1sm2: Difference between revisions

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|SITE=  
|SITE=  
|LIGAND= <scene name='pdbligand=STU:STAUROSPORINE'>STU</scene>
|LIGAND= <scene name='pdbligand=STU:STAUROSPORINE'>STU</scene>
|ACTIVITY= [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]  
|ACTIVITY= <span class='plainlinks'>[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] </span>
|GENE= ITK, LYK, EMT ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= ITK, LYK, EMT ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|DOMAIN=
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1sm2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1sm2 OCA], [http://www.ebi.ac.uk/pdbsum/1sm2 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1sm2 RCSB]</span>
}}
}}


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==Overview==
==Overview==
Interleukin-2 tyrosine kinase, Itk, is an important member of the Tec family of non-receptor tyrosine kinases that play a central role in signaling through antigen receptors such as the T-cell receptor, B-cell receptor, and Fcepsilon. Selective inhibition of Itk may be an important way of modulating many diseases involving heightened or inappropriate activation of the immune system. In addition to an unliganded nonphophorylated Itk catalytic kinase domain, we determined the crystal structures of the phosphorylated and nonphosphorylated kinase domain bound to staurosporine, a potent broad-spectrum kinase inhibitor. These structures are useful for the design of novel, highly potent and selective Itk inhibitors and provide insight into the influence of inhibitor binding and phosphorylation on the conformation of Itk.
Interleukin-2 tyrosine kinase, Itk, is an important member of the Tec family of non-receptor tyrosine kinases that play a central role in signaling through antigen receptors such as the T-cell receptor, B-cell receptor, and Fcepsilon. Selective inhibition of Itk may be an important way of modulating many diseases involving heightened or inappropriate activation of the immune system. In addition to an unliganded nonphophorylated Itk catalytic kinase domain, we determined the crystal structures of the phosphorylated and nonphosphorylated kinase domain bound to staurosporine, a potent broad-spectrum kinase inhibitor. These structures are useful for the design of novel, highly potent and selective Itk inhibitors and provide insight into the influence of inhibitor binding and phosphorylation on the conformation of Itk.
==Disease==
Known disease associated with this structure: Polyhydramnios, megalencephaly, and symptomatic epilepsy OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=608626 608626]]


==About this Structure==
==About this Structure==
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[[Category: Tanner, A J.]]
[[Category: Tanner, A J.]]
[[Category: Vial, S C.M.]]
[[Category: Vial, S C.M.]]
[[Category: STU]]
[[Category: immunology]]
[[Category: immunology]]
[[Category: protein kinase]]
[[Category: protein kinase]]


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