8BVI

Crystal structure of the METTL9-like histidine methyltransferase from Ostreococcus tauri

8BVI の概要

• エントリーDOI: 10.2210/pdb8bvi/pdb
• 分子名称: DREV methyltransferase (2 entities in total)
• 機能のキーワード: methyltransferase, histidine methyltransferase, rossmann fold, transferase
• 由来する生物種: Ostreococcus tauri
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 33902.30

構造登録者

Hammerstad, M.,Schroer, L.,Hersleth, H.-P. (登録日: 2022-12-04, 公開日: 2023-12-13, 最終更新日: 2025-07-09)

主引用文献

Schroer, L.,Weirich, S.,Hammerstad, M.,Hersleth, H.P.,Gronsberg, I.A.,Hagen, L.,Slupphaug, G.,Malecki, J.M.,Jeltsch, A.,Falnes, P.O.,Davydova, E.
Orthologues of the human protein histidine methyltransferase METTL9 display distinct substrate specificities.
J.Biol.Chem., :110318-110318, 2025

PubMed Abstract: The human (Homo sapiens; Hs) methyltransferase (MTase) METTL9 is the first enzyme shown to generate 1-methylhistidine (π-methylhistidine) in proteins. METTL9 preferentially methylates an alternating histidine (HxH) motif, where "x" is a small, uncharged amino acid, and multiple substrates have been identified. Putative METTL9 orthologues are found in most eukaryotes, and we have here investigated the activity of such enzymes from several species, representing all five eukaryotic supergroups. The majority of the tested enzymes demonstrated in vitro MTase activity on the prototype HsMETTL9 substrates ARMC6 and DNAJB12. We also detected protein methylation activity of the Caenorhabditis elegans METTL9 which had previously been suggested to be a DNA MTase. However, METTL9 from the fruit fly (Drosophila melanogaster; Dm) and the picoplankton Ostreococcus tauri (Ot) displayed distinct substrate specificities, differing from each other and from that of HsMETTL9. These differences were observed when recombinant proteins and short peptides were used as METTL9 substrates. To further analyze substrate specificity, we used peptide arrays to systematically replace the "x" residue and the residues flanking the HxH motif in a substrate peptide. This revealed varying degrees of tolerance among the METTL9 orthologues (Hs > Dm > Ot) for substitutions at these positions. Our results show that the METTL9 orthologues, although requiring an HxH target site, have evolved different substrate specificities, likely due to differing biologically relevant substrates in the respective organisms. Furthermore, we solved the X-ray structure of OtMETTL9, revealing several differences from the previously published HsMETTL9 structures that may explain its distinct substrate specificity.

PubMed: 40451431
DOI: 10.1016/j.jbc.2025.110318

実験手法

X-RAY DIFFRACTION (3.1 Å)