Structural characterization of the transmembrane domain from subunit e of yeast F1Fo-ATP synthase: A helical GXXXG motif located just under the micelle surface

Biochemistry

Volumn 47, Issue 7, 2008, Pages 1910-1917

  Yao, Huili ^a   Stuart, Rosemary A ^a   Cai, Sheng ^a   Sem, Daniel S ^a  

^a Marquette University   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL MEMBRANES; ENZYMES; MICELLES; MOLECULAR STRUCTURE; SURFACE CHEMISTRY;

CRISTAE MEMBRANE ARCHITECTURE; MICELLE SURFACE; MULTIPROTEIN COMPLEXES;

YEAST;

ALANINE; ARGININE; DIMETHYL SULFOXIDE; GLYCINE; IRON; MEMBRANE PROTEIN; PEPTIDE; PHOSPHATE; PROTEIN SUBUNIT; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE; SULFUR; TRIFLUOROETHANOL; WATER;

ARTICLE; CARBOXY TERMINAL SEQUENCE; CIRCULAR DICHROISM; DIMERIZATION; ENZYME STABILITY; MEASUREMENT; MEMBRANE POTENTIAL; MICELLE; MOLECULE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PARAMETER; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN DOMAIN; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN MOTIF; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ACTIVITY RELATION; SURFACE PROPERTY;

AMINO ACID SEQUENCE; MICELLES; MOLECULAR SEQUENCE DATA; PROTEIN CONFORMATION; PROTON-TRANSLOCATING ATPASES; SACCHAROMYCES CEREVISIAE;

EID: 39649105224     PISSN: 00062960     EISSN: None     Source Type: Journal    
DOI: 10.1021/bi7015475     Document Type: Article

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