Lipopolysaccharide binding protein

 Lipopolysaccharide binding protein is a protein that in humans is encoded by the LBP gene.[5][6]

LBP
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesLBP, BPIFD2, lipopolysaccharide binding protein
External IDsOMIM151990 MGI1098776 HomoloGene3055 GeneCardsLBP
Gene location (Human)
Chromosome 20 (human)
Chr.Chromosome 20 (human)[1]
Chromosome 20 (human)
Genomic location for LBP
Genomic location for LBP
Band20q11.23Start38,346,482 bp[1]
End38,377,013 bp[1]
RNA expression pattern
PBB GE LBP 211652 s at fs.png

PBB GE LBP 214461 at fs.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004139

NM_008489

RefSeq (protein)

NP_004130

NP_032515

Location (UCSC)Chr 20: 38.35 – 38.38 MbChr 2: 158.31 – 158.33 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

LBP is a soluble acute-phase protein that binds to bacterial lipopolysaccharide (or LPS) to elicit immune responses by presenting the LPS to important cell surface pattern recognition receptors called CD14 and TLR4.[7]

The protein encoded by this gene is involved in the acute-phase immunologic response to gram-negative bacterial infections. Gram-negative bacteria contain a glycolipid, lipopolysaccharide (LPS), on their outer cell wall. Together with bactericidal permeability-increasing protein (BPI), the encoded protein binds LPS and interacts with the CD14 receptor, probably playing a role in regulating LPS-dependent monocyte responses. Studies in mice suggest that the encoded protein is necessary for the rapid acute-phase response to LPS but not for the clearance of LPS from circulation. This protein is part of a family of structurally and functionally related proteins, including BPI, plasma cholesteryl ester transfer protein (CETP), and phospholipid transfer protein (PLTP). Finally, this gene is found on chromosome 20, immediately downstream of the BPI gene.[6]

InteractionsEdit

Lipopolysaccharide-binding protein has been shown to interact with CD14TLR2TLR4 and the co-receptor MD-2.[8][9][10]

This article uses material from the Wikipedia article
 Metasyntactic variable, which is released under the 
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Attribution-ShareAlike 3.0 Unported License
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