Homo sapiens Protein: MTO1
Summary
InnateDB Protein IDBP-92383.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MTO1
Protein Name mitochondrial translation optimization 1 homolog (S. cerevisiae)
Synonyms COXPD10;
Species Homo sapiens
Ensembl Protein ENSP00000359323
InnateDB Gene IDBG-92375 (MTO1)
Protein Structure
UniProt Annotation
Function Involved in the 5-carboxymethylaminomethyl modification (mnm(5)s(2)U34) of the wobble uridine base in mitochondrial tRNAs. {ECO:0000269PubMed:12011058}.
Subcellular Localization Mitochondrion {ECO:0000250}.
Disease Associations Combined oxidative phosphorylation deficiency 10 (COXPD10) [MIM:614702]: An autosomal recessive disorder resulting in variable defects of mitochondrial oxidative respiration. Affected individuals present in infancy with hypertrophic cardiomyopathy and lactic acidosis. The severity is variable, but can be fatal in the most severe cases. {ECO:0000269PubMed:22608499}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Ubiquitously expressed in various tissues, but with a markedly elevated expression in tissues of high metabolic rates including cochlea. {ECO:0000269PubMed:12011058}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
Experimentally validated
Total 5 [view]
Protein-Protein 5 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0044822 poly(A) RNA binding
GO:0050660 flavin adenine dinucleotide binding
Biological Process
GO:0008033 tRNA processing
GO:0055114 oxidation-reduction process
Cellular Component
GO:0005739 mitochondrion
Protein Structure and Domains
PDB ID
InterPro IPR002218 Glucose-inhibited division protein A-related
IPR003953 FAD binding domain
IPR013027 FAD-dependent pyridine nucleotide-disulphide oxidoreductase
PFAM PF01134
PF00890
PRINTS PR00368
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9Y2Z2
PhosphoSite PhosphoSite-Q9Y2Z2
TrEMBL
UniProt Splice Variant
Entrez Gene 25821
UniGene Hs.347614
RefSeq NP_598400
HUGO HGNC:19261
OMIM 614667
CCDS CCDS4979
HPRD 17611
IMGT
EMBL AF132937 AF319422 AF442963 AF469110 AF469111 AK074625 AK225828 AL603910 AL833823 AY078985 AY078986 BC005808 BC011051 CH471051
GenPept AAD27712 AAG42814 AAH05808 AAH11051 AAL35894 AAL82394 AAL82395 AAL85490 AAL85491 BAG51977 CAD38685 CAI14880 CAI14881 CAI14882 EAW48762