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7OWN

HsNMT1 in complex with both MyrCoA and peptide AKSFSKPR

7OWN の概要
エントリーDOI10.2210/pdb7own/pdb
分子名称Glycylpeptide N-tetradecanoyltransferase 1, ALA-LYS-SER-PHE-SER-LYS-PRO-ARG, GLYCEROL, ... (5 entities in total)
機能のキーワードe-myristoylation, nmt, myristoyltransferase type1, acyltransferase, gnat, gcn5-related n-acetyltransferases, transferase
由来する生物種Homo sapiens (Human)
詳細
タンパク質・核酸の鎖数3
化学式量合計96178.07
構造登録者
Dian, C.,Giglione, C.,Meinnel, T. (登録日: 2021-06-18, 公開日: 2022-12-21, 最終更新日: 2024-01-31)
主引用文献Riviere, F.,Dian, C.,Dutheil, R.F.,Monassa, P.,Giglione, C.,Meinnel, T.
Structural and Large-scale Analysis Unveil the Intertwined Paths Promoting NMT-catalyzed Lysine and Glycine Myristoylation.
J.Mol.Biol., 434:167843-167843, 2022
Cited by
PubMed Abstract: N-myristoyltransferases (NMTs) catalyze protein myristoylation, a lipid modification crucial for cell survival and a range of pathophysiological processes. Originally thought to modify only N-terminal glycine α-amino groups (G-myristoylation), NMTs were recently shown to also modify lysine ε-amino groups (K-myristoylation). However, the clues ruling NMT-dependent K-myristoylation and the full range of targets are currently unknown. Here we combine mass spectrometry, kinetic studies, in silico analysis, and crystallography to identify the specific features driving each modification. We show that direct interactions between the substrate's reactive amino group and the NMT catalytic base promote K-myristoylation but with poor efficiency compared to G-myristoylation, which instead uses a water-mediated interaction. We provide evidence of depletion of proteins with NMT-dependent K-myristoylation motifs in humans, suggesting evolutionary pressure to prevent this modification in favor of G-myristoylation. In turn, we reveal that K-myristoylation may only result from post-translational events. Our studies finally unravel the respective paths towards K-myristoylation or G-myristoylation, which rely on a very subtle tradeoff embracing the chemical landscape around the reactive group.
PubMed: 36181773
DOI: 10.1016/j.jmb.2022.167843
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.1 Å)
構造検証レポート
Validation report summary of 7own
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-11-06に公開中

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