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3WCD

The complex structure of HsSQS wtih ligand, WC-9

3WCD の概要
エントリーDOI10.2210/pdb3wcd/pdb
関連するPDBエントリー3WC9 3WCA 3WCB 3WCC 3WCE 3WCF 3WCG 3WCH 3WCI 3WCJ 3WCL 3WCM
分子名称Squalene synthase, 2-(4-phenoxyphenoxy)ethyl thiocyanate (3 entities in total)
機能のキーワードisoprenoids, drug discovery, transferase, wc-9
由来する生物種Homo sapiens (human)
細胞内の位置Endoplasmic reticulum membrane; Multi-pass membrane protein: P37268
タンパク質・核酸の鎖数6
化学式量合計248819.26
構造登録者
Shang, N.,Li, Q.,Ko, T.P.,Chan, H.C.,Huang, C.H.,Ren, F.,Zheng, Y.,Zhu, Z.,Chen, C.C.,Guo, R.T. (登録日: 2013-05-27, 公開日: 2014-06-18, 最終更新日: 2023-11-08)
主引用文献Shang, N.,Li, Q.,Ko, T.P.,Chan, H.C.,Li, J.,Zheng, Y.,Huang, C.H.,Ren, F.,Chen, C.C.,Zhu, Z.,Galizzi, M.,Li, Z.H.,Rodrigues-Poveda, C.A.,Gonzalez-Pacanowska, D.,Veiga-Santos, P.,de Carvalho, T.M.,de Souza, W.,Urbina, J.A.,Wang, A.H.,Docampo, R.,Li, K.,Liu, Y.L.,Oldfield, E.,Guo, R.T.
Squalene synthase as a target for Chagas disease therapeutics.
Plos Pathog., 10:e1004114-e1004114, 2014
Cited by
PubMed Abstract: Trypanosomatid parasites are the causative agents of many neglected tropical diseases and there is currently considerable interest in targeting endogenous sterol biosynthesis in these organisms as a route to the development of novel anti-infective drugs. Here, we report the first x-ray crystallographic structures of the enzyme squalene synthase (SQS) from a trypanosomatid parasite, Trypanosoma cruzi, the causative agent of Chagas disease. We obtained five structures of T. cruzi SQS and eight structures of human SQS with four classes of inhibitors: the substrate-analog S-thiolo-farnesyl diphosphate, the quinuclidines E5700 and ER119884, several lipophilic bisphosphonates, and the thiocyanate WC-9, with the structures of the two very potent quinuclidines suggesting strategies for selective inhibitor development. We also show that the lipophilic bisphosphonates have low nM activity against T. cruzi and inhibit endogenous sterol biosynthesis and that E5700 acts synergistically with the azole drug, posaconazole. The determination of the structures of trypanosomatid and human SQS enzymes with a diverse set of inhibitors active in cells provides insights into SQS inhibition, of interest in the context of the development of drugs against Chagas disease.
PubMed: 24789335
DOI: 10.1371/journal.ppat.1004114
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.75 Å)
構造検証レポート
Validation report summary of 3wcd
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2024-10-30に公開中

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