1qwe: Difference between revisions

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New page: left|200px<br /><applet load="1qwe" size="450" color="white" frame="true" align="right" spinBox="true" caption="1qwe" /> '''C-SRC SH3 DOMAIN COMPLEXED WITH LIGAND APP12...
 
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[[Image:1qwe.jpg|left|200px]]<br /><applet load="1qwe" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1qwe.jpg|left|200px]]<br /><applet load="1qwe" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1qwe" />
caption="1qwe" />
'''C-SRC SH3 DOMAIN COMPLEXED WITH LIGAND APP12'''<br />
'''C-SRC SH3 DOMAIN COMPLEXED WITH LIGAND APP12'''<br />


==Overview==
==Overview==
Two dodecapeptides belonging to distinct classes of Src homology 3 (SH3), ligands and selected from biased phage display libraries were used to, investigate interactions between a specificity pocket in the Src SH3, domain and ligant residues flanking the proline-rich core. The solution, structures of c-Src SH3 complexed with these peptides were solved by NMR., In addition to proline-rich, polyproline type II helix-forming core, the, class I and II ligands each possesses a flanking sequence that occupies a, large pocket between the RT and n-Src loops of the SH3 domain. Structural, and mutational analyses illustrate how the two classes of SH3 ligands, exploit a specificity pocket on the receptor differently to increase, binding affinity and specificity.
Two dodecapeptides belonging to distinct classes of Src homology 3 (SH3) ligands and selected from biased phage display libraries were used to investigate interactions between a specificity pocket in the Src SH3 domain and ligant residues flanking the proline-rich core. The solution structures of c-Src SH3 complexed with these peptides were solved by NMR. In addition to proline-rich, polyproline type II helix-forming core, the class I and II ligands each possesses a flanking sequence that occupies a large pocket between the RT and n-Src loops of the SH3 domain. Structural and mutational analyses illustrate how the two classes of SH3 ligands exploit a specificity pocket on the receptor differently to increase binding affinity and specificity.


==About this Structure==
==About this Structure==
1QWE is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Avian_sarcoma_virus Avian sarcoma virus]. Active as [http://en.wikipedia.org/wiki/Transferase Transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.10.1 and 2.7.10.2 2.7.10.1 and 2.7.10.2] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1QWE OCA].  
1QWE is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Avian_sarcoma_virus Avian sarcoma virus]. Active as [http://en.wikipedia.org/wiki/Transferase Transferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.10.1 and 2.7.10.2 2.7.10.1 and 2.7.10.2] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1QWE OCA].  


==Reference==
==Reference==
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[[Category: Chiyoshi, K.]]
[[Category: Chiyoshi, K.]]
[[Category: Feng, S.]]
[[Category: Feng, S.]]
[[Category: Rickles, R.J.]]
[[Category: Rickles, R J.]]
[[Category: Schreiber, S.L.]]
[[Category: Schreiber, S L.]]
[[Category: class ii ligand complex]]
[[Category: class ii ligand complex]]
[[Category: src sh3 domain]]
[[Category: src sh3 domain]]


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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:44:24 2008''