COX10 / YPL172C Overview


Standard Name
COX10 1
Systematic Name
YPL172C
SGD ID
SGD:S000006093
Feature Type
ORF , Verified
Description
Heme A:farnesyltransferase; catalyzes first step in conversion of protoheme to heme A prosthetic group required for cytochrome c oxidase activity; human ortholog COX10 can complement yeast cox10 null mutant; human ortholog COX10 is associated with mitochondrial disorders 2 3
Name Description
Cytochrome c OXidase 1
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
COX10/YPL172C is located on the left arm of chromosome XVI between MRPL40 mitochondrial ribosomal protein and OYE3 NADPH oxidoreductase; coding sequence is 1389 nucleotides long with 10 SNPs, 3 of which cause amino acid polymorphisms
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
Cox10p is 462 amino acids long; contains a UbiA prenyltransferase conserved site near the middle of the protein
Length (a.a.)
462
Mol. Weight (Da)
52176.4
Isoelectric Point
10.33

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 COX10 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
Putative protoheme IX farnesyltransferase, catalyzes conversion of protoheme to heme A in heme A biosynthesis; localized to mitochondria in high-throughput experiments

View computational annotations

Molecular Function

Manually Curated

Biological Process

Manually Curated

Cellular Component

Manually Curated
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
COX10/YPL172C is a non-essential gene; null mutant fails to respire; in large-scale studies, the null mutant shows reduced competitive fitness and chronological lifespan, sensitivity to desiccation, starvation, and oxidative stress, small cell size, increased biofilm formation, and altered resistance to various chemicals
Disease Details

Disease

Disease Annotations consist of three mandatory components: a gene product, a term from the Disease Ontology (DO) controlled vocabulary and an evidence code. SGD provides manually curated DO Annotations derived from the literature. Click "Disease Details" to view all Disease information and evidence for this locus as well as diseases it shares with other genes.


Summary
Yeast COX10 is homologous to human COX10, and has been used to study Leigh syndrome, a cytochrome-c oxidase deficiency disease characterized by progressive loss of mental and movement abilities
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
Cox10p interacts physically with proteins involved in RNA catabolism and translation regulation; COX10 interacts genetically with genes involved in transcription

557 total interactions for 432 unique genes

Physical Interactions

  • Affinity Capture-RNA: 10
  • Affinity Capture-Western: 2
  • Biochemical Activity: 1
  • Co-localization: 1
  • Proximity Label-MS: 5

Genetic Interactions

  • Dosage Lethality: 1
  • Dosage Rescue: 4
  • Negative Genetic: 481
  • Phenotypic Enhancement: 1
  • Positive Genetic: 43
  • Synthetic Growth Defect: 4
  • Synthetic Rescue: 4
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.


Summary
COX10 promoter is bound by Uga3p in response to heat; COX10 transcription is regulated by Sfp1p in response to stress; COX10 mRNA is stabilized by Pbp1p
Regulators
5
Targets
0
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.


Last Updated: 2006-07-20

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.


Primary
20
Additional
38
Reviews
19

Resources