LTB
Lymphotoxin-beta
Also known as: p33, TNFC, TNFC_HUMAN, TNFSF3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q06643
- Gene
- LTB
- Ensembl
- ENSG00000227507
- Chromosome
- 6
- Canonical length
- 244 aa
- Protein class
- Cancer-related genes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Centrosome
OverviewNCBI Gene
Lymphotoxin beta is a type II membrane protein of the TNF family. It anchors lymphotoxin-alpha to the cell surface through heterotrimer formation. The predominant form on the lymphocyte surface is the lymphotoxin-alpha 1/beta 2 complex (e.g. 1 molecule alpha/2 molecules beta) and this complex is the primary ligand for the lymphotoxin-beta receptor. The minor complex is lymphotoxin-alpha 2/beta 1. LTB is an inducer of the inflammatory response system and involved in normal development of lymphoid tissue. Lymphotoxin-beta isoform b is unable to complex with lymphotoxin-alpha suggesting a function for lymphotoxin-beta which is independent of lympyhotoxin-alpha. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
244 residues, UniProt reviewed canonical sequence.
>Q06643|LTB
1 MGALGLEGRG GRLQGRGSLL LAVAGATSLV TLLLAVPITV LAVLALVPQD QGGLVTETAD
61 PGAQAQQGLG FQKLPEEEPE TDLSPGLPAA HLIGAPLKGQ GLGWETTKEQ AFLTSGTQFS
121 DAEGLALPQD GLYYLYCLVG YRGRAPPGGG DPQGRSVTLR SSLYRAGGAY GPGTPELLLE
181 GAETVTPVLD PARRQGYGPL WYTSVGFGGL VQLRRGERVY VNISHPDMVD FARGKTFFGA
241 VMVGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LTB 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.43
- Highest tissue expression
- 220 nTPM
Expression across tissuesHPA
Tissue
- spleen: 220 nTPM
- lymph node: 97 nTPM
- appendix: 78 nTPM
- thymus: 78 nTPM
- small intestine: 62 nTPM
- tonsil: 45 nTPM
Single-cell type
- b-cells: 35 nCPM
- innate lymphoid cells: 19 nCPM
- pdcs: 12 nCPM
- t-cells: 11 nCPM
- papillary tip epithelial cells: 5.5 nCPM
- neutrophils: 3.7 nCPM
Immune cell
- memory B-cell: 1,028 nTPM
- naive B-cell: 1,022 nTPM
- memory CD4 T-cell: 938 nTPM
- naive CD4 T-cell: 727 nTPM
- T-reg: 672 nTPM
- MAIT T-cell: 649 nTPM
Brain region
- medulla oblongata: 0.6 nTPM
- basal ganglia: 0.4 nTPM
- pons: 0.4 nTPM
- thalamus: 0.4 nTPM
- cerebral cortex: 0.3 nTPM
- choroid plexus: 0.3 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)
- 1.92
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.79
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- none
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
- cell surface receptor signaling pathway
- cell-cell signaling
- gene expression
- immune response
- lymph node development
- positive regulation of canonical NF-kappaB signal transduction
- positive regulation of extrinsic apoptotic signaling pathway
- positive regulation of interleukin-12 production
- signal transduction
- skin development
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads LTB as an antibody target. Whether an autoantibody or antibody against LTB could matter depends on whether native LTB is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LTB is annotated at the cell surface, where native LTB is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label LTB as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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