4B2D
human PKM2 with L-serine and FBP bound.
4B2D の概要
エントリーDOI | 10.2210/pdb4b2d/pdb |
関連するPDBエントリー | 1T5A |
分子名称 | PYRUVATE KINASE ISOZYMES M1/M2, SERINE, 1,6-di-O-phosphono-beta-D-fructofuranose, ... (6 entities in total) |
機能のキーワード | transferase, tumour, pkm2, glycolysis |
由来する生物種 | HOMO SAPIENS (HUMAN) 詳細 |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 241156.73 |
構造登録者 | Chaneton, B.,Hillmann, P.,Zheng, L.,Martin, A.C.L.,Maddocks, O.D.K.,Chokkathukalam, A.,Coyle, J.E.,Jankevics, A.,Holding, F.P.,Vousden, K.H.,Frezza, C.,O'Reilly, M.,Gottlieb, E. (登録日: 2012-07-13, 公開日: 2012-10-10, 最終更新日: 2023-12-20) |
主引用文献 | Chaneton, B.,Hillmann, P.,Zheng, L.,Martin, A.C.L.,Maddocks, O.D.K.,Chokkathukalam, A.,Coyle, J.E.,Jankevics, A.,Holding, F.P.,Vousden, K.H.,Frezza, C.,O'Reilly, M.,Gottlieb, E. Serine is a natural ligand and allosteric activator of pyruvate kinase M2. Nature, 491:458-462, 2012 Cited by PubMed Abstract: Cancer cells exhibit several unique metabolic phenotypes that are critical for cell growth and proliferation. Specifically, they overexpress the M2 isoform of the tightly regulated enzyme pyruvate kinase (PKM2), which controls glycolytic flux, and are highly dependent on de novo biosynthesis of serine and glycine. Here we describe a new rheostat-like mechanistic relationship between PKM2 activity and serine biosynthesis. We show that serine can bind to and activate human PKM2, and that PKM2 activity in cells is reduced in response to serine deprivation. This reduction in PKM2 activity shifts cells to a fuel-efficient mode in which more pyruvate is diverted to the mitochondria and more glucose-derived carbon is channelled into serine biosynthesis to support cell proliferation. PubMed: 23064226DOI: 10.1038/nature11540 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.3 Å) |
構造検証レポート
検証レポート(詳細版)をダウンロード