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  2. Aromatic L-amino acid decarboxylase - Wikipedia

    en.wikipedia.org/wiki/Aromatic_L-amino_acid...

    Aromatic L-amino acid decarboxylase is active as a homodimer. Before addition of the pyridoxal phosphate cofactor, the apoenzyme exists in an open conformation. Upon cofactor binding, a large structural transformation occurs as the subunits pull closer and close the active site. This conformational change results in the active, closed ...

  3. Aromatic L-amino acid decarboxylase inhibitor - Wikipedia

    en.wikipedia.org/wiki/Aromatic_L-amino_acid...

    An aromatic L-amino acid decarboxylase inhibitor (synonyms: DOPA decarboxylase inhibitor, extracerebral decarboxylase inhibitor, DDCI and AAADI) is a medication of type enzyme inhibitor which inhibits the synthesis of dopamine by the enzyme aromatic L-amino acid decarboxylase (AADC, AAAD, or DOPA decarboxylase).

  4. Autosomal dominant GTP cyclohydrolase I deficiency

    en.wikipedia.org/wiki/Autosomal_dominant_GTP_cyc...

    Patients are prescribed L-dopa in conjunction with a DC inhibitor such as carbidopa or benserazide. [2] If symptoms persist, dopamine agonists such as pramipexole, bromocriptine, or cabergoline could be considered as a second line of treatment. [2] Anticholinergic drugs or COMT inhibitors could be considered as a third line of treatment. [2]

  5. Dihydropteridine reductase deficiency - Wikipedia

    en.wikipedia.org/wiki/Dihydropteridine_reductase...

    Dihydropteridine reductase deficiency (DHPRD) is a genetic disorder affecting the tetrahydrobiopterin (BH4) synthesis pathway, inherited in the autosomal recessive pattern. It is one of the six known disorders causing tetrahydrobiopterin deficiency , and occurs in patients with mutations of the QDPR gene.

  6. Aromatic L-amino acid decarboxylase deficiency - Wikipedia

    en.wikipedia.org/wiki/Aromatic_L-amino_acid...

    Aromatic L-amino acid decarboxylase deficiency has an autosomal recessive pattern of inheritance. Aromatic L-amino acid decarboxylase deficiency is an autosomal recessive condition, meaning an individual needs to have two faulty copies of the DDC gene in order to be affected. Usually, one copy is inherited from each parent. [3]

  7. L-DOPA - Wikipedia

    en.wikipedia.org/wiki/L-DOPA

    l-DOPA can be manufactured and in its pure form is sold as a drug with the INN Tooltip International Nonproprietary Name levodopa. Trade names include Sinemet, Pharmacopa, Atamet, and Stalevo. As a drug, it is used in the clinical treatment of Parkinson's disease and dopamine-responsive dystonia. l-DOPA has a counterpart with opposite chirality ...

  8. Tyrosine hydroxylase deficiency - Wikipedia

    en.wikipedia.org/.../Tyrosine_hydroxylase_deficiency

    Tyrosine hydroxylase deficiency; Simplified overview of the biosynthesis and catabolism of serotonin and the catecholamines, with tyrosine hydroxylase (TH) and its cofactor tetrahydrobiopterin (BH 4) circled in red. Note that different parts of these processes take place in different tissues.

  9. Levodopa - Wikipedia

    en.wikipedia.org/wiki/Levodopa

    Once levodopa has entered the central nervous system, it is converted into dopamine by the enzyme aromatic l-amino acid decarboxylase (AAAD), also known as DOPA decarboxylase (DDC). Pyridoxal phosphate (vitamin B 6) is a required cofactor in this reaction, and may occasionally be administered along with levodopa, usually in the form of pyridoxine.