Abstract
A gene named stp1+, coding for a 17.5-kDa protein, that rescues cdc25-22 when overexpressed, has been previously isolated from fission yeast. Here we describe the expression and purification of Stp1 protein as a fusion with the glutathione S-transferase in E. coli and its kinetic characterisation. Stp1 deduced protein sequence shows an high homology to members of a class of cytosolic low M(r) protein phosphatase previously known to exist only in mammalian species. Stp1 has a kinetic behaviour that appears to be intermediate with respect to the two isoenzymatic forms of low M(r) protein tyrosine phosphatases present in mammalian tissues. These differing kinetic characteristics are mainly due to the sequence 45-56 that is spatially close to the active site pocket.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Base Sequence
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Binding Sites
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Cloning, Molecular
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Cytosol / enzymology
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Escherichia coli
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Humans
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Kinetics
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Molecular Sequence Data
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Mutagenesis, Site-Directed
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Nuclear Proteins / biosynthesis
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Nuclear Proteins / metabolism
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Oligodeoxyribonucleotides
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Protein Tyrosine Phosphatases / biosynthesis
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Protein Tyrosine Phosphatases / isolation & purification*
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Protein Tyrosine Phosphatases / metabolism*
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RNA-Binding Proteins*
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Recombinant Fusion Proteins / biosynthesis
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Recombinant Fusion Proteins / isolation & purification
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Recombinant Fusion Proteins / metabolism
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Saccharomyces cerevisiae / enzymology*
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Saccharomyces cerevisiae / genetics
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Saccharomyces cerevisiae / metabolism
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Saccharomyces cerevisiae Proteins*
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Sequence Homology, Amino Acid
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Substrate Specificity
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Transcription Factors*
Substances
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Nuclear Proteins
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Oligodeoxyribonucleotides
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RNA-Binding Proteins
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Recombinant Fusion Proteins
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STP1 protein, S cerevisiae
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Saccharomyces cerevisiae Proteins
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Transcription Factors
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Protein Tyrosine Phosphatases