Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 3.4.13.9 extracted from

  • Klar, A.; Navon-Elkan, P.; Rubinow, A.; Branski, D.; Hurvitz, H.; Christensen, E.; Khayat, M.; Falik-Zaccai, T.C.
    Prolidase deficiency: it looks like systemic lupus erythematosus but it is not (2010), Eur. J. Pediatr., 169, 727-732.
    View publication on PubMed

Protein Variants

Protein Variants Comment Organism
Y256X a homozygous nonsense C > G transition at nucleotide 768 is a naturally occuring mutation, which leads to recalcitrant leg ulceration, splenomegaly, and photosensitive rash due to prolidase deficiency, phenotype, overview Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
fibroblast
-
Homo sapiens
-

Synonyms

Synonyms Comment Organism
prolidase
-
Homo sapiens