Importance of the GP dipeptide of the antiporter motif and other membrane-embedded proline and glycine residues in tetracycline efflux protein Tet(L)

Biochemistry

Volumn 44, Issue 38, 2005, Pages 12896-12904

  De Jesus, Magdia ^a,b   Jin, Jie ^a,c   Guffanti, Arthur A ^a   Krulwich, Terry A ^a  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^b ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^c BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL MEMBRANES; HYDROPHOBICITY; MUTAGENESIS; PROTEINS; SUBSTRATES;

GLYCIN RESIDUES; HYDROPHOBIC DOMAINS; MEMBRANE TRANSPORT PROTEINS; MUTATIONAL CHANGES;

POLYPEPTIDES;

DIPEPTIDE; GLYCINE; GLYCYLPROLINE; PROLINE; TETRACYCLINE;

ARTICLE; CONFORMATIONAL TRANSITION; CONTROLLED STUDY; HYDROPHOBICITY; MEMBRANE BINDING; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN DOMAIN; PROTEIN MOTIF;

AMINO ACID MOTIFS; AMINO ACID SEQUENCE; ANTIPORTERS; ARGININE; BACTERIAL PROTEINS; DIPEPTIDES; GLUTAMIC ACID; GLYCINE; ION TRANSPORT; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; POTASSIUM; PROLINE; RUBIDIUM; TETRACYCLINE; TETRACYCLINE RESISTANCE;

EID: 25444499137     PISSN: 00062960     EISSN: None     Source Type: Journal    
DOI: 10.1021/bi050762c     Document Type: Article

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