1opk: Difference between revisions

New page: left|200px<br /><applet load="1opk" size="450" color="white" frame="true" align="right" spinBox="true" caption="1opk, resolution 1.80Å" /> '''Structural basis for...
 
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[[Image:1opk.gif|left|200px]]<br /><applet load="1opk" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1opk.gif|left|200px]]<br /><applet load="1opk" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1opk, resolution 1.80&Aring;" />
caption="1opk, resolution 1.80&Aring;" />
'''Structural basis for the auto-inhibition of c-Abl tyrosine kinase'''<br />
'''Structural basis for the auto-inhibition of c-Abl tyrosine kinase'''<br />


==Overview==
==Overview==
c-Abl is normally regulated by an autoinhibitory mechanism, the disruption, of which leads to chronic myelogenous leukemia. The details of this, mechanism have been elusive because c-Abl lacks a phosphotyrosine residue, that triggers the assembly of the autoinhibited form of the closely, related Src kinases by internally engaging the SH2 domain. Crystal, structures of c-Abl show that the N-terminal myristoyl modification of, c-Abl 1b binds to the kinase domain and induces conformational changes, that allow the SH2 and SH3 domains to dock onto it. Autoinhibited c-Abl, forms an assembly that is strikingly similar to that of inactive Src, kinases but with specific differences that explain the differential, ability of the drug STI-571/Gleevec/imatinib (STI-571) to inhibit the, catalytic activity of Abl, but not that of c-Src.
c-Abl is normally regulated by an autoinhibitory mechanism, the disruption of which leads to chronic myelogenous leukemia. The details of this mechanism have been elusive because c-Abl lacks a phosphotyrosine residue that triggers the assembly of the autoinhibited form of the closely related Src kinases by internally engaging the SH2 domain. Crystal structures of c-Abl show that the N-terminal myristoyl modification of c-Abl 1b binds to the kinase domain and induces conformational changes that allow the SH2 and SH3 domains to dock onto it. Autoinhibited c-Abl forms an assembly that is strikingly similar to that of inactive Src kinases but with specific differences that explain the differential ability of the drug STI-571/Gleevec/imatinib (STI-571) to inhibit the catalytic activity of Abl, but not that of c-Src.


==About this Structure==
==About this Structure==
1OPK is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with MYR, P16 and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. 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=1OPK OCA].  
1OPK is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with <scene name='pdbligand=MYR:'>MYR</scene>, <scene name='pdbligand=P16:'>P16</scene> and <scene name='pdbligand=GOL:'>GOL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. 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=1OPK OCA].  


==Reference==
==Reference==
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[[Category: Superti-Furga, G.]]
[[Category: Superti-Furga, G.]]
[[Category: Veach, D.]]
[[Category: Veach, D.]]
[[Category: Young, M.A.]]
[[Category: Young, M A.]]
[[Category: GOL]]
[[Category: GOL]]
[[Category: MYR]]
[[Category: MYR]]
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[[Category: transferase]]
[[Category: transferase]]


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