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2q54
From Proteopedia
(New page: 200px<br /> <applet load="2q54" size="450" color="white" frame="true" align="right" spinBox="true" caption="2q54, resolution 1.85Å" /> '''Crystal structure o...) |
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| - | [[Image:2q54. | + | [[Image:2q54.jpg|left|200px]]<br /><applet load="2q54" size="350" color="white" frame="true" align="right" spinBox="true" |
| - | <applet load="2q54" size=" | + | |
caption="2q54, resolution 1.85Å" /> | caption="2q54, resolution 1.85Å" /> | ||
'''Crystal structure of KB73 bound to HIV-1 protease'''<br /> | '''Crystal structure of KB73 bound to HIV-1 protease'''<br /> | ||
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==About this Structure== | ==About this Structure== | ||
| - | 2Q54 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1] with PO4, ACT and MU1 as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http:// | + | 2Q54 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1] with <scene name='pdbligand=PO4:'>PO4</scene>, <scene name='pdbligand=ACT:'>ACT</scene> and <scene name='pdbligand=MU1:'>MU1</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2Q54 OCA]. |
==Reference== | ==Reference== | ||
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[[Category: protease inhibitors]] | [[Category: protease inhibitors]] | ||
| - | ''Page seeded by [http:// | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 13:37:32 2008'' |
Revision as of 11:37, 23 January 2008
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Crystal structure of KB73 bound to HIV-1 protease
Overview
A series of novel HIV-1 protease inhibitors based on two pseudosymmetric, dipeptide isosteres have been synthesized and evaluated. The inhibitors, were designed by incorporating N-phenyloxazolidinone-5-carboxamides into, the hydroxyethylene and (hydroxyethyl)hydrazine dipeptide isosteres as P2, and P2' ligands. Compounds with (S)-phenyloxazolidinones attached at a, position proximal to the central hydroxyl group showed low nM inhibitory, activities against wild-type HIV-1 protease. Selected compounds were, further evaluated for their inhibitory activities against a panel of, multidrug-resistant protease variants and for their antiviral potencies in, MT-4 cells. The crystal structures of lopinavir (LPV) and two new, inhibitors containing phenyloxazolidinone-based ligands in complex with, wild-type HIV-1 protease have been determined. A comparison of the, inhibitor-protease structures with the LPV-protease structure provides, valuable insight into the binding mode of the new inhibitors to the, protease enzyme. Based on the crystal structures and knowledge of, structure-activity relationships, new inhibitors can be designed with, enhanced enzyme inhibitory and antiviral potencies.
About this Structure
2Q54 is a Single protein structure of sequence from Human immunodeficiency virus 1 with , and as ligands. Full crystallographic information is available from OCA.
Reference
Design and Synthesis of HIV-1 Protease Inhibitors Incorporating Oxazolidinones as P2/P2' Ligands in Pseudosymmetric Dipeptide Isosteres., Reddy GS, Ali A, Nalam MN, Anjum SG, Cao H, Nathans RS, Schiffer CA, Rana TM, J Med Chem. 2007 Sep 6;50(18):4316-28. Epub 2007 Aug 16. PMID:17696512
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