LAMTOR3
Ragulator complex protein LAMTOR3
Also known as: LTOR3_HUMAN, MAP2K1IP1, MAPBP, MAPKSP1, MP1, Ragulator3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UHA4
- Gene
- LAMTOR3
- Ensembl
- ENSG00000109270
- Chromosome
- 4
- Canonical length
- 124 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a scaffold protein that functions in the extracellular signal-regulated kinase (ERK) cascade. The protein is localized to late endosomes by the mitogen-activated protein-binding protein-interacting protein, and binds specifically to MAP kinase kinase MAP2K1/MEK1, MAP kinase MAPK3/ERK1, and MAP kinase MAPK1/ERK2. Studies of the orthologous gene in mouse indicate that it regulates late endosomal traffic and cell proliferation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. A pseudogene of this gene is located on the long arm of chromosome 13. [provided by RefSeq, Aug 2011]
Canonical amino-acid sequenceUniProt
124 residues, UniProt reviewed canonical sequence.
>Q9UHA4|LAMTOR3
1 MADDLKRFLY KKLPSVEGLH AIVVSDRDGV PVIKVANDNA PEHALRPGFL STFALATDQG
61 SKLGLSKNKS IICYYNTYQV VQFNRLPLVV SFIASSSANT GLIVSLEKEL APLFEELRQV
121 VEVSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LAMTOR3 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.3
- Highest tissue expression
- 37 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 37 nTPM
- kidney: 36 nTPM
- parathyroid gland: 34 nTPM
- thyroid gland: 32 nTPM
- bone marrow: 31 nTPM
- esophagus: 28 nTPM
Single-cell type
- esophageal apical cells: 321 nCPM
- neutrophils: 184 nCPM
- esophageal suprabasal cells: 137 nCPM
- oocytes: 120 nCPM
- parietal cells: 115 nCPM
- hofbauer cells: 111 nCPM
Immune cell
- neutrophil: 59 nTPM
- basophil: 44 nTPM
- eosinophil: 39 nTPM
- non-classical monocyte: 29 nTPM
- intermediate monocyte: 27 nTPM
- myeloid DC: 19 nTPM
Brain region
- cerebellum: 21 nTPM
- cerebral cortex: 21 nTPM
- midbrain: 20 nTPM
- hypothalamus: 19 nTPM
- thalamus: 18 nTPM
- pons: 18 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)
- 0.55
- gnomAD pLI
- 0.73
- gnomAD missense Z
- 0.04
- DepMap mean gene effect
- -0.58
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to amino acid stimulus
- intracellular protein localization
- positive regulation of MAPK cascade
- positive regulation of TOR signaling
- positive regulation of TORC1 signaling
- protein localization to cell junction
- TORC1 signaling
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Ragulator complex protein LAMTOR3
- Mitogen-activated protein kinase kinase 1 interacting
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LAMTOR3 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 LAMTOR3 as an antibody target. Whether an autoantibody or antibody against LAMTOR3 could matter depends on whether native LAMTOR3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LAMTOR3 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 LAMTOR3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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