PDR15 / YDR406W Overview


Standard Name
PDR15 1
Systematic Name
YDR406W
SGD ID
SGD:S000002814
Feature Type
ORF , Verified
Description
Plasma membrane ATP binding cassette (ABC) transporter; multidrug transporter and general stress response factor implicated in cellular detoxification; regulated by Pdr1p, Pdr3p and Pdr8p; promoter contains a PDR responsive element; PDR15 has a paralog, PDR5, that arose from the whole genome duplication 1 2 3 4 5
Name Description
Pleiotropic Drug Resistance 1
Paralog
PDR5 5
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.


Summary
PDR15/YDR406W is located on the right arm of chromosome IV between mitochondrial ribosomal protein MRP20 and TRAPP complex component TRS120; coding sequence is 4590 nucleotides long with insertions in alternative reference strains SK1 and Y55, has 14 synonymous and 7 nonsynonymous SNPs; PDR15 has a paralog, PDR5, that arose from the whole genome duplication
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.


Summary
Pdr15p is 1529 amino acids long, low in abundance and slightly shorter-lived; phosphorylated on 9 residues and ubiquitinylated on K441 and K857
AlphaFold predicted structure of PDR15
Length (a.a.)
1529
Mol. Weight (Da)
172264.5
Isoelectric Point
8.0
Median Abundance (molecules/cell)
2838 +/- 1372
Half-life (hr)
8.1

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 PDR15 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
ATPase-coupled transmembrane transporter of the cell periphery; involved in response to xenobiotic stimuli

View computational annotations

Molecular Function

Manually Curated

Biological Process

Manually Curated

Cellular Component

High-Throughput
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
Non-essential gene in reference strain S288C; null mutant displays decreased resistance to 2,4-dichlorophenol and wighteone; overexpression causes decreased resistance to DMSO; is haploinsufficient; in W303, null mutant displays decreased resistance to 2,4-dichlorophenol; the pdr15 null mutant is viable; the null mutant of paralog pdr5 is viable; the pdr15 pdr5 double mutant displays a phenotypic enhancement
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.


Summary
Pdr15p interacts physically with proteins involved in mitochondrial translation; PDR15 interacts genetically with genes involved in DNA repair

89 total interactions for 80 unique genes

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.


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.


Literature Details

All Curated Literature

All manually curated literature for the specified gene, shown as a count of references by year of publication followed by the most recent papers. Click "Literature Details" or "See all" to view all literature information for this locus, organized into topics according to their relevance to the gene (Primary Literature, Additional Literature, or Review).


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Resources