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MSS1 Mss1p [ Saccharomyces cerevisiae S288C ]

Gene ID: 855037, updated on 2-Nov-2024

Summary

Official Symbol
MSS1
Official Full Name
Mss1p
Primary source
SGD:S000004625
Locus tag
YMR023C
See related
AllianceGenome:SGD:S000004625; FungiDB:YMR023C; VEuPathDB:YMR023C
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Saccharomyces cerevisiae S288C (strain: S288C)
Lineage
Eukaryota; Fungi; Dikarya; Ascomycota; Saccharomycotina; Saccharomycetes; Saccharomycetales; Saccharomycetaceae; Saccharomyces
Also known as
PET53
Summary
Predicted to enable GTP binding activity. Involved in mitochondrial tRNA wobble uridine modification. Located in mitochondrial inner membrane. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 23. Orthologous to human GTPBP3 (GTP binding protein 3, mitochondrial). [provided by Alliance of Genome Resources, Nov 2024]
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Genomic context

See MSS1 in Genome Data Viewer
Location:
chromosome: XIII
Exon count:
1
Sequence:
Chromosome: XIII; NC_001145.3 (319437..321017, complement)

Chromosome XIII - NC_001145.3Genomic Context describing neighboring genes Neighboring gene Mac1p Neighboring gene E2 ubiquitin-conjugating protein UBC7 Neighboring gene tRNA-Ala Neighboring gene mitochondrial 54S ribosomal protein YmL3

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Pathways from PubChem

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Gene Ontology Provided by SGD

Function Evidence Code Pubs
enables GTP binding IEA
Inferred from Electronic Annotation
more info
 
enables GTP binding ISS
Inferred from Sequence or Structural Similarity
more info
PubMed 
enables GTPase activity IEA
Inferred from Electronic Annotation
more info
 
Process Evidence Code Pubs
involved_in mitochondrial tRNA wobble uridine modification IMP
Inferred from Mutant Phenotype
more info
PubMed 
involved_in tRNA methylation IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in tRNA modification IEA
Inferred from Electronic Annotation
more info
 
involved_in tRNA processing IEA
Inferred from Electronic Annotation
more info
 
involved_in tRNA wobble uridine modification IBA
Inferred from Biological aspect of Ancestor
more info
 
Component Evidence Code Pubs
is_active_in cytoplasm IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in cytosol HDA PubMed 
located_in mitochondrial inner membrane IDA
Inferred from Direct Assay
more info
PubMed 
located_in mitochondrion HDA PubMed 
is_active_in mitochondrion IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in mitochondrion IEA
Inferred from Electronic Annotation
more info
 

General protein information

Preferred Names
Mss1p
NP_013736.1
  • Mitochondrial protein; forms a heterodimer complex with Mto1p that performs the 5-carboxymethylaminomethyl modification of the wobble uridine base in mitochondrial tRNAs; similar to human GTPBP3

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_001145.3 Reference assembly

    Range
    319437..321017 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_001182519.1NP_013736.1  TPA: Mss1p [Saccharomyces cerevisiae S288C]

    See identical proteins and their annotated locations for NP_013736.1

    Status: REVIEWED

    UniProtKB/Swiss-Prot
    D6VZJ7, P32559, Q0PHA7
    UniProtKB/TrEMBL
    A6ZM85, B3LLS4, C7GL96, C8ZEN0, N1NY71
    Conserved Domains (1) summary
    COG0486
    Location:38526
    MnmE; tRNA U34 5-carboxymethylaminomethyl modifying GTPase MnmE/TrmE [Translation, ribosomal structure and biogenesis]