LGMN

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Legumain is a protein that in humans is encoded by the LGMN gene.[5][6][7]

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LGMN
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesLGMN, AEP, LGMN1, PRSC1, legumain
External IDsOMIM: 602620; MGI: 1330838; HomoloGene: 38075; GeneCards: LGMN; OMA:LGMN - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001008530
NM_005606
NM_001363696
NM_001363699

NM_011175
NM_001378875

RefSeq (protein)

NP_001008530
NP_005597
NP_001350625
NP_001350628

NP_035305
NP_001365804

Location (UCSC)Chr 14: 92.7 – 92.75 MbChr 12: 102.36 – 102.41 Mb
PubMed search[3][4]
Wikidata
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This gene encodes a cysteine protease, legumain, 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.[7]

References

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