1V49
Solution structure of microtubule-associated protein light chain-3
1V49 の概要
エントリーDOI | 10.2210/pdb1v49/pdb |
NMR情報 | BMRB: 5958 |
分子名称 | Microtubule-associated proteins 1A/1B light chain 3B (1 entity in total) |
機能のキーワード | ubiquitin fold, structural protein |
由来する生物種 | Homo sapiens (human) |
細胞内の位置 | Cytoplasm, cytoskeleton: Q9GZQ8 |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 14150.28 |
構造登録者 | Kouno, T.,Mizuguchi, M.,Tanida, I.,Ueno, T.,Kominami, E.,Kawano, K. (登録日: 2003-11-11, 公開日: 2004-12-28, 最終更新日: 2023-12-27) |
主引用文献 | Kouno, T.,Mizuguchi, M.,Tanida, I.,Ueno, T.,Kanematsu, T.,Mori, Y.,Shinoda, H.,Hirata, M.,Kominami, E.,Kawano, K. Solution structure of microtubule-associated protein light chain 3 and identification of its functional subdomains. J.Biol.Chem., 280:24610-24617, 2005 Cited by PubMed Abstract: Microtubule-associated protein (MAP) light chain 3 (LC3) is a human homologue of yeast Apg8/Aut7/Cvt5 (Atg8), which is essential for autophagy. MAP-LC3 is cleaved by a cysteine protease to produce LC3-I, which is located in cytosolic fraction. LC3-I, in turn, is converted to LC3-II through the actions of E1- and E2-like enzymes. LC3-II is covalently attached to phosphatidylethanolamine on its C terminus, and it binds tightly to autophagosome membranes. We determined the solution structure of LC3-I and found that it is divided into N- and C-terminal subdomains. Additional analysis using a photochemically induced dynamic nuclear polarization technique also showed that the N-terminal subdomain of LC3-I makes contact with the surface of the C-terminal subdomain and that LC3-I adopts a single compact conformation in solution. Moreover, the addition of dodecylphosphocholine into the LC3-I solution induced chemical shift perturbations primarily in the C-terminal subdomain, which implies that the two subdomains have different sensitivities to dodecylphosphocholine micelles. On the other hand, deletion of the N-terminal subdomain abolished binding of tubulin and microtubules. Thus, we showed that two subdomains of the LC3-I structure have distinct functions, suggesting that MAP-LC3 can act as an adaptor protein between microtubules and autophagosomes. PubMed: 15857831DOI: 10.1074/jbc.M413565200 主引用文献が同じPDBエントリー |
実験手法 | SOLUTION NMR |
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