AGP1 / YCL025C Overview
- Standard Name
- AGP1 1
- Systematic Name
- YCL025C
- SGD ID
- SGD:S000000530
- Aliases
- YCC5 1 , WAP1 4
- Feature Type
- ORF , Verified
- Description
- Broad-specificity, low-affinity amino acid permease; minor serine permease with major contributions from paralog Gnp1p; involved in uptake of asparagine, glutamine, and other amino acids; expression induced by amino acids and regulated by SPS plasma membrane amino acid sensor system (Ssy1p-Ptr3p-Ssy5p) 1 2 3 4
- Name Description
- high-Affinity Glutamine Permease 1
- Paralog
- GNP1
- 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.
- Summary
- AGP1 has a paralog, GNP1, that arose from the whole genome duplication
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.)
- 633
- Mol. Weight (Da)
- 69669.0
- Isoelectric Point
- 6.97
- Median Abundance (molecules/cell)
- 4012 +/- 3797
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 AGP1 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
- Transmembrane transporter of L-proline; localizes to plasma membrane
View computational annotations
Molecular Function
- Manually Curated
Biological Process
- Manually Curated
- involved in amino acid transport (IDA)
- involved in serine import across plasma membrane (IMP, IGI)
- involved in transmembrane transport (IDA)
Cellular Component
- Manually Curated
- located in endoplasmic reticulum (HDA)
- located in plasma 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 mutant has increased competitive fitness in minimal medium; homozygous diploid null mutant has an elevated chronological lifespan and accumulated glycogen; null mutant displays reduced apoptosis after a ramped heat stimulus, and has increased resistance to quinine, camptothecin and hydroxyurea; heterozygous null mutant is haploproficient; overexpression results in a decreased growth rate and increased invasive growth
Classical Genetics
- null
- 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.
- Summary
- The agp1 null mutant is viable; the null mutant of paralog gnp1 is viable; the agp1 gnp1 double mutant displays growth defects.
353 total interactions for 285 unique genes
Physical Interactions
- Affinity Capture-MS: 7
- Affinity Capture-RNA: 6
- PCA: 39
Genetic Interactions
- Dosage Rescue: 1
- Negative Genetic: 249
- Phenotypic Enhancement: 3
- Positive Genetic: 37
- Synthetic Growth Defect: 10
- Synthetic Lethality: 1
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
- 26
- 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.