Matches in DBpedia 2014 for { <http://dbpedia.org/resource/PEPD> ?p ?o. }
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- PEPD abstract "Xaa-Pro dipeptidase, also known as prolidase, is an enzyme that in humans is encoded by the PEPD gene.Xaa-Pro dipeptidase is a cytosolic dipeptidase that hydrolyzes dipeptides with proline or hydroxyproline at the carboxy terminus (but not Pro-Pro). It is important in collagen metabolism because of the high levels of imino acids. Mutations at the PEPD locus cause prolidase deficiency. This is characterised by Iminodipeptidurea, Skin ulcers, mental retardation and recurrent infections.".
- PEPD entrezgene "5184".
- PEPD wikiPageID "14762138".
- PEPD wikiPageRevisionID "592763943".
- PEPD hasPhotoCollection PEPD.
- PEPD requireManualInspection "no".
- PEPD summaryText "Xaa-Pro dipeptidase is a cytosolic dipeptidase that hydrolyzes dipeptides with proline or hydroxyproline at the carboxy terminus . It is important in collagen metabolism because of the high levels of imino acids. Mutations at the PEPD locus cause prolidase deficiency. This is characterised by Iminodipeptidurea, Skin ulcers, mental retardation and recurrent infections.".
- PEPD updateCitations "yes".
- PEPD updatePage "yes".
- PEPD updateProteinBox "yes".
- PEPD updateSummary "yes".
- PEPD type Biomolecule.
- PEPD type Protein.
- PEPD type BiologicalObject.
- PEPD comment "Xaa-Pro dipeptidase, also known as prolidase, is an enzyme that in humans is encoded by the PEPD gene.Xaa-Pro dipeptidase is a cytosolic dipeptidase that hydrolyzes dipeptides with proline or hydroxyproline at the carboxy terminus (but not Pro-Pro). It is important in collagen metabolism because of the high levels of imino acids. Mutations at the PEPD locus cause prolidase deficiency. This is characterised by Iminodipeptidurea, Skin ulcers, mental retardation and recurrent infections.".
- PEPD label "PEPD".
- PEPD sameAs m.03gx30t.
- PEPD sameAs Q7118991.
- PEPD sameAs Q7118991.
- PEPD sameAs PEPD.
- PEPD wasDerivedFrom PEPD?oldid=592763943.
- PEPD isPrimaryTopicOf PEPD.