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EMI1 [ Saccharomyces cerevisiae S288C ]

Gene ID: 852125, updated on 22-Aug-2024

Summary

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Official Symbol
EMI1
Primary source
FungiDB:YDR512C
Locus tag
YDR512C
See related
SGD:S000002920; AllianceGenome:SGD:S000002920; VEuPathDB:YDR512C
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Saccharomyces cerevisiae S288C (strain: S288C)
Lineage
Eukaryota; Fungi; Dikarya; Ascomycota; Saccharomycotina; Saccharomycetes; Saccharomycetales; Saccharomycetaceae; Saccharomyces
Summary
Involved in mitochondrion organization. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

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Location:
chromosome: IV
Exon count:
1
Sequence:
Chromosome: IV; NC_001136.10 (1470500..1471063, complement)

Chromosome IV - NC_001136.10Genomic Context describing neighboring genes Neighboring gene SUMO family protein SMT3 Neighboring gene Sdh7p Neighboring gene dithiol glutaredoxin GRX2 Neighboring gene uncharacterized protein Neighboring gene Slf1p

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_001136.10

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Complementation of coenzyme Q-deficient yeast by coenzyme Q analogues requires the isoprenoid side chain. James AM, et al. FEBS J, 2010 May. PMID 20345901
  2. Systematic analysis of the twin cx(9)c protein family. Longen S, et al. J Mol Biol, 2009 Oct 23. PMID 19703468
  3. Large-scale functional genomic analysis of sporulation and meiosis in Saccharomyces cerevisiae. Enyenihi AH, et al. Genetics, 2003 Jan. PMID 12586695, Free PMC Article
  4. FMP30 is required for the maintenance of a normal cardiolipin level and mitochondrial morphology in the absence of mitochondrial phosphatidylethanolamine synthesis. Kuroda T, et al. Mol Microbiol, 2011 Apr. PMID 21306442
  5. The yeast oligopeptide transporter Opt2 is localized to peroxisomes and affects glutathione redox homeostasis. Elbaz-Alon Y, et al. FEMS Yeast Res, 2014 Nov. PMID 25130273

See all (41) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Loss of Mdm35, Emi1, and Mrp10 leads to abnormal mitochondrial morphology
    Title: Systematic analysis of the twin cx(9)c protein family.
Submit: New GeneRIF Correction

Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Homology

Gene Ontology Provided by SGD

Function Evidence Code Pubs
enables molecular_function ND
No biological Data available
more info
  
Process Evidence Code Pubs
involved_in ascospore formation HMP PubMed 
involved_in meiotic cell cycle IEA
Inferred from Electronic Annotation
more info
  
involved_in mitochondrion organization IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in sporulation resulting in formation of a cellular spore IEA
Inferred from Electronic Annotation
more info
  
Component Evidence Code Pubs
is_active_in cellular_component ND
No biological Data available
more info
  

General protein information

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Preferred Names
Emi1p
NP_010800.3
  • Non-essential hypothetical protein; required for transcriptional induction of the early meiotic-specific transcription factor IME1, also required for sporulation; contains twin cysteine-x9-cysteine motifs; deletion affects mitochondrial morphology

NCBI Reference Sequences (RefSeq)

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Genome Annotation

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference assembly

Genomic

  1. NC_001136.10 Reference assembly

    Range
    1470500..1471063 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001180820.3 → NP_010800.3  TPA: Emi1p [Saccharomyces cerevisiae S288C]

    See identical proteins and their annotated locations for NP_010800.3

    Status: REVIEWED

    UniProtKB/Swiss-Prot
    D6VTD3, Q04406
    UniProtKB/TrEMBL
    G2WBN9, N1P7Q1
    Conserved Domains (1) summary
    pfam11326
    Location:104 → 181
    DUF3128; Protein of unknown function (DUF3128)
Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
Q04406.1

Gene LinkOut

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