CTSD
Identifiers | |
---|---|
EC number | 3.4.23.5 |
CAS number | 9001-01-8 |
Alt. names | |
IntEnz | IntEnz view |
BRENDA | BRENDA entry |
ExPASy | NiceZyme view |
KEGG | KEGG entry |
MetaCyc | metabolic pathway |
Cathepsin D is a lysosomal aspartic protease that is important in the degradation of proteins. It is encoded by the CTSD gene in humans.
Function[edit | edit source]
Cathepsin D is involved in the proteolytic processing of proteins within the lysosome. It plays a role in the breakdown of intracellular and extracellular proteins, which is crucial for cellular homeostasis.
Clinical significance[edit | edit source]
Mutations in the CTSD gene can lead to a variety of diseases. For example, deficiency of cathepsin D is associated with neurodegenerative disorders such as neuronal ceroid lipofuscinosis.
Cathepsin D is also implicated in cancer progression. It is often overexpressed in breast cancer and is thought to contribute to tumor invasion and metastasis.
Structure[edit | edit source]
Cathepsin D is synthesized as an inactive zymogen and is activated in the acidic environment of the lysosome. It consists of a single polypeptide chain that is cleaved into two chains, which form the active enzyme.
See also[edit | edit source]
References[edit | edit source]
External links[edit | edit source]
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Contributors: Prab R. Tumpati, MD