2gkw: Difference between revisions

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New page: left|200px<br /> <applet load="2gkw" size="450" color="white" frame="true" align="right" spinBox="true" caption="2gkw, resolution 2.70Å" /> '''Key contacts promot...
 
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[[Image:2gkw.gif|left|200px]]<br />
[[Image:2gkw.gif|left|200px]]<br /><applet load="2gkw" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="2gkw" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="2gkw, resolution 2.70&Aring;" />
caption="2gkw, resolution 2.70&Aring;" />
'''Key contacts promote recongnito of BAFF-R by TRAF3'''<br />
'''Key contacts promote recongnito of BAFF-R by TRAF3'''<br />


==Overview==
==Overview==
B cell-activating factor belonging to the TNF family receptor (BAFF-R), a, member of the TNFR superfamily, plays a role in autoimmunity after, ligation with BAFF ligand (also called TALL-1, BLyS, THANK, or zTNF4)., BAFF/BAFF-R interactions are critical for B cell regulation, and signaling, from this ligand-receptor complex results in NF-kappaB activation. Most, TNFRs transmit signals intracellularly by recruitment of adaptor proteins, called TNFR-associated factors (TRAFs). However, BAFF-R binds only one, TRAF adaptor, TRAF3, and this interaction negatively regulates activation, of NF-kappaB. In this study, we report the crystal structure of a, 24-residue fragment of the cytoplasmic portion of BAFF-R bound in complex, with TRAF3. The recognition motif (162)PVPAT(166) in BAFF-R is, accommodated in the same binding crevice on TRAF3 that binds two related, TNFRs, CD40 and LTbetaR, but is presented in a completely different, structural framework. This region of BAFF-R assumes an open conformation, with two extended strands opposed at right angles that each make contacts, with TRAF3. The recognition motif is located in the N-terminal arm and, intermolecular contacts mediate TRAF recognition. In the C-terminal arm, key stabilizing contacts are made, including critical hydrogen bonds with, Gln(379) in TRAF3 that define the molecular basis for selective binding of, BAFF-R solely to this member of the TRAF family. A dynamic conformational, adjustment of Tyr(377) in TRAF3 occurs forming a new intermolecular, contact with BAFF-R that stabilizes the complex. The structure of the, complex provides a molecular explanation for binding affinities and, selective protein interactions in TNFR-TRAF interactions.
B cell-activating factor belonging to the TNF family receptor (BAFF-R), a member of the TNFR superfamily, plays a role in autoimmunity after ligation with BAFF ligand (also called TALL-1, BLyS, THANK, or zTNF4). BAFF/BAFF-R interactions are critical for B cell regulation, and signaling from this ligand-receptor complex results in NF-kappaB activation. Most TNFRs transmit signals intracellularly by recruitment of adaptor proteins called TNFR-associated factors (TRAFs). However, BAFF-R binds only one TRAF adaptor, TRAF3, and this interaction negatively regulates activation of NF-kappaB. In this study, we report the crystal structure of a 24-residue fragment of the cytoplasmic portion of BAFF-R bound in complex with TRAF3. The recognition motif (162)PVPAT(166) in BAFF-R is accommodated in the same binding crevice on TRAF3 that binds two related TNFRs, CD40 and LTbetaR, but is presented in a completely different structural framework. This region of BAFF-R assumes an open conformation with two extended strands opposed at right angles that each make contacts with TRAF3. The recognition motif is located in the N-terminal arm and intermolecular contacts mediate TRAF recognition. In the C-terminal arm, key stabilizing contacts are made, including critical hydrogen bonds with Gln(379) in TRAF3 that define the molecular basis for selective binding of BAFF-R solely to this member of the TRAF family. A dynamic conformational adjustment of Tyr(377) in TRAF3 occurs forming a new intermolecular contact with BAFF-R that stabilizes the complex. The structure of the complex provides a molecular explanation for binding affinities and selective protein interactions in TNFR-TRAF interactions.


==About this Structure==
==About this Structure==
2GKW is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence 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=2GKW OCA].  
2GKW is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence 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=2GKW OCA].  


==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Ely, K.R.]]
[[Category: Ely, K R.]]
[[Category: baff receptor]]
[[Category: baff receptor]]
[[Category: cd40]]
[[Category: cd40]]
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[[Category: traf3]]
[[Category: traf3]]


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