Gene Ontology annotation through association of InterPro records with GO terms
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Combined Automated Annotation using Multiple IEA Methods
An mRNA from human brain encodes an isoform of the B subunit of the vacuolar H(+)-ATPase.
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First identification of the brain B subunit isoform (B2) of V-ATPase; established that brain and kidney B subunit cDNAs represent different isoforms.
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The B subunit is one of the two major subunits of the hydrophilic catalytic complex of V-ATPase.
Proteomic analysis of early melanosomes: identification of novel melanosomal proteins.
Integral and associated lysosomal membrane proteins.
Large-scale proteomics and phosphoproteomics of urinary exosomes.
Proteomic analysis of human parotid gland exosomes by multidimensional protein identification technology (MudPIT).
Lipofuscin is formed independently of macroautophagy and lysosomal activity in stress-induced prematurely senescent human fibroblasts.
In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.
A proteome-scale map of the human interactome network.
H(+)-ATPase B1 subunit localizes to thick ascending limb and distal convoluted tubule of rodent and human kidney.
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B1 subunit localizes to apical membrane domains of thick ascending limb and distal convoluted tubule in human kidney.
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B2 subunit is also expressed in TAL, DCT, and CNT in addition to intercalated cells; it colocalizes with B1 in early distal nephron.
Structure and Roles of V-type ATPases.
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Comprehensive review of V-ATPase structure, function, and disease associations.
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V-ATPase is the primary organellar acidification system in eukaryotes.
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.
Structures of a Complete Human V-ATPase Reveal Mechanisms of Its Assembly.
Nsp2 has the potential to be a drug target revealed by global identification of SARS-CoV-2 Nsp2-interacting proteins.
Intraphagosomal pH is lowered to 5 by V-ATPase
Acidification of Tf:TfR1 containing endosome
RRAGC,D exchanges GTP for GDP
RRAGA,B exchanges GDP for GTP
v-ATPase:Ragulator:RRAGA,B:GTP:RRAGC,D:GDP:SLC38A9:Arginine dissociates yielding v-ATPase:Ragulator:RRAGA,B:GTP:RRAGC,D:GDP and SLC38A9:Arginine
v-ATPase:Ragulator:RagA,B:GDP:RagC,D:GDP binds SLC38A9:Arginine
v-ATPase:Ragulator:RRAGA,B:GTP:RRAGC,D:GDP binds mTORC1
MITF-M-dependent ATP6V1B2 gene expression