PEPD peptidase D [ Homo sapiens (human) ]
Source: NCBI Gene (ID 5184)
Source: NCBI Gene (ID 5184)
Symbol: PEPD
Full name: peptidase D
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: PROLIDASE
Summary: This gene encodes a member of the peptidase family. The protein forms a homodimer that hydrolyzes dipeptides or tripeptides with C-terminal proline or hydroxyproline residues. The enzyme serves an important role in the recycling of proline, and may be rate limiting for the production of collagen. Mutations in this gene result in prolidase deficiency, which is characterized by the excretion of large amount of di- and tri-peptides containing proline. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]
Expression: Broad expression in kidney (RPKM 221.6), small intestine (RPKM 95.0) and 19 other tissues
Orthologs: mouse
Gene size: 134842bp
Exon count: 15