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1 Clinical relevance  





2 References  





3 Further reading  





4 External links  














Mitochondrial ribosomal protein L3






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From Wikipedia, the free encyclopedia
 


MRPL3
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMRPL3, COXPD9, MRL3, RPML3, mitochondrial ribosomal protein L3
External IDsOMIM: 607118; MGI: 2137204; HomoloGene: 31431; GeneCards: MRPL3; OMA:MRPL3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_007208

NM_053159
NM_001364512
NM_001364513

RefSeq (protein)

NP_009139

NP_444389
NP_001351441
NP_001351442

Location (UCSC)Chr 3: 131.46 – 131.5 MbChr 9: 104.93 – 104.96 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Mitochondrial ribosomal protein L3 is a protein that in humans is encoded by the MRPL3 gene.[5]

Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% proteintorRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein that belongs to the L3P ribosomal protein family. A pseudogene corresponding to this gene is found on chromosome 13q. [provided by RefSeq, Jul 2008].[5]

Clinical relevance[edit]

Mutations in this gene have been shown to cause mitochondrial cardiomyopathy.[6]

References[edit]

  • ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  • ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  • ^ a b "Entrez Gene: Mitochondrial ribosomal protein L3". Retrieved 2011-12-30.
  • ^ Galmiche L, Serre V, Beinat M, Assouline Z, Lebre AS, Chretien D, Nietschke P, Benes V, Boddaert N, Sidi D, Brunelle F, Rio M, Munnich A, Rötig A (November 2011). "Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy". Hum. Mutat. 32 (11): 1225–31. doi:10.1002/humu.21562. PMID 21786366. S2CID 46713472.
  • Further reading[edit]

    • Kenmochi, N.; Suzuki, T.; Uechi, T.; Magoori, M.; Kuniba, M.; Higa, S.; Watanabe, K.; Tanaka, T. (2001). "The Human Mitochondrial Ribosomal Protein Genes: Mapping of 54 Genes to the Chromosomes and Implications for Human Disorders". Genomics. 77 (1–2): 65–70. doi:10.1006/geno.2001.6622. PMID 11543634.
  • Ou, J. H.; Yen, T. S.; Wang, Y. F.; Kam, W. K.; Rutter, W. J. (1987). "Cloning and characterization of a human ribosomal protein gene with enhanced expression in fetal and neoplastic cells". Nucleic Acids Research. 15 (21): 8919–8934. doi:10.1093/nar/15.21.8919. PMC 306413. PMID 2891103.
  • External links[edit]

  • t
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  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Mitochondrial_ribosomal_protein_L3&oldid=1142697697"

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    This page was last edited on 3 March 2023, at 22:14 (UTC).

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