CPD (gene) explained

Carboxypeptidase D is an enzyme that in humans is encoded by the CPD gene.[1] [2]

Function

The metallocarboxypeptidase family of enzymes is divided into 2 subfamilies based on sequence similarities: the pancreatic carboxypeptidase-like and the regulatory B-type carboxypeptidase subfamilies. Carboxypeptidase D has been identified as a regulatory B-type carboxypeptidase. CPD is a homolog of duck gp180, a hepatitis B virus binding protein. Transcript variants utilizing alternative polyadenylation signals exist for this gene.[3]

Further reading

Notes and References

  1. Riley DA, Tan F, Miletich DJ, Skidgel RA . Chromosomal localization of the genes for human carboxypeptidase D (CPD) and the active 50-kilodalton subunit of human carboxypeptidase N (CPN1) . Genomics . 50 . 1 . 105–8 . May 1998 . 9628828 . 10.1006/geno.1998.5295 .
  2. Tan F, Rehli M, Krause SW, Skidgel RA . Sequence of human carboxypeptidase D reveals it to be a member of the regulatory carboxypeptidase family with three tandem active site domains . The Biochemical Journal . 327 (Pt 1) . Pt 1 . 81–7 . Oct 1997 . 9355738 . 1218766 . 10.1042/bj3270081.
  3. Web site: Entrez Gene: CPD carboxypeptidase D.