MRPL11
Large ribosomal subunit protein uL11m
Also known as: RM11_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y3B7
- Gene
- MRPL11
- Ensembl
- ENSG00000174547
- Chromosome
- 11
- Canonical length
- 192 aa
- Protein class
- Predicted intracellular proteins, Ribosomal proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
This nuclear gene encodes a 39S subunit component of the mitochondial ribosome. Alternative splicing results in multiple transcript variants. Pseudogenes for this gene are found on chromosomes 5 and 12. [provided by RefSeq, May 2014]
Canonical amino-acid sequenceUniProt
192 residues, UniProt reviewed canonical sequence.
>Q9Y3B7|MRPL11
1 MSKLGRAARG LRKPEVGGVI RAIVRAGLAM PGPPLGPVLG QRGVSINQFC KEFNERTKDI
61 KEGIPLPTKI LVKPDRTFEI KIGQPTVSYF LKAAAGIEKG ARQTGKEVAG LVTLKHVYEI
121 ARIKAQDEAF ALQDVPLSSV VRSIIGSARS LGIRVVKDLS SEELAAFQKE RAIFLAAQKE
181 ADLAAQEEAA KKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MRPL11 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)
- 0.38
- Highest tissue expression
- 46 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 46 nTPM
- tongue: 34 nTPM
- rectum: 22 nTPM
- bone marrow: 22 nTPM
- ovary: 22 nTPM
- liver: 21 nTPM
Single-cell type
- esophageal basal cells: 259 nCPM
- migrating cytotrophoblasts: 219 nCPM
- extravillous trophoblasts: 217 nCPM
- enteric transient amplifying cells: 179 nCPM
- enteric stem cells: 165 nCPM
- cytotrophoblasts: 160 nCPM
Immune cell
- myeloid DC: 55 nTPM
- memory B-cell: 52 nTPM
- intermediate monocyte: 45 nTPM
- T-reg: 44 nTPM
- total PBMC: 43 nTPM
- naive CD4 T-cell: 41 nTPM
Brain region
- choroid plexus: 13 nTPM
- thalamus: 13 nTPM
- cerebral cortex: 12 nTPM
- basal ganglia: 10 nTPM
- cerebellum: 10 nTPM
- medulla oblongata: 10 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)
- 1.88
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.19
- DepMap mean gene effect
- -0.27
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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
- Ribosomal protein uL11
- Large ribosomal subunit protein uL11, C-terminal
- Large ribosomal subunit protein uL11, N-terminal
- Large ribosomal subunit protein uL11, C-terminal domain superfamily
- Large ribosomal subunit protein uL11, N-terminal domain superfamily
- Ribosomal protein L11, RNA binding domain
- Ribosomal protein L11, N-terminal domain
- Large ribosomal subunit protein uL11, bacteria
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MRPL11 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 MRPL11 as an antibody target. Whether an autoantibody or antibody against MRPL11 could matter depends on whether native MRPL11 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MRPL11 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 MRPL11 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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