(Q33946526)

English

N-linked glycosylation at Asn3 and the positively charged residues within the amino-terminal domain of the c1 inhibitor are required for interaction of the C1 Inhibitor with Salmonella enterica serovar typhimurium lipopolysaccharide and lipid A.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

N-linked glycosylation at Asn3 and the positively charged residues within the amino-terminal domain of the c1 inhibitor are required for interaction of the C1 Inhibitor with Salmonella enterica serovar typhimurium lipopolysaccharide and lipid A. (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Salmonella enterica

0 references

lipopolysaccharide

0 references

1 reference

based on heuristic

inferred from title

author name string

Dongxu Liu

1

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Cort C Cramer

2

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Jennifer Scafidi

3

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Alvin E Davis

4

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

language of work or name

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publication date

1 August 2005

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Europe PubMed Central

PubMed publication ID

30 July 2017

Infection and Immunity

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Europe PubMed Central

PubMed publication ID

30 July 2017

73

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

4478-4487

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC1201182/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Structural model of MD-2 and functional role of its basic amino acid clusters involved in cellular lipopolysaccharide recognition

1 reference

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5 July 2018

N-linked glycosylation is required for c1 inhibitor-mediated protection from endotoxin shock in mice

1 reference

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5 July 2018

Separate Functional Domains of Human MD-2 Mediate Toll-Like Receptor 4-Binding and Lipopolysaccharide Responsiveness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Lysines 128 and 132 enable lipopolysaccharide binding to MD-2, leading to Toll-like receptor-4 aggregation and signal transduction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

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Augmentation of the lipopolysaccharide-neutralizing activities of human cathelicidin CAP18/LL-37-derived antimicrobial peptides by replacement with hydrophobic and cationic amino acid residues

1 reference

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5 July 2018

Identification of single amino acid residues essential for the binding of lipopolysaccharide (LPS) to LPS binding protein (LBP) residues 86-99 by using an Ala-scanning library

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

MD-2 and TLR4 N-linked glycosylations are important for a functional lipopolysaccharide receptor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

N-linked glycosylations at Asn(26) and Asn(114) of human MD-2 are required for toll-like receptor 4-mediated activation of NF-kappaB by lipopolysaccharide

1 reference

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Cathelicidin family of antibacterial peptides CAP18 and CAP11 inhibit the expression of TNF-alpha by blocking the binding of LPS to CD14(+) cells

1 reference

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5 July 2018

Toll-like receptors in the induction of the innate immune response

1 reference

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5 July 2018

A conserved structural motif for lipopolysaccharide recognition by procaryotic and eucaryotic proteins

1 reference

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5 July 2018

C1-Esterase inhibitor: an anti-inflammatory agent and its potential use in the treatment of diseases other than hereditary angioedema.

1 reference

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5 July 2018

Structure-function analysis of CD14 as a soluble receptor for lipopolysaccharide

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Interpretation of biological activity data of bacterial endotoxins by simple molecular models of mechanism of action

1 reference

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5 July 2018

Cutting edge: cationic antimicrobial peptides block the binding of lipopolysaccharide (LPS) to LPS binding protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Role of CD14 in cellular recognition of bacterial lipopolysaccharides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Lipopolysaccharide-binding protein.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Solution structure of polymyxins B and E and effect of binding to lipopolysaccharide: an NMR and molecular modeling study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

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Defective LPS Signaling in C3H/HeJ and C57BL/10ScCr Mice: Mutations in Tlr4 Gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

LPS-binding proteins and receptors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

The BPI/LBP family of proteins: a structural analysis of conserved regions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

N-terminal stretch Arg2, Arg3, Arg4 and Arg5 of human lactoferrin is essential for binding to heparin, bacterial lipopolysaccharide, human lysozyme and DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Mutation of amino acids 39-44 of human CD14 abrogates binding of lipopolysaccharide and Escherichia coli.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Effects of site-directed mutagenesis of basic residues (Arg 94, Lys 95, Lys 99) of lipopolysaccharide (LPS)-binding protein on binding and transfer of LPS and subsequent immune cell activation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Titration calorimetric studies to elucidate the specificity of the interactions of polymyxin B with lipopolysaccharides and lipid A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Antibacterial activity of peptides homologous to a loop region in human lactoferrin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

The myeloid differentiation antigen CD14 is N- and O-glycosylated. Contribution of N-linked glycosylation to different soluble CD14 isoforms.

1 reference

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Crystal structure of an endotoxin-neutralizing protein from the horseshoe crab, Limulus anti-LPS factor, at 1.5 A resolution.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Protein glycosylation. Structural and functional aspects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Lactoferrin is a lipid A-binding protein.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Complete cDNA encoding human phospholipid transfer protein from human endothelial cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

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Bacterial endotoxin: molecular relationships of structure to activity and function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

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Point mutagenesis of positively charged amino acids of cholesteryl ester transfer protein: conserved residues within the lipid transfer/lipopolysaccharide binding protein gene family essential for function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Peptide derivatives of three distinct lipopolysaccharide binding proteins inhibit lipopolysaccharide-induced tumor necrosis factor-alpha secretion in vitro*

1 reference

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5 July 2018

Receptor-dependent mechanisms of cell stimulation by bacterial endotoxin

1 reference

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5 July 2018

Identification of a lipopolysaccharide binding domain in CD14 between amino acids 57 and 64.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

A region of human CD14 required for lipopolysaccharide binding

1 reference

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Proteolytic cleavage and inactivation of alpha 2-plasmin inhibitor and C1 inactivator by human polymorphonuclear leukocyte elastase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

5 July 2018

Inactivation of factor XII active fragment in normal plasma. Predominant role of C-1-inhibitor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

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Contribution of Plasma Protease Inhibitors to the Inactivation of Kallikrein in Plasma

1 reference

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Cloning and sequencing of human cholesteryl ester transfer protein cDNA

1 reference

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Proteolysis and deglycosylation of human C1 inhibitor. Effect on functional properties

1 reference

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1 reference

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1 reference

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Proteolytic inactivation of plasma C1- inhibitor in sepsis

1 reference

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Structural requirements of lipid A for endotoxicity and other biological activities

1 reference

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The role of the asparagine-linked oligosaccharides of the alpha subunit in the secretion and assembly of human chorionic gonadotrophin

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Endotoxic lipid A interaction with human platelets. Structure-function analysis of lipid A homologs obtained from Salmonella minnesota Re595 lipopolysaccharide.

1 reference

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Septic shock: pathogenesis

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Interaction of 125I-labelled complement subcomponents C-1r and C-1s with protease inhibitors in plasma

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Interactions of lactoferricin-derived peptides with LPS and antimicrobial activity

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29 October 2018

C1 inhibitor prevents endotoxin shock via a direct interaction with lipopolysaccharide

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1201182

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Interchangeable endotoxin-binding domains in proteins with opposite lipopolysaccharide-dependent activities.

1 reference

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1 reference

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Differential impact of substitution of amino acids 9-13 and 91-101 of human CD14 on soluble CD14-dependent activation of cells by lipopolysaccharide

1 reference

https://pubmed.ncbi.nlm.nih.gov/16040958

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Biologic activities of the contact factors in vivo--potentiation of hypotension, inflammation, and fibrinolysis, and inhibition of cell adhesion, angiogenesis and thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16040958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

N-terminal modifications of Polymyxin B nonapeptide and their effect on antibacterial activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/16040958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of LPS-Binding Peptide Fragment of MD-2, a Toll-Receptor Accessory Protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/16040958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional analysis of the serpin domain of C1 inhibitor

1 reference

https://pubmed.ncbi.nlm.nih.gov/16040958

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based on heuristic

inferred from PubMed ID database lookup

Lipopolysaccharide (LPS) neutralizing peptides reveal a lipid A binding site of LPS binding protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/16040958

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/IAI.73.8.4478-4487.2005

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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