Arginine 336 and Asparagine 333 of the Human Cholecystokinin-A Receptor Binding Site Interact with the Penultimate Aspartic Acid and the C-terminal Amide of Cholecystokinin-Reference-Cited by-同舟云学术

Arginine 336 and Asparagine 333 of the Human Cholecystokinin-A Receptor Binding Site Interact with the Penultimate Aspartic Acid and the C-terminal Amide of Cholecystokinin

Published:1999-07 Issue:29 Volume:274 Page:20457-20464
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Gigoux Véronique,Escrieut Chantal,Fehrentz Jean-Alain,Poirot Sandrine,Maigret Bernard,Moroder Luis,Gully Danielle,Martinez Jean,Vaysse Nicole,Fourmy Daniel

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference48 articles.

1. Molecular Cloning, Functional Expression and Chromosomal Localization of the Human Cholecystokinin Type A Receptor

2. Molecular Cloning and Functional Expression of the Human Gallbladder Cholecystokinin A Receptor

3. The peripheral cholecystokinin receptors

4. Human Cholecystokinin Type A Receptor Gene: Cytogenetic Localization, Physical Mapping, and Identification of Two Missense Variants in Patients with Obesity and Non-Insulin-Dependent Diabetes Mellitus (NIDDM)

Cited by 75 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ligand recognition and G-protein coupling selectivity of cholecystokinin A receptor;Nature Chemical Biology;2021-09-23

2. Structures of the human cholecystokinin 1 (CCK1) receptor bound to Gs and Gq mimetic proteins provide insight into mechanisms of G protein selectivity;PLOS Biology;2021-06-04

3. Structural basis for ligand recognition and G protein-coupling promiscuity of the cholecystokinin A receptor;2021-05-10

4. Structures of the human cholecystokinin 1 (CCK1) receptor bound to Gs and Gq mimetic proteins: insight into mechanisms of G protein selectivity;2021-05-06

5. Triazolo-Peptidomimetics: Novel Radiolabeled Minigastrin Analogs for Improved Tumor Targeting;Journal of Medicinal Chemistry;2020-04-17