Competition for binding sites on C3b by CR1, CR2, MCP, factor B and factor H.

No abstract is available for this paper.

• Publication year

  1990

• Venue

  Complement and Inflammation

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine, Chemistry

• Identifiers
  DOI 10.1159/000463124PMID 2138950
• 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.

• No references are available for this paper.

• Inhibition of acute complement responses towards bolus-injected nanoparticles using targeted short-circulating regulatory proteins

  2023influential citation
• Early Diagnostic Ability of Human Complement Factor B in Pancreatic Cancer Is Partly Linked to Its Potential Tumor-Promoting Role.

  2021cites this paper
• Candida and Complement: New Aspects in an Old Battle

  2020cites this paper
• Complement Factor H

  2020cites this paper
• Complement C3

  2020influential citation
• Two distinct conformations of factor H regulate discrete complement-binding functions in the fluid phase and at cell surfaces

  2018cites this paper
• Detection of microbial proteases by the Toll pathway during innate immune responses in Drosophila melanogaster

  2018cites this paper
• Complement Component C3 is a Critical Point in Aged Choroidal Vessels in the Complement Factor H knock Out Model of Retinal Degeneration.

  2017cites this paper
• Viral-derived complement inhibitors: current status and potential role in immunomodulation

  2017cites this paper
• Immune factors guiding Listeria monocytogenes infection

  2016cites this paper
• A Familial C3GN Secondary to Defective C3 Regulation by Complement Receptor 1 and Complement Factor H.

  2016cites this paper
• Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome.

  2015cites this paper
• Role of leukocytes, complement system and endothelium in rat renal ischaemia-reperfusion injury

  2015cites this paper
• The complement system: history, pathways, cascade and inhibitors.

  2012cites this paper
• Complement factor H dysfunction in atypical hemolytic uremic syndrome

  2011cites this paper
• Solution structures of gycosaminoglycans and theirinteractions with complement factor H

  2011cites this paper
• The role of lipo-oligosaccharide ganglioside mimicry on the interaction of Guillain-Barré syndrome associated strains of Campylobacter jejuni with the immune system

  2010cites this paper
• Transcriptional control of genes for soluble complement cascade regulatory proteins.

  2010cites this paper
• Complement Factor H Binds at Two Independent Sites to C-reactive Protein in Acute Phase Concentrations*♦

  2009cites this paper
• Loa loa Microfilariae Evade Complement Attack In Vivo by Acquiring Regulatory Proteins from Host Plasma

  2009cites this paper
• Electrostatic interactions contribute to the folded-back conformation of wild type human factor H.

  2009cites this paper
• Complement Factor H: solution structures and interactions with ligands

  2009cites this paper
• Multimeric interactions between complement factor H and its C3d ligand provide new insight on complement regulation.

  2009influential citation
• Implications of the progressive self-association of wild-type human factor H for complement regulation and disease.

  2008cites this paper
• Uncontrolled zinc- and copper-induced oligomerisation of the human complement regulator factor H and its possible implications for function and disease.

  2008cites this paper
• The regulatory SCR-1/5 and cell surface-binding SCR-16/20 fragments of factor H reveal partially folded-back solution structures and different self-associative properties.

  2008cites this paper
• Complement factor H: using atomic resolution structure to illuminate disease mechanisms.

  2008cites this paper
• Defective B cell ontogeny and immune response in human complement receptor 2 (CR2, CD21) transgenic mice is partially recovered in the absence of C3.

  2007cites this paper
• The Opportunistic Human Pathogenic Fungus Aspergillus fumigatus Evades the Host Complement System

  2007cites this paper
• Where next with atypical hemolytic uremic syndrome?

  2007cites this paper
• Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome.

  2007cites this paper
• Selective and efficient inhibition of the alternative pathway of complement by a mAb that recognizes C3b/iC3b.

  2006cites this paper
• Localization of the third heparin-binding site in the human complement regulator factor H1.

  2006cites this paper
• Molecular Dissection of Interactions between Components of the Alternative Pathway of Complement and Decay Accelerating Factor (CD55)*

  2005cites this paper
• Structural stability and heat‐induced conformational change of two complement inhibitors: C4b‐binding protein and factor H

  2004cites this paper
• Funktionelle Charakterisierung des Faktor H-verwandten Proteins 1 (FHR-1) im Komplementsystem

  2003cites this paper
• The Yeast Candida albicans Binds Complement Regulators Factor H and FHL-1

  2002cites this paper
• Bacterial expression and membrane targeting of the rat complement regulator Crry: A new model anticomplement therapeutic

  2002cites this paper
• CR1 and CR1‐like: the primate immune adherence receptors

  2001cites this paper
• Identification of Residues within the 727–767 Segment of Human Complement Component C3 Important for Its Interaction with Factor H and with Complement Receptor 1 (CR1, CD35)*

  1999cites this paper
• Components and Reactivity

  1998cites this paper
• Complement-inhibiting peptides identified by proximity to indels in the C3/4/5 protein family.

  1997cites this paper
• Erythrocyte complement receptors.

  1995cites this paper
• Interactions of human complement component C3 with factor B and with complement receptors type 1 (CR1, CD35) and type 3 (CR3, CD11b/CD18) involve an acidic sequence at the N-terminus of C3 alpha'-chain.

  1994cites this paper
• Herpes simplex virus glycoprotein C: molecular mimicry of complement regulatory proteins by a viral protein.

  1993cites this paper
• Third component of trout complement. cDNA cloning and conservation of functional sites.

  1993cites this paper
• Primary structure of cobra complement component C3.

  1992cites this paper
• Segment spanning residues 727-768 of the complement C3 sequence contains a neoantigenic site and accommodates the binding of CR1, factor H, and factor B.

  1992cites this paper
• Phylogeny of the third component of complement, C3: analysis of the conservation of human CR1, CR2, H, and B binding sites, concanavalin A binding sites, and thiolester bond in the C3 from different species.

  1992cites this paper
• Complement C3: a molecular mosaic of binding sites.

  1991cites this paper
• Evolution of the complement system.

  1991cites this paper
• Contribution of the repeating domains of membrane cofactor protein (CD46) of the complement system to ligand binding and cofactor activity.

  1991cites this paper
• Sites within the complement C3b/C4b receptor important for the specificity of ligand binding.

  1991cites this paper