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PUBMED FOR HANDHELDS

Journal Abstract Search


223 related items for PubMed ID: 11242518

  • 21.
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  • 22.
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  • 23. Role of the fusion peptide and membrane-proximal domain in HIV-1 envelope glycoprotein-mediated membrane fusion.
    Dimitrov AS, Rawat SS, Jiang S, Blumenthal R.
    Biochemistry; 2003 Dec 09; 42(48):14150-8. PubMed ID: 14640682
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  • 24.
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  • 25. A large HIV gp41 construct with trimer-of-hairpins structure exhibits V2E mutation-dominant attenuation of vesicle fusion and helicity very similar to V2E attenuation of HIV fusion and infection and supports: (1) hairpin stabilization of membrane apposition with larger distance for V2E; and (2) V2E dominance by an antiparallel β sheet with interleaved fusion peptide strands from two gp41 trimers.
    Rokonujjaman M, Sahyouni A, Wolfe R, Jia L, Ghosh U, Weliky DP.
    Biophys Chem; 2023 Feb 09; 293():106933. PubMed ID: 36508984
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  • 26.
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  • 27. A leucine zipper-like sequence from the cytoplasmic tail of the HIV-1 envelope glycoprotein binds and perturbs lipid bilayers.
    Kliger Y, Shai Y.
    Biochemistry; 1997 Apr 29; 36(17):5157-69. PubMed ID: 9136877
    [Abstract] [Full Text] [Related]

  • 28. A novel bispecific peptide HIV-1 fusion inhibitor targeting the N-terminal heptad repeat and fusion peptide domains in gp41.
    Jiang X, Jia Q, Lu L, Yu F, Zheng J, Shi W, Cai L, Jiang S, Liu K.
    Amino Acids; 2016 Dec 29; 48(12):2867-2873. PubMed ID: 27631437
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  • 29. How structure correlates to function for membrane associated HIV-1 gp41 constructs corresponding to the N-terminal half of the ectodomain.
    Sackett K, Shai Y.
    J Mol Biol; 2003 Oct 10; 333(1):47-58. PubMed ID: 14516742
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  • 30. The role of the N-terminal heptad repeat of HIV-1 in the actual lipid mixing step as revealed by its substitution with distant coiled coils.
    Wexler-Cohen Y, Sackett K, Shai Y.
    Biochemistry; 2005 Apr 19; 44(15):5853-61. PubMed ID: 15823044
    [Abstract] [Full Text] [Related]

  • 31. Identification of membrane-active regions of the HIV-1 envelope glycoprotein gp41 using a 15-mer gp41-peptide scan.
    Moreno MR, Pascual R, Villalaín J.
    Biochim Biophys Acta; 2004 Feb 10; 1661(1):97-105. PubMed ID: 14967479
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  • 32. Conformational mapping of the N-terminal peptide of HIV-1 gp41 in lipid detergent and aqueous environments using 13C-enhanced Fourier transform infrared spectroscopy.
    Gordon LM, Mobley PW, Lee W, Eskandari S, Kaznessis YN, Sherman MA, Waring AJ.
    Protein Sci; 2004 Apr 10; 13(4):1012-30. PubMed ID: 15044732
    [Abstract] [Full Text] [Related]

  • 33. Solid-state nuclear magnetic resonance measurements of HIV fusion peptide 13CO to lipid 31P proximities support similar partially inserted membrane locations of the α helical and β sheet peptide structures.
    Gabrys CM, Qiang W, Sun Y, Xie L, Schmick SD, Weliky DP.
    J Phys Chem A; 2013 Oct 03; 117(39):9848-59. PubMed ID: 23418890
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  • 34. Design of potent inhibitors of HIV-1 entry from the gp41 N-peptide region.
    Eckert DM, Kim PS.
    Proc Natl Acad Sci U S A; 2001 Sep 25; 98(20):11187-92. PubMed ID: 11572974
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  • 35.
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  • 36. Functional and structural characterization of HIV-1 gp41 ectodomain regions in phospholipid membranes suggests that the fusion-active conformation is extended.
    Korazim O, Sackett K, Shai Y.
    J Mol Biol; 2006 Dec 15; 364(5):1103-17. PubMed ID: 17045292
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  • 37.
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  • 38. Hydrophobic mutations in buried polar residues enhance HIV-1 gp41 N-terminal heptad repeat-C-terminal heptad repeat interactions and C-peptides' anti-HIV activity.
    Zheng B, Wang K, Lu L, Yu F, Cheng M, Jiang S, Liu K, Cai L.
    AIDS; 2014 Jun 01; 28(9):1251-60. PubMed ID: 24625369
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  • 39. HIV-1 membrane fusion mechanism: structural studies of the interactions between biologically-active peptides from gp41.
    Lawless MK, Barney S, Guthrie KI, Bucy TB, Petteway SR, Merutka G.
    Biochemistry; 1996 Oct 22; 35(42):13697-708. PubMed ID: 8885850
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  • 40.
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