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Initial studies indicated that dopamine activates PLM via a conformational movement of transmembrane helix #6 that exposes the active methionine residue (#313 in the D4.4R) 1 , and more recent x-ray crystallography studies subsequently confirmed this large agonist-induced rotational movement for the equivalent leucine residue in β-2 adrenergic receptors

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4 (January/February 2004), each of which is hereby incorporated by reference for such disclosure