1nd3

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Revision as of 23:02, 20 November 2007 by OCA (talk | contribs) (New page: left|200px<br /><applet load="1nd3" size="450" color="white" frame="true" align="right" spinBox="true" caption="1nd3, resolution 2.8Å" /> '''The structure of HRV1...)
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File:1nd3.jpg


1nd3, resolution 2.8Å

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The structure of HRV16, when complexed with pleconaril, an antiviral compound

OverviewOverview

Pleconaril is a broad-spectrum antirhinovirus and antienterovirus compound, that binds into a hydrophobic pocket within viral protein 1, stabilizing, the capsid and resulting in the inhibition of cell attachment and RNA, uncoating. When crystals of human rhinovirus 16 (HRV16) and HRV14 are, incubated with pleconaril, drug occupancy in the binding pocket is lower, than when pleconaril is introduced during assembly prior to, crystallization. This effect is far more marked in HRV16 than in HRV14 and, is more marked with pleconaril than with other compounds. These, observations are consistent with virus yield inhibition studies and, radiolabeled drug binding studies showing that the antiviral effect of, pleconaril against HRV16 is greater on the infectivity of progeny virions, than the parent input viruses. These data suggest that drug integration, into the binding pocket during assembly, or at some other late stage in, virus replication, may contribute to the antiviral activity of capsid, binding compounds.

About this StructureAbout this Structure

1ND3 is a Protein complex structure of sequences from Human rhinovirus 2 with ZN and W11 as ligands. Full crystallographic information is available from OCA.

ReferenceReference

Structural and virological studies of the stages of virus replication that are affected by antirhinovirus compounds., Zhang Y, Simpson AA, Ledford RM, Bator CM, Chakravarty S, Skochko GA, Demenczuk TM, Watanyar A, Pevear DC, Rossmann MG, J Virol. 2004 Oct;78(20):11061-9. PMID:15452226

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