1r2d: Difference between revisions

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New page: left|200px<br /> <applet load="1r2d" size="450" color="white" frame="true" align="right" spinBox="true" caption="1r2d, resolution 1.95Å" /> '''Structure of Human ...
 
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[[Image:1r2d.gif|left|200px]]<br />
[[Image:1r2d.gif|left|200px]]<br /><applet load="1r2d" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1r2d" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1r2d, resolution 1.95&Aring;" />
caption="1r2d, resolution 1.95&Aring;" />
'''Structure of Human Bcl-XL at 1.95 Angstroms'''<br />
'''Structure of Human Bcl-XL at 1.95 Angstroms'''<br />


==Overview==
==Overview==
Cells expressing high levels of the BCL-X(L) anti-apoptotic protein are, preferentially killed by the mitochondrial inhibitor antimycin A (AA)., Computational modeling predicts a binding site for AA in the extended, hydrophobic groove on BCL-X(L), previously identified as an interface for, dimerization to BAX and related proapoptotic proteins. Here, we identify, BCL-X(L) hydrophobic groove mutants with normal cellular anti-apoptotic, function but suppressed sensitivity to AA. The LD(50) of AA for cells, expressing BCL-X(L) mutants directly correlates with the measured in vitro, dissociation constants for AA binding. These results indicate that, BCL-X(L) is a principal target mediating AA cytotoxicity.
Cells expressing high levels of the BCL-X(L) anti-apoptotic protein are preferentially killed by the mitochondrial inhibitor antimycin A (AA). Computational modeling predicts a binding site for AA in the extended hydrophobic groove on BCL-X(L), previously identified as an interface for dimerization to BAX and related proapoptotic proteins. Here, we identify BCL-X(L) hydrophobic groove mutants with normal cellular anti-apoptotic function but suppressed sensitivity to AA. The LD(50) of AA for cells expressing BCL-X(L) mutants directly correlates with the measured in vitro dissociation constants for AA binding. These results indicate that BCL-X(L) is a principal target mediating AA cytotoxicity.


==About this Structure==
==About this Structure==
1R2D 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=1R2D OCA].  
1R2D 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=1R2D OCA].  


==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Giedt, C.D.]]
[[Category: Giedt, C D.]]
[[Category: Hockenbery, D.M.]]
[[Category: Hockenbery, D M.]]
[[Category: Kim, K.M.]]
[[Category: Kim, K M.]]
[[Category: Manion, M.K.]]
[[Category: Manion, M K.]]
[[Category: Neill, J.W.O.]]
[[Category: Neill, J W.O.]]
[[Category: Zhang, K.Y.]]
[[Category: Zhang, K Y.]]
[[Category: alpha-helical]]
[[Category: alpha-helical]]
[[Category: apoptosis]]
[[Category: apoptosis]]
[[Category: monomeric]]
[[Category: monomeric]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 18:58:53 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:46:18 2008''