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Description for Protein TUFM

Tu translation elongation factor, mitochondrial
4 total interacting proteins; 2 platelet interacting proteins
Icon Book Platelet Evidence (proteome studies/others : 7/1)
(membrane: 1; microparticles: 1; platelet: 5; undefined: 1)
Summary:
This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17. [provided by RefSeq] (PubMed Links)
Domains and Motifs:
None Available
Gene Ontology:
Gene Ontology Annotations
KEGG - Enzyme ID(s):
3.6.5.3
KEGG - Orthology:
K02358
KEGG - Pathway(s):
None Available
Nomenclature / Alternative Names:
Elongation factor Tu mitochondrial; EFTU; EF TuMT; EF Tu mitochondrial; Tu translation elongation factor mitochondrial
Approved Symbol:
TUFM
(De-) Phosphorylations:
Total (de-) phosphorylation sites: 1
Human (de-) phosphorylation sites: 1; No platelet phosphorylation sites
Phosphorylation Targets:
Total phosphorylation targets: 0
Human phosphorylation targets: 0;Predicted platelet targets: 0
Protein Characteristics:
Isoform-specific Information
Icon DrugsAssociated Drugs (DrugBank Accession):

  • Guanosine-5'-Diphosphate(db)

    Associated Genetic Diseases:

  • Combined oxidative phosphorylation deficiency 4(Pd)
    		• Predicted Transmembrane Domains:
  • Isoform 1 : 0
    • Additional Identifiers:

    HPRD: 03861 Entrez Gene ID: 7284 OMIM ID: 602389 Swissprot Accession: P49411;