1nd2

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(New page: 200px<br /><applet load="1nd2" size="450" color="white" frame="true" align="right" spinBox="true" caption="1nd2, resolution 2.5&Aring;" /> '''The structure of Rhin...)
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[[Image:1nd2.jpg|left|200px]]<br /><applet load="1nd2" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1nd2, resolution 2.5&Aring;" />
caption="1nd2, resolution 2.5&Aring;" />
'''The structure of Rhinovirus 16'''<br />
'''The structure of Rhinovirus 16'''<br />
==Overview==
==Overview==
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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.
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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 Structure==
==About this Structure==
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1ND2 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Human_rhinovirus_2 Human rhinovirus 2] with ZN and MYR as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1ND2 OCA].
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1ND2 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Human_rhinovirus_2 Human rhinovirus 2] with <scene name='pdbligand=ZN:'>ZN</scene> and <scene name='pdbligand=MYR:'>MYR</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1ND2 OCA].
==Reference==
==Reference==
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[[Category: Human rhinovirus 2]]
[[Category: Human rhinovirus 2]]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Bator, C.M.]]
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[[Category: Bator, C M.]]
[[Category: Chakravarty, S.]]
[[Category: Chakravarty, S.]]
[[Category: Diana, G.]]
[[Category: Diana, G.]]
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[[Category: Pevear, D.C.]]
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[[Category: Pevear, D C.]]
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[[Category: Rossmann, M.G.]]
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[[Category: Rossmann, M G.]]
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[[Category: Simpson, A.A.]]
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[[Category: Simpson, A A.]]
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[[Category: Skochko, G.A.]]
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[[Category: Skochko, G A.]]
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[[Category: Tull, T.M.]]
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[[Category: Tull, T M.]]
[[Category: Zhang, Y.]]
[[Category: Zhang, Y.]]
[[Category: MYR]]
[[Category: MYR]]
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[[Category: rhinovirus]]
[[Category: rhinovirus]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 22:09:08 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:04:47 2008''

Revision as of 12:04, 21 February 2008


1nd2, resolution 2.5Å

Drag the structure with the mouse to rotate

The structure of Rhinovirus 16

Overview

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 Structure

1ND2 is a Protein complex structure of sequences from Human rhinovirus 2 with and as ligands. Full crystallographic information is available from OCA.

Reference

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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