Tau-tubulin kinase

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== Relevance ==
== Relevance ==
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TTBK1 inhibitors are promising candidates for Alzheimer Disease therapy<ref>PMID:37621404</ref>. TTBK1 phosphorylates TDP-43 and thus its inhibitors can be promising therapeutic targets for treatment of ALS<ref>PMID:34978799</ref>.
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TTBK1 inhibitors are promising candidates for Alzheimer Disease therapy<ref>PMID:37621404</ref>. TTBK1 phosphorylates TDP-43 and thus its inhibitors can be promising therapeutic targets for treatment of ALS<ref>PMID:34978799</ref>.
== Structural highlights ==
== Structural highlights ==
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<scene name='10/1042598/Cv/3'>TTBK1 inhibitor interacts with residues which are in the ATP-binding pocket of the protein</scene><ref>PMID:24039150</ref>.
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<scene name='10/1042598/Cv/4'>TTBK1 inhibitor interacts with residues which are in the ATP-binding pocket of the protein</scene><ref>PMID:24039150</ref>.
==Tau-tubulin kinase 3D structures==
==Tau-tubulin kinase 3D structures==

Revision as of 16:22, 14 April 2024

Human tau-tubulin kinase kinase domain complex with inhibitor, glycerol, sulfate and dimethyl sulfoxide (PDB code 4btm)

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Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Alexander Berchansky

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