Homo sapiens Protein: TSFM
Summary
InnateDB Protein IDBP-379173.4
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TSFM
Protein Name Ts translation elongation factor, mitochondrial
Synonyms EFTS; EFTSMT;
Species Homo sapiens
Ensembl Protein ENSP00000388330
InnateDB Gene IDBG-43934 (TSFM)
Protein Structure
UniProt Annotation
Function Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome. {ECO:0000255HAMAP-Rule:MF_03135}.
Subcellular Localization Mitochondrion.
Disease Associations Combined oxidative phosphorylation deficiency 3 (COXPD3) [MIM:610505]: A mitochondrial disease resulting in severe metabolic acidosis with encephalomyopathy or with hypertrophic cardiomyopathy. Patients show a severe defect in mitochondrial translation leading to a failure to assemble adequate amounts of three of the oxidative phosphorylation complexes. {ECO:0000269PubMed:17033963, ECO:0000269PubMed:22499341}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Expressed in all tissues, with the highest levels of expression in skeletal muscle, liver and kidney.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 9 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 9 [view]
Protein-Protein 9 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003746 translation elongation factor activity
GO:0005515 protein binding
GO:0044822 poly(A) RNA binding
Biological Process
GO:0006414 translational elongation
GO:0032784 regulation of DNA-templated transcription, elongation
Cellular Component
GO:0005622 intracellular
GO:0005634 nucleus
GO:0005739 mitochondrion
Protein Structure and Domains
PDB ID
InterPro IPR000449 Ubiquitin-associated domain/translation elongation factor EF-Ts, N-terminal
IPR009060 UBA-like
IPR014039 Translation elongation factor EFTs/EF1B, dimerisation
PFAM PF00627
PF00889
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P43897
PhosphoSite PhosphoSite-P43897
TrEMBL E5KS95
UniProt Splice Variant
Entrez Gene 10102
UniGene
RefSeq NP_005717
HUGO HGNC:12367
OMIM 604723
CCDS CCDS8958
HPRD 05285
IMGT
EMBL AC025165 AF110399 AK304621 AK308981 BC022862 BC093068 CH471054 HQ205906 HQ205907 HQ205908 HQ205909 HQ205910 HQ205911 HQ205912 HQ205913 HQ205914 HQ205915 HQ205916 HQ205917 HQ205918 HQ205919 HQ205920 HQ205921 HQ205922 HQ205923 HQ205924 HQ205925 HQ205926 HQ205927 HQ205928 HQ205929 HQ205930 HQ205931 HQ205932 HQ205933 HQ205934 HQ205935 HQ205936 HQ205937 HQ205938 HQ205939 HQ205940 HQ205941 HQ205942 HQ205943 HQ205944 HQ205945 L37936
GenPept AAC37577 AAD20224 AAH22862 AAH93068 ADP91774 ADP91775 ADP91776 ADP91777 ADP91778 ADP91779 ADP91780 ADP91781 ADP91782 ADP91783 ADP91784 ADP91785 ADP91786 ADP91787 ADP91788 ADP91789 ADP91790 ADP91791 ADP91792 ADP91793 ADP91794 ADP91795 ADP91796 ADP91797 ADP91798 ADP91799 ADP91800 ADP91801 ADP91802 ADP91803 ADP91804 ADP91805 ADP91806 ADP91807 ADP91808 ADP91809 ADP91810 ADP91811 ADP91812 ADP91813 BAG65403 EAW97075