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2a0z

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(New page: 200px<br /> <applet load="2a0z" size="450" color="white" frame="true" align="right" spinBox="true" caption="2a0z, resolution 2.400&Aring;" /> '''The molecular stru...)
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<applet load="2a0z" size="450" color="white" frame="true" align="right" spinBox="true"
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'''The molecular structure of toll-like receptor 3 ligand binding domain'''<br />
'''The molecular structure of toll-like receptor 3 ligand binding domain'''<br />
==Overview==
==Overview==
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Innate immunity is the first line of defense against invading pathogens., Toll-like receptors (TLRs) act as sentinels of the innate immune system, sensing a variety of ligands from lipopolysaccharide to flagellin to dsRNA, through their ligand-binding domain that is composed of leucine-rich, repeats (LRRs). Ligand binding initiates a signaling cascade that leads to, the up-regulation of inflammation mediators. In this study, we have, expressed and crystallized the ectodomain (ECD) of human TLR3, which, recognizes dsRNA, a molecular signature of viruses, and have determined, the molecular structure to 2.4-A resolution. The overall horseshoe-shaped, structure of the TLR3-ECD is formed by 23 repeating LRRs that are capped, at each end by specialized non-LRR domains. The extensive beta-sheet on, the molecule's concave surface forms a platform for several modifications, including insertions in the LRRs and 11 N-linked glycans. The TLR3-ECD, structure indicates how LRR loops can establish distinct pathogen, recognition receptors.
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Innate immunity is the first line of defense against invading pathogens. Toll-like receptors (TLRs) act as sentinels of the innate immune system, sensing a variety of ligands from lipopolysaccharide to flagellin to dsRNA through their ligand-binding domain that is composed of leucine-rich repeats (LRRs). Ligand binding initiates a signaling cascade that leads to the up-regulation of inflammation mediators. In this study, we have expressed and crystallized the ectodomain (ECD) of human TLR3, which recognizes dsRNA, a molecular signature of viruses, and have determined the molecular structure to 2.4-A resolution. The overall horseshoe-shaped structure of the TLR3-ECD is formed by 23 repeating LRRs that are capped at each end by specialized non-LRR domains. The extensive beta-sheet on the molecule's concave surface forms a platform for several modifications, including insertions in the LRRs and 11 N-linked glycans. The TLR3-ECD structure indicates how LRR loops can establish distinct pathogen recognition receptors.
==About this Structure==
==About this Structure==
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2A0Z is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with NAG, GLC, SO4 and BME as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2A0Z OCA].
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2A0Z is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=NAG:'>NAG</scene>, <scene name='pdbligand=GLC:'>GLC</scene>, <scene name='pdbligand=SO4:'>SO4</scene> and <scene name='pdbligand=BME:'>BME</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2A0Z OCA].
==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Askins, J.]]
[[Category: Askins, J.]]
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[[Category: Bell, J.K.]]
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[[Category: Bell, J K.]]
[[Category: Botos, I.]]
[[Category: Botos, I.]]
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[[Category: Davies, D.R.]]
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[[Category: Davies, D R.]]
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[[Category: Hall, P.R.]]
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[[Category: Hall, P R.]]
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[[Category: Segal, D.M.]]
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[[Category: Segal, D M.]]
[[Category: Shiloach, J.]]
[[Category: Shiloach, J.]]
[[Category: BME]]
[[Category: BME]]
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[[Category: solenoid]]
[[Category: solenoid]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 20:44:17 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:22:32 2008''

Revision as of 14:22, 21 February 2008


2a0z, resolution 2.400Å

Drag the structure with the mouse to rotate

The molecular structure of toll-like receptor 3 ligand binding domain

Overview

Innate immunity is the first line of defense against invading pathogens. Toll-like receptors (TLRs) act as sentinels of the innate immune system, sensing a variety of ligands from lipopolysaccharide to flagellin to dsRNA through their ligand-binding domain that is composed of leucine-rich repeats (LRRs). Ligand binding initiates a signaling cascade that leads to the up-regulation of inflammation mediators. In this study, we have expressed and crystallized the ectodomain (ECD) of human TLR3, which recognizes dsRNA, a molecular signature of viruses, and have determined the molecular structure to 2.4-A resolution. The overall horseshoe-shaped structure of the TLR3-ECD is formed by 23 repeating LRRs that are capped at each end by specialized non-LRR domains. The extensive beta-sheet on the molecule's concave surface forms a platform for several modifications, including insertions in the LRRs and 11 N-linked glycans. The TLR3-ECD structure indicates how LRR loops can establish distinct pathogen recognition receptors.

About this Structure

2A0Z is a Single protein structure of sequence from Homo sapiens with , , and as ligands. Full crystallographic information is available from OCA.

Reference

The molecular structure of the Toll-like receptor 3 ligand-binding domain., Bell JK, Botos I, Hall PR, Askins J, Shiloach J, Segal DM, Davies DR, Proc Natl Acad Sci U S A. 2005 Aug 2;102(31):10976-80. Epub 2005 Jul 25. PMID:16043704

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