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.

CTSA
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1IVY, 3BP4, 3BP7, 3BXN, 4AZ0, 4AZ3, 4CI9, 4CIA, 4CIB, 4MWS, 4MWT
Identifiers
Aliases	CTSA, GLB2, GSL, NGBE, PPCA, PPGB, cathepsin A
External IDs	OMIM: 613111; MGI: 97748; HomoloGene: 80163; GeneCards: CTSA; OMA:CTSA - orthologs
Gene location (Human) Chr. Chromosome 20 (human) Band 20q13.12 Start 45,890,144 bp End 45,898,949 bp
Gene location (Mouse) Chr. Chromosome 2 (mouse) Band 2 H3|2 85.27 cM Start 164,674,793 bp End 164,682,952 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in right adrenal gland right adrenal cortex left adrenal gland left adrenal cortex mucosa of transverse colon stromal cell of endometrium monocyte rectum human kidney gallbladder Top expressed in stroma of bone marrow decidua calvaria lip right kidney yolk sac vestibular sensory epithelium proximal tubule skin of external ear uterus More reference expression data BioGPS More reference expression data
Gene ontology Molecular function peptidase activity carboxypeptidase activity enzyme activator activity hydrolase activity exo-alpha-sialidase activity serine-type carboxypeptidase activity 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 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 positive regulation of catalytic activity neutrophil degranulation negative regulation of chaperone-mediated autophagy Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 5476 19025 Ensembl ENSG00000064601 ENSMUSG00000017760 UniProt P10619 P16675 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 Mb Chr 2: 164.67 – 164.68 Mb PubMed search
Wikidata
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Function

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.

Clinical significance

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

Interactions

Cathepsin A has been shown to interact with NEU1.

Further reading

• Morreau H, Galjart NJ, Willemsen R, et al. (1992). "Human lysosomal protective protein. Glycosylation, intracellular transport, and association with beta-galactosidase in the endoplasmic reticulum". J. Biol. Chem. 267 (25): 17949–56. doi:10.1016/S0021-9258(19)37135-2. PMID 1387645.
• Halal F, Chitayat D, Parikh H, et al. (1992). "Ring chromosome 20 and possible assignment of the structural gene encoding human carboxypeptidase-L to the distal segment of the long arm of chromosome 20". Am. J. Med. Genet. 43 (3): 576–9. doi:10.1002/ajmg.1320430314. PMID 1605251.
• Jackman HL, Tan FL, Tamei H, et al. (1990). "A peptidase in human platelets that deamidates tachykinins. Probable identity with the lysosomal "protective protein"". J. Biol. Chem. 265 (19): 11265–72. doi:10.1016/S0021-9258(19)38586-2. PMID 1694176.
• Zhou XY, Galjart NJ, Willemsen R, et al. (1992). "A mutation in a mild form of galactosialidosis impairs dimerization of the protective protein and renders it unstable". EMBO J. 10 (13): 4041–8. doi:10.1002/j.1460-2075.1991.tb04980.x. PMC 453152. PMID 1756715.
• Galjart NJ, Morreau H, Willemsen R, et al. (1991). "Human lysosomal protective protein has cathepsin A-like activity distinct from its protective function". J. Biol. Chem. 266 (22): 14754–62. doi:10.1016/S0021-9258(18)98751-X. PMID 1907282.
• Yoshida K, Oshima A, Shimmoto M, et al. (1991). "Human beta-galactosidase gene mutations in GM1-gangliosidosis: a common mutation among Japanese adult/chronic cases". Am. J. Hum. Genet. 49 (2): 435–42. PMC 1683306. PMID 1907800.
• Wiegant J, Galjart NJ, Raap AK, d'Azzo A (1991). "The gene encoding human protective protein (PPGB) is on chromosome 20". Genomics. 10 (2): 345–9. doi:10.1016/0888-7543(91)90318-9. PMID 2071143.
• Strisciuglio P, Sly WS, Dodson WE, et al. (1991). "Combined deficiency of beta-galactosidase and neuraminidase: natural history of the disease in the first 18 years of an American patient with late infantile onset form". Am. J. Med. Genet. 37 (4): 573–7. doi:10.1002/ajmg.1320370431. PMID 2148053.
• Kase R, Itoh K, Takiyama N, et al. (1990). "Galactosialidosis: simultaneous deficiency of esterase, carboxy-terminal deamidase and acid carboxypeptidase activities". Biochem. Biophys. Res. Commun. 172 (3): 1175–9. doi:10.1016/0006-291X(90)91572-A. PMID 2244901.
• Willemsen R, Hoogeveen AT, Sips HJ, et al. (1986). "Immunoelectron microscopical localization of lysosomal beta-galactosidase and its precursor forms in normal and mutant human fibroblasts". Eur. J. Cell Biol. 40 (1): 9–15. PMID 3084261.
• Verheijen FW, Palmeri S, Galjaard H (1987). "Purification and partial characterization of lysosomal neuraminidase from human placenta". Eur. J. Biochem. 162 (1): 63–7. doi:10.1111/j.1432-1033.1987.tb10542.x. PMID 3102233.
• Nanba E, Tsuji A, Omura K, Suzuki Y (1987). "Galactosialidosis: a direct evidence that a 46-kilodalton protein restores deficient enzyme activities in fibroblasts". Biochem. Biophys. Res. Commun. 144 (1): 138–42. doi:10.1016/S0006-291X(87)80486-2. PMID 3107551.
• Galjart NJ, Gillemans N, Harris A, et al. (1988). "Expression of cDNA encoding the human "protective protein" associated with lysosomal beta-galactosidase and neuraminidase: homology to yeast proteases". Cell. 54 (6): 755–64. doi:10.1016/S0092-8674(88)90999-3. PMID 3136930. S2CID 21504892.
• Chitayat D, Applegarth DA, Lewis J, et al. (1989). "Juvenile galactosialidosis in a white male: a new variant". Am. J. Med. Genet. 31 (4): 887–901. doi:10.1002/ajmg.1320310423. PMID 3149149.
• Verheijen FW, Palmeri S, Hoogeveen AT, Galjaard H (1985). "Human placental neuraminidase. Activation, stabilization and association with beta-galactosidase and its protective protein". Eur. J. Biochem. 149 (2): 315–21. doi:10.1111/j.1432-1033.1985.tb08928.x. PMID 3922758.
• van der Horst GT, Kleijer WJ, Hoogeveen AT, et al. (1984). "Morquio B syndrome: a primary defect in beta-galactosidase". Am. J. Med. Genet. 16 (2): 261–75. doi:10.1002/ajmg.1320160215. PMID 6418007.
• Maire I, Nivelon-Chevallier AR (1982). "Combined deficiency of beta-galactosidase and neuraminidase: three affected siblings in a French family". J. Inherit. Metab. Dis. 4 (4): 221–3. doi:10.1007/BF02263656. PMID 6796775. S2CID 38676707.
• Pshezhetsky AV, Potier M (1994). "Direct affinity purification and supramolecular organization of human lysosomal cathepsin A.". Arch. Biochem. Biophys. 313 (1): 64–70. doi:10.1006/abbi.1994.1359. PMID 8053688.
• Ishii N, Oshima A, Sakuraba H, et al. (1994). "Normal serum beta-galactosidase in juvenile GM1 gangliosidosis". Pediatr. Neurol. 10 (4): 317–9. doi:10.1016/0887-8994(94)90129-5. PMID 8068159.
• Chakraborty S, Rafi MA, Wenger DA (1994). "Mutations in the lysosomal beta-galactosidase gene that cause the adult form of GM1 gangliosidosis". Am. J. Hum. Genet. 54 (6): 1004–13. PMC 1918177. PMID 8198123.

External links

• Cathepsin+A at the U.S. National Library of Medicine Medical Subject Headings (MeSH)