Sequential tyrosine sulfation of CXCR4 by tyrosylprotein sulfotransferases. - Wikidata - wikimedia - TriplyDB

Sequential tyrosine sulfation of CXCR4 by tyrosylprotein sulfotransferases.

Sequential tyrosine sulfation of CXCR4 by tyrosylprotein sulfotransferases.

http://www.wikidata.org/entity/Q37143965

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Catalytic mechanism of Golgi-resident human tyrosylprotein sulfotransferase-2: a mass spectrometry approach Diversity and Inter-Connections in the CXCR4 Chemokine Receptor/Ligand Family: Molecular Perspectives Intermonomer Interactions Are Essential for Lysosomal Enzyme Binding by the Cation-Dependent Mannose 6-Phosphate Receptor Targeting SDF-1/CXCL12 with a ligand that prevents activation of CXCR4 through structure-based drug design CKR-L3, a deletion version CCR6-isoform shows coreceptor-activity for limited human and simian immunodeficiency viruses.A genome-wide CRISPR screen identifies a restricted set of HIV host dependency factors.A competitive binding study of chemokine, sulfated receptor, and glycosaminoglycan interactions by nano-electrospray ionization mass spectrometry.Fragment-based optimization of small molecule CXCL12 inhibitors for antagonizing the CXCL12/CXCR4 interaction.Tyrosylprotein sulfotransferase-1 and tyrosine sulfation of chemokine receptor 4 are induced by Epstein-Barr virus encoded latent membrane protein 1 and associated with the metastatic potential of human nasopharyngeal carcinoma.NMR in the Analysis of Functional Chemokine Interactions and Drug Discovery Heparin oligosaccharides inhibit chemokine (CXC motif) ligand 12 (CXCL12) cardioprotection by binding orthogonal to the dimerization interface, promoting oligomerization, and competing with the chemokine (CXC motif) receptor 4 (CXCR4) N terminus Tyrosine sulfation of chemokine receptor CCR2 enhances interactions with both monomeric and dimeric forms of the chemokine monocyte chemoattractant protein-1 (MCP-1)Preparation and Analysis of N-Terminal Chemokine Receptor Sulfopeptides Using Tyrosylprotein Sulfotransferase Enzymes.Macrophage Migration Inhibitory Factor-CXCR4 Receptor Interactions: EVIDENCE FOR PARTIAL ALLOSTERIC AGONISM IN COMPARISON WITH CXCL12 CHEMOKINE.Regulation of chemokine recognition by site-specific tyrosine sulfation of receptor peptides.Sulfopeptide probes of the CXCR4/CXCL12 interface reveal oligomer-specific contacts and chemokine allostery.Pattern and temporal sequence of sulfation of CCR5 N-terminal peptides by tyrosylprotein sulfotransferase-2: an assessment of the effects of N-terminal residues The role of tyrosine sulfation in the dimerization of the CXCR4:SDF-1 complex.International 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.Emerging sulfated flavonoids and other polyphenols as drugs: nature as an inspiration.The structural role of receptor tyrosine sulfation in chemokine recognition.Novel roles and therapeutic targets of Epstein-Barr virus-encoded latent membrane protein 1-induced oncogenesis in nasopharyngeal carcinoma.CCR7 Sulfotyrosine Enhances CCL21 Binding.New paradigms in chemokine receptor signal transduction: Moving beyond the two-site model.Synthesis of Sulfotyrosine-Containing Peptides by Incorporating Fluorosulfated Tyrosine Using an Fmoc-Based Solid-Phase Strategy.Structural basis for the broad substrate specificity of the human tyrosylprotein sulfotransferase-1.Differences in Sulfotyrosine Binding amongst CXCR1 and CXCR2 Chemokine Ligands.Chapter 3. Lymphotactin structural dynamics.Sulfotyrosine recognition as marker for druggable sites in the extracellular space.Modelling binding between CCR5 and CXCR4 receptors and their ligands suggests the surface electrostatic potential of the co-receptor to be a key player in the HIV-1 tropism.Recent Advances in the Application of Solution NMR Spectroscopy to Multi-Span Integral Membrane Proteins.Identification of an Arg-Leu-Arg tripeptide that contributes to the binding interface between the cytokine MIF and the chemokine receptor CXCR4.Explaining the Paucity of Intratumoral T Cells: A Construction Out of Known Entities.New tools for evaluating protein tyrosine sulfation: tyrosylprotein sulfotransferases (TPSTs) are novel targets for RAF protein kinase inhibitors

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Sequential tyrosine sulfation of CXCR4 by tyrosylprotein sulfotransferases.

http://www.wikidata.org/entity/Q37143965

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 04 October 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Sequential tyrosine sulfation of CXCR4 by tyrosylprotein sulfotransferases.

@en

Sequential tyrosine sulfation of CXCR4 by tyrosylprotein sulfotransferases.

@nl

type

label

Sequential tyrosine sulfation of CXCR4 by tyrosylprotein sulfotransferases.

@en

Sequential tyrosine sulfation of CXCR4 by tyrosylprotein sulfotransferases.

@nl

prefLabel

Sequential tyrosine sulfation of CXCR4 by tyrosylprotein sulfotransferases.

@en

Sequential tyrosine sulfation of CXCR4 by tyrosylprotein sulfotransferases.

@nl

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Sequential tyrosine sulfation of CXCR4 by tyrosylprotein sulfotransferases.

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Brian F Volkman

http://www.w3.org/2001/XMLSchema#string

Brian T Chait

http://www.w3.org/2001/XMLSchema#string

Christoph Seibert

http://www.w3.org/2001/XMLSchema#string

Christopher T Veldkamp

http://www.w3.org/2001/XMLSchema#string

Francis C Peterson

http://www.w3.org/2001/XMLSchema#string

Thomas P Sakmar

http://www.w3.org/2001/XMLSchema#string

P2860

HIV-1 Entry Cofactor: Functional cDNA Cloning of a Seven-Transmembrane, G Protein-Coupled Receptor

Involvement of chemokine receptors in breast cancer metastasis

Existence of distinct tyrosylprotein sulfotransferase genes: molecular characterization of tyrosylprotein sulfotransferase-2

The lymphocyte chemoattractant SDF-1 is a ligand for LESTR/fusin and blocks HIV-1 entry

Tyrosylprotein sulfotransferase: purification and molecular cloning of an enzyme that catalyzes tyrosine O-sulfation, a common posttranslational modification of eukaryotic proteins

Cloning of a human seven-transmembrane domain receptor, LESTR, that is highly expressed in leukocytes

Tyrosine sulfation of CCR5 N-terminal peptide by tyrosylprotein sulfotransferases 1 and 2 follows a discrete pattern and temporal sequence.

Tyrosine sulfation is a trans-Golgi-specific protein modification

Insights into the molecular basis of leukocyte tethering and rolling revealed by structures of P- and E-selectin bound to SLe(X) and PSGL-1

Structures of the CCR5 N Terminus and of a Tyrosine-Sulfated Antibody with HIV-1 gp120 and CD4

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11251-11262

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scholarly article

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10.1021/BI800965M

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P433

43

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47

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2008-10-04T00:00:00Z

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23298707

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18834145

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2662774

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