Histone methyltransferase: Difference between revisions

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== Relevance ==
== Relevance ==
Inhibitors of the histone-lysine N-methyltransferase SMYD2 which represses the tumor-suppressing activities of p53 are studied as cancer therapy drug<ref>PMID:21782458</ref>.s.
Inhibitors of the histone-lysine N-methyltransferase SMYD2 which represses the tumor-suppressing activities of p53 are studied as cancer therapy drugs<ref>PMID:21782458</ref>.


== Disease ==
== Disease ==
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*Histone-lysine N-methyltransferase binary complexes
*Histone-lysine N-methyltransferase binary complexes


**[[2kkf]] – hKHMT Hrx CxxC domain +_DNA – NMR<br />
**[[2kkf]] – hKHMT Hrx CxxC domain + DNA – NMR<br />
**[[4nw3]] – hKHMT Mll CxxC domain + DNA <br />
**[[4nw3]] – hKHMT Mll CxxC domain + DNA <br />
**[[4pzi]] – hKHMT CxxC domain + DNA <br />
**[[4pzi]] – hKHMT CxxC domain + DNA <br />
**[[3q0b]], [[3q0c]], [[3q0d]], [[3q0f]] – hKHMT SRA domain +_DNA <br />
**[[3q0b]], [[3q0c]], [[3q0d]], [[3q0f]] – hKHMT SRA domain + DNA <br />
**[[3qow]] – hKHMT + SAM <br />
**[[3qow]] – hKHMT + SAM <br />
**[[4fmu]] – hKHMT SETD2 + inhibitor <br />
**[[4fmu]] – hKHMT SETD2 + inhibitor <br />

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

Michal Harel, Alexander Berchansky, Joel L. Sussman