Envelope surface glycoprotein gp160, precursor
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env
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HIV-1 gp160 is identified to have a physical interaction with adaptor-related protein complex 1, mu 1 subunit (AP1M1) in human HEK293 and/or Jurkat cell lines by using affinity tagging and purification mass spectrometry analyses |
PubMed
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env
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Two tyrosine-based endocytic signals (residues 704-710 and 760-766) in the cytosolic tail (gp41) of the HIV-1 envelope glycoprotein (Env) complex interact with members of the adaptor medium chain family, AP-1 mu1, AP-2 mu2 and AP-3 mu3A |
PubMed
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Envelope transmembrane glycoprotein gp41
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env
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The cytoplasmic domain (residues 707-856) of HIV-1 gp41 interacts with whole clathrin-associated AP-1 and AP-2 adaptor complexes |
PubMed
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env
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The highly conserved C-terminal dileucine motif (residues 851-856) in the cytosolic domain of HIV-1 gp41 interacts with clathrin-associated AP-1 adaptor complexes |
PubMed
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env
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Two tyrosine-based endocytic signals (residues 704-710 and 760-766) in the cytosolic tail (gp41) of the HIV-1 envelope glycoprotein (Env) complex interact with members of the adaptor medium chain family, AP-1 mu1, AP-2 mu2 and AP-3 mu3A |
PubMed
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Nef
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nef
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HIV-1 Nef downregulates CD4 and MHC I by connecting these receptors with the endocytic machinery through direct interactions between Nef and the mu medium chains of AP complexes, essential components of clathrin-coated pits |
PubMed
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nef
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Two distinct regions in Nef, from amino acids 140-150 and from 180-190, can both interact with the mu subunit of the adaptor protein complex 1 (AP-1) |
PubMed
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nef
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A leucine-based motif near the C-terminus of HIV-1 Nef interacts with AP-1 complexes; residues 164 and 165 in Nef are required for the interaction with AP-1 |
PubMed
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nef
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Adaptor-related protein complex 1 (AP-1) is necessary for cross-presentation by MHC-I HLA-A and HLA-B molecules containing a cytoplasmic tail tyrosine signal and that HIV-1 Nef inhibits the cross-presentation in antigen-presenting cells |
PubMed
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nef
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Dominant active ARF1 (Q71L) potently stabilizes interactions among AP-1 mu1, HIV-1 Nef, and HLA-A2 and that the formation of a static complex sequesters necessary trafficking components |
PubMed
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nef
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A quadruple mutation of mu 1 (K274E/K298E/K302E/R303D) abolishes binding to HIV-1 Nef, but a complementary mutation in the acidic cluster in Nef (62EEEE65 to 62KKKK65) restores their interaction |
PubMed
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nef
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Asp327 and Tyr320 of MHC-I, Asp123 of Nef, and Arg225, Arg393, Lys396, Arg211, and Arg246 of mu 1 are involved in a crucial three-way electrostatic network, which results in the Nef-MHC-I CD-mu 1 complex formation |
PubMed
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nef
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Exogenous Nef and TNF-alpha synergistically activate NF-kappaB and AP-1 resulting in enhancing viral replication in both chronically infected promonocytic cells and acutely infected primary macrophages |
PubMed
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nef
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HIV-1 Nef acidic (Glu62-65) and polyproline domains (Pro75/78) stabilize the interaction between the HLA-A2/Nef fusion protein and AP-1 mu1 |
PubMed
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nef
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The mu1 subunit of AP-1 uses its canonical tyrosine binding pocket for Nef-induced downregulation of HLA-A2. M20 is the only amino acid in the N-terminal domain of Nef needed for HLA-A2 downregulation |
PubMed
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nef
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Mutating three amino acids (Y320, A324, and D327) in the cytoplasmic tail of HLA-A2 abrogates Nef-induced downregulation of HLA-A2 through a failuer to recruit the mu1 or gamma subunits of AP-1 |
PubMed
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nef
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Knocking down either AP-1 gamma, AP-1 mu1, or clathrin strongly inhibits Nef-induced downregulation of HLA-A2 |
PubMed
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nef
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A fusion protein, composed of the cytoplasmic domain (CD) of MHC-I and HIV-1 Nef, shows its binding to the mu subunit of AP-1, which requires the tyrosine residue of the YSQA sequence in the MHC-I CD and Nef residues E62-65 and P78 |
PubMed
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nef
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HIV-1 Nef acts in cis to induce the rapid endocytosis of CD8-Nef fusion proteins via binding to the mu 1 chain of the adaptor protein type 1 (AP1) complex |
PubMed
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nef
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HIV-1 Nef stabilizes AP-1 complexes on endosomal membranes after ADP-ribosylation factor-1 (ARF1) -dependent attachment |
PubMed
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Pr55(Gag)
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gag
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HIV-1 Gag mutant lacking the matrix domain is insensitive to AP-1 mu depletion, suggesting that AP-1 mu participates in HIV-1 release through a direct interaction with the MA domain of Gag |
PubMed
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gag
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HIV-1 Gag interacts with adaptor complex AP-1 mu in vitro. The release of HIV-1 Gag is inhibited by silencing AP-1 mu in cells |
PubMed
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Vpu
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vpu
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HIV-1 Vpu physically interacts with the mu subunit of adaptor-related protein complex 1 (AP1) in cells, and Vpu R44 and L/I45 potentially interact with the mu 1 subunit |
PubMed
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vpu
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Fusion of the Vpu cytoplasmic domain (residues 28-80) to the BST2 cytoplasmic domain (residues 1-21) enhances binding to the beta, mu, and sigma subunits of adaptor-related protein complex 1 (AP1) in cells |
PubMed
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