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1tdq

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(New page: 200px<br /><applet load="1tdq" size="450" color="white" frame="true" align="right" spinBox="true" caption="1tdq, resolution 2.60&Aring;" /> '''Structural basis for...)
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[[Image:1tdq.gif|left|200px]]<br /><applet load="1tdq" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1tdq.gif|left|200px]]<br /><applet load="1tdq" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1tdq, resolution 2.60&Aring;" />
caption="1tdq, resolution 2.60&Aring;" />
'''Structural basis for the interactions between tenascins and the C-type lectin domains from lecticans: evidence for a cross-linking role for tenascins'''<br />
'''Structural basis for the interactions between tenascins and the C-type lectin domains from lecticans: evidence for a cross-linking role for tenascins'''<br />
==Overview==
==Overview==
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The C-terminal G3 domains of lecticans mediate crosslinking to diverse, extracellular matrix (ECM) proteins during ECM assembly, through their, C-type lectin (CLD) subdomains. The structure of the rat aggrecan CLD in a, Ca(2+)-dependent complex with fibronectin type III repeats 3-5 of rat, tenascin-R provides detailed support for such crosslinking. The CLD loops, bind Ca2+ like other CLDs, but no carbohydrate binding is observed or, possible. This is thus the first example of a direct Ca(2+)-dependent, protein-protein interaction of a CLD. Surprisingly, tenascin-R does not, coordinate the Ca2+ ions directly. Electron microscopy confirms that, full-length tenascin-R and tenascin-C crosslink hyaluronan-aggrecan, complexes. The results are significant for the binding of all lectican, CLDs to tenascin-R and tenascin-C. Comparison of the protein interaction, surface with that of P-selectin in complex with the PGSL-1 peptide, suggests that direct protein-protein interactions of Ca(2+)-binding CLDs, may be more widespread than previously appreciated.
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The C-terminal G3 domains of lecticans mediate crosslinking to diverse extracellular matrix (ECM) proteins during ECM assembly, through their C-type lectin (CLD) subdomains. The structure of the rat aggrecan CLD in a Ca(2+)-dependent complex with fibronectin type III repeats 3-5 of rat tenascin-R provides detailed support for such crosslinking. The CLD loops bind Ca2+ like other CLDs, but no carbohydrate binding is observed or possible. This is thus the first example of a direct Ca(2+)-dependent protein-protein interaction of a CLD. Surprisingly, tenascin-R does not coordinate the Ca2+ ions directly. Electron microscopy confirms that full-length tenascin-R and tenascin-C crosslink hyaluronan-aggrecan complexes. The results are significant for the binding of all lectican CLDs to tenascin-R and tenascin-C. Comparison of the protein interaction surface with that of P-selectin in complex with the PGSL-1 peptide suggests that direct protein-protein interactions of Ca(2+)-binding CLDs may be more widespread than previously appreciated.
==About this Structure==
==About this Structure==
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1TDQ is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus] with CA as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1TDQ OCA].
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1TDQ is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus] with <scene name='pdbligand=CA:'>CA</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1TDQ OCA].
==Reference==
==Reference==
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[[Category: Rattus norvegicus]]
[[Category: Rattus norvegicus]]
[[Category: Aspberg, A.]]
[[Category: Aspberg, A.]]
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[[Category: Logan, D.T.]]
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[[Category: Logan, D T.]]
[[Category: Lundell, A.]]
[[Category: Lundell, A.]]
[[Category: Moergelin, M.]]
[[Category: Moergelin, M.]]
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[[Category: Olin, A.I.]]
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[[Category: Olin, A I.]]
[[Category: al-Karadaghi, S.]]
[[Category: al-Karadaghi, S.]]
[[Category: CA]]
[[Category: CA]]
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[[Category: tenascins]]
[[Category: tenascins]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 03:11:17 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:12:30 2008''

Revision as of 13:12, 21 February 2008


1tdq, resolution 2.60Å

Drag the structure with the mouse to rotate

Structural basis for the interactions between tenascins and the C-type lectin domains from lecticans: evidence for a cross-linking role for tenascins

Overview

The C-terminal G3 domains of lecticans mediate crosslinking to diverse extracellular matrix (ECM) proteins during ECM assembly, through their C-type lectin (CLD) subdomains. The structure of the rat aggrecan CLD in a Ca(2+)-dependent complex with fibronectin type III repeats 3-5 of rat tenascin-R provides detailed support for such crosslinking. The CLD loops bind Ca2+ like other CLDs, but no carbohydrate binding is observed or possible. This is thus the first example of a direct Ca(2+)-dependent protein-protein interaction of a CLD. Surprisingly, tenascin-R does not coordinate the Ca2+ ions directly. Electron microscopy confirms that full-length tenascin-R and tenascin-C crosslink hyaluronan-aggrecan complexes. The results are significant for the binding of all lectican CLDs to tenascin-R and tenascin-C. Comparison of the protein interaction surface with that of P-selectin in complex with the PGSL-1 peptide suggests that direct protein-protein interactions of Ca(2+)-binding CLDs may be more widespread than previously appreciated.

About this Structure

1TDQ is a Protein complex structure of sequences from Rattus norvegicus with as ligand. Full crystallographic information is available from OCA.

Reference

Structural basis for interactions between tenascins and lectican C-type lectin domains: evidence for a crosslinking role for tenascins., Lundell A, Olin AI, Morgelin M, al-Karadaghi S, Aspberg A, Logan DT, Structure. 2004 Aug;12(8):1495-506. PMID:15296743

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