RSP5 / YER125W Overview
- Standard Name
- RSP5
1
- Systematic Name
- YER125W
- SGD ID
- S000000927
- Aliases
-
SMM1
2
,
MDP1
3
,
MUT2
,
NPI1
4
,
UBY1
- Feature Type
- ORF
, Verified
- Description
-
NEDD4 family E3 ubiquitin ligase; regulates processes including: MVB sorting, the heat shock response, transcription, endocytosis and ribosome stability; ubiquitinates Sec23p, Sna3p, Ste4p, Nfi1p, Rpo21p and Sem1p; autoubiquitinates; deubiquitinated by Ubp2p; regulated by SUMO ligase Siz1p, in turn regulates Siz1p SUMO ligase activity; required for efficient Golgi-to-ER trafficking in COPI mutants; mutant tolerates aneuploidy; human homolog implicated in Liddle syndrome
5
6
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10
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12
13
14
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18
19
20
- Name Description
- Reverses Spt- Phenotype
21
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.
Protein Details
Protein
Basic information about the protein. Click "Protein Details" for further information about the protein
such as abundance data, domains, shared domains with other proteins, protein sequence retrieval for
various strains, sequence-based physico-chemical proterties, protein modification sites sites, and
external identifiers for the protein.
- Length (a.a.)
- 809
- Mol. Weight (Da)
- 91810.2
- Isoelectric Point
- 6.67
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
- E3 ubiquitin ligase that conjugates ubiquitin to proteins to target them for degradation; known to ubiquitinate Ste4p; involved in regulating a variety of processes via ubiquitin-dependent catabolism including organization of the mitochondrion, multivesilular body size, initiation of the mating tip projection and actin cytoskeletal organization; positively regulates dolichol and fatty acid biosynthesis; localized throughout the cell
View computational annotations
Molecular Function
- Manually Curated
Biological Process
- Manually Curated
-
cellular response to UV
(IMP)
-
chromatin assembly or disassembly
(IMP)
-
late endosome to vacuole transport via multivesicular body sorting pathway
(IMP,
IPI)
-
mitochondrion organization
(IGI,
IMP)
-
poly(A)+ mRNA export from nucleus
(IMP)
-
positive regulation of endocytosis
(IMP)
-
positive regulation of fatty acid biosynthetic process
(IMP)
-
positive regulation of proteasomal ubiquitin-dependent protein catabolic process
(IMP)
-
positive regulation of receptor-mediated endocytosis
(IMP)
-
positive regulation of transcription from RNA polymerase II promoter
(IMP)
-
proteasome-mediated ubiquitin-dependent protein catabolic process
(IPI)
-
protein autoubiquitination
(IGI)
-
protein monoubiquitination
(IDA,
IGI,
IMP)
-
protein polyubiquitination
(IDA,
IMP)
-
protein ubiquitination
(IDA)
-
protein ubiquitination involved in ubiquitin-dependent protein catabolic process
(IMP)
-
regulation of actin cytoskeleton organization
(IGI)
-
regulation of dolichol biosynthetic process
(IGI,
IMP)
-
regulation of ergosterol biosynthetic process
(IGI,
IMP)
-
regulation of initiation of mating projection growth
(IMP)
-
regulation of mRNA export from nucleus
(IMP,
IPI)
-
regulation of multivesicular body size
(IMP)
-
regulation of nitrogen utilization
(IGI)
-
regulation of phosphate metabolic process
(IGI)
-
regulation of protein localization
(IPI,
IMP)
-
regulation of ribosomal large subunit export from nucleus
(IMP)
-
regulation of rRNA processing
(IMP)
-
regulation of tRNA export from nucleus
(IMP)
-
regulation of tRNA processing
(IMP)
-
regulation of ubiquinone biosynthetic process
(IGI,
IMP)
-
response to drug
(IMP,
IPI)
-
ribophagy
(IGI)
-
ubiquitin-dependent endocytosis
(IMP)
-
ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway
(IMP)
Cellular Component
- Manually Curated
- 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
- Essential gene; conditional (ts) mutations lead to buildup of unprocessed reporter proteins normally targeted for degradation and to defects in processing of mRNA, rRNA and tRNA precursors; reduction of function causes higher sensitivity to cell wall-affecting chemicals (caffeine, Calcofluor White); repression results in opi- phenotype (overproduction and excretion of inositol in the absence of inositol and choline); overexpression causes slow growth
Classical Genetics
- repressible
- conditional
- overexpression
- unspecified
- reduction of function
Large-scale Survey
- reduction of function
- null
- overexpression
- repressible
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.
824 total interactions for 446 unique genes
Physical Interactions
- Affinity Capture-MS: 156
- Affinity Capture-RNA: 2
- Affinity Capture-Western: 66
- Biochemical Activity: 114
- Co-crystal Structure: 2
- Co-fractionation: 2
- Co-localization: 1
- Co-purification: 1
- Far Western: 2
- PCA: 1
- Protein-peptide: 122
- Reconstituted Complex: 114
- Two-hybrid: 34
Genetic Interactions
- Dosage Growth Defect: 6
- Dosage Lethality: 16
- Dosage Rescue: 27
- Negative Genetic: 79
- Phenotypic Enhancement: 25
- Phenotypic Suppression: 12
- Positive Genetic: 14
- Synthetic Growth Defect: 11
- Synthetic Lethality: 5
- Synthetic Rescue: 12
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.
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.
Literature Details
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.