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 |
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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. |
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ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1006/bbrc.1993.2034 |