2008
DOI: 10.1016/j.gene.2008.07.004
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Functionally important residues of the Tet repressor inducing peptide TIP determined by a complete mutational analysis

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Cited by 3 publications
(2 citation statements)
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“…A similar result was found for the TetR inducing peptides TIP and TIP2, since the crystal structures of both, [TetR⋅TIP] and [TetR⋅TIP2], revealed tryptophan residues localized within the tc-binding pocket forming crucial interactions to residues of TetR [28], [30]. For both peptides, the activity was lost when the tryptophan residues were exchanged to alanine [29], [31].…”
Section: Resultssupporting
confidence: 76%
“…A similar result was found for the TetR inducing peptides TIP and TIP2, since the crystal structures of both, [TetR⋅TIP] and [TetR⋅TIP2], revealed tryptophan residues localized within the tc-binding pocket forming crucial interactions to residues of TetR [28], [30]. For both peptides, the activity was lost when the tryptophan residues were exchanged to alanine [29], [31].…”
Section: Resultssupporting
confidence: 76%
“…Increasing the inducer to TetR ratio is one promising way, since strains with less TetR, controlling the P xyl/tet promoter upstream of gfpmut2 , putatively respond better to lower levels of Tip‐tagged proteins ( Klotzsche et al ., 2005 ). To this end, S. aureus strains bearing autoregulated tetR , which generally ensures a balanced level of repressor molecules, might be exploited ( Gründling and Schneewind, 2007 ), optionally combined with improved TetR/Tip pairs ( Klotzsche et al ., 2005 ; Klotzsche et al ., 2007 ; Daam et al ., 2008 ). Taken together, proof‐of‐concept for a functional Tip‐tagging architecture in S. aureus was achieved using mCherry as a carrier protein.…”
mentioning
confidence: 99%