VMA3 / YEL027W Overview


Standard Name
VMA3 1 2
Systematic Name
YEL027W
SGD ID
SGD:S000000753
Aliases
CUP5 11 , CLS7 12 , GEF2
Feature Type
ORF , Verified
Description
Proteolipid subunit c of the V0 domain of vacuolar H(+)-ATPase; dicyclohexylcarbodiimide binding subunit; required for vacuolar acidification and important for copper and iron metal ion homeostasis 3 4
Name Description
Vacuolar Membrane Atpase
Comparative Info
Sequence Details

Sequence

The S. cerevisiae Reference Genome sequence is derived from laboratory strain S288C. Download DNA or protein sequence, view genomic context and coordinates. Click "Sequence Details" to view all sequence information for this locus, including that for other strains.


Protein Details

Protein

Basic sequence-derived (length, molecular weight, isoelectric point) and experimentally-determined (median abundance, median absolute deviation) protein information. Click "Protein Details" for further information about the protein such as half-life, abundance, domains, domains shared with other proteins, protein sequence retrieval for various strains, physico-chemical properties, protein modification sites, and external identifiers for the protein.


Length (a.a.)
160
Mol. Weight (Da)
16352.8
Isoelectric Point
8.1
Median Abundance (molecules/cell)
5416 +/- 2701
Half-life (hr)
>= 100

Alleles

Curated mutant alleles for the specified gene, listed alphabetically. Click on the allele name to open the allele page. Click "SGD search" to view all alleles in search results.


View all VMA3 alleles in SGD search

Gene Ontology Details

Gene Ontology

GO Annotations consist of four mandatory components: a gene product, a term from one of the three Gene Ontology (GO) controlled vocabularies (Molecular Function, Biological Process, and Cellular Component), a reference, and an evidence code. SGD has manually curated and high-throughput GO Annotations, both derived from the literature, as well as computational, or predicted, annotations. Click "Gene Ontology Details" to view all GO information and evidence for this locus as well as biological processes it shares with other genes.


Summary
Subunit of vacuolar proton-transporting V-type ATPase involved in endocytosis, vacuolar protein targeting, vacuole acidification, and metal ion homeostasis

View computational annotations

Molecular Function

Manually Curated

Biological Process

Manually Curated

Cellular Component

Manually Curated

Complex

Macromolecular complex annotations are imported from the Complex Portal. These annotations have been derived from physical molecular interaction evidence extracted from the literature and cross-referenced in the entry, or by curator inference from information on homologs in closely related species or by inference from scientific background.


Phenotype Details

Phenotype

Phenotype annotations for a gene are curated single mutant phenotypes that require an observable (e.g., "cell shape"), a qualifier (e.g., "abnormal"), a mutant type (e.g., null), strain background, and a reference. In addition, annotations are classified as classical genetics or high-throughput (e.g., large scale survey, systematic mutation set). Whenever possible, allele information and additional details are provided. Click "Phenotype Details" to view all phenotype annotations and evidence for this locus as well as phenotypes it shares with other genes.


Summary
VMA3/YEL027W is a non-essential gene; null mutants are viable but exhibit a range of phenotypic changes including altered chemical compound accumulation, decreased metal resistance, decreased oxidative stress resistance, increased protein/peptide accumulation, abnormal protein/peptide distribution, decreased resistance to chemicals, absent respiratory growth, decreased small molecule transport, decreased vegetative growth rate, decreased alkaline pH resistance, auxotrophy, abnormal budding pattern, increased duration of cell cycle progression in the G1 phase, abnormal cell shape, decreased chronological lifespan, decreased competitive fitness, decreased desiccation resistance, decreased freeze-thaw resistance, increased heat sensitivity, decreased hyperosmotic stress resistance, abnormal mitochondrial morphology, increased mitophagy, decreased protein/peptide modification, decreased resistance to enzymatic treatment, altered toxin resistance, decreased utilization rates of carbon and iron sources, and decreased vegetative growth. Overexpression of VMA3 results in decreased vegetative growth.
Disease Details

Disease

Disease Annotations consist of three mandatory components: a gene product, a term from the Disease Ontology (DO) controlled vocabulary and an evidence code. SGD provides manually curated DO Annotations derived from the literature. Click "Disease Details" to view all Disease information and evidence for this locus as well as diseases it shares with other genes.


Summary
Yeast VMA3 is homologous to human ATP6V0C, and has been used to study ATP6V0C variants that cause a human syndrome of developmental delay, epilepsy and intellectual disability

Manually Curated

Interaction Details

Interaction

Interaction annotations are curated by BioGRID and include physical or genetic interactions observed between at least two genes. An interaction annotation is composed of the interaction type, name of the interactor, assay type (e.g., Two-Hybrid), annotation type (e.g., manual or high-throughput), and a reference, as well as other experimental details. Click "Interaction Details" to view all interaction annotations and evidence for this locus, including an interaction visualization.


486 total interactions for 397 unique genes

Physical Interactions

  • Affinity Capture-MS: 7
  • Affinity Capture-RNA: 5
  • Affinity Capture-Western: 8
  • Co-fractionation: 1
  • Co-localization: 1
  • Co-purification: 3
  • PCA: 14
  • Protein-peptide: 1
  • Reconstituted Complex: 2
  • Two-hybrid: 1

Genetic Interactions

  • Dosage Rescue: 1
  • Negative Genetic: 265
  • Phenotypic Enhancement: 2
  • Phenotypic Suppression: 2
  • Positive Genetic: 136
  • Synthetic Growth Defect: 17
  • Synthetic Haploinsufficiency: 11
  • Synthetic Lethality: 6
  • Synthetic Rescue: 3
Regulation Details

Regulation

The number of putative Regulators (genes that regulate it) and Targets (genes it regulates) for the given locus, based on experimental evidence. This evidence includes data generated through high-throughput techniques. Click "Regulation Details" to view all regulation annotations, shared GO enrichment among regulation Targets, and a regulator/target diagram for the locus.


Regulators
4
Targets
0
Expression Details

Expression

Expression data are derived from records contained in the Gene Expression Omnibus (GEO), and are first log2 transformed and normalized. Referenced datasets may contain one or more condition(s), and as a result there may be a greater number of conditions than datasets represented in a single clickable histogram bar. The histogram division at 0.0 separates the down-regulated (green) conditions and datasets from those that are up-regulated (red). Click "Expression Details" to view all expression annotations and details for this locus, including a visualization of genes that share a similar expression pattern.


Summary Paragraph

A summary of the locus, written by SGD Biocurators following a thorough review of the literature. Links to gene names and curated GO terms are included within the Summary Paragraphs.


Last Updated: 2000-05-18

Literature Details

Literature

All manually curated literature for the specified gene, organized into topics according to their relevance to the gene (Primary Literature, Additional Literature, or Review). Click "Literature Details" to view all literature information for this locus, including shared literature between genes.


Primary
88
Additional
111
Reviews
38

Resources