Identification of a ligand binding site in the human neutrophil formyl peptide receptor using a site-specific fluorescent photoaffinity label and mass spectrometry.
about
International Union of Basic and Clinical Pharmacology. LXXIII. Nomenclature for the formyl peptide receptor (FPR) familyStructure modeling of all identified G protein-coupled receptors in the human genomeThe role of water in activation mechanism of human N-formyl peptide receptor 1 (FPR1) based on molecular dynamics simulationsHuman formyl peptide receptor function role of conserved and nonconserved charged residuesFunctional characterization of three mouse formyl peptide receptorsPhotoaffinity labeling combined with mass spectrometric approaches as a tool for structural proteomics.Cgamma H2 of Met174 side chain is the site of covalent attachment of a substance P analog photoactivable in position 5.Chemical cross-linking with thiol-cleavable reagents combined with differential mass spectrometric peptide mapping--a novel approach to assess intermolecular protein contacts.Involvement of the second extracellular loop (E2) of the neurokinin-1 receptor in the binding of substance P. Photoaffinity labeling and modeling studies.Mapping ligand-receptor interfaces: approaching the resolution limit of benzophenone-based photoaffinity scanningPeptides derived from HIV-1, HIV-2, Ebola virus, SARS coronavirus and coronavirus 229E exhibit high affinity binding to the formyl peptide receptor.Chemotaxis inhibitory protein of Staphylococcus aureus, a bacterial antiinflammatory agent.Identification of formyl peptides from Listeria monocytogenes and Staphylococcus aureus as potent chemoattractants for mouse neutrophils.Structural determinants for the interaction of formyl peptide receptor 2 with peptide ligands.Mass spectrometry based tools to investigate protein-ligand interactions for drug discovery.Enemy attraction: bacterial agonists for leukocyte chemotaxis receptors.The Formyl Peptide Receptors: Diversity of Ligands and Mechanism for Recognition.The annexin I sequence gln(9)-ala(10)-trp(11)-phe(12) is a core structure for interaction with the formyl peptide receptor 1.Identification of ligand effector binding sites in transmembrane regions of the human G protein-coupled C3a receptor.Mutations of F110 and C126 of the formyl peptide receptor interfere with G-protein coupling and chemotaxis.Recognition-driven chemical labeling of endogenous proteins in multi-molecular crowding in live cells.G protein-coupled receptors. I. Diversity of receptor-ligand interactions.
P2860
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P2860
Identification of a ligand binding site in the human neutrophil formyl peptide receptor using a site-specific fluorescent photoaffinity label and mass spectrometry.
description
1998 nî lūn-bûn
@nan
1998 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Identification of a ligand bin ...... y label and mass spectrometry.
@ast
Identification of a ligand bin ...... y label and mass spectrometry.
@en
type
label
Identification of a ligand bin ...... y label and mass spectrometry.
@ast
Identification of a ligand bin ...... y label and mass spectrometry.
@en
prefLabel
Identification of a ligand bin ...... y label and mass spectrometry.
@ast
Identification of a ligand bin ...... y label and mass spectrometry.
@en
P2093
P2860
P356
P1476
Identification of a ligand bin ...... ty label and mass spectrometry
@en
P2093
D Barnidge
H M Miettinen
M J Vlases
S Wimer-Mackin
P2860
P304
10428-10435
P356
10.1074/JBC.273.17.10428
P407
P577
1998-04-01T00:00:00Z