3AEA

Crystal structure of porcine heart mitochondrial complex II bound with N-(3-Dimethylaminomethyl-phenyl)-2-trifluoromethyl-benzamide

3AEA の概要

• エントリーDOI: 10.2210/pdb3aea/pdb
• 関連するPDBエントリー: 3ABV 3AE1 3AE2 3AE3 3AE4 3AE5 3AE6 3AE7 3AE8 3AE9 3AEB 3AEC 3AED 3AEE 3AEF 3AEG
• 分子名称: Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial, PROTOPORPHYRIN IX CONTAINING FE, N-{3-[(dimethylamino)methyl]phenyl}-2-(trifluoromethyl)benzamide, ... (12 entities in total)
• 機能のキーワード: respiratory complex ii, inhibitors, electron transport, iron, iron-sulfur, metal-binding, mitochondrion, mitochondrion inner membrane, oxidoreductase, transit peptide, transport, tricarboxylic acid cycle, heme, transmembrane, fad-binding protein, oxidoreductase-oxidoreductase inhibitor complex, oxidoreductase/oxidoreductase inhibitor
• 由来する生物種: Sus scrofa (Pig); 詳細
• 細胞内の位置: Mitochondrion inner membrane ; Peripheral membrane protein ; Matrix side : Q0QF01 Q007T0; Mitochondrion inner membrane ; Multi-pass membrane protein : D0VWV4 A5GZW8
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 126677.82

構造登録者

Harada, S.,Sasaki, T.,Shindo, M.,Kido, Y.,Inaoka, D.K.,Omori, J.,Osanai, A.,Sakamoto, K.,Mao, J.,Matsuoka, S.,Inoue, M.,Honma, T.,Tanaka, A.,Kita, K. (登録日: 2010-02-04, 公開日: 2011-02-09, 最終更新日: 2024-10-16)

主引用文献

Inaoka, D.K.,Shiba, T.,Sato, D.,Balogun, E.O.,Sasaki, T.,Nagahama, M.,Oda, M.,Matsuoka, S.,Ohmori, J.,Honma, T.,Inoue, M.,Kita, K.,Harada, S.
Structural Insights into the Molecular Design of Flutolanil Derivatives Targeted for Fumarate Respiration of Parasite Mitochondria
Int J Mol Sci, 16:15287-15308, 2015

PubMed Abstract: Recent studies on the respiratory chain of Ascaris suum showed that the mitochondrial NADH-fumarate reductase system composed of complex I, rhodoquinone and complex II plays an important role in the anaerobic energy metabolism of adult A. suum. The system is the major pathway of energy metabolism for adaptation to a hypoxic environment not only in parasitic organisms, but also in some types of human cancer cells. Thus, enzymes of the pathway are potential targets for chemotherapy. We found that flutolanil is an excellent inhibitor for A. suum complex II (IC50 = 0.058 μM) but less effectively inhibits homologous porcine complex II (IC50 = 45.9 μM). In order to account for the specificity of flutolanil to A. suum complex II from the standpoint of structural biology, we determined the crystal structures of A. suum and porcine complex IIs binding flutolanil and its derivative compounds. The structures clearly demonstrated key interactions responsible for its high specificity to A. suum complex II and enabled us to find analogue compounds, which surpass flutolanil in both potency and specificity to A. suum complex II. Structures of complex IIs binding these compounds will be helpful to accelerate structure-based drug design targeted for complex IIs.

PubMed: 26198225
DOI: 10.3390/ijms160715287

実験手法

X-RAY DIFFRACTION (3.39 Å)