CXCR3 requires tyrosine sulfation for ligand binding and a second extracellular loop arginine residue for ligand-induced chemotaxis.
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Catalytic mechanism of Golgi-resident human tyrosylprotein sulfotransferase-2: a mass spectrometry approachGliadin induces an increase in intestinal permeability and zonulin release by binding to the chemokine receptor CXCR3Detection and purification of tyrosine-sulfated proteins using a novel anti-sulfotyrosine monoclonal antibody.CXCR3 in carcinoma progressionA novel CXCL10-based GPI-anchored fusion protein as adjuvant in NK-based tumor therapyStructure of the Tyrosine-sulfated C5a Receptor N Terminus in Complex with Chemotaxis Inhibitory Protein of Staphylococcus aureusImmunopathogenic Mechanisms of Autoimmune Hepatitis: How Much Do We Know from Animal Models?Lack of tyrosylprotein sulfotransferase-2 activity results in altered sperm-egg interactions and loss of ADAM3 and ADAM6 in epididymal spermArginine mimetics using α-guanidino acids: introduction of functional groups and stereochemistry adjacent to recognition guanidiniums in peptidesCXCL10 Acts as a Bifunctional Antimicrobial Molecule against Bacillus anthracis.Mammalian target of rapamycin and Rictor control neutrophil chemotaxis by regulating Rac/Cdc42 activity and the actin cytoskeletonHydrogen Peroxide Triggers a Dual Signaling Axis To Selectively Suppress Activated Human T Lymphocyte Migration.Incomplete posttranslational prohormone modifications in hyperactive neuroendocrine cells.CXC chemokine ligand (CXCL) 9 and CXCL10 are antagonistic costimulation molecules during the priming of alloreactive T cell effectorsSmall molecule chemokine mimetics suggest a molecular basis for the observation that CXCL10 and CXCL11 are allosteric ligands of CXCR3A competitive binding study of chemokine, sulfated receptor, and glycosaminoglycan interactions by nano-electrospray ionization mass spectrometry.Structural Analysis of Chemokine Receptor-Ligand Interactions.Fragment-based optimization of small molecule CXCL12 inhibitors for antagonizing the CXCL12/CXCR4 interaction.Prolongation of cardiac and islet allograft survival by a blocking hamster anti-mouse CXCR3 monoclonal antibody.CXCR3 signaling in BRAFWT melanoma increases IL-8 expression and tumorigenicity.NMR in the Analysis of Functional Chemokine Interactions and Drug DiscoveryIdentification of key regulatory pathways of myeloid differentiation using an mESC-based karyotypically normal cell model.Tyrosine sulfation of chemokine receptor CCR2 enhances interactions with both monomeric and dimeric forms of the chemokine monocyte chemoattractant protein-1 (MCP-1)Glucocorticoids enhance the in vivo migratory response of human monocytesSulfopeptide probes of the CXCR4/CXCL12 interface reveal oligomer-specific contacts and chemokine allostery.Pediatric Kawasaki Disease and Adult Human Immunodeficiency Virus Kawasaki-Like Syndrome Are Likely the Same Malady.Pattern and temporal sequence of sulfation of CCR5 N-terminal peptides by tyrosylprotein sulfotransferase-2: an assessment of the effects of N-terminal residuesInternational Union of Basic and Clinical Pharmacology. [corrected]. LXXXIX. Update on the extended family of chemokine receptors and introducing a new nomenclature for atypical chemokine receptors.CXCL11-dependent induction of FOXP3-negative regulatory T cells suppresses autoimmune encephalomyelitis.Sulfated tyrosines 27 and 29 in the N-terminus of human CXCR3 participate in binding native IP-10.Tyrosine sulfation in N-terminal domain of human C5a receptor is necessary for binding of chemotaxis inhibitory protein of Staphylococcus aureus.CXCR3 ligands: redundant, collaborative and antagonistic functions.Targeting chemokine receptors in allergic disease.Pharmacological modulation of chemokine receptor function.The structural role of receptor tyrosine sulfation in chemokine recognition.Understanding and applying tyrosine biochemical diversity.Tyrosine sulfation as a protein post-translational modification.Role of tyrosine-sulfated proteins in retinal structure and functionTyrosine sulfation is prevalent in human chemokine receptors important in lung disease.Biased signaling pathways via CXCR3 control the development and function of CD4+ T cell subsets.
P2860
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P2860
CXCR3 requires tyrosine sulfation for ligand binding and a second extracellular loop arginine residue for ligand-induced chemotaxis.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
CXCR3 requires tyrosine sulfat ...... for ligand-induced chemotaxis.
@en
type
label
CXCR3 requires tyrosine sulfat ...... for ligand-induced chemotaxis.
@en
prefLabel
CXCR3 requires tyrosine sulfat ...... for ligand-induced chemotaxis.
@en
P2093
P2860
P356
P1476
CXCR3 requires tyrosine sulfat ...... for ligand-induced chemotaxis.
@en
P2093
Andrew D Luster
Gabriele S V Campanella
Lindsay A Manice
Richard A Colvin
P2860
P304
P356
10.1128/MCB.00556-06
P407
P577
2006-08-01T00:00:00Z