3ao4: Difference between revisions

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m Protected "3ao4" [edit=sysop:move=sysop]
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[[Image:3ao4.jpg|left|200px]]
[[Image:3ao4.png|left|200px]]


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{{STRUCTURE_3ao4|  PDB=3ao4  |  SCENE=  }}  
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==Reference==
==Reference==
<ref group="xtra">PMID:21275048</ref><references group="xtra"/>
<ref group="xtra">PMID:021275048</ref><references group="xtra"/>
[[Category: Human immunodeficiency virus 1]]
[[Category: Human immunodeficiency virus 1]]
[[Category: Chalmers, D K.]]
[[Category: Chalmers, D K.]]
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[[Category: Scanlon, M J.]]
[[Category: Scanlon, M J.]]
[[Category: Wielens, J.]]
[[Category: Wielens, J.]]
[[Category: Aid]]
[[Category: Dna binding]]
[[Category: Dna integration]]
[[Category: Endonuclease]]
[[Category: Fragment binding]]
[[Category: Integrase]]
[[Category: Polynucleotidyl transferase]]
[[Category: Rnaseh]]
[[Category: Viral protein]]
[[Category: Viral protein-transferase inhibitor complex]]

Revision as of 16:19, 6 February 2013

File:3ao4.png

Template:STRUCTURE 3ao4

Fragment-based approach to the design of ligands targeting a novel site on HIV-1 integraseFragment-based approach to the design of ligands targeting a novel site on HIV-1 integrase

About this StructureAbout this Structure

3ao4 is a 2 chain structure with sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.

ReferenceReference

[xtra 1]

  1. Wielens J, Headey SJ, Deadman JJ, Rhodes DI, Parker MW, Chalmers DK, Scanlon MJ. Fragment-based design of ligands targeting a novel site on the integrase enzyme of human immunodeficiency virus 1. ChemMedChem. 2011 Feb 7;6(2):258-61. doi: 10.1002/cmdc.201000483. Epub, 2010 Dec 16. PMID:21275048 doi:10.1002/cmdc.201000483

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