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6A2M

Crystal structure of wild type Plasmodium falciparum DHFR-TS complexed with BT2, NADPH, and dUMP

6A2M の概要
エントリーDOI10.2210/pdb6a2m/pdb
分子名称Bifunctional dihydrofolate reductase-thymidylate synthase, 5-(4-{3-[(2,4-diamino-6-ethylpyrimidin-5-yl)oxy]propoxy}phenyl)-6-ethylpyrimidine-2,4-diamine, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, ... (6 entities in total)
機能のキーワードrossmann fold, dual-binding inhibitor, oxidoreductase
由来する生物種Plasmodium falciparum (malaria parasite P. falciparum)
タンパク質・核酸の鎖数2
化学式量合計146798.11
構造登録者
Chitnumsub, P.,Jaruwat, A.,Tarnchampoo, B.,Yuthavong, Y. (登録日: 2018-06-12, 公開日: 2019-04-24, 最終更新日: 2023-11-22)
主引用文献Tarnchompoo, B.,Chitnumsub, P.,Jaruwat, A.,Shaw, P.J.,Vanichtanankul, J.,Poen, S.,Rattanajak, R.,Wongsombat, C.,Tonsomboon, A.,Decharuangsilp, S.,Anukunwithaya, T.,Arwon, U.,Kamchonwongpaisan, S.,Yuthavong, Y.
Hybrid Inhibitors of Malarial Dihydrofolate Reductase with Dual Binding Modes That Can Forestall Resistance.
ACS Med Chem Lett, 9:1235-1240, 2018
Cited by
PubMed: 30613332
DOI: 10.1021/acsmedchemlett.8b00389
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.2 Å)
構造検証レポート
Validation report summary of 6a2m
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2024-04-17に公開中

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