3drs

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m (Protected "3drs" [edit=sysop:move=sysop])
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[[Image:3drs.png|left|200px]]
[[Image:3drs.png|left|200px]]
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{{STRUCTURE_3drs| PDB=3drs | SCENE= }}
{{STRUCTURE_3drs| PDB=3drs | SCENE= }}
===HIV reverse transcriptase K103N mutant in complex with inhibitor R8D===
===HIV reverse transcriptase K103N mutant in complex with inhibitor R8D===
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{{ABSTRACT_PUBMED_18826204}}
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==See Also==
==See Also==
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*[[Reverse transcriptase]]
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*[[Reverse transcriptase|Reverse transcriptase]]
==Reference==
==Reference==
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<ref group="xtra">PMID:18826204</ref><references group="xtra"/>
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<ref group="xtra">PMID:018826204</ref><references group="xtra"/>
[[Category: Human immunodeficiency virus 1]]
[[Category: Human immunodeficiency virus 1]]
[[Category: Prasad, S.]]
[[Category: Prasad, S.]]

Revision as of 09:22, 26 July 2012

Template:STRUCTURE 3drs

Contents

HIV reverse transcriptase K103N mutant in complex with inhibitor R8D

Template:ABSTRACT PUBMED 18826204

About this Structure

3drs is a 2 chain structure of Reverse transcriptase with sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.

See Also

Reference

  • Tucker TJ, Sisko JT, Tynebor RM, Williams TM, Felock PJ, Flynn JA, Lai MT, Liang Y, McGaughey G, Liu M, Miller M, Moyer G, Munshi V, Perlow-Poehnelt R, Prasad S, Reid JC, Sanchez R, Torrent M, Vacca JP, Wan BL, Yan Y. Discovery of 3-{5-[(6-Amino-1H-pyrazolo[3,4-b]pyridine-3-yl)methoxy]-2-chlorophenoxy}-5 -chlorobenzonitrile (MK-4965): A Potent, Orally Bioavailable HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitor with Improved Potency against Key Mutant Viruses. J Med Chem. 2008 Oct 1. PMID:18826204 doi:10.1021/jm800856c

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