8TZ8
Cryo-EM structure of bovine concentrative nucleoside transporter 3 in complex with Molnupiravir, condition 1, INT1-INT1-INT3 conformation
8TZ8 の概要
エントリーDOI | 10.2210/pdb8tz8/pdb |
EMDBエントリー | 41737 |
分子名称 | Sodium/nucleoside cotransporter, N-hydroxy-5'-O-(2-methylpropanoyl)cytidine, 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (3 entities in total) |
機能のキーワード | membrane protein, transporter, nucleoside, transport protein |
由来する生物種 | Bos taurus (cattle) |
タンパク質・核酸の鎖数 | 3 |
化学式量合計 | 240638.39 |
構造登録者 | |
主引用文献 | Wright, N.J.,Zhang, F.,Suo, Y.,Kong, L.,Yin, Y.,Fedor, J.G.,Sharma, K.,Borgnia, M.J.,Im, W.,Lee, S.Y. Antiviral drug recognition and elevator-type transport motions of CNT3. Nat.Chem.Biol., 20:1144-1153, 2024 Cited by PubMed Abstract: Nucleoside analogs have broad clinical utility as antiviral drugs. Key to their systemic distribution and cellular entry are human nucleoside transporters. Here, we establish that the human concentrative nucleoside transporter 3 (CNT3) interacts with antiviral drugs used in the treatment of coronavirus infections. We report high-resolution single-particle cryo-electron microscopy structures of bovine CNT3 complexed with antiviral nucleosides N-hydroxycytidine, PSI-6206, GS-441524 and ribavirin, all in inward-facing states. Notably, we found that the orally bioavailable antiviral molnupiravir arrests CNT3 in four distinct conformations, allowing us to capture cryo-electron microscopy structures of drug-loaded outward-facing and drug-loaded intermediate states. Our studies uncover the conformational trajectory of CNT3 during membrane transport of a nucleoside analog antiviral drug, yield new insights into the role of interactions between the transport and the scaffold domains in elevator-like domain movements during drug translocation, and provide insights into the design of nucleoside analog antiviral prodrugs with improved oral bioavailability. PubMed: 38418906DOI: 10.1038/s41589-024-01559-8 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (3.19 Å) |
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