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Journal Abstract Search

166 related items for PubMed ID: 15047193

  • 1. Fusogenic domain and lysines in saposin C.
    Qi X, Chu Z.
    Arch Biochem Biophys; 2004 Apr 15; 424(2):210-8. PubMed ID: 15047193
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  • 2. Role of lysine residues in membrane anchoring of saposin C.
    Liu A, Wenzel N, Qi X.
    Arch Biochem Biophys; 2005 Nov 15; 443(1-2):101-12. PubMed ID: 16256068
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  • 3. Solution structure of human saposin C: pH-dependent interaction with phospholipid vesicles.
    de Alba E, Weiler S, Tjandra N.
    Biochemistry; 2003 Dec 23; 42(50):14729-40. PubMed ID: 14674747
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  • 6. The N370S (Asn370-->Ser) mutation affects the capacity of glucosylceramidase to interact with anionic phospholipid-containing membranes and saposin C.
    Salvioli R, Tatti M, Scarpa S, Moavero SM, Ciaffoni F, Felicetti F, Kaneski CR, Brady RO, Vaccaro AM.
    Biochem J; 2005 Aug 15; 390(Pt 1):95-103. PubMed ID: 15826241
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  • 7. Functional characterization of the postulated intramolecular sphingolipid activator protein domain of human acid sphingomyelinase.
    Kölzer M, Ferlinz K, Bartelsen O, Hoops SL, Lang F, Sandhoff K.
    Biol Chem; 2004 Dec 15; 385(12):1193-5. PubMed ID: 15653433
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  • 9. A novel saposin-like protein of Entamoeba histolytica with membrane-fusogenic activity.
    Winkelmann J, Leippe M, Bruhn H.
    Mol Biochem Parasitol; 2006 May 15; 147(1):85-94. PubMed ID: 16529828
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  • 10. Conformational and amino acid residue requirements for the saposin C neuritogenic effect.
    Qi X, Kondoh K, Krusling D, Kelso GJ, Leonova T, Grabowski GA.
    Biochemistry; 1999 May 11; 38(19):6284-91. PubMed ID: 10320358
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  • 11. An Asn > Lys substitution in saposin B involving a conserved amino acidic residue and leading to the loss of the single N-glycosylation site in a patient with metachromatic leukodystrophy and normal arylsulphatase A activity.
    Regis S, Filocamo M, Corsolini F, Caroli F, Keulemans JL, van Diggelen OP, Gatti R.
    Eur J Hum Genet; 1999 May 11; 7(2):125-30. PubMed ID: 10196694
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  • 14. Brucella abortus MFP: a trimeric coiled-coil protein with membrane fusogenic activity.
    Carrica Mdel C, Craig PO, Alonso Sdel V, Goldbaum FA, Cravero SL.
    Biochemistry; 2008 Aug 05; 47(31):8165-75. PubMed ID: 18616282
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  • 15. The interaction of the Bax C-terminal domain with negatively charged lipids modifies the secondary structure and changes its way of insertion into membranes.
    Ausili A, Torrecillas A, Martínez-Senac MM, Corbalán-García S, Gómez-Fernández JC.
    J Struct Biol; 2008 Oct 05; 164(1):146-52. PubMed ID: 18672068
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  • 16. Glycosidase-induced fusion of isoprenoid gentiobiosyl lipid membranes at acidic pH.
    Sprott GD, Côté JP, Jarrell HC.
    Glycobiology; 2009 Mar 05; 19(3):267-76. PubMed ID: 19029107
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  • 17. Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse.
    Matsuda J, Kido M, Tadano-Aritomi K, Ishizuka I, Tominaga K, Toida K, Takeda E, Suzuki K, Kuroda Y.
    Hum Mol Genet; 2004 Nov 01; 13(21):2709-23. PubMed ID: 15345707
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  • 18. Structural and membrane-binding properties of saposin D.
    Tatti M, Salvioli R, Ciaffoni F, Pucci P, Andolfo A, Amoresano A, Vaccaro AM.
    Eur J Biochem; 1999 Jul 01; 263(2):486-94. PubMed ID: 10406958
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  • 19. Secondary structure, phospholipid membrane interactions, and fusion activity of two glutamate-rich analogs of influenza hemagglutinin fusion peptide.
    Kantchev EA, Cheng SF, Wu CW, Huang HJ, Chang DK.
    Arch Biochem Biophys; 2004 May 15; 425(2):173-83. PubMed ID: 15111125
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  • 20. Saposin B mobilizes lipids from cholesterol-poor and bis(monoacylglycero)phosphate-rich membranes at acidic pH. Unglycosylated patient variant saposin B lacks lipid-extraction capacity.
    Remmel N, Locatelli-Hoops S, Breiden B, Schwarzmann G, Sandhoff K.
    FEBS J; 2007 Jul 15; 274(13):3405-20. PubMed ID: 17561962
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