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1oqd

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(New page: 200px<br /> <applet load="1oqd" size="450" color="white" frame="true" align="right" spinBox="true" caption="1oqd, resolution 2.60&Aring;" /> '''Crystal structure o...)
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<applet load="1oqd" size="450" color="white" frame="true" align="right" spinBox="true"
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'''Crystal structure of sTALL-1 and BCMA'''<br />
'''Crystal structure of sTALL-1 and BCMA'''<br />
==Overview==
==Overview==
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The tumour necrosis factor (TNF) ligand TALL-1 and its cognate receptors, BCMA, TACI and BAFF-R, were recently identified as members of the TNF, superfamily, which are essential factors contributing to B-cell, maturation. The functional, soluble fragment of TALL-1 (sTALL-1) forms a, virus-like assembly for its proper function. Here we determine the crystal, structures of sTALL-1 complexed with the extracellular domains of BCMA and, BAFF-R at 2.6 and 2.5 A, respectively. The single cysteine-rich domain of, BCMA and BAFF-R both have saddle-like architectures, which sit on the, horseback-like surface formed by four coil regions on each individual, sTALL-1 monomer. Three novel structural modules, D2, X2 and N, were, revealed from the current structures. Sequence alignments, structural, modelling and mutagenesis revealed that one disulphide bridge in BAFF-R is, critical for determining the binding specificity of the extracellular, domain eBAFF-R to TALL-1 instead of APRIL, a closely related ligand of, TALL-1, which was confirmed by binding experiments in vitro.
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The tumour necrosis factor (TNF) ligand TALL-1 and its cognate receptors, BCMA, TACI and BAFF-R, were recently identified as members of the TNF superfamily, which are essential factors contributing to B-cell maturation. The functional, soluble fragment of TALL-1 (sTALL-1) forms a virus-like assembly for its proper function. Here we determine the crystal structures of sTALL-1 complexed with the extracellular domains of BCMA and BAFF-R at 2.6 and 2.5 A, respectively. The single cysteine-rich domain of BCMA and BAFF-R both have saddle-like architectures, which sit on the horseback-like surface formed by four coil regions on each individual sTALL-1 monomer. Three novel structural modules, D2, X2 and N, were revealed from the current structures. Sequence alignments, structural modelling and mutagenesis revealed that one disulphide bridge in BAFF-R is critical for determining the binding specificity of the extracellular domain eBAFF-R to TALL-1 instead of APRIL, a closely related ligand of TALL-1, which was confirmed by binding experiments in vitro.
==About this Structure==
==About this Structure==
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1OQD is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1OQD OCA].
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1OQD is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1OQD OCA].
==Reference==
==Reference==
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[[Category: ligand receptor complex]]
[[Category: ligand receptor complex]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 18:35:22 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:20:25 2008''

Revision as of 12:20, 21 February 2008


1oqd, resolution 2.60Å

Drag the structure with the mouse to rotate

Crystal structure of sTALL-1 and BCMA

Overview

The tumour necrosis factor (TNF) ligand TALL-1 and its cognate receptors, BCMA, TACI and BAFF-R, were recently identified as members of the TNF superfamily, which are essential factors contributing to B-cell maturation. The functional, soluble fragment of TALL-1 (sTALL-1) forms a virus-like assembly for its proper function. Here we determine the crystal structures of sTALL-1 complexed with the extracellular domains of BCMA and BAFF-R at 2.6 and 2.5 A, respectively. The single cysteine-rich domain of BCMA and BAFF-R both have saddle-like architectures, which sit on the horseback-like surface formed by four coil regions on each individual sTALL-1 monomer. Three novel structural modules, D2, X2 and N, were revealed from the current structures. Sequence alignments, structural modelling and mutagenesis revealed that one disulphide bridge in BAFF-R is critical for determining the binding specificity of the extracellular domain eBAFF-R to TALL-1 instead of APRIL, a closely related ligand of TALL-1, which was confirmed by binding experiments in vitro.

About this Structure

1OQD is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Ligand-receptor binding revealed by the TNF family member TALL-1., Liu Y, Hong X, Kappler J, Jiang L, Zhang R, Xu L, Pan CH, Martin WE, Murphy RC, Shu HB, Dai S, Zhang G, Nature. 2003 May 1;423(6935):49-56. PMID:12721620

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