Cathepsin A is an enzyme that is classified both as a cathepsin and a carboxypeptidase. In humans, it is encoded by the CTSA gene.[5]
| CTSA |
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| Available structures |
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| PDB | Ortholog search: PDBe RCSB |
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| List of PDB id codes |
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1IVY, 3BP4, 3BP7, 3BXN, 4AZ0, 4AZ3, 4CI9, 4CIA, 4CIB, 4MWS, 4MWT |
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| Identifiers |
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| Aliases | CTSA, GLB2, GSL, NGBE, PPCA, PPGB, cathepsin A |
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| External IDs | OMIM: 613111 MGI: 97748 HomoloGene: 80163 GeneCards: CTSA |
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| Gene location (Human) |
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 | | Chr. | Chromosome 20 (human)[1] |
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| | Band | 20q13.12 | Start | 45,890,144 bp[1] |
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| End | 45,898,820 bp[1] |
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| Gene location (Mouse) |
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 | | Chr. | Chromosome 2 (mouse)[2] |
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| | Band | 2 H3|2 85.27 cM | Start | 164,832,873 bp[2] |
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| End | 164,841,032 bp[2] |
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| RNA expression pattern |
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 | | More reference expression data |
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| Gene ontology |
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| Molecular function | • peptidase activity • carboxypeptidase activity • GO:0010577 enzyme activator activity • hydrolase activity • exo-alpha-sialidase activity • serine-type carboxypeptidase activity
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| Cellular component | • membrane • intracellular membrane-bounded organelle • nucleoplasm • lysosomal lumen • endoplasmic reticulum • lysosome • lumenal side of lysosomal membrane • extracellular exosome • extracellular region • azurophil granule lumen
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| Biological process | • regulation of protein stability • glycosphingolipid metabolic process • proteolysis • regulation of chaperone-mediated autophagy • proteolysis involved in cellular protein catabolic process • intracellular protein transport • GO:0048554 positive regulation of catalytic activity • neutrophil degranulation • negative regulation of chaperone-mediated autophagy
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| Sources:Amigo / QuickGO |
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| Orthologs |
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| Species | Human | Mouse |
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| Entrez | | |
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| Ensembl | | |
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| UniProt | | |
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| RefSeq (mRNA) | |
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NM_001167594 NM_000308 NM_001127695 |
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| RefSeq (protein) | |
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NP_000299 NP_001121167 NP_001161066 |
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| Location (UCSC) | Chr 20: 45.89 – 45.9 Mb | Chr 2: 164.83 – 164.84 Mb |
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| PubMed search | [3] | [4] |
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| Wikidata |
| View/Edit Human | View/Edit Mouse |
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FunctionEditThis gene encodes a glycoprotein that associates with lysosomal enzymes beta-galactosidase and neuraminidase to form a complex of high-molecular-weight multimers. The formation of this complex provides a protective role for stability and activity. It is protective for β-galactosidase and neuraminidase.[6]
Clinical significanceEditDeficiencies in this gene are linked to multiple forms of galactosialidosis.[5]
InteractionsEditCathepsin A has been shown to interact with NEU1.[7]