$VAR1 = undef;
Summary for peptidase M24.007: Xaa-Pro dipeptidase (eukaryote-type)
| Names | |
|---|---|
| MEROPS Name | Xaa-Pro dipeptidase (eukaryote-type) |
| Other names | peptidase D, PEPD g.p. (Homo sapiens), prolidase I, proline dipeptidase, peptidase 4 (Mus musculus), X-Pro dipeptidase |
| Domain architecture |
|---|
| MEROPS Classification | |
|---|---|
| Classification | Clan MG >> Subclan (none) >> Family M24 >> Subfamily B >> M24.007 |
| Holotype | Xaa-Pro dipeptidase (eukaryote-type) (Homo sapiens), Uniprot accession P12955 (peptidase unit: 225-477), MERNUM MER0001248 |
| History | Identifier created: MEROPS 3.03 (10 September 1998) |
| Activity | |||
|---|---|---|---|
| Catalytic type | Metallo | ||
| Peplist | Included in the Peplist with identifier PL00241 | ||
| NC-IUBMB | Not yet included in IUBMB recommendations. | ||
| Activity status | human: active (Mock, 2004) mouse: active (by similarity to rat) (Hu et al., 2003) | ||
| Knockout | Prolidase deficiency is an autosomal recessive disorder with highly variable penetrance characterized by massive urinary excretion of imidodipeptides X-Pro and X-Hyp (Ledoux et al., 1996; Mandel et al., 2000). Prolidase deficiency is a risk factor for the development of systemic lupus erythematosus (Shrinath et al., 1997). | ||
| Pharmaceutical relevance | Recombinant prolidase is capable of destroying the organophosphorus toxin, soman (Wang et al., 2005). | ||
| Other databases | TREEFAM | http://www.treefam.org/family/TF313396 | |
| Human genetics | ||||||
|---|---|---|---|---|---|---|
| Gene symbol | Locus | Megabases | Ensembl | Entrez gene | Gene Cards | OMIM |
| PEPD | 19cen-q13.11 | ENSG00000124299 | 5184 | PEPD | 170100 | |
| Mouse genetics | ||||||
| Gene symbol | Position | Megabases | Ensembl | Entrez gene | MGI | |
| Pep4 | 7:A3 | ENSMUSG00000001779 | 18624 | MGI:97542 | ||
