PMID:12374816: Difference between revisions

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<span style = 'font-size: large'> '''Pi, J, Chow, H and Pittard, AJ'''  (2002) Study of second-site suppression in the pheP gene for the phenylalanine transporter of Escherichia coli.''J. Bacteriol.'' '''184''':5842-7</span>
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!align=left  |Citation
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'''Pi, J, Chow, H and Pittard, AJ'''  (2002) Study of second-site suppression in the pheP gene for the phenylalanine transporter of Escherichia coli. ''J. Bacteriol.'' '''184''':5842-7
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!align=left  |Abstract
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Site-directed mutagenesis was used to investigate a region of the PheP protein corresponding to the postulated consensus amphipathic region (CAR) in the GabP protein. Whereas some critical residues are conserved in both proteins, there are major differences between the two proteins which may reflect different functions for this region. Replacement of R317, Y313, or P341 by a number of other amino acids destroyed the PheP function. An R317E-E234R double mutant exhibited low levels of PheP transport activity, indicating that there is a possible interaction between these two residues in the wild-type protein. E234 is highly conserved in members of the superfamily of amino acid-polyamine-organocation transporters and also is critical for PheP function in the wild-type protein. Second-site suppressors were isolated for mutants with mutations in E234, Y313, R317, and P341. Most suppressor mutations were found to cluster towards the extracellular face of spans III, IX, and X. Some mutations, such as changes at M116, were able to suppress each of the primary changes at positions E234, Y313, R317, and P341 but were unable to restore function to a number of other primary mutants. The possible implications of these results for the tertiary structure of the protein are discussed.
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!align=left  |Links
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[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=12374816 PubMed] [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC135400 PMC135400]


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|{{TableHeadingColor}} |'''Abstract''' || Site-directed mutagenesis was used to investigate a region of the PheP protein corresponding to the postulated consensus amphipathic region (CAR) in the GabP protein. Whereas some critical residues are conserved in both proteins, there are major differences between the two proteins which may reflect different functions for this region. Replacement of R317, Y313, or P341 by a number of other amino acids destroyed the PheP function. An R317E-E234R double mutant exhibited low levels of PheP transport activity, indicating that there is a possible interaction between these two residues in the wild-type protein. E234 is highly conserved in members of the superfamily of amino acid-polyamine-organocation transporters and also is critical for PheP function in the wild-type protein. Second-site suppressors were isolated for mutants with mutations in E234, Y313, R317, and P341. Most suppressor mutations were found to cluster towards the extracellular face of spans III, IX, and X. Some mutations, such as changes at M116, were able to suppress each of the primary changes at positions E234, Y313, R317, and P341 but were unable to restore function to a number of other primary mutants. The possible implications of these results for the tertiary structure of the protein are discussed.
!align=left  |Keywords
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Amino Acid Sequence; Amino Acid Transport Systems, Neutral/genetics; Bacterial Proteins/genetics; Consensus Sequence; Escherichia coli/enzymology; Escherichia coli/genetics; Escherichia coli Proteins; GABA Plasma Membrane Transport Proteins; Genes, Bacterial; Glutamic Acid/genetics; Molecular Sequence Data; Mutagenesis, Site-Directed; Organic Anion Transporters/genetics; Phenylalanine/metabolism; Proline/genetics; Tyrosine/genetics
|{{TableHeadingColor}} nowrap |'''Links''' ||  [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=12374816 PubMed]
 
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Latest revision as of 04:18, 15 September 2013

Citation

Pi, J, Chow, H and Pittard, AJ (2002) Study of second-site suppression in the pheP gene for the phenylalanine transporter of Escherichia coli. J. Bacteriol. 184:5842-7

Abstract

Site-directed mutagenesis was used to investigate a region of the PheP protein corresponding to the postulated consensus amphipathic region (CAR) in the GabP protein. Whereas some critical residues are conserved in both proteins, there are major differences between the two proteins which may reflect different functions for this region. Replacement of R317, Y313, or P341 by a number of other amino acids destroyed the PheP function. An R317E-E234R double mutant exhibited low levels of PheP transport activity, indicating that there is a possible interaction between these two residues in the wild-type protein. E234 is highly conserved in members of the superfamily of amino acid-polyamine-organocation transporters and also is critical for PheP function in the wild-type protein. Second-site suppressors were isolated for mutants with mutations in E234, Y313, R317, and P341. Most suppressor mutations were found to cluster towards the extracellular face of spans III, IX, and X. Some mutations, such as changes at M116, were able to suppress each of the primary changes at positions E234, Y313, R317, and P341 but were unable to restore function to a number of other primary mutants. The possible implications of these results for the tertiary structure of the protein are discussed.

Links

PubMed PMC135400

Keywords

Amino Acid Sequence; Amino Acid Transport Systems, Neutral/genetics; Bacterial Proteins/genetics; Consensus Sequence; Escherichia coli/enzymology; Escherichia coli/genetics; Escherichia coli Proteins; GABA Plasma Membrane Transport Proteins; Genes, Bacterial; Glutamic Acid/genetics; Molecular Sequence Data; Mutagenesis, Site-Directed; Organic Anion Transporters/genetics; Phenylalanine/metabolism; Proline/genetics; Tyrosine/genetics

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