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M12: Astacin/Adamalysin C

Unless otherwise stated all data on this page refer to the human proteins. Gene information is provided for human (Hs), mouse (Mm) and rat (Rn).

Overview

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ADAM (A Disintegrin And Metalloproteinase domain containing proteins) metalloproteinases cleave cell-surface or transmembrane proteins to generate soluble and membrane-limited products.

ADAMTS (with thrombospondin motifs) metalloproteinases cleave cell-surface or transmembrane proteins to generate soluble and membrane-limited products.

Enzymes

1685
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ADAM2 Show summary »

ADAM7 Show summary »

ADAM8 Show summary » More detailed page go icon to follow link

ADAM9 Show summary » More detailed page go icon to follow link

ADAM10 Show summary » More detailed page go icon to follow link

ADAM11 Show summary »

ADAM12 Show summary » More detailed page go icon to follow link

ADAM15 Show summary »

ADAM17 Show summary » More detailed page go icon to follow link

ADAM18 Show summary »

ADAM19 Show summary »

ADAM20 Show summary »

ADAM21 Show summary »

ADAM22 Show summary »

ADAM23 Show summary »

ADAM28 Show summary »

ADAM29 Show summary »

ADAM30 Show summary »

ADAM32 Show summary »

ADAM33 Show summary » More detailed page go icon to follow link

ADAMTS1 Show summary » More detailed page go icon to follow link

ADAMTS2 Show summary »

ADAMTS3 Show summary »

ADAMTS4 Show summary » More detailed page go icon to follow link

ADAMTS5 Show summary » More detailed page go icon to follow link

ADAMTS6 Show summary »

ADAMTS7 Show summary »

ADAMTS8 Show summary »

ADAMTS9 Show summary »

ADAMTS10 Show summary »

ADAMTS12 Show summary »

ADAMTS13 Show summary »


Target Id 1685
Nomenclature ADAMTS13
Previous and unofficial names von Willebrand factor-cleaving protease | a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 13 | TTP | VWFCP | ADAM metallopeptidase with thrombospondin type 1 motif | a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif
Genes ADAMTS13 (Hs), Adamts13 (Mm), Adamts13 (Rn)
Ensembl ID ENSG00000160323 (Hs), ENSMUSG00000014852 (Mm), ENSRNOG00000005780 (Rn)
UniProtKB AC Q76LX8 (Hs), Q769J6 (Mm)
Comment Loss-of-function mutations in ADAMTS13 and autoimmune anti-ADAMTS13 antibodies are identified causes of thrombotic thrombocytopenic purpura (TTP). A recombinant version of ADAMTS13 (Adzynma®) was approved as an enzyme replacement therapy for patients with the congeital form of TTP in late 2023.

ADAMTS14 Show summary »

ADAMTS15 Show summary »

ADAMTS16 Show summary »

ADAMTS17 Show summary »

ADAMTS18 Show summary »

ADAMTS19 Show summary »

ADAMTS20 Show summary »

bone morphogenetic protein 1 Show summary » More detailed page go icon to follow link

Comments

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References

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How to cite this family page

Database page citation:

M12: Astacin/Adamalysin. Accessed on 25/04/2024. IUPHAR/BPS Guide to PHARMACOLOGY, http://www.guidetopharmacology.org/GRAC/FamilyDisplayForward?familyId=739.

Concise Guide to PHARMACOLOGY citation:

Alexander SPH, Fabbro D, Kelly E, Mathie AA, Peters JA, Veale EL, Armstrong JF, Faccenda E, Harding SD, Davies JA et al. (2023) The Concise Guide to PHARMACOLOGY 2023/24: Enzymes. Br J Pharmacol. 180 Suppl 2:S289-373.