MRPL54
Large ribosomal subunit protein mL54
Also known as: RM54_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6P161
- Gene
- MRPL54
- Ensembl
- ENSG00000183617
- Chromosome
- 19
- Canonical length
- 138 aa
- Protein class
- Predicted intracellular proteins, Ribosomal proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
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. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
138 residues, UniProt reviewed canonical sequence.
>Q6P161|MRPL54
1 MATKRLFGAT RTWAGWGAWE LLNPATSGRL LARDYAKKPV MKGAKSGKGA VTSEALKDPD
61 VCTDPVQLTT YAMGVNIYKE GQDVPLKPDA EYPEWLFEMN LGPPKTLEEL DPESREYWRR
121 LRKQNIWRHN RLSKNKRLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MRPL54 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.61
- Highest tissue expression
- 121 nTPM
Expression across tissuesHPA
Tissue
- liver: 121 nTPM
- bone marrow: 103 nTPM
- choroid plexus: 99 nTPM
- adrenal gland: 85 nTPM
- pancreas: 84 nTPM
- kidney: 81 nTPM
Single-cell type
- hepatocytes: 291 nCPM
- esophageal suprabasal cells: 269 nCPM
- esophageal basal cells: 241 nCPM
- late primary spermatocytes: 227 nCPM
- parietal cells: 216 nCPM
- oocytes: 212 nCPM
Immune cell
- T-reg: 169 nTPM
- total PBMC: 144 nTPM
- memory B-cell: 140 nTPM
- myeloid DC: 135 nTPM
- non-classical monocyte: 135 nTPM
- NK-cell: 133 nTPM
Brain region
- white matter: 38 nTPM
- cerebellum: 35 nTPM
- choroid plexus: 35 nTPM
- hypothalamus: 35 nTPM
- thalamus: 35 nTPM
- medulla oblongata: 34 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.44
- gnomAD pLI
- 0.02
- gnomAD missense Z
- 0.06
- DepMap mean gene effect
- -0.34
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Large ribosomal subunit protein mL54
- Mitochondrial ribosomal protein L37
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MRPL54 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MRPL54 as an antibody target. Whether an autoantibody or antibody against MRPL54 could matter depends on whether native MRPL54 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MRPL54 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label MRPL54 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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