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Journal Abstract Search


208 related items for PubMed ID: 17176088

  • 1. Glycine-rich transmembrane helix 10 in the staphylococcal tetracycline transporter TetA(K) lines a solvent-accessible channel.
    Hassan KA, Robinson KL, Smith AN, Gibson JH, Skurray RA, Brown MH.
    Biochemistry; 2006 Dec 26; 45(51):15661-9. PubMed ID: 17176088
    [Abstract] [Full Text] [Related]

  • 2. Roles of conserved arginine residues in the metal-tetracycline/H+ antiporter of Escherichia coli.
    Kimura T, Nakatani M, Kawabe T, Yamaguchi A.
    Biochemistry; 1998 Apr 21; 37(16):5475-80. PubMed ID: 9548929
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  • 3. Determination of a transmembrane segment using cysteine-scanning mutants of transposon Tn10-encoded metal-tetracycline/H+ antiporter.
    Kimura T, Suzuki M, Sawai T, Yamaguchi A.
    Biochemistry; 1996 Dec 10; 35(49):15896-9. PubMed ID: 8961955
    [Abstract] [Full Text] [Related]

  • 4. His257 is a uniquely important histidine residue for tetracycline/H+ antiport function but not mandatory for full activity of the transposon Tn10-encoded metal-tetracycline/H+ antiporter.
    Yamaguchi A, Samejima T, Kimura T, Sawai T.
    Biochemistry; 1996 Apr 09; 35(14):4359-64. PubMed ID: 8605184
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  • 7. Functions of tetracycline efflux proteins that do not involve tetracycline.
    Krulwich TA, Jin J, Guffanti AA, Bechhofer H.
    J Mol Microbiol Biotechnol; 2001 Apr 09; 3(2):237-46. PubMed ID: 11321579
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  • 9. The TetA(K) tetracycline/H(+) antiporter from Staphylococcus aureus: mutagenesis and functional analysis of motif C.
    Ginn SL, Brown MH, Skurray RA.
    J Bacteriol; 2000 Mar 09; 182(6):1492-8. PubMed ID: 10692352
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  • 10. Substrate-induced tryptophan fluorescence changes in EmrE, the smallest ion-coupled multidrug transporter.
    Elbaz Y, Tayer N, Steinfels E, Steiner-Mordoch S, Schuldiner S.
    Biochemistry; 2005 May 17; 44(19):7369-77. PubMed ID: 15882076
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  • 11. Mutational analysis of tetracycline resistance protein transmembrane segment insertion.
    Lewis GS, Jewell JE, Phang T, Miller KW.
    Arch Biochem Biophys; 2002 Aug 15; 404(2):317-25. PubMed ID: 12147271
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  • 12. Functional importance of GGXG sequence motifs in putative reentrant loops of 2HCT and ESS transport proteins.
    Dobrowolski A, Lolkema JS.
    Biochemistry; 2009 Aug 11; 48(31):7448-56. PubMed ID: 19594131
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  • 13. Mercaptide formed between the residue Cys70 and Hg2+ or Co2+ behaves as a functional positively charged side chain operative in the Arg70-->Cys mutant of the metal-tetracycline/H+ antiporter of Escherichia coli.
    Someya Y, Yamaguchi A.
    Biochemistry; 1996 Jul 23; 35(29):9385-91. PubMed ID: 8755716
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  • 14. Importance of the GP dipeptide of the antiporter motif and other membrane-embedded proline and glycine residues in tetracycline efflux protein Tet(L).
    De Jesus M, Jin J, Guffanti AA, Krulwich TA.
    Biochemistry; 2005 Sep 27; 44(38):12896-904. PubMed ID: 16171405
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  • 16. Arrangement of core membrane segments in the MotA/MotB proton-channel complex of Escherichia coli.
    Braun TF, Al-Mawsawi LQ, Kojima S, Blair DF.
    Biochemistry; 2004 Jan 13; 43(1):35-45. PubMed ID: 14705929
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  • 17. The tet(K) gene of plasmid pT181 of Staphylococcus aureus encodes an efflux protein that contains 14 transmembrane helices.
    Guay GG, Khan SA, Rothstein DM.
    Plasmid; 1993 Sep 13; 30(2):163-6. PubMed ID: 8234490
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  • 18. The transmembrane domains of the ABC multidrug transporter LmrA form a cytoplasmic exposed, aqueous chamber within the membrane.
    Poelarends GJ, Konings WN.
    J Biol Chem; 2002 Nov 08; 277(45):42891-8. PubMed ID: 12183459
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  • 19. A fluorescence method to define transmembrane alpha-helices in membrane proteins: studies with bacterial diacylglycerol kinase.
    Jittikoon J, East JM, Lee AG.
    Biochemistry; 2007 Sep 25; 46(38):10950-9. PubMed ID: 17722884
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  • 20. Functional effects of intramembranous proline substitutions in the staphylococcal multidrug transporter QacA.
    Hassan KA, Galea M, Wu J, Mitchell BA, Skurray RA, Brown MH.
    FEMS Microbiol Lett; 2006 Oct 25; 263(1):76-85. PubMed ID: 16958854
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