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Literature summary for 3.1.3.43 extracted from

  • Maj, M.C.; MacKay, N.; Levandovskiy, V.; Addis, J.; Baumgartner, E.R.; Baumgartner, M.R.; Robinson, B.H.; Cameron, J.M.
    Pyruvate dehydrogenase phosphatase deficiency: identification of the first mutation in two brothers and restoration of activity by protein complementation (2005), J. Clin. Endocrinol. Metab., 90, 4101-4107.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
His-tag fusion protein, expression in Escherichia coli BL21(DE3) Homo sapiens

Metals/Ions

Metals/Ions Comment Organism Structure
Ca2+ 2 mM required for optimal phosphorylase activity Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Purification (Commentary)

Purification (Comment) Organism
75% purity after Ni-affinity chromatography Homo sapiens

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
[pyruvate dehydrogenase (lipoamide)]-phosphate + H2O pyruvate dehydrogenase activity is only 25% in patients carrying a deletion mutation of L213 of PDP1 Homo sapiens [pyruvate dehydrogenase (lipoamide)] + phosphate
-
?

Synonyms

Synonyms Comment Organism
PDP1
-
Homo sapiens
pyruvate dehydrogenase phosphatase
-
Homo sapiens