3ul7
From Proteopedia
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{{STRUCTURE_3ul7| PDB=3ul7 | SCENE= }} | {{STRUCTURE_3ul7| PDB=3ul7 | SCENE= }} | ||
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===Crystal structure of the TV3 mutant F63W=== | ===Crystal structure of the TV3 mutant F63W=== | ||
| + | {{ABSTRACT_PUBMED_22363519}} | ||
| + | ==Disease== | ||
| + | [[http://www.uniprot.org/uniprot/TLR4_HUMAN TLR4_HUMAN]] Genetic variation in TLR4 is associated with age-related macular degeneration type 10 (ARMD10) [MIM:[http://omim.org/entry/611488 611488]]. ARMD is a multifactorial eye disease and the most common cause of irreversible vision loss in the developed world. In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid that lie beneath the retinal pigment epithelium and within an elastin-containing structure known as Bruch membrane. | ||
| - | + | ==Function== | |
| - | + | [[http://www.uniprot.org/uniprot/TLR4_HUMAN TLR4_HUMAN]] Cooperates with LY96 and CD14 to mediate the innate immune response to bacterial lipopolysaccharide (LPS). Acts via MYD88, TIRAP and TRAF6, leading to NF-kappa-B activation, cytokine secretion and the inflammatory response. Also involved in LPS-independent inflammatory responses triggered by Ni(2+). These responses require non-conserved histidines and are, therefore, species-specific.<ref>PMID:20711192</ref> | |
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==About this Structure== | ==About this Structure== | ||
| - | [[3ul7]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/ | + | [[3ul7]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Eptatretus_burgeri Eptatretus burgeri]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3UL7 OCA]. |
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID:022363519</ref><references group="xtra"/> | + | <ref group="xtra">PMID:022363519</ref><references group="xtra"/><references/> |
| - | [[Category: | + | [[Category: Eptatretus burgeri]] |
[[Category: Cheong, H K.]] | [[Category: Cheong, H K.]] | ||
[[Category: Jeon, Y H.]] | [[Category: Jeon, Y H.]] | ||
Revision as of 21:48, 24 March 2013
Contents |
Crystal structure of the TV3 mutant F63W
Template:ABSTRACT PUBMED 22363519
Disease
[TLR4_HUMAN] Genetic variation in TLR4 is associated with age-related macular degeneration type 10 (ARMD10) [MIM:611488]. ARMD is a multifactorial eye disease and the most common cause of irreversible vision loss in the developed world. In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid that lie beneath the retinal pigment epithelium and within an elastin-containing structure known as Bruch membrane.
Function
[TLR4_HUMAN] Cooperates with LY96 and CD14 to mediate the innate immune response to bacterial lipopolysaccharide (LPS). Acts via MYD88, TIRAP and TRAF6, leading to NF-kappa-B activation, cytokine secretion and the inflammatory response. Also involved in LPS-independent inflammatory responses triggered by Ni(2+). These responses require non-conserved histidines and are, therefore, species-specific.[1]
About this Structure
3ul7 is a 1 chain structure with sequence from Eptatretus burgeri. Full crystallographic information is available from OCA.
Reference
- Han J, Kim HJ, Lee SC, Hong S, Park K, Jeon YH, Kim D, Cheong HK, Kim HS. Structure-based rational design of a Toll-like receptor 4 (TLR4) decoy receptor with high binding affinity for a target protein. PLoS One. 2012;7(2):e30929. Epub 2012 Feb 17. PMID:22363519 doi:10.1371/journal.pone.0030929
- ↑ Schmidt M, Raghavan B, Muller V, Vogl T, Fejer G, Tchaptchet S, Keck S, Kalis C, Nielsen PJ, Galanos C, Roth J, Skerra A, Martin SF, Freudenberg MA, Goebeler M. Crucial role for human Toll-like receptor 4 in the development of contact allergy to nickel. Nat Immunol. 2010 Sep;11(9):814-9. doi: 10.1038/ni.1919. Epub 2010 Aug 15. PMID:20711192 doi:10.1038/ni.1919
