Site-directed mutagenesis identifies residues involved in ligand recognition in the human A2a adenosine receptor (Q24612312)

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J Wess

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A M van Rhee

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T Schöneberg

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K A Jacobson

Journal of Biological Chemistry

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language of work or name

English

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publication date

9 June 1995

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published in

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volume

270

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page(s)

13987-97

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issue

23

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cites work

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Crossref

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Projection structure of rhodopsin

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Antagonistic interaction between adenosine A2A receptors and dopamine D2 receptors in the ventral striopallidal system. Implications for the treatment of schizophrenia

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Pharmacological characterization of the D2 dopamine receptor negatively coupled with adenylate cyclase in rat anterior pituitary

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Identification of two serine residues involved in agonist activation of the beta-adrenergic receptor

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125I-2-[4-[2-[2-[(4-azidophenyl)methylcarbonylamino] ethylaminocarbonyl]ethyl]phenyl] ethylamino-5'-N-ethylcarboxamidoadenosine labels transmembrane span V of the A2a adenosine receptor

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Role of histidine residues in the adenosine A2a receptor ligand binding site

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Molecular modeling of adenosine receptors. The ligand binding site on the rat adenosine A2A receptor

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Identifiers

DOI

10.1074/JBC.270.23.13987

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5120559

5120559

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