6CDJ

HIV-1 wild type protease with GRL-03314A, 6-5-5-ring fused umbrella-like tetrahydropyranofuran as the P2-ligand, a cyclopropylaminobenzothiazole as the P2'-ligand and 3,5-difluorophenylmethyl as the P1-ligand

6CDJ の概要

• エントリーDOI: 10.2210/pdb6cdj/pdb
• 関連するPDBエントリー: 2IEN 6BZ2
• 分子名称: Protease, (2aS,4R,4aS,7aS,7bS)-octahydro-2H-1,7-dioxacyclopenta[cd]inden-4-yl [(2S,3R)-4-[{[2-(cyclopropylamino)-1,3-benzothiazol-6-yl]sulfonyl}(2-methylpropyl)amino]-1-(3,5-difluorophenyl)-3-hydroxybutan-2-yl]carbamate, SODIUM ION, ... (7 entities in total)
• 機能のキーワード: aspartic acid protease, hiv-1 protease inhibitor of grl-03314a, umb-thf, antiviral, multidrug-resistant, synthesis, backbone binding, hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
• 由来する生物種: Human immunodeficiency virus 1
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 22541.73

構造登録者

Wang, Y.-F.,Agniswamy, J.,Weber, I.T. (登録日: 2018-02-08, 公開日: 2018-05-30, 最終更新日: 2023-10-04)

• 主引用文献: Ghosh, A.K.,R Nyalapatla, P.,Kovela, S.,Rao, K.V.,Brindisi, M.,Osswald, H.L.,Amano, M.,Aoki, M.,Agniswamy, J.,Wang, Y.F.,Weber, I.T.,Mitsuya, H.; Design and Synthesis of Highly Potent HIV-1 Protease Inhibitors Containing Tricyclic Fused Ring Systems as Novel P2 Ligands: Structure-Activity Studies, Biological and X-ray Structural Analysis.; J. Med. Chem., 61:4561-4577, 2018; PubMed: 29763303; DOI: 10.1021/acs.jmedchem.8b00298

実験手法

X-RAY DIFFRACTION (1.13 Å)