Binding of the second generation non-nucleoside inhibitor S-1153 to HIV-1 reverse transcriptase involves extensive main chain hydrogen bonding

被引:130
作者
Ren, JS
Nichols, C
Bird, LE
Fujiwara, T
Sugimoto, H
Stuart, DI
Stammers, DK
机构
[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Struct Biol Div, Oxford OX3 7BN, England
[2] Shionogi & Co Ltd, Discovery Res Labs, Fukushima Ku, Osaka 5530002, Japan
[3] Oxford Ctr Mol Sci, Oxford OX1 3QY, England
关键词
D O I
10.1074/jbc.275.19.14316
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
S-1153 (AG1549) is perhaps the most promising nonnucleoside inhibitor of HIV-1 reverse transcriptase currently under development as a potential anti-AIDS drug, because it has a favorable profile of resilience to many drug resistance mutations. We have determined the crystal structure of S-1153 in a complex with HIV-1 reverse transcriptase, The complex possesses some novel features, including an extensive network of hydrogen bonds involving the main chain of residues 101, 103, and 236 of the p66 reverse transcriptase subunit, Such interactions are unlikely to be disrupted by side chain mutations. The reverse transcriptase/S-1153 complex suggests different ways in which resilience to mutations in the non-nucleoside inhibitors of reverse transcriptase binding site can be achieved.
引用
收藏
页码:14316 / 14320
页数:5
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