DOPA decarboxylase

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==Introduction==
==Introduction==
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{{STRUCTURE_1js3 | PDB=1js3 | SCENE= }}'''[http://en.wikipedia.org/wiki/DOPA_decarboxylase ''DOPA decarboxylase'']''' (DDC, aromatic L-amino acid decarboxylase, tryptophan decarboxylase, 5-hydroxytryptophan decarboxylase, AAAD) is an approximately 52 kDa protein that belongs to the aspartate aminotransferase family (fold type 1) of [http://en.wikipedia.org/wiki/Pyridoxal_phosphate ''PLP'']-dependent enzymes. The catalytically active form of the enzyme exists as a homodimer, typical of this class of enzymes. The homodimeric form of the enzyme purified from [http://en.wikipedia.org/wiki/Sus_scrofa ''sus scrofa''] is shown in complex with the inhibitor [http://en.wikipedia.org/wiki/Carbidopa ''carbidopa''] to the right. DOPA decarboxylase is responsible for the synthesis of [http://en.wikipedia.org/wiki/Dopamine ''dopamine''] and [http://en.wikipedia.org/wiki/Serotoninn ''serotonin''] from [http://en.wikipedia.org/wiki/L-dopa ''L-DOPA''] and [http://en.wikipedia.org/wiki/L-5-Hydroxytryptophan ''L-5;hydroxytryptophan''], respectively. Due to its role in neurotransmitter synthesis, DOPA decarboxylase has been implicated in [http://en.wikipedia.org/wiki/Parkinson%27s_disease ''Parkinson's disease''], a disease thought to be the result of the degeneration of dopamine-producing cells in the brain. Currently, treatment for the disease is aimed at DOPA decarboxylase inhibition, which would allow greater amounts of exogenously administered L-DOPA to reach the brain.
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{{STRUCTURE_1js3 | PDB=1js3 | SCENE= }}'''[http://en.wikipedia.org/wiki/DOPA_decarboxylase ''DOPA decarboxylase'']''' (DDC, aromatic L-amino acid decarboxylase, tryptophan decarboxylase, 5-hydroxytryptophan decarboxylase, AAAD) is an approximately 52 kDa protein that belongs to the aspartate aminotransferase family (fold type 1) of [http://en.wikipedia.org/wiki/Pyridoxal_phosphate ''PLP'']-dependent enzymes. The catalytically active form of the enzyme exists as a homodimer, typical of this class of enzymes.<ref name="schneider">PMID:10673430 </ref> The homodimeric form of the enzyme purified from [http://en.wikipedia.org/wiki/Sus_scrofa ''sus scrofa''] is shown in complex with the inhibitor [http://en.wikipedia.org/wiki/Carbidopa ''carbidopa''] to the right. DOPA decarboxylase is responsible for the synthesis of [http://en.wikipedia.org/wiki/Dopamine ''dopamine''] and [http://en.wikipedia.org/wiki/Serotoninn ''serotonin''] from [http://en.wikipedia.org/wiki/L-dopa ''L-DOPA''] and [http://en.wikipedia.org/wiki/L-5-Hydroxytryptophan ''L-5;hydroxytryptophan''], respectively. Due to its role in neurotransmitter synthesis, DOPA decarboxylase has been implicated in [http://en.wikipedia.org/wiki/Parkinson%27s_disease ''Parkinson's disease''], a disease thought to be the result of the degeneration of dopamine-producing cells in the brain. Currently, treatment for the disease is aimed at DOPA decarboxylase inhibition, which would allow greater amounts of exogenously administered L-DOPA to reach the brain.
[[Image:dopa.png]]
[[Image:dopa.png]]

Revision as of 23:33, 3 May 2011

Introduction


PDB ID 1js3

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1js3, resolution 2.25Å ()
Ligands: , ,
Activity: Aromatic-L-amino-acid decarboxylase, with EC number 4.1.1.28
Related: 1js6
Resources: FirstGlance, OCA, RCSB, PDBsum
Coordinates: save as pdb, mmCIF, xml


DOPA decarboxylase (DDC, aromatic L-amino acid decarboxylase, tryptophan decarboxylase, 5-hydroxytryptophan decarboxylase, AAAD) is an approximately 52 kDa protein that belongs to the aspartate aminotransferase family (fold type 1) of PLP-dependent enzymes. The catalytically active form of the enzyme exists as a homodimer, typical of this class of enzymes.[1] The homodimeric form of the enzyme purified from sus scrofa is shown in complex with the inhibitor carbidopa to the right. DOPA decarboxylase is responsible for the synthesis of dopamine and serotonin from L-DOPA and L-5;hydroxytryptophan, respectively. Due to its role in neurotransmitter synthesis, DOPA decarboxylase has been implicated in Parkinson's disease, a disease thought to be the result of the degeneration of dopamine-producing cells in the brain. Currently, treatment for the disease is aimed at DOPA decarboxylase inhibition, which would allow greater amounts of exogenously administered L-DOPA to reach the brain.

Image:dopa.png

Structure


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