Proteopedia:Featured JRN/0

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<tr><td>[[Image:Anim_Journal-JBIC-2_Hydrophobic_interactions.gif|center]]</td></tr>
<tr><td>[[Image:Anim_Journal-JBIC-2_Hydrophobic_interactions.gif|center]]</td></tr>
<tr><td><div class="scrolling">'''Structure of Anticancer Ruthenium Half-Sandwich Complex Bound to Glycogen Synthase Kinase 3ß'''<br>
<tr><td><div class="scrolling">'''Structure of Anticancer Ruthenium Half-Sandwich Complex Bound to Glycogen Synthase Kinase 3ß'''<br>
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''G. Atilla-Gocumen, L. Di Costanzo, E. Meggers''. J Biol Inorg Chem. 2010 doi: [http://dx.doi.org/10.1007/s00775-010-0699-x 10.1007/s00775-010-0699-x] <br>
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''G Atilla-Gocumen, L Di Costanzo, E Meggers''. ''J Biol Inorg Chem.'' 2010 doi: [http://dx.doi.org/10.1007/s00775-010-0699-x 10.1007/s00775-010-0699-x] <br>
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A crystal structure of an organometallic half-sandwich ruthenium complex bound to the protein kinase glycogen synthase kinase 3ß (GSK-3ß) has been determined and reveals that the inhibitor binds to the ATP binding site via an induced fit mechanism utlizing several hydrogen bonds and hydrophobic interactions. Importantly, the metal is not involved in any direct interaction with the protein kinase but fulfills a purely structural role.
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A crystal structure of an organometallic half-sandwich ruthenium complex bound to glycogen synthase kinase 3ß (GSK-3ß) reveals that the inhibitor binds to the ATP binding site via an induced fit mechanism utilizing several hydrogen bonds and hydrophobic interactions. Importantly, the metal is not involved in any direct interaction with the protein kinase but fulfills a purely structural role.
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Revision as of 19:03, 18 October 2018

Structure of Anticancer Ruthenium Half-Sandwich Complex Bound to Glycogen Synthase Kinase 3ß

G Atilla-Gocumen, L Di Costanzo, E Meggers. J Biol Inorg Chem. 2010 doi: 10.1007/s00775-010-0699-x
A crystal structure of an organometallic half-sandwich ruthenium complex bound to glycogen synthase kinase 3ß (GSK-3ß) reveals that the inhibitor binds to the ATP binding site via an induced fit mechanism utilizing several hydrogen bonds and hydrophobic interactions. Importantly, the metal is not involved in any direct interaction with the protein kinase but fulfills a purely structural role.

>>> Visit this I3DC complement >>>

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