Conformational analysis of the human chemokine receptor CXCR3

No abstract is available for this paper.

• Publication year

  2017

• Venue

  Molecular Immunology

• Publication date

  2017-12-01

• Fields of study

  Medicine, Chemistry

• Identifiers
  DOI 10.1016/j.molimm.2017.10.010PMID 29054054
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Structural basis of ligand interaction with atypical chemokine receptor 3

  2017cited by this paper
• Structure-Based Identification of Novel Ligands Targeting Multiple Sites within a Chemokine-G-Protein-Coupled-Receptor Interface.

  2016cited by this paper
• An overview of the sequence features of N- and C-terminal segments of the human chemokine receptors.

  2014influential reference
• Closing the Ring: A Fourth Extracellular Loop in Chemokine Receptors

  2014influential reference
• cytoHubba: identifying hub objects and sub-networks from complex interactome

  2014cited by this paper
• Interaction of chemokines with their receptors--from initial chemokine binding to receptor activating steps.

  2014cited by this paper
• N-terminal region of human chemokine receptor CXCR3: Structural analysis of CXCR3(1-48) by experimental and computational studies.

  2014influential reference
• Conformations of intrinsically disordered proteins are influenced by linear sequence distributions of oppositely charged residues

  2013influential reference
• Molecular Dynamics Simulation of Chemokine Receptors in Lipid Bilayer: A Case Study on C–C Chemokine Receptor Type 2

  2013influential reference
• The N‐terminal Region of CXCL11 as Structural Template for CXCR3 Molecular Recognition: Synthesis, Conformational Analysis, and Binding Studies

  2012cited by this paper
• COCOMAPS: a web application to analyze and visualize contacts at the interface of biomolecular complexes

  2011cited by this paper
• Analyzing and visualizing residue networks of protein structures.

  2011cited by this paper
• Structures of the CXCR4 Chemokine GPCR with Small-Molecule and Cyclic Peptide Antagonists

  2010cited by this paper
• Modelling of the membrane receptor CXCR3 and its complexes with CXCL9, CXCL10 and CXCL11 chemokines: putative target for new drug design.

  2009cited by this paper
• ESBRI: A web server for evaluating salt bridges in proteins

  2008cited by this paper
• GROMACS 4:  Algorithms for Highly Efficient, Load-Balanced, and Scalable Molecular Simulation.

  2008cited by this paper
• Computing topological parameters of biological networks

  2008cited by this paper
• CXCR3 Requires Tyrosine Sulfation for Ligand Binding and a Second Extracellular Loop Arginine Residue for Ligand-Induced Chemotaxis

  2006cited by this paper
• Scalable molecular dynamics with NAMD

  2005influential reference
• PatchDock and SymmDock: servers for rigid and symmetric docking

  2005cited by this paper
• NMR structure of CXCR3 binding chemokine CXCL11 (ITAC)

  2004influential reference
• Molecular characterization of the chemokine receptor CXCR3: evidence for the involvement of distinct extracellular domains in a multi‐step model of ligand binding and receptor activation

  2003influential reference
• Two Novel Fully Functional Isoforms of CX3CR1 Are Potent HIV Coreceptors 1

  2003cited by this paper
• Strategies for chemokine antagonists as therapeutics.

  2003cited by this paper
• Chemokines and chemokine receptors in leukocyte trafficking.

  2002cited by this paper
• Structure of a CXC chemokine-receptor fragment in complex with interleukin-8.

  1999cited by this paper
• VMD: visual molecular dynamics.

  1996influential reference
• Structure‐activity relationships of chemokines

  1995influential reference
• Satisfying hydrogen bonding potential in proteins.

  1994cited by this paper
• Supplementary Information Supplementary Methods : DNA preparation

  year unknowncited by this paper

• The Model Structures of the Complement Component 5a Receptor (C5aR) Bound to the Native and Engineered hC5a

  2018cites this paper