ATG40 / YOR152C Overview
- Standard Name
- ATG40 1
- Systematic Name
- YOR152C
- SGD ID
- SGD:S000005678
- Feature Type
- ORF , Verified
- Description
- Autophagy receptor with a role in endoplasmic reticulum degradation; involved specifically in autophagy of cortical and cytoplasmic ER in response to nitrogen starvation or rapamycin treatment; acts with COPII subunit Sfb3p; localizes to the cortical and cytoplasmic ER; similar to human FAM134B, which is also involved in ER autophagy and is associated with sensory neuropathy 1 2
- Name Description
- AuTophaGy related 1
- Comparative Info
-
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.
Analyze Sequence
S288C only
BLASTN | BLASTP | Design Primers | Restriction Fragment Map | Restriction Fragment Sizes | Six-Frame Translation
S288C vs. other species
BLASTN vs. fungi | BLASTP at NCBI | BLASTP vs. fungi
S288C vs. other strains
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.)
- 256
- Mol. Weight (Da)
- 29685.9
- Isoelectric Point
- 4.55
- Median Abundance (molecules/cell)
- 1890 +/- 1228
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 ATG40 alleles in SGD search
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
- Protein involved in autophagic degradation of the endoplasmic reticulum in response to nitrogen starvation; binds to Atg8p during autophagy; localized to the cortical ER
View computational annotations
Molecular Function
- Manually Curated
- enables protein-macromolecule adaptor activity (IGI, IMP)
Biological Process
- Manually Curated
- involved in cellular response to nitrogen starvation (IGI, IMP)
- involved in reticulophagy (IMP, IGI)
Cellular Component
- Manually Curated
- located in cortical endoplasmic reticulum (IDA)
- located in membrane (IDA)
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
- Non-essential gene; null mutation causes abnormal ER morphology, delayed autophagy and reduced reticulophagy; in systematic studies null mutants have abnormal vacuolar morphology and reduced competitive fitness
Classical Genetics
- null
- competitive fitness: decreased
- competitive fitness: increased
- heat sensitivity: increased
- killer toxin resistance: increased
- resistance to chemicals: decreased
- resistance to chemicals: increased
- reticulophagy: decreased
- toxin resistance: decreased
- utilization of nitrogen source: decreased rate
- vacuolar morphology: abnormal
- viable
- overexpression
Large-scale Survey
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.
56 total interactions for 44 unique genes
Physical Interactions
- Affinity Capture-MS: 2
- Affinity Capture-RNA: 4
- Affinity Capture-Western: 8
- Co-crystal Structure: 2
- Co-localization: 4
- Protein-peptide: 1
- Reconstituted Complex: 1
- Two-hybrid: 2
Genetic Interactions
- Negative Genetic: 22
- Phenotypic Enhancement: 3
- Positive Genetic: 7
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
- 7
- Targets
- 0
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.
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.