Vacuolar ATPases play major roles in endomembrane and plasma membrane proton transport in eukaryotes. A Drosophila melanogaster cDNA encoding vha55, the 55-kDa vacuolar ATPase (V-ATPase) regulatory B-subunit, was characterized and mapped to 87C2-4 on chromosome 3R. A fly line was identified that carried a single lethal P-element insertion within the coding portion of gene, and its LacZ reporter gene revealed elevated expression in Malpighian tubules, rectum, antennal palps, and oviduct, regions where V-ATPases are believed to play a plasma membrane, rather than an endomembrane, role. The P-element vha55 insertion was shown to be allelic to a known lethal complementation group l(3)SzA (= l(3)87Ca) at 87C, for which many alleles have been des...
Mitochondrial disorders associated with genetic defects of the ATP synthase are among the most delet...
AbstractVDAC, a major protein of the mitochondrial outer membrane, forms voltage-dependent, anion-se...
VDACs (voltage-dependent anion-selective channels) or mitochondrial PORINS are transmembrane protein...
V-ATPases play multiple roles in eukaryotes: in Drosophila, null mutations are recessive lethal. Her...
Vacuolar H+-ATPases (V-ATPases) are multi-subunit enzymes which pump protons across cellular membran...
The function and the molecular properties of the Rpt1/p48B ATPase subunit of the regulatory particle...
We have studied the spatio-temporal pattern of expression of the gene encoding the H+ adenosine trip...
The V-ATPase is a highly conserved enzymatic complex that ensures appropriate levels of organelle ac...
The V(0) complex forms the proteolipid pore of an ATPase that acidifies vesicles. In addition, an in...
SummaryThe V0 complex forms the proteolipid pore of an ATPase that acidifies vesicles. In addition, ...
The vital task of vectorial solute transport is often energised by a plasma membrane, proton-motive ...
Mitochondrial disorders associated with genetic defects of the ATP synthase are among the most delet...
Mitochondrial disorders associated with genetic defects of the ATP synthase are among the most delet...
International audienceEukaryotes possess multiple isoforms of the a subunit of the V(0) complex of v...
This work is licensed under a Creative Commons Attribution 3.0 Unported license.Vacuolar-type H+ ATP...
Mitochondrial disorders associated with genetic defects of the ATP synthase are among the most delet...
AbstractVDAC, a major protein of the mitochondrial outer membrane, forms voltage-dependent, anion-se...
VDACs (voltage-dependent anion-selective channels) or mitochondrial PORINS are transmembrane protein...
V-ATPases play multiple roles in eukaryotes: in Drosophila, null mutations are recessive lethal. Her...
Vacuolar H+-ATPases (V-ATPases) are multi-subunit enzymes which pump protons across cellular membran...
The function and the molecular properties of the Rpt1/p48B ATPase subunit of the regulatory particle...
We have studied the spatio-temporal pattern of expression of the gene encoding the H+ adenosine trip...
The V-ATPase is a highly conserved enzymatic complex that ensures appropriate levels of organelle ac...
The V(0) complex forms the proteolipid pore of an ATPase that acidifies vesicles. In addition, an in...
SummaryThe V0 complex forms the proteolipid pore of an ATPase that acidifies vesicles. In addition, ...
The vital task of vectorial solute transport is often energised by a plasma membrane, proton-motive ...
Mitochondrial disorders associated with genetic defects of the ATP synthase are among the most delet...
Mitochondrial disorders associated with genetic defects of the ATP synthase are among the most delet...
International audienceEukaryotes possess multiple isoforms of the a subunit of the V(0) complex of v...
This work is licensed under a Creative Commons Attribution 3.0 Unported license.Vacuolar-type H+ ATP...
Mitochondrial disorders associated with genetic defects of the ATP synthase are among the most delet...
AbstractVDAC, a major protein of the mitochondrial outer membrane, forms voltage-dependent, anion-se...
VDACs (voltage-dependent anion-selective channels) or mitochondrial PORINS are transmembrane protein...