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6VZW

TTLL6 bound to the initiation analog

6VZW の概要
エントリーDOI10.2210/pdb6vzw/pdb
分子名称Tubulin polyglutamylase TTLL6, (2~{S})-2-[[[(3~{R})-3-acetamido-4-(ethylamino)-4-oxidanylidene-butyl]-phosphonooxy-phosphoryl]methyl]pentanedioic acid, GLYCEROL, ... (6 entities in total)
機能のキーワードttll6, initiation, glutamylase, phosphinic acid, ligase
由来する生物種Mus musculus (Mouse)
タンパク質・核酸の鎖数4
化学式量合計219079.92
構造登録者
Mahalingan, K.K.,Keenen, E.K.,Strickland, M.,Li, Y.,Liu, Y.,Ball, H.L.,Tanner, T.E.,Tjandra, N.,Roll-Mecak, A. (登録日: 2020-02-28, 公開日: 2020-08-12, 最終更新日: 2023-10-11)
主引用文献Mahalingan, K.K.,Keith Keenan, E.,Strickland, M.,Li, Y.,Liu, Y.,Ball, H.L.,Tanner, M.E.,Tjandra, N.,Roll-Mecak, A.
Structural basis for polyglutamate chain initiation and elongation by TTLL family enzymes.
Nat.Struct.Mol.Biol., 27:802-813, 2020
Cited by
PubMed Abstract: Glutamylation, introduced by tubulin tyrosine ligase-like (TTLL) enzymes, is the most abundant modification of brain tubulin. Essential effector proteins read the tubulin glutamylation pattern, and its misregulation causes neurodegeneration. TTLL glutamylases post-translationally add glutamates to internal glutamates in tubulin carboxy-terminal tails (branch initiation, through an isopeptide bond), and additional glutamates can extend these (elongation). TTLLs are thought to specialize in initiation or elongation, but the mechanistic basis for regioselectivity is unknown. We present cocrystal structures of murine TTLL6 bound to tetrahedral intermediate analogs that delineate key active-site residues that make this enzyme an elongase. We show that TTLL4 is exclusively an initiase and, through combined structural and phylogenetic analyses, engineer TTLL6 into a branch-initiating enzyme. TTLL glycylases add glycines post-translationally to internal glutamates, and we find that the same active-site residues discriminate between initiase and elongase glycylases. These active-site specializations of TTLL glutamylases and glycylases ultimately yield the chemical complexity of cellular microtubules.
PubMed: 32747782
DOI: 10.1038/s41594-020-0462-0
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.5 Å)
構造検証レポート
Validation report summary of 6vzw
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2026-04-22に公開中

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