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Literature summary extracted from

  • Ambrus, A.; Adam-Vizi, V.
    Molecular dynamics study of the structural basis of dysfunction and the modulation of reactive oxygen species generation by pathogenic mutants of human dihydrolipoamide dehydrogenase (2013), Arch. Biochem. Biophys., 538, 145-155 .
    View publication on PubMed

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
1.8.1.4 dihydrolipoamide + NAD+ Homo sapiens
-
lipoamide + NADH + H+
-
r

Organism

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

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.8.1.4 dihydrolipoamide + NAD+
-
Homo sapiens lipoamide + NADH + H+
-
r

Subunits

EC Number Subunits Comment Organism
1.8.1.4 homodimer
-
Homo sapiens

Synonyms

EC Number Synonyms Comment Organism
1.8.1.4 dihydrolipoamide dehydrogenase
-
Homo sapiens
1.8.1.4 DLD
-
Homo sapiens
1.8.1.4 E3
-
Homo sapiens
1.8.1.4 E3 component
-
Homo sapiens
1.8.1.4 LADH
-
Homo sapiens

Cofactor

EC Number Cofactor Comment Organism Structure
1.8.1.4 flavin flavoprotein Homo sapiens

General Information

EC Number General Information Comment Organism
1.8.1.4 malfunction pathogenic mutations of LADH cause severe metabolic disturbances, called E3 deficiency that often involve cardiological and neurological symptoms and premature death. Some of the known pathogenic mutations augment the reactive oxygen species (ROS) generation capacity of LADH, which may contribute to the clinical presentations. Structural changes are likely to turn the physiological LADH conformation to its ROS-generating conformation Homo sapiens
1.8.1.4 additional information molecular dynamics simulation the conformation of enzyme LADH that is proposed to be compatible with the reactive oxygen species (ROS) generation Homo sapiens
1.8.1.4 physiological function dihydrolipoamide dehydrogenase is a component in the pyruvate-, 2-oxooglutarate- and branched-chain oxoacid dehydrogenase complexes and in the glycine cleavage system Homo sapiens