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Literature summary for 3.4.24.87 extracted from
- Genetic and Functional Characterization of ADAMTS13 variants in a patient cohort with Upshaw-Schulman syndrome investigated in Germany (2018), Thromb. Haemost., 118, 709-722 .
Natural Substrates/ Products (Substrates)
| Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| von Willebrand factor + H2O | Homo sapiens | - |
? | - |
? |  |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Homo sapiens | - |
- |
- |
Substrates and Products (Substrate)
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| von Willebrand factor + H2O | - |
Homo sapiens | ? | - |
? | |
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 | - |
Homo sapiens |
| ADAMTS13 | - |
Homo sapiens |
General Information
| General Information | Comment | Organism |
|---|---|---|
| malfunction | Upshaw-Schulman syndrome is caused by severe enzyme deficiency | Homo sapiens |
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Release 2023.1 (January 2023)
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