LGMN
Legumain
Also known as: LGMN_HUMAN, LGMN1, PRSC1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q99538
- Gene
- LGMN
- Ensembl
- ENSG00000100600
- Chromosome
- 14
- Canonical length
- 433 aa
- Protein class
- Cancer-related genes, Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles
- Secretome location
- Intracellular and membrane
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a cysteine protease that has a strict specificity for hydrolysis of asparaginyl bonds. This enzyme may be involved in the processing of bacterial peptides and endogenous proteins for MHC class II presentation in the lysosomal/endosomal systems. Enzyme activation is triggered by acidic pH and appears to be autocatalytic. Protein expression occurs after monocytes differentiate into dendritic cells. A fully mature, active enzyme is produced following lipopolysaccharide expression in mature dendritic cells. Overexpression of this gene may be associated with the majority of solid tumor types. This gene has a pseudogene on chromosome 13. Several alternatively spliced transcript variants have been described, but the biological validity of only two has been determined. These two variants encode the same isoform. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
433 residues, UniProt reviewed canonical sequence.
>Q99538|LGMN
1 MVWKVAVFLS VALGIGAVPI DDPEDGGKHW VVIVAGSNGW YNYRHQADAC HAYQIIHRNG
61 IPDEQIVVMM YDDIAYSEDN PTPGIVINRP NGTDVYQGVP KDYTGEDVTP QNFLAVLRGD
121 AEAVKGIGSG KVLKSGPQDH VFIYFTDHGS TGILVFPNED LHVKDLNETI HYMYKHKMYR
181 KMVFYIEACE SGSMMNHLPD NINVYATTAA NPRESSYACY YDEKRSTYLG DWYSVNWMED
241 SDVEDLTKET LHKQYHLVKS HTNTSHVMQY GNKTISTMKV MQFQGMKRKA SSPVPLPPVT
301 HLDLTPSPDV PLTIMKRKLM NTNDLEESRQ LTEEIQRHLD ARHLIEKSVR KIVSLLAASE
361 AEVEQLLSER APLTGHSCYP EALLHFRTHC FNWHSPTYEY ALRHLYVLVN LCEKPYPLHR
421 IKLSMDHVCL GHYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LGMN 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)
- 0.23
- Highest tissue expression
- 246 nTPM
Expression across tissuesHPA
Tissue
- placenta: 246 nTPM
- parathyroid gland: 232 nTPM
- kidney: 192 nTPM
- spleen: 191 nTPM
- lymph node: 166 nTPM
- adipose tissue: 162 nTPM
Single-cell type
- hofbauer cells: 2,621 nCPM
- kupffer cells: 1,061 nCPM
- macrophages: 653 nCPM
- syncytiotrophoblasts: 585 nCPM
- esophageal apical cells: 404 nCPM
- enterocytes: 316 nCPM
Immune cell
- plasmacytoid DC: 209 nTPM
- myeloid DC: 19 nTPM
- memory B-cell: 17 nTPM
- naive CD4 T-cell: 15 nTPM
- naive B-cell: 15 nTPM
- T-reg: 9.7 nTPM
Brain region
- thalamus: 95 nTPM
- choroid plexus: 65 nTPM
- white matter: 62 nTPM
- pons: 47 nTPM
- hypothalamus: 44 nTPM
- cerebral cortex: 40 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)
- 0.69
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.22
- DepMap mean gene effect
- 0.11
- DepMap dependency class
- none
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
- antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent
- antigen processing and presentation of exogenous peptide antigen via MHC class II
- associative learning
- cellular response to amyloid-beta
- cellular response to calcium ion
- cellular response to hepatocyte growth factor stimulus
- dendritic spine organization
- memory
- negative regulation of ERBB signaling pathway
- negative regulation of gene expression
- negative regulation of multicellular organism growth
- negative regulation of neuron apoptotic process
- positive regulation of cell population proliferation
- positive regulation of endothelial cell chemotaxis
- positive regulation of long-term synaptic potentiation
- positive regulation of mitotic cell cycle
- positive regulation of monocyte chemotaxis
- protein maturation
- proteolysis
- proteolysis involved in protein catabolic process
- receptor catabolic process
- renal system process
- response to acidic pH
- vacuolar protein processing
- vitamin D metabolic process
Molecular functions
- cysteine-type endopeptidase activity
- endopeptidase activator activity
- peptidase activity
- tau protein binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Peptidase C13, legumain
- Peptidase C13 family
- Asparaginyl endopeptidase
- Legumain prodomain superfamily
- Legumain, prodomain
- Legumain, prodomain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LGMN 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 LGMN as an antibody target. Whether an autoantibody or antibody against LGMN could matter depends on whether native LGMN is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LGMN 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 LGMN as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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