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3ao1

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[[Image:3ao1.png|left|200px]]
 
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{{STRUCTURE_3ao1| PDB=3ao1 | SCENE= }}
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==Fragment-based approach to the design of ligands targeting a novel site in HIV-1 integrase==
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<StructureSection load='3ao1' size='340' side='right'caption='[[3ao1]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
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===Fragment-based approach to the design of ligands targeting a novel site in HIV-1 integrase===
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== Structural highlights ==
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<table><tr><td colspan='2'>[[3ao1]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3AO1 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3AO1 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.9&#8491;</td></tr>
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==About this Structure==
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=BZX:1,3-BENZODIOXOL-5-OL'>BZX</scene>, <scene name='pdbligand=CD:CADMIUM+ION'>CD</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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[[3ao1]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3AO1 OCA].
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3ao1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3ao1 OCA], [https://pdbe.org/3ao1 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3ao1 RCSB], [https://www.ebi.ac.uk/pdbsum/3ao1 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3ao1 ProSAT]</span></td></tr>
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</table>
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==Reference==
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== Function ==
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<ref group="xtra">PMID:021275048</ref><references group="xtra"/>
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[https://www.uniprot.org/uniprot/Q72498_9HIV1 Q72498_9HIV1]
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__TOC__
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</StructureSection>
[[Category: Human immunodeficiency virus 1]]
[[Category: Human immunodeficiency virus 1]]
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[[Category: Chalmers, D K.]]
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[[Category: Large Structures]]
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[[Category: Parker, M W.]]
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[[Category: Chalmers DK]]
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[[Category: Scanlon, M J.]]
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[[Category: Parker MW]]
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[[Category: Wielens, J.]]
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[[Category: Scanlon MJ]]
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[[Category: Aid]]
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[[Category: Wielens J]]
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[[Category: Dna binding]]
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[[Category: Dna integration]]
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[[Category: Endonuclease]]
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[[Category: Fragment binding]]
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[[Category: Integrase]]
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[[Category: Polynucleotidyl transferase]]
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[[Category: Rnaseh]]
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[[Category: Viral protein]]
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[[Category: Viral protein-transferase inhibitor complex]]
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Current revision

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

PDB ID 3ao1

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