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Literature summary for 3.5.3.18 extracted from

  • Zhang, P.; Hu, X.; Xu, X.; Chen, Y.; Bache, R.J.
    Dimethylarginine dimethylaminohydrolase 1 modulates endothelial cell growth through nitric oxide and Akt (2011), Arterioscler. Thromb. Vasc. Biol., 31, 890-897.
    View publication on PubMedView publication on EuropePMC

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
additional information Homo sapiens DDAH1 forms a protein complex with Ras ?
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?

Organism

Organism UniProt Comment Textmining
Homo sapiens
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-
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Mus musculus
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-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information DDAH1 forms a protein complex with Ras Homo sapiens ?
-
?

Synonyms

Synonyms Comment Organism
DDAH1
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Mus musculus
DDAH1
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Homo sapiens
dimethylarginine dimethylaminohydrolase
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Mus musculus
dimethylarginine dimethylaminohydrolase
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Homo sapiens

General Information

General Information Comment Organism
malfunction DDAH1 knockout impairs endothelial sprouting from cultured aortic rings, and overexpression of constitutively active Akt or DDAH1 rescues endothelial sprouting in the aortic rings from these mice Mus musculus
malfunction using selective gene silencing of DDAH1 with small interfering RNA and overexpression of DDAH1 in HUVEC, it is shown that DDAH1 acts to promote endothelial cell proliferation, migration and tube formation both by Akt phosphorylation as well as through the traditional role of degrading ADMA. DDAH1 overexpression increases Ras activity Homo sapiens