Sandbox Reserved 691

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== Function ==
== Function ==
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Through the binding of two sodium ions, dopamine can then bind after which the protein undergoes a conformational change to allow for the sodium and dopamine to enter the cell. Similar to other ionic pumps, the flow of sodium is coupled with the flow of a chlorine ion, in order to balance the charge build up. The internalization of dopamine into neural cells allows for the clearing of dopamine from the synapse and the termination of dopamine signaling pathways.
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Through the binding of two sodium <scene name='Sandbox_Reserved_691/2a65_ions3/1'>ions</scene> represented in purple, dopamine can then bind after which the protein undergoes a conformational change to allow for the sodium and dopamine to enter the cell. Similar to other ionic pumps, the flow of sodium is coupled with the flow of a chlorine ion, represented in green, in order to balance the charge build up. The internalization of dopamine into neural cells allows for the clearing of dopamine from the synapse and the termination of dopamine signaling pathways. <scene name='Sandbox_Reserved_691/2a65_leucine/2'>Leucine</scene>, shown here highlighted in yellow and stabilized by two sodium atoms, is being transported across the cell membrane by the LEUTAA transporter.
== Amphetamines ==
== Amphetamines ==
Amphetamines are a class of chemical compounds derived from amphetamine ((RS)-1-phenylpropan-2-amine) and are used both recreationally to induce euphoria and clinically to treat disorders, notably Attention Deficit Hyperactivity Disorder (ADHD). While amphetamines bear structural similarities to dopamine, they are not true competitive inhibitors of the dopamine transporter. Amphetamines instead work by binding to an unknown receptor that initiates phosphorylation of the N-terminus once Ca2+/calmodulin-dependent protein kinase II (CamKII) binds to the C-terminus. This causes DAT to conform to a "willing" conformation and results in DAT effluxing into the cell through the formation of an intercellular endosome. This reduces the expression of DAT in the surface of the cell membrane, reducing the rate at which dopamine is cleared from the synapse.
Amphetamines are a class of chemical compounds derived from amphetamine ((RS)-1-phenylpropan-2-amine) and are used both recreationally to induce euphoria and clinically to treat disorders, notably Attention Deficit Hyperactivity Disorder (ADHD). While amphetamines bear structural similarities to dopamine, they are not true competitive inhibitors of the dopamine transporter. Amphetamines instead work by binding to an unknown receptor that initiates phosphorylation of the N-terminus once Ca2+/calmodulin-dependent protein kinase II (CamKII) binds to the C-terminus. This causes DAT to conform to a "willing" conformation and results in DAT effluxing into the cell through the formation of an intercellular endosome. This reduces the expression of DAT in the surface of the cell membrane, reducing the rate at which dopamine is cleared from the synapse.
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<scene name='Sandbox_Reserved_691/2a65_default/2'>DEFAULT</scene>
 
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<scene name='Sandbox_Reserved_691/2a65_ions3/1'>IONS</scene>
 
<scene name='Sandbox_Reserved_691/2a65_leucine/2'>LEUCINE</scene>
<scene name='Sandbox_Reserved_691/2a65_leucine/2'>LEUCINE</scene>

Revision as of 00:14, 1 May 2013

This Sandbox is Reserved from 30/01/2013, through 30/12/2013 for use in the course "Biochemistry II" taught by Hannah Tims at the Messiah College. This reservation includes Sandbox Reserved 686 through Sandbox Reserved 700.
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Dopamine Active Transporter

Dopamine Active Transporter (DAT) is a transmembrane protein found in human neurons, that is responsible for the reuptake of the neurotransmitter dopamine from the synapse back into synaptic vesicles for storage and later release. The action of this protein is responsible for the termination of signaling in dopaminergic pathways, which are responsible for many important biological functions such as cognition, motor control, sleep, and emotion.

LEUTAA, a bacterial homolog for human Na+/Cl- dependent neurotransmitter transporters such as DAT

Drag the structure with the mouse to rotate

Function

Through the binding of two sodium represented in purple, dopamine can then bind after which the protein undergoes a conformational change to allow for the sodium and dopamine to enter the cell. Similar to other ionic pumps, the flow of sodium is coupled with the flow of a chlorine ion, represented in green, in order to balance the charge build up. The internalization of dopamine into neural cells allows for the clearing of dopamine from the synapse and the termination of dopamine signaling pathways. , shown here highlighted in yellow and stabilized by two sodium atoms, is being transported across the cell membrane by the LEUTAA transporter.

Amphetamines

Amphetamines are a class of chemical compounds derived from amphetamine ((RS)-1-phenylpropan-2-amine) and are used both recreationally to induce euphoria and clinically to treat disorders, notably Attention Deficit Hyperactivity Disorder (ADHD). While amphetamines bear structural similarities to dopamine, they are not true competitive inhibitors of the dopamine transporter. Amphetamines instead work by binding to an unknown receptor that initiates phosphorylation of the N-terminus once Ca2+/calmodulin-dependent protein kinase II (CamKII) binds to the C-terminus. This causes DAT to conform to a "willing" conformation and results in DAT effluxing into the cell through the formation of an intercellular endosome. This reduces the expression of DAT in the surface of the cell membrane, reducing the rate at which dopamine is cleared from the synapse.


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