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

BRENDA support

Literature summary extracted from

  • Hassenpflug, W.A.; Obser, T.; Bode, J.; Oyen, F.; Budde, U.; Schneppenheim, S.; Schneppenheim, R.; Brehm, M.A.
    Genetic and Functional Characterization of ADAMTS13 variants in a patient cohort with Upshaw-Schulman syndrome investigated in Germany (2018), Thromb. Haemost., 118, 709-722 .
    View publication on PubMed

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
3.4.24.87 von Willebrand factor + H2O Homo sapiens
-
?
-
?

Organism

EC Number Organism UniProt Comment Textmining
3.4.24.87 Homo sapiens
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.4.24.87 von Willebrand factor + H2O
-
Homo sapiens ?
-
?

Synonyms

EC Number Synonyms Comment Organism
3.4.24.87 a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13
-
Homo sapiens
3.4.24.87 ADAMTS13
-
Homo sapiens

General Information

EC Number General Information Comment Organism
3.4.24.87 malfunction Upshaw-Schulman syndrome is caused by severe enzyme deficiency Homo sapiens