(Q38352900)

2 September 2017

Constitutive activation of the angiotensin II type 1 receptor alters the spatial proximity of transmembrane 7 to the ligand-binding pocket (English)

1 reference

2 September 2017

transmembrane protein

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1 reference

1 reference

Marie-Eve Beaulieu

3

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Emanuel Escher

object named as

Emanuel Escher

5

0 references

Antony A. Boucard

1

object named as

Antony A Boucard

1 reference

2 September 2017

Marise Roy

2

1 reference

2 September 2017

Pierre Lavigne

4

1 reference

2 September 2017

Gaetan Guillemette

6

1 reference

2 September 2017

Richard Leduc

7

1 reference

2 September 2017

language of work or name

English

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publication date

3 July 2003

1 reference

Journal of Biological Chemistry

2 September 2017

1 reference

2 September 2017

278

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2 September 2017

38

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2 September 2017

36628-36636

1 reference

G protein-coupled receptors. II. Mechanism of agonist activation.

2 September 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Agonist-induced conformational changes in the G-protein-coupling domain of the beta 2 adrenergic receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Structure and function in rhodopsin: mapping light-dependent changes in distance between residue 65 in helix TM1 and residues in the sequence 306-319 at the cytoplasmic end of helix TM7 and in helix H8.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Structure and function in rhodopsin: mapping light-dependent changes in distance between residue 316 in helix 8 and residues in the sequence 60-75, covering the cytoplasmic end of helices TM1 and TM2 and their connection loop CL1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

A review of mutagenesis studies of angiotensin II type 1 receptor, the three-dimensional receptor model in search of the agonist and antagonist binding site and the hypothesis of a receptor activation mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Constitutive activation of angiotensin II type 1 receptor alters the orientation of transmembrane Helix-2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Use of the substituted cysteine accessibility method to study the structure and function of G protein-coupled receptors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Protein and cell membrane iodinations with a sparingly soluble chloroamide, 1,3,4,6-tetrachloro-3a,6a-diphenylglycoluril

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Photolabelling the rat urotensin II/GPR14 receptor identifies a ligand-binding site in the fourth transmembrane domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

A cysteine residue in the third membrane-spanning segment of the human D2 dopamine receptor is exposed in the binding-site crevice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Structure and energetics of ligand binding to proteins: Escherichia coli dihydrofolate reductase-trimethoprim, a drug-receptor system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Disulfide bridges in extracellular domains of angiotensin II receptor type IA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Residues in the seventh membrane-spanning segment of the dopamine D2 receptor accessible in the binding-site crevice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Use of an in situ disulfide cross-linking strategy to map proximities between amino acid residues in transmembrane domains I and VII of the M3 muscarinic acetylcholine receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Crystal structure of rhodopsin: A G protein-coupled receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Residues 293 and 294 are ligand contact points of the human angiotensin type 1 receptor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

The ligand binding site of the angiotensin AT1 receptor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Angiotensin IV is a potent agonist for constitutive active human AT1 receptors. Distinct roles of the N-and C-terminal residues of angiotensin II during AT1 receptor activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

TM2-TM7 interaction in coupling movement of transmembrane helices to activation of the angiotensin II type-1 receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Constitutive activity of G-protein-coupled receptors: cause of disease and common property of wild-type receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Rhodopsin activation blocked by metal-ion-binding sites linking transmembrane helices C and F.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Role of the conserved NPxxY(x)5,6F motif in the rhodopsin ground state and during activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

Conserved helix 7 tyrosine acts as a multistate conformational switch in the 5HT2C receptor. Identification of a novel "locked-on" phenotype and double revertant mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

A Conserved NPLFY Sequence Contributes to Agonist Binding and Signal Transduction but Is Not an Internalization Signal for the Type 1 Angiotensin II Receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M305952200

21 January 2018

Identifiers

DOI

10.1074/JBC.M305952200

1 reference

2 September 2017

1 reference