Molecular Basis of Receptor/G Protein Coupling Selectivity Studied by Coexpression of Wild Type and Mutant m2 Muscarinic Receptors with Mutant Gαq Subunits-Reference-Cited by-同舟云学术

Molecular Basis of Receptor/G Protein Coupling Selectivity Studied by Coexpression of Wild Type and Mutant m2 Muscarinic Receptors with Mutant Gαq Subunits

Published:1997-02-01 Issue:6 Volume:36 Page:1487-1495
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Kostenis Evi¹,Conklin Bruce R.¹,Wess Jürgen¹

Affiliation:

1. Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892, and the Departments of Medicine and Pharmacology, Gladstone Institute of Cardiovascular Disease, University of California, San Francisco, California 94141-9100

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi962554d

Reference42 articles.

1. The probable arrangement of the helices in G protein-coupled receptors.

2. Reconstitution of agonist-stimulated phosphatidylinositol 4,5-bisphosphate hydrolysis using purified m1 muscarinic receptor, Gq/11, and phospholipase C-beta 1.

3. Mapping of Single Amino Acid Residues Required for Selective Activation of G by the m3 Muscarinic Acetylcholine Receptor

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