1gh6

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(New page: 200px<br /> <applet load="1gh6" size="450" color="white" frame="true" align="right" spinBox="true" caption="1gh6, resolution 3.2&Aring;" /> '''RETINOBLASTOMA POCKE...)
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caption="1gh6, resolution 3.2&Aring;" />
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'''RETINOBLASTOMA POCKET COMPLEXED WITH SV40 LARGE T ANTIGEN'''<br />
'''RETINOBLASTOMA POCKET COMPLEXED WITH SV40 LARGE T ANTIGEN'''<br />
==Overview==
==Overview==
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Inactivation of the retinoblastoma (Rb) tumor suppressor by Simian virus, 40 (SV40) large T antigen is one of the central features of tumorigenesis, induced by SV40. Both the N-terminal J domain and the LxCxE motif of large, T antigen are required for inactivation of Rb. The crystal structure of, the N-terminal region (residues 7-117) of SV40 large T antigen bound to, the pocket domain of Rb reveals that large T antigen contains a four-helix, bundle, and residues from helices alpha2 and alpha4 and from a loop, containing the LxCxE motif participate in the interactions with Rb. The, two central helices and a connecting loop in large T antigen have, structural similarities with the J domains of the molecular chaperones, DnaJ and HDJ-1, suggesting that large T antigen may use a chaperone, mechanism for its biological function. However, there are significant, differences between large T antigen and the molecular chaperones in other, regions and these differences are likely to provide the specificity needed, for large T antigen to inactivate Rb.
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Inactivation of the retinoblastoma (Rb) tumor suppressor by Simian virus 40 (SV40) large T antigen is one of the central features of tumorigenesis induced by SV40. Both the N-terminal J domain and the LxCxE motif of large T antigen are required for inactivation of Rb. The crystal structure of the N-terminal region (residues 7-117) of SV40 large T antigen bound to the pocket domain of Rb reveals that large T antigen contains a four-helix bundle, and residues from helices alpha2 and alpha4 and from a loop containing the LxCxE motif participate in the interactions with Rb. The two central helices and a connecting loop in large T antigen have structural similarities with the J domains of the molecular chaperones DnaJ and HDJ-1, suggesting that large T antigen may use a chaperone mechanism for its biological function. However, there are significant differences between large T antigen and the molecular chaperones in other regions and these differences are likely to provide the specificity needed for large T antigen to inactivate Rb.
==Disease==
==Disease==
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==About this Structure==
==About this Structure==
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1GH6 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/Simian_virus_40 Simian virus 40]. The following page contains interesting information on the relation of 1GH6 with [[http://pdb.rcsb.org/pdb/static.do?p=education_discussion/molecule_of_the_month/pdb47_1.html Simian Virus 40]]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1GH6 OCA].
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1GH6 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/Simian_virus_40 Simian virus 40]. The following page contains interesting information on the relation of 1GH6 with [[http://pdb.rcsb.org/pdb/static.do?p=education_discussion/molecule_of_the_month/pdb47_1.html Simian Virus 40]]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1GH6 OCA].
==Reference==
==Reference==
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[[Category: Simian virus 40]]
[[Category: Simian virus 40]]
[[Category: Cho, Y.]]
[[Category: Cho, Y.]]
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[[Category: Kim, H.Y.]]
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[[Category: Kim, H Y.]]
[[Category: oncoprotein]]
[[Category: oncoprotein]]
[[Category: tumor suppressor]]
[[Category: tumor suppressor]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 17:05:16 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:50:02 2008''

Revision as of 10:50, 21 February 2008


1gh6, resolution 3.2Å

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RETINOBLASTOMA POCKET COMPLEXED WITH SV40 LARGE T ANTIGEN

Contents

Overview

Inactivation of the retinoblastoma (Rb) tumor suppressor by Simian virus 40 (SV40) large T antigen is one of the central features of tumorigenesis induced by SV40. Both the N-terminal J domain and the LxCxE motif of large T antigen are required for inactivation of Rb. The crystal structure of the N-terminal region (residues 7-117) of SV40 large T antigen bound to the pocket domain of Rb reveals that large T antigen contains a four-helix bundle, and residues from helices alpha2 and alpha4 and from a loop containing the LxCxE motif participate in the interactions with Rb. The two central helices and a connecting loop in large T antigen have structural similarities with the J domains of the molecular chaperones DnaJ and HDJ-1, suggesting that large T antigen may use a chaperone mechanism for its biological function. However, there are significant differences between large T antigen and the molecular chaperones in other regions and these differences are likely to provide the specificity needed for large T antigen to inactivate Rb.

Disease

Known diseases associated with this structure: Bladder cancer OMIM:[180200], Osteosarcoma OMIM:[180200], Pinealoma with bilateral retinoblastoma OMIM:[180200], Retinoblastoma OMIM:[180200]

About this Structure

1GH6 is a Protein complex structure of sequences from Homo sapiens and Simian virus 40. The following page contains interesting information on the relation of 1GH6 with [Simian Virus 40]. Full crystallographic information is available from OCA.

Reference

Structural basis for the inactivation of retinoblastoma tumor suppressor by SV40 large T antigen., Kim HY, Ahn BY, Cho Y, EMBO J. 2001 Jan 15;20(1-2):295-304. PMID:11226179

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