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4MUB

Schistosoma mansoni (Blood Fluke) Sulfotransferase/Oxamniquine Complex

4MUB の概要
エントリーDOI10.2210/pdb4mub/pdb
分子名称Sulfotransferase, ADENOSINE-3'-5'-DIPHOSPHATE, {(2S)-7-nitro-2-[(propan-2-ylamino)methyl]-1,2,3,4-tetrahydroquinolin-6-yl}methanol, ... (4 entities in total)
機能のキーワードpap, oxamniquine, parasite, helminth, drug resistance, transferase
由来する生物種Schistosoma mansoni (Blood fluke)
タンパク質・核酸の鎖数1
化学式量合計30683.10
構造登録者
主引用文献Valentim, C.L.,Cioli, D.,Chevalier, F.D.,Cao, X.,Taylor, A.B.,Holloway, S.P.,Pica-Mattoccia, L.,Guidi, A.,Basso, A.,Tsai, I.J.,Berriman, M.,Carvalho-Queiroz, C.,Almeida, M.,Aguilar, H.,Frantz, D.E.,Hart, P.J.,LoVerde, P.T.,Anderson, T.J.
Genetic and molecular basis of drug resistance and species-specific drug action in schistosome parasites.
Science, 342:1385-1389, 2013
Cited by
PubMed Abstract: Oxamniquine resistance evolved in the human blood fluke (Schistosoma mansoni) in Brazil in the 1970s. We crossed parental parasites differing ~500-fold in drug response, determined drug sensitivity and marker segregation in clonally derived second-generation progeny, and identified a single quantitative trait locus (logarithm of odds = 31) on chromosome 6. A sulfotransferase was identified as the causative gene by using RNA interference knockdown and biochemical complementation assays, and we subsequently demonstrated independent origins of loss-of-function mutations in field-derived and laboratory-selected resistant parasites. These results demonstrate the utility of linkage mapping in a human helminth parasite, while crystallographic analyses of protein-drug interactions illuminate the mode of drug action and provide a framework for rational design of oxamniquine derivatives that kill both S. mansoni and S. haematobium, the two species responsible for >99% of schistosomiasis cases worldwide.
PubMed: 24263136
DOI: 10.1126/science.1243106
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.75 Å)
構造検証レポート
Validation report summary of 4mub
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2026-04-15に公開中

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