F-box protein component of an SCF ubiquitin-ligase complex; modular substrate specificity factor which associates with core SCF (Cdc53p, Skp1p and Hrt1p/Rbx1p) to form the SCF(Grr1) complex; SCF(Grr1) acts as a ubiquitin-protein ligase directing ubiquitination of substrates such as: Gic2p, Mks1p, Mth1p, Cln1p, Cln2p and Cln3p; involved in carbon catabolite repression, glucose-dependent divalent cation transport, glucose transport, morphogenesis, and sulfite detoxification
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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
GRR1/YJR090C is located on the right arm of chromosome X between BIR1 and JSN1; coding sequence is 3456 nucleotides long with a variable AAC trinucleotide repeat and 34 SNPs, 13 of which cause amino acid polymorphisms
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
Grr1p is 1151 amino acids long, extremely low in abundance; contains disordered regions at both termini, an F-box domain, 11 cysteine-containing leucine-rich repeats, and a variable stretch of Asn residues; ubiquitinylated on K567 and K622; phosphorylated on 10 residues
Length (a.a.)
1151
Mol. Weight (Da)
132722.7
Isoelectric Point
6.48
Median Abundance (molecules/cell)
780 +/- 664
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.
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 SCF ubiquitin ligase complex; involved in SCF-dependent proteasomal ubiquitin-dependent protein catabolism, pheromone-responsive mitotic cell cycle G1 arrest, and cellular responses to DNA damage stimulus and methylmercury; localizes to nucleus, cytoplasm, and bud neck contractile ring
Functional Networks display how gene products work together in biological systems. The Shared Annotations
network shows genes with similar GO annotations, suggesting functional relationships. GO-CAMs (Gene
Ontology Causal Activity Models) are manually curated pathway models that illustrate how molecular
activities of multiple gene products connect through causal relationships to carry out biological
processes. GO-CAMs integrate Molecular Function, Biological Process, and Cellular Component information
into unified pathway representations based on published experimental evidence. Click "View GO-CAM at Gene
Ontology" to explore the interactive model at AmiGO.
Click on a gene or Biological Process GO term name to go to its specific page within SGD; drag any of the gene or GO
term name objects around within the visualization for easier viewing; click “Reset” to automatically redraw the
diagram; filter the genes that share GO Biological Process terms with the given gene by the number of terms they
share by clicking anywhere on the slider bar or dragging the tab to the desired filter number.
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 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
GRR1/YJR090C is a non-essential gene; null mutants are viable, slow-growing, and associated with a range of mutant phenotypes that significantly impact cellular functions and overall fitness. Mutants lacking GRR1 exhibit decreased resistance to both acidic and alkaline pH levels, which may hinder their survival in varying environmental conditions. These mutants show an increased ability to form biofilms, which could affect their interactions with surfaces and other cells. The budding pattern in null mutants is abnormal, characterized by bipolar budding, and bud morphology is also disrupted, indicating potential issues with cell division. Competitive fitness is diminished, leading to reduced viability in resource-limited environments, while desiccation resistance is decreased, making them more vulnerable to dry conditions. The rate of fermentative growth is reduced, and these mutants also exhibit decreased resistance to freeze-thaw cycles. Invasive growth is increased, suggesting an enhanced ability to penetrate surfaces or tissues. Resistance to killer toxins is decreased, and lipid particle morphology is abnormal, which may impact cellular metabolism. Furthermore, oxidative stress resistance is diminished, and respiratory growth is absent, indicating a reliance on fermentation for energy production. UV resistance is also decreased, further underscoring their vulnerability to environmental stressors. Reduced function mutants show an increased rate of fermentative metabolism, suggesting a compensatory mechanism in response to the loss of function. However, when GRR1 is overexpressed, competitive fitness is again decreased, and UV resistance is diminished, indicating that excessive levels of the gene or gene product may also be detrimental.
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
Grr1p interacts physically with proteins involved in mitotic cell cycle; GRR1 interacts genetically with genes involved in mitotic cell cycle
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.
Summary
GRR1/YJR090C promoter is bound by Tfc7p and Yap6p in response to heat
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.
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).