2h2j: Difference between revisions
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{{STRUCTURE_2h2j| PDB=2h2j | SCENE= }} | |||
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'''Structure of Rubisco LSMT bound to Sinefungin and Monomethyllysine''' | '''Structure of Rubisco LSMT bound to Sinefungin and Monomethyllysine''' | ||
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[[Category: Pisum sativum]] | [[Category: Pisum sativum]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Couture, J F.]] | [[Category: Couture, J F.]] | ||
[[Category: Hauk, G.]] | [[Category: Hauk, G.]] | ||
[[Category: Trievel, R C.]] | [[Category: Trievel, R C.]] | ||
[[Category: | [[Category: Protein lysine methyltransferase]] | ||
[[Category: | [[Category: Set domain]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 05:47:49 2008'' | |||
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Revision as of 05:47, 4 May 2008
Structure of Rubisco LSMT bound to Sinefungin and Monomethyllysine
OverviewOverview
SET domain enzymes represent a distinct family of protein lysine methyltransferases in eukaryotes. Recent studies have yielded significant insights into the structural basis of substrate recognition and the product specificities of these enzymes. However, the mechanism by which SET domain methyltransferases catalyze the transfer of the methyl group from S-adenosyl-L-methionine to the lysine epsilon-amine has remained unresolved. To elucidate this mechanism, we have determined the structures of the plant SET domain enzyme, pea ribulose-1,5 bisphosphate carboxylase/oxygenase large subunit methyltransferase, bound to S-adenosyl-L-methionine, and its non-reactive analogs Aza-adenosyl-L-methionine and Sinefungin, and characterized the binding of these ligands to a homolog of the enzyme. The structural and biochemical data collectively reveal that S-adenosyl-L-methionine is selectively recognized through carbon-oxygen hydrogen bonds between the cofactor's methyl group and an array of structurally conserved oxygens that comprise the methyl transfer pore in the active site. Furthermore, the structure of the enzyme co-crystallized with the product epsilon-N-trimethyllysine reveals a trigonal array of carbon-oxygen interactions between the epsilon-ammonium methyl groups and the oxygens in the pore. Taken together, these results establish a central role for carbon-oxygen hydrogen bonding in aligning the cofactor's methyl group for transfer to the lysine epsilon-amine and in coordinating the methyl groups after transfer to facilitate multiple rounds of lysine methylation.
About this StructureAbout this Structure
2H2J is a Single protein structure of sequence from Pisum sativum. Full crystallographic information is available from OCA.
ReferenceReference
Catalytic roles for carbon-oxygen hydrogen bonding in SET domain lysine methyltransferases., Couture JF, Hauk G, Thompson MJ, Blackburn GM, Trievel RC, J Biol Chem. 2006 Jul 14;281(28):19280-7. Epub 2006 May 8. PMID:16682405 Page seeded by OCA on Sun May 4 05:47:49 2008