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      Inhibitors of the interactions between HIV-1 IN and the cofactor LEDGF/p75.

      Chemmedchem
      Benzoates, chemistry, pharmacology, HIV Integrase, metabolism, HIV Integrase Inhibitors, HIV-1, enzymology, Humans, Indoles, Intercellular Signaling Peptides and Proteins, Peptides, Protein Interaction Domains and Motifs, drug effects, Quinolines, Thiazolidinediones

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          Abstract

          The replication cycle of human immunodeficiency virus type 1 (HIV-1) is a complex multistep process that depends on both viral and host cell factors. The nuclear protein lens epithelium-derived growth factor (LEDGF/p75) is a multidomain protein, present in host cells, which plays an important role in the integration process. LEDGF/p75 not only binds HIV-1 integrase (IN) at its IN binding domain (IBD) but also contains several motifs that function in DNA and chromatin binding. The demonstrated importance of the association between IN and LEDGF/p75 in HIV-1 integration suggests the possibility that this protein-protein interaction (PPI) could be exploited as an antiviral target. We describe herein the progress to date in developing inhibitors of this promising target. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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