(Q40150862)

English

Systematic analysis of the entire second extracellular loop of the V(1a) vasopressin receptor: key residues, conserved throughout a G-protein-coupled receptor family, identified.

scientific article published on 2 April 2007

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17403667%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Systematic analysis of the entire second extracellular loop of the V(1a) vasopressin receptor: key residues, conserved throughout a G-protein-coupled receptor family, identified (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17403667%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

G protein-coupled receptor

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3

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28 December 2019

4

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28 December 2019

8

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28 December 2019

author name string

Matthew Conner

1

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28 December 2019

Stuart R Hawtin

2

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28 December 2019

Zoe Lawson

5

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28 December 2019

Alex C Conner

6

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28 December 2019

Rosemary A Parslow

7

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28 December 2019

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2 April 2007

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28 December 2019

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8

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Journal of Biological Chemistry

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28 December 2019

282

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28 December 2019

24

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28 December 2019

17405-17412

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Seven-transmembrane receptors: crystals clarify

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The basic and clinical pharmacology of nonpeptide vasopressin receptor antagonists

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Molecular pharmacology of V1a vasopressin receptors.

1 reference

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Functional architecture of vasopressin/oxytocin receptors

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The binding site of neuropeptide vasopressin V1a receptor. Evidence for a major localization within transmembrane regions

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A Gly/Ala switch contributes to high affinity binding of benzoxazinone-based non-peptide oxytocin receptor antagonists.

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Molecular recognition of peptide and non-peptide ligands by the extracellular domains of neurohypophysial hormone receptors

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A single residue (arg46) located within the N-terminus of the V1a vasopressin receptor is critical for binding vasopressin but not peptide or nonpeptide antagonists

1 reference

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The N-terminal juxtamembrane segment of the V1a vasopressin receptor provides two independent epitopes required for high-affinity agonist binding and signaling

1 reference

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Agonist-specific, high-affinity binding epitopes are contributed by an arginine in the N-terminus of the human oxytocin receptor

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The binding site of aminergic G protein-coupled receptors: the transmembrane segments and second extracellular loop

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Refinement of the conformation of a critical region of charge-charge interaction between cholecystokinin and its receptor

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Mutations of the second extracellular loop of the human lutropin receptor emphasize the importance of receptor activation and de-emphasize the importance of receptor phosphorylation in agonist-induced internalization

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A radioiodinated linear vasopressin antagonist: a ligand with high affinity and specificity for V1a receptors

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Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction

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Charged extracellular residues, conserved throughout a G-protein-coupled receptor family, are required for ligand binding, receptor activation, and cell-surface expression

1 reference

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21 January 2018

Critical role of a subdomain of the N-terminus of the V1a vasopressin receptor for binding agonists but not antagonists; functional rescue by the oxytocin receptor N-terminus.

1 reference

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Biochemical and pharmacological properties of SR 49059, a new, potent, nonpeptide antagonist of rat and human vasopressin V1a receptors

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Solution structure of the second extracellular loop of human thromboxane A2 receptor

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NMR and modeling studies of a synthetic extracellular loop II of the kappa opioid receptor in a DPC micelle

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Molecular characterization of the substance P*neurokinin-1 receptor complex: development of an experimentally based model.

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Involvement of the second extracellular loop (E2) of the neurokinin-1 receptor in the binding of substance P. Photoaffinity labeling and modeling studies

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Structure and function in rhodopsin: replacement by alanine of cysteine residues 110 and 187, components of a conserved disulfide bond in rhodopsin, affects the light-activated metarhodopsin II state

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Peptide receptors. Stepping up the pressure

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Coupling of retinal isomerization to the activation of rhodopsin

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Coupling of canine serotonin 5-HT(1B) and 5-HT(1D) receptor subtypes to the formation of inositol phosphates by dual interactions with endogenous G(i/o) and recombinant G(alpha15) proteins.

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Structure of cholecystokinin receptor binding sites and mechanism of activation/inactivation by agonists/antagonists.

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Structural and functional characterization of human CXCR4 as a chemokine receptor and HIV-1 co-receptor by mutagenesis and molecular modeling studies

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Vasopressin receptor mutations and nephrogenic diabetes insipidus

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Changes in interhelical hydrogen bonding upon rhodopsin activation

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Evolutionary trace of G protein-coupled receptors reveals clusters of residues that determine global and class-specific functions

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Essential role for the second extracellular loop in C5a receptor activation

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Contacts between extracellular loop two and transmembrane helix six determine basal activity of the thyroid-stimulating hormone receptor

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Palmitoylation of the vasopressin V1a receptor reveals different conformational requirements for signaling, agonist-induced receptor phosphorylation, and sequestration.

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10.1074/JBC.M702151200

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17403667%20AND%20SRC:MED&resulttype=core&format=json

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24 November 2022

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28 December 2019

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