: Artikel
Sprache:eng
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Zusammenfassung:The role of Cys-138 in the catalysis of the skeletal muscle 6-phosphofructo-2-kinase reaction was investigated by mutating this residue to serine, glutamine and alanine, expressing the mutants in E. coli with a T7 RNA polymerase-based expression system, and analyzing their kinetic properties. The Cys138Ala mutant had greatly diminished activity, while the Cys138Ser and Cys138Gln mutants had maximal velocities 2-3 fold higher than the wild-type enzyme. It was concluded that Cys-138 does not act as a base catalyst in the kinase reaction, but that it plays a significant structural role in the enzyme′s active site.
ISSN:0006-291X
1090-2104
DOI:10.1006/bbrc.1993.2034