Cathepsin A

 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
Protein CTSA PDB 1ivy.png
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCTSA, GLB2, GSL, NGBE, PPCA, PPGB, cathepsin A
External IDsOMIM613111 MGI97748 HomoloGene80163 GeneCardsCTSA
Gene location (Human)
Chromosome 20 (human)
Chr.Chromosome 20 (human)[1]
Chromosome 20 (human)
Genomic location for CTSA
Genomic location for CTSA
Band20q13.12Start45,890,144 bp[1]
End45,898,820 bp[1]
RNA expression pattern
PBB GE CTSA 200661 at fs.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001167594
NM_000308
NM_001127695

NM_001038492
NM_008906

RefSeq (protein)

NP_000299
NP_001121167
NP_001161066

NP_001033581
NP_032932

Location (UCSC)Chr 20: 45.89 – 45.9 MbChr 2: 164.83 – 164.84 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

FunctionEdit

This 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 significanceEdit

Deficiencies in this gene are linked to multiple forms of galactosialidosis.[5]

InteractionsEdit

Cathepsin A has been shown to interact with NEU1.[7]

This article uses material from the Wikipedia article
 Metasyntactic variable, which is released under the 
Creative Commons
Attribution-ShareAlike 3.0 Unported License
.