Mitochondrial translational release factor 1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Mitochondrial translational release factor 1, also known as MTRF1 is a human gene.[5][6]

AliasesMTRF1, MRF1, MTTRF1, RF1, mitochondrial translational release factor 1, mitochondrial translation release factor 1
End41,263,577 bp[1]
Quick facts MTRF1, Identifiers ...
MTRF1
Identifiers
AliasesMTRF1, MRF1, MTTRF1, RF1, mitochondrial translational release factor 1, mitochondrial translation release factor 1
External IDsOMIM: 604601; MGI: 2384815; HomoloGene: 20903; GeneCards: MTRF1; OMA:MTRF1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004294
NM_001354073
NM_001354074
NM_001354076

NM_145960

RefSeq (protein)

NP_004285
NP_001341002
NP_001341003
NP_001341005

NP_666072

Location (UCSC)Chr 13: 41.22 – 41.26 MbChr 14: 79.64 – 79.66 Mb
PubMed search[3][4]
Wikidata
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The protein encoded by this gene directs the termination of translation in response to the peptide chain termination codons. Initially thought to have a role in the termination of mitochondria protein synthesis. mtRF1 has been hypothesized to recognize non-standard stop codons AGA and AGG in vertebrates. Alternatively, based on detailed 3D modelling, it has been proposed to recognize stalled ribosomes in which a tRNA is still bound to the peptide chain, but in which the A-site of the ribosome is empty.

References

Further reading

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