Abstract

S-1153 (AG1549) is perhaps the most promising non-nucleoside 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.

Highlights

  • 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

  • Given the substantial data base of structures of RT/nucleoside inhibitors of reverse transcriptase (NNRTIs) complexes, we are in a position to dissect out structural features responsible for the resilience of S-1153 to drug resistance mutations within RT

  • The most remarkable feature of the interaction of S-1153 with HIV RT is the network of three hydrogen-bonding interactions with the main chain, two of which are direct to the protein, whereas one is mediated by a water molecule

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Summary

Introduction

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. 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. More recently structural studies have revealed some common factors that contribute to the second generation properties of UC-781 [21]. Such factors include a combination of a nonaromatic moiety of optimal size that contacts the aromatic residues Tyr-181, Tyr188, and Trp-229 at the top of the NNRTI pocket. High level resistance to S-1153 requires at least two mutations

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