Identification of a key region of kinin B(1) receptor for high affinity binding of peptide antagonists (Q73487312)

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4 November 2019

title

Identification of a key region of kinin B(1) receptor for high affinity binding of peptide antagonists (English)

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4 November 2019

author name string

S Bastian

1

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4 November 2019

D Pruneau

2

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4 November 2019

B Loillier

3

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4 November 2019

C Robert

4

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4 November 2019

J C Bonnafous

5

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4 November 2019

J L Paquet

6

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4 November 2019

language of work or name

English

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publication date

1 March 2000

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Journal of Biological Chemistry

4 November 2019

published in

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4 November 2019

volume

275

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4 November 2019

issue

9

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4 November 2019

page(s)

6107-6113

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Kinin formation: mechanisms and role in inflammatory disorders

4 November 2019

cites work

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Bradykinin receptors: pharmacological properties and biological roles

21 January 2018

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Cloning and pharmacological characterization of a human bradykinin (BK-2) receptor

21 January 2018

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Delineation of a region in the B2 bradykinin receptor that is essential for high-affinity agonist binding

21 January 2018

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Mutation of aspartate residues in the third extracellular loop of the rat B2 bradykinin receptor decreases affinity for bradykinin

21 January 2018

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Extracellular domains of the bradykinin B2 receptor involved in ligand binding and agonist sensing defined by anti-peptide antibodies

21 January 2018

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The N terminus of bradykinin when bound to the human bradykinin B2 receptor is adjacent to extracellular Cys20 and Cys277 in the receptor

21 January 2018

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Mutations in the B2 bradykinin receptor reveal a different pattern of contacts for peptidic agonists and peptidic antagonists

21 January 2018

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The sixth transmembrane domains of the human B1 and B2 bradykinin receptors are structurally compatible and involved in discriminating between subtype-selective agonists

21 January 2018

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A single position in the third transmembrane domains of the human B1 and B2 bradykinin receptors is adjacent to and discriminates between the C-terminal residues of subtype-selective ligands

21 January 2018

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High-efficiency transformation of mammalian cells by plasmid DNA

21 January 2018

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Mutation of Asn111 in the third transmembrane domain of the AT1A angiotensin II receptor induces its constitutive activation.

21 January 2018

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Stable expression of human kinin B1 receptor in 293 cells: pharmacological and functional characterization

21 January 2018

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A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

21 January 2018

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Lithium amplifies agonist-dependent phosphatidylinositol responses in brain and salivary glands

21 January 2018

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Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

21 January 2018

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The N-terminal extracellular segments of the chemokine receptors CCR1 and CCR3 are determinants for MIP-1alpha and eotaxin binding, respectively, but a second domain is essential for efficient receptor activation

21 January 2018

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The key amino acid residue of prostaglandin EP3 receptor for governing G protein association and activation steps

21 January 2018

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The deletion of 14 amino acids in the seventh transmembrane domain of a naturally occurring calcitonin receptor isoform alters ligand binding and selectively abolishes coupling to phospholipase C

21 January 2018

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Influence of the cytosolic carboxyl termini of human B1 and B2 kinin receptors on receptor sequestration, ligand internalization, and signal transduction

21 January 2018

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Effects of intracellular tyrosine residue mutation and carboxyl terminus truncation on signal transduction and internalization of the rat bradykinin B2 receptor

21 January 2018

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Motif mutation of bradykinin B2 receptor second intracellular loop and proximal C terminus is critical for signal transduction, internalization, and resensitization.

21 January 2018

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Hoe 140 a new potent and long acting bradykinin-antagonist: in vitro studies

21 January 2018

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A single amino-acid difference confers major pharmacological variation between human and rodent 5-HT1B receptors

21 January 2018

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A single point mutation increases the affinity of serotonin 5-HT1D alpha, 5-HT1D beta, 5-HT1E and 5-HT1F receptors for beta-adrenergic antagonists

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.275.9.6107

21 January 2018

Identifiers

DOI

10.1074/JBC.275.9.6107

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10692400%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference