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4M8Y

GS-8374, a Novel Phosphonate-Containing Inhibitor of HIV-1 Protease, Effectively Inhibits HIV PR Mutants with Amino Acid Insertions

4M8Y の概要
エントリーDOI10.2210/pdb4m8y/pdb
関連するPDBエントリー2RKF 2RKG 4M8X
分子名称Protease, DIETHYL ({4-[(2S,3R)-2-({[(3R,3AS,6AR)-HEXAHYDROFURO[2,3-B]FURAN-3-YLOXY]CARBONYL}AMINO)-3-HYDROXY-4-{ISOBUTYL[(4-METHOXYPHENYL)SULFONYL]AMINO}BUTYL]PHENOXY}METHYL)PHOSPHONATE (3 entities in total)
機能のキーワードhiv-1 protease, aspartic protease, amino acid insertion, 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23283.12
構造登録者
Grantz saskova, K.,Brynda, J.,Rezacova, P.,Kozisek, M.,Konvalinka, J. (登録日: 2013-08-14, 公開日: 2014-05-07, 最終更新日: 2023-09-20)
主引用文献Grantz Saskova, K.,Kozisek, M.,Stray, K.,de Jong, D.,Rezaova, P.,Brynda, J.,van Maarseveen, N.M.,Nijhuis, M.,Cihlar, T.,Konvalinka, J.
GS-8374, a prototype phosphonate-containing inhibitor of HIV-1 protease, effectively inhibits protease mutants with amino acid insertions.
J.Virol., 88:3586-3590, 2014
Cited by
PubMed Abstract: Insertions in the protease (PR) region of human immunodeficiency virus (HIV) represent an interesting mechanism of antiviral resistance against HIV PR inhibitors (PIs). Here, we demonstrate the improved ability of a phosphonate-containing experimental HIV PI, GS-8374, relative to that of other PIs, to effectively inhibit patient-derived recombinant HIV strains bearing PR insertions and numerous other mutations. We correlate enzyme inhibition with the catalytic activities of corresponding recombinant PRs in vitro and provide a biochemical and structural analysis of the PR-inhibitor complex.
PubMed: 24371077
DOI: 10.1128/JVI.02688-13
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.22 Å)
構造検証レポート
Validation report summary of 4m8y
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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