LAMTOR5
Ragulator complex protein LAMTOR5
Also known as: HBXIP, LTOR5_HUMAN, MGC71071, XIP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43504
- Gene
- LAMTOR5
- Ensembl
- ENSG00000134248
- Chromosome
- 1
- Canonical length
- 91 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a protein that specifically complexes with the C-terminus of hepatitis B virus X protein (HBx). The function of this protein is to negatively regulate HBx activity and thus to alter the replication life cycle of the virus. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
91 residues, UniProt reviewed canonical sequence.
>O43504|LAMTOR5
1 MEATLEQHLE DTMKNPSIVG VLCTDSQGLN LGCRGTLSDE HAGVISVLAQ QAAKLTSDPT
61 DIPVVCLESD NGNIMIQKHD GITVAVHKMA SLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LAMTOR5 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)
- 0.34
- Highest tissue expression
- 431 nTPM
Expression across tissuesHPA
Tissue
- kidney: 431 nTPM
- heart muscle: 265 nTPM
- skeletal muscle: 260 nTPM
- tongue: 259 nTPM
- bone marrow: 236 nTPM
- choroid plexus: 209 nTPM
Single-cell type
- oocytes: 898 nCPM
- esophageal apical cells: 666 nCPM
- parietal cells: 631 nCPM
- syncytiotrophoblasts: 567 nCPM
- hofbauer cells: 558 nCPM
- esophageal suprabasal cells: 557 nCPM
Immune cell
- eosinophil: 487 nTPM
- neutrophil: 350 nTPM
- memory B-cell: 346 nTPM
- naive B-cell: 324 nTPM
- plasmacytoid DC: 322 nTPM
- basophil: 297 nTPM
Brain region
- choroid plexus: 100 nTPM
- cerebellum: 99 nTPM
- white matter: 98 nTPM
- spinal cord: 94 nTPM
- hypothalamus: 90 nTPM
- thalamus: 88 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)
- 1.77
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.91
- DepMap mean gene effect
- -0.28
- 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
- cellular response to amino acid stimulus
- negative regulation of apoptotic process
- positive regulation of canonical NF-kappaB signal transduction
- positive regulation of gene expression
- positive regulation of interleukin-8 production
- positive regulation of protein localization to nucleus
- positive regulation of TOR signaling
- positive regulation of TORC1 signaling
- protein localization to lysosome
- regulation of cell size
- response to virus
- TORC1 signaling
- viral genome replication
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Ragulator complex protein LAMTOR5
- Ragulator complex protein LAMTOR5
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LAMTOR5 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 LAMTOR5 as an antibody target. Whether an autoantibody or antibody against LAMTOR5 could matter depends on whether native LAMTOR5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LAMTOR5 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 LAMTOR5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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