4B0C
Crystal Structure of 3-hydroxydecanoyl-Acyl Carrier Protein Dehydratase (FabA) from Pseudomonas aeruginosa in complex with 3-(pentylthio)-4H-1,2,4-triazole
4B0C の概要
エントリーDOI | 10.2210/pdb4b0c/pdb |
関連するPDBエントリー | 4B0B 4B0I 4B8U 4FQ9 |
分子名称 | 3-HYDROXYDECANOYL-[ACYL-CARRIER-PROTEIN] DEHYDRATASE, 5-(pentylsulfanyl)-1H-1,2,4-triazole (3 entities in total) |
機能のキーワード | lyase, fatty acid biosynthesis, bacterial virulence, drug discovery |
由来する生物種 | PSEUDOMONAS AERUGINOSA |
細胞内の位置 | Cytoplasm (By similarity): O33877 |
タンパク質・核酸の鎖数 | 5 |
化学式量合計 | 94698.98 |
構造登録者 | Moynie, L.,McMahon, S.A.,Duthie, F.G.,Naismith, J.H. (登録日: 2012-07-01, 公開日: 2012-11-28, 最終更新日: 2023-12-20) |
主引用文献 | Moynie, L.,Leckie, S.M.,Mcmahon, S.A.,Duthie, F.G.,Koehnke, A.,Taylor, J.W.,Alphey, M.S.,Brenk, R.,Smith, A.D.,Naismith, J.H. Structural Insights Into the Mechanism and Inhibition of the Beta-Hydroxydecanoyl-Acyl Carrier Protein Dehydratase from Pseudomonasaeruginosa. J.Mol.Biol., 425:365-, 2013 Cited by PubMed Abstract: Fatty acid biosynthesis is an essential component of metabolism in both eukaryotes and prokaryotes. The fatty acid biosynthetic pathway of Gram-negative bacteria is an established therapeutic target. Two homologous enzymes FabA and FabZ catalyze a key step in fatty acid biosynthesis; both dehydrate hydroxyacyl fatty acids that are coupled via a phosphopantetheine to an acyl carrier protein (ACP). The resulting trans-2-enoyl-ACP is further polymerized in a processive manner. FabA, however, carries out a second reaction involving isomerization of trans-2-enoyl fatty acid to cis-3-enoyl fatty acid. We have solved the structure of Pseudomonas aeruginosa FabA with a substrate allowing detailed molecular insight into the interactions of the active site. This has allowed a detailed examination of the factors governing the second catalytic step. We have also determined the structure of FabA in complex with small molecules (so-called fragments). These small molecules occupy distinct regions of the active site and form the basis for a rational inhibitor design program. PubMed: 23174186DOI: 10.1016/J.JMB.2012.11.017 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.7 Å) |
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