Tyrosine sulfation is prevalent in human chemokine receptors important in lung disease.
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Structural Basis of CXCR4 Sulfotyrosine Recognition by the Chemokine SDF-1/CXCL12Structure of the Tyrosine-sulfated C5a Receptor N Terminus in Complex with Chemotaxis Inhibitory Protein of Staphylococcus aureusSmall changes huge impact: the role of protein posttranslational modifications in cellular homeostasis and diseasePredicting sulfotyrosine sites using the random forest algorithm with significantly improved prediction accuracy.Neisseria meningitidis Opc invasin binds to the sulphated tyrosines of activated vitronectin to attach to and invade human brain endothelial cells.Structural Analysis of Chemokine Receptor-Ligand Interactions.Fragment-based optimization of small molecule CXCL12 inhibitors for antagonizing the CXCL12/CXCR4 interaction.Attachment of Chlamydia trachomatis L2 to host cells requires sulfation.NMR in the Analysis of Functional Chemokine Interactions and Drug DiscoveryA Multifeatures Fusion and Discrete Firefly Optimization Method for Prediction of Protein Tyrosine Sulfation Residues.Tyrosine sulfation of chemokine receptor CCR2 enhances interactions with both monomeric and dimeric forms of the chemokine monocyte chemoattractant protein-1 (MCP-1)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.Binding thermodynamics of the N-terminal peptide of the CCR5 coreceptor to HIV-1 envelope glycoprotein gp120Position weight matrix, gibbs sampler, and the associated significance tests in motif characterization and predictionSulfated 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.Novel roles and therapeutic targets of Epstein-Barr virus-encoded latent membrane protein 1-induced oncogenesis in nasopharyngeal carcinoma.What Do Structures Tell Us About Chemokine Receptor Function and Antagonism?Synthesis of polymers and nanoparticles bearing polystyrene sulfonate brushes for chemokine binding.Differences in Sulfotyrosine Binding amongst CXCR1 and CXCR2 Chemokine Ligands.Post-translational Modifications of Natural Antimicrobial Peptides and Strategies for Peptide Engineering.Sulfotyrosine recognition as marker for druggable sites in the extracellular space.Sulfonation, an underexploited area: from skeletal development to infectious diseases and cancer.Metabolomic fingerprint in patients at high risk of cardiovascular disease by cocoa intervention.
P2860
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P2860
Tyrosine sulfation is prevalent in human chemokine receptors important in lung disease.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
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2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
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2008年學術文章
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name
Tyrosine sulfation is prevalent in human chemokine receptors important in lung disease.
@en
type
label
Tyrosine sulfation is prevalent in human chemokine receptors important in lung disease.
@en
prefLabel
Tyrosine sulfation is prevalent in human chemokine receptors important in lung disease.
@en
P2093
P2860
P356
P1476
Tyrosine sulfation is prevalent in human chemokine receptors important in lung disease.
@en
P2093
Grace L Rosenquist
Hugh B Nicholas
Justin Liu
Kristine M Yu
Samuel Louie
P2860
P304
P356
10.1165/RCMB.2007-0118OC
P577
2008-01-24T00:00:00Z