Concanamycin and indolyl pentadieneamide inhibitors of the vacuolar H+-ATPase bind with high affinity to the purified proteolipid subunit of the membrane domain.
Whyteside, Graham
Concanamycin and indolyl pentadieneamide inhibitors of the vacuolar H+-ATPase bind with high affinity to the purified proteolipid subunit of the membrane domain. [electronic resource] - Biochemistry Nov 2005 - 15024-31 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0006-2960
10.1021/bi051529h doi
Binding Sites
Enzyme Inhibitors--chemistry
Fluorescent Dyes
Indoles--chemistry
Macrolides--chemistry
Piperidines--chemistry
Protein Structure, Tertiary
Protein Subunits--chemistry
Proteolipids--chemistry
Pyrenes--chemistry
Saccharomyces cerevisiae--enzymology
Spectrometry, Fluorescence
Vacuolar Proton-Translocating ATPases--chemistry
Concanamycin and indolyl pentadieneamide inhibitors of the vacuolar H+-ATPase bind with high affinity to the purified proteolipid subunit of the membrane domain. [electronic resource] - Biochemistry Nov 2005 - 15024-31 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0006-2960
10.1021/bi051529h doi
Binding Sites
Enzyme Inhibitors--chemistry
Fluorescent Dyes
Indoles--chemistry
Macrolides--chemistry
Piperidines--chemistry
Protein Structure, Tertiary
Protein Subunits--chemistry
Proteolipids--chemistry
Pyrenes--chemistry
Saccharomyces cerevisiae--enzymology
Spectrometry, Fluorescence
Vacuolar Proton-Translocating ATPases--chemistry