1gux: Difference between revisions

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New page: left|200px<br /> <applet load="1gux" size="450" color="white" frame="true" align="right" spinBox="true" caption="1gux, resolution 1.85Å" /> '''RB POCKET BOUND TO ...
 
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[[Image:1gux.gif|left|200px]]<br />
[[Image:1gux.gif|left|200px]]<br /><applet load="1gux" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1gux" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1gux, resolution 1.85&Aring;" />
caption="1gux, resolution 1.85&Aring;" />
'''RB POCKET BOUND TO E7 LXCXE MOTIF'''<br />
'''RB POCKET BOUND TO E7 LXCXE MOTIF'''<br />


==Overview==
==Overview==
The pocket domain of the retinoblastoma (Rb) tumour suppressor is central, to Rb function, and is frequently inactivated by the binding of the human, papilloma virus E7 oncoprotein in cervical cancer. The crystal structure, of the Rb pocket bound to a nine-residue E7 peptide containing the LxCxE, motif, shared by other Rb-binding viral and cellular proteins, shows that, the LxCxE peptide binds a highly conserved groove on the B-box portion of, the pocket; the A-box portion appears to be required for the stable, folding of the B box. Also highly conserved is the extensive A-B, interface, suggesting that it may be an additional protein-binding site., The A and B boxes each contain the cyclin-fold structural motif, with the, LxCxE-binding site on the B-box cyclin fold being similar to a, Cdk2-binding site of cyclin A and to a TBP-binding site of TFIIB.
The pocket domain of the retinoblastoma (Rb) tumour suppressor is central to Rb function, and is frequently inactivated by the binding of the human papilloma virus E7 oncoprotein in cervical cancer. The crystal structure of the Rb pocket bound to a nine-residue E7 peptide containing the LxCxE motif, shared by other Rb-binding viral and cellular proteins, shows that the LxCxE peptide binds a highly conserved groove on the B-box portion of the pocket; the A-box portion appears to be required for the stable folding of the B box. Also highly conserved is the extensive A-B interface, suggesting that it may be an additional protein-binding site. The A and B boxes each contain the cyclin-fold structural motif, with the LxCxE-binding site on the B-box cyclin fold being similar to a Cdk2-binding site of cyclin A and to a TBP-binding site of TFIIB.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1GUX is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [http://en.wikipedia.org/wiki/Human_papillomavirus Human papillomavirus]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1GUX OCA].  
1GUX is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [http://en.wikipedia.org/wiki/Human_papillomavirus Human papillomavirus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1GUX OCA].  


==Reference==
==Reference==
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[[Category: Human papillomavirus]]
[[Category: Human papillomavirus]]
[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Lee, J.O.]]
[[Category: Lee, J O.]]
[[Category: Pavletich, N.P.]]
[[Category: Pavletich, N P.]]
[[Category: Russo, A.A.]]
[[Category: Russo, A A.]]
[[Category: complex (transcription regulation/peptide)]]
[[Category: complex (transcription regulation/peptide)]]
[[Category: retinoblastoma]]
[[Category: retinoblastoma]]
[[Category: tumor suppressor protein]]
[[Category: tumor suppressor protein]]


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