Mitochondrial ribosomal protein L19

(Redirected from MRPL19)

39S ribosomal protein L19, mitochondrial is a protein that in humans is encoded by the MRPL19 gene.[5][6][7]

MRPL19
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMRPL19, L19mt, MRP-L15, MRP-L19, MRPL15, RLX1, RPML15, mitochondrial ribosomal protein L19
External IDsOMIM: 611832; MGI: 1926274; HomoloGene: 8851; GeneCards: MRPL19; OMA:MRPL19 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_014763

NM_026490

RefSeq (protein)

NP_055578

NP_080766

Location (UCSC)Chr 2: 75.65 – 75.69 MbChr 6: 81.93 – 81.94 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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% protein to rRNA 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.[7]

References

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  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000115364 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000030045 Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Kenmochi N, Suzuki T, Uechi T, Magoori M, Kuniba M, Higa S, et al. (Sep 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.
  6. Anthoni H, Zucchelli M, Matsson H, Muller-Myhsok B, Fransson I, Schumacher J, et al. (Apr 2007). "A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia". Human Molecular Genetics. 16 (6): 667–677. doi:10.1093/hmg/ddm009. PMID 17309879.
  7. 1 2 "Entrez Gene: MRPL19 mitochondrial ribosomal protein L19".

Further reading

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