Binding site of AChR: Difference between revisions

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This notion is supported by recent studies on charge reversal mutations of basic residues on loop 2 of α-neurotoxin.
This notion is supported by recent studies on charge reversal mutations of basic residues on loop 2 of α-neurotoxin.
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The possible formation of an intermolecular salt bridge between AChR and α-BTX at that positionmay provide further explanation to the high affinity of binding of the toxin to the receptor.This notion is supported by recent studies on charge reversal mutations of basic residues on loop 2 of α-neurotoxin
The possible formation of an intermolecular salt bridge between AChR and α-BTX at that positionmay provide further explanation to the high affinity of binding of the toxin to the receptor.This notion is supported by recent studies on charge reversal mutations of basic residues on loop 2 of α-neurotoxin
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</StructureSection>
</StructureSection>
== References ==
== References ==
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<references/>

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