NMR solution structure and receptor peptide binding of the CC chemokine eotaxin-2
about
Structural rearrangement of human lymphotactin, a C chemokine, under physiological solution conditionsMonomeric solution structure of the prototypical 'C' chemokine lymphotactinStructural basis for differential binding of the interleukin-8 monomer and dimer to the CXCR1 N-domain: role of coupled interactions and dynamicsMolecular determinants for CC-chemokine recognition by a poxvirus CC-chemokine inhibitorMolecular cloning, characterization and expression analysis of a CC chemokine gene from miiuy croaker (Miichthys miiuy).Solution structure of the complex between poxvirus-encoded CC chemokine inhibitor vCCI and human MIP-1beta.Design and receptor interactions of obligate dimeric mutant of chemokine monocyte chemoattractant protein-1 (MCP-1).Structural basis of chemokine receptor function--a model for binding affinity and ligand selectivityTyrosine sulfation of chemokine receptor CCR2 enhances interactions with both monomeric and dimeric forms of the chemokine monocyte chemoattractant protein-1 (MCP-1)Chemokine CXCL1 dimer is a potent agonist for the CXCR2 receptor.Thermodynamic characterization of interleukin-8 monomer binding to CXCR1 receptor N-terminal domain.Regulation of chemokine recognition by site-specific tyrosine sulfation of receptor peptides.Chemokine oligomerization in cell signaling and migration.The structural role of receptor tyrosine sulfation in chemokine recognition.Characterization of the interactions of vMIP-II, and a dimeric variant of vMIP-II, with glycosaminoglycans.The binding surface and affinity of monomeric and dimeric chemokine macrophage inflammatory protein 1 beta for various glycosaminoglycan disaccharides.New paradigms in chemokine receptor signal transduction: Moving beyond the two-site model.Kinetic and thermodynamic studies reveal chemokine homologues CC11 and CC24 with an almost identical tertiary structure have different folding pathways.Sulfotyrosine recognition as marker for druggable sites in the extracellular space.Identification of receptor binding and activation determinants in the N-terminal and N-loop regions of the CC chemokine eotaxin.Solution structure of CXCL13 and heparan sulfate binding show that GAG binding site and cellular signalling rely on distinct domains.Eotaxin-3/CCL26 is a natural antagonist for CC chemokine receptors 1 and 5. A human chemokine with a regulatory role.The human CC chemokine MIP-1beta dimer is not competent to bind to the CCR5 receptor.PDBe: Protein Data Bank in Europe
P2860
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P2860
NMR solution structure and receptor peptide binding of the CC chemokine eotaxin-2
description
2000 nî lūn-bûn
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2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2000年の論文
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2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
NMR solution structure and receptor peptide binding of the CC chemokine eotaxin-2
@ast
NMR solution structure and receptor peptide binding of the CC chemokine eotaxin-2
@en
NMR solution structure and receptor peptide binding of the CC chemokine eotaxin-2
@nl
type
label
NMR solution structure and receptor peptide binding of the CC chemokine eotaxin-2
@ast
NMR solution structure and receptor peptide binding of the CC chemokine eotaxin-2
@en
NMR solution structure and receptor peptide binding of the CC chemokine eotaxin-2
@nl
prefLabel
NMR solution structure and receptor peptide binding of the CC chemokine eotaxin-2
@ast
NMR solution structure and receptor peptide binding of the CC chemokine eotaxin-2
@en
NMR solution structure and receptor peptide binding of the CC chemokine eotaxin-2
@nl
P356
P1433
P1476
NMR solution structure and receptor peptide binding of the CC chemokine eotaxin-2
@en
P2093
P304
P356
10.1021/BI000523J
P407
P577
2000-07-25T00:00:00Z