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Structural and functional analyses of a conserved hydrophobic pocket of flavivirus methyltransferase.

ABSTRACT: The flavivirus methyltransferase (MTase) sequentially methylates the N7 and 2'-O positions of the viral RNA cap (GpppA-RNA ? m(7)GpppA-RNA ? m(7)GpppAm-RNA), using S-adenosyl-l-methionine (AdoMet) as a methyl donor. We report here that sinefungin (SIN), an AdoMet analog, inhibits several flaviviruses through suppression of viral MTase. The crystal structure of West Nile virus MTase in complex with SIN inhibitor at 2.0-Å resolution revealed a flavivirus-conserved hydrophobic pocket located next to the AdoMet-binding site. The pocket is functionally critical in the viral replication and cap methylations. In addition, the N7 methylation efficiency was found to correlate with the viral replication ability. Thus, SIN analogs with modifications that interact with the hydrophobic pocket are potential specific inhibitors of flavivirus MTase.

SUBMITTER: Dong H

PROVIDER: S-EPMC2952261 | biostudies-literature | 2010 Oct

REPOSITORIES: biostudies-literature

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Structural and functional analyses of a conserved hydrophobic pocket of flavivirus methyltransferase.

Dong Hongping H Liu Lihui L Zou Gang G Zhao Yiwei Y Li Zhong Z Lim Siew Pheng SP Shi Pei-Yong PY Li Hongmin H

The Journal of biological chemistry 20100804 42

The flavivirus methyltransferase (MTase) sequentially methylates the N7 and 2'-O positions of the viral RNA cap (GpppA-RNA → m(7)GpppA-RNA → m(7)GpppAm-RNA), using S-adenosyl-l-methionine (AdoMet) as a methyl donor. We report here that sinefungin (SIN), an AdoMet analog, inhibits several flaviviruses through suppression of viral MTase. The crystal structure of West Nile virus MTase in complex with SIN inhibitor at 2.0-Å resolution revealed a flavivirus-conserved hydrophobic pocket located next t ...[more]

PMID: 20685660

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