PDR5 / YOR153W Overview
- Standard Name
- PDR5 1
- Systematic Name
- YOR153W
- SGD ID
- SGD:S000005679
- Aliases
- LEM1 30 , YDR1 31 , STS1 4
- Feature Type
- ORF , Verified
- Description
- Plasma membrane ATP-binding cassette (ABC) transporter; multidrug transporter actively regulated by Pdr1p; also involved in steroid transport, cation resistance, and cellular detoxification during exponential growth; PDR5 has a paralog, PDR15, that arose from the whole genome duplication 2 3 4 5 6 7 8 9 10 11
- Name Description
- Pleiotropic Drug Resistance 1
- Paralog
- PDR15 11
- 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.
- Summary
- Pdr5p is 1511 amino acids long, shorter-lived, moderate in abundance; contains 2 ATP-binding domains; N-glycosylated on N57 and N734, succinylated on K232, ubiquitinylated on 5 lysines, phosphorylated on 34 residues
- Length (a.a.)
- 1511
- Mol. Weight (Da)
- 170444.9
- Isoelectric Point
- 7.87
- Median Abundance (molecules/cell)
- 10371 +/- 4608
- Half-life (hr)
- 8.2
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 PDR5 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
- Plasma membrane ATP-binding cassette (ABC) transporter involved in resistance to multiple drugs; facilitates drug removal from the cell
View computational annotations
Molecular Function
- Manually Curated
- enables ABC-type xenobiotic transporter activity (IMP, IDA)
Biological Process
- Manually Curated
- involved in intracellular monoatomic cation homeostasis (IGI, IMP)
- involved in response to xenobiotic stimulus (IMP)
- involved in xenobiotic detoxification by transmembrane export across the plasma membrane (IMP)
Cellular Component
- Manually Curated
- located in cell periphery (HDA)
- located in mitochondrion (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 and point mutations confer resistance or sensitivity to various drugs; in large-scale studies, null mutation confers a filamentous growth defect, increased competitive fitness in minimal medium, and altered resistance to a wide variety of drugs
Classical Genetics
- null
- overexpression
- activation
- reduction of function
- null
- chemical compound accumulation: abnormal
- competitive fitness: increased
- filamentous growth: decreased
- haploinsufficient
- invasive growth: absent
- oxidative stress resistance: decreased
- resistance to chemicals: decreased
- resistance to chemicals: increased
- utilization of nitrogen source: decreased rate
- vacuolar morphology: abnormal
- viable
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
- Pdr5p interacts physically with proteins involved in transmembrane transport, PDR5 interacts genetically with genes involved in transcription; the pdr5 null mutant is viable, the null mutant of paralog pdr15 is viable, the pdr5 pdr15 double mutant displays a phenotypic enhancement
230 total interactions for 166 unique genes
Physical Interactions
- Affinity Capture-MS: 58
- Affinity Capture-RNA: 10
- Affinity Capture-Western: 4
- Biochemical Activity: 2
- Co-fractionation: 10
- PCA: 54
- Proximity Label-MS: 1
- Two-hybrid: 13
Genetic Interactions
- Dosage Rescue: 6
- Negative Genetic: 22
- Phenotypic Enhancement: 16
- Phenotypic Suppression: 8
- Synthetic Growth Defect: 21
- Synthetic Rescue: 5
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
- 20
- 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.
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: 2007-11-06
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.