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1oit
From Proteopedia
(Difference between revisions)
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==Imidazopyridines: a potent and selective class of Cyclin-dependent Kinase inhibitors identified through Structure-based hybridisation== | ==Imidazopyridines: a potent and selective class of Cyclin-dependent Kinase inhibitors identified through Structure-based hybridisation== | ||
| - | <StructureSection load='1oit' size='340' side='right' caption='[[1oit]], [[Resolution|resolution]] 1.60Å' scene=''> | + | <StructureSection load='1oit' size='340' side='right'caption='[[1oit]], [[Resolution|resolution]] 1.60Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1oit]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1OIT OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1OIT FirstGlance]. <br> | <table><tr><td colspan='2'>[[1oit]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1OIT OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1OIT FirstGlance]. <br> | ||
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</div> | </div> | ||
<div class="pdbe-citations 1oit" style="background-color:#fffaf0;"></div> | <div class="pdbe-citations 1oit" style="background-color:#fffaf0;"></div> | ||
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| + | ==See Also== | ||
| + | *[[Cyclin-dependent kinase 3D structures|Cyclin-dependent kinase 3D structures]] | ||
== References == | == References == | ||
<references/> | <references/> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Human]] | [[Category: Human]] | ||
| + | [[Category: Large Structures]] | ||
[[Category: Transferase]] | [[Category: Transferase]] | ||
[[Category: Beattie, J F]] | [[Category: Beattie, J F]] | ||
Revision as of 18:09, 20 November 2019
Imidazopyridines: a potent and selective class of Cyclin-dependent Kinase inhibitors identified through Structure-based hybridisation
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