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Journal Abstract Search


149 related items for PubMed ID: 8630037

  • 21. Restoration of defective mechanochemical properties of cleaved actins by native tropomyosin: involvement of the 40-50 loop in subdomain 2 of actin in interaction with myosin and tropomyosin.
    Higashi-Fujime S, Hozumi T.
    Biochem Biophys Res Commun; 1997 Aug 08; 237(1):121-5. PubMed ID: 9266842
    [Abstract] [Full Text] [Related]

  • 22. Interaction between actin and HMM.
    Borejdo J, Giordano M.
    Biochem Biophys Res Commun; 1986 Dec 15; 141(2):541-6. PubMed ID: 3541936
    [Abstract] [Full Text] [Related]

  • 23. The amounts of adenosine di- and triphosphates bound to H-meromyosin and the adenosinetriphosphatase activity of the H-meromyosin-F-actin-relaxing protein system in the presence and absence of calcium ions. The physiological functions of the two routes of myosin adenosinetriphosphatase in muscle contraction.
    Inoue A, Tonomura Y.
    J Biochem; 1975 Jul 15; 78(1):83-92. PubMed ID: 127789
    [Abstract] [Full Text] [Related]

  • 24. Activation of regulated actin by SH1-modified myosin subfragment 1.
    Bobkov AA, Bobkova EA, Homsher E, Reisler E.
    Biochemistry; 1997 Jun 24; 36(25):7733-8. PubMed ID: 9201914
    [Abstract] [Full Text] [Related]

  • 25. Comparison of the binding of heavy meromyosin and myosin subfragment 1 in F-actin.
    Greene LE.
    Biochemistry; 1981 Apr 14; 20(8):2120-6. PubMed ID: 7016172
    [Abstract] [Full Text] [Related]

  • 26. Reaction mechanism of Mn2+-ATPase of acto-H-meromyosin in 0.1 M KCl at 5 degrees C: evidence for the Lymn-Taylor mechanism.
    Ikebe M, Inoue A, Tonomura Y.
    J Biochem; 1980 Dec 14; 88(6):1653-62. PubMed ID: 6450754
    [Abstract] [Full Text] [Related]

  • 27. Addition of lysines to the 50/20 kDa junction of myosin strengthens weak binding to actin without affecting the maximum ATPase activity.
    Joel PB, Sweeney HL, Trybus KM.
    Biochemistry; 2003 Aug 05; 42(30):9160-6. PubMed ID: 12885250
    [Abstract] [Full Text] [Related]

  • 28. Delayed dissociation of in vitro moving actin filaments from heavy meromyosin induced by low concentrations of Triton X-100.
    Kellermayer MS.
    Biophys Chem; 1997 Sep 01; 67(1-3):199-210. PubMed ID: 9397525
    [Abstract] [Full Text] [Related]

  • 29. Mutual sensitization of ATP and GTP in driving F-actin on the surface-fixed H-meromyosin.
    Oda T, Shikata Y, Mihashi K.
    Biophys Chem; 1996 Oct 30; 61(2-3):63-72. PubMed ID: 8956480
    [Abstract] [Full Text] [Related]

  • 30. Maximum limit to the number of myosin II motors participating in processive sliding of actin.
    Rastogi K, Puliyakodan MS, Pandey V, Nath S, Elangovan R.
    Sci Rep; 2016 Aug 24; 6():32043. PubMed ID: 27554800
    [Abstract] [Full Text] [Related]

  • 31. Myosin step size. Estimation from slow sliding movement of actin over low densities of heavy meromyosin.
    Uyeda TQ, Kron SJ, Spudich JA.
    J Mol Biol; 1990 Aug 05; 214(3):699-710. PubMed ID: 2143785
    [Abstract] [Full Text] [Related]

  • 32. Inhibition of sliding movement of F-actin by crosslinking emphasizes the role of actin structure in the mechanism of motility.
    Prochniewicz E, Yanagida T.
    J Mol Biol; 1990 Dec 05; 216(3):761-72. PubMed ID: 2147958
    [Abstract] [Full Text] [Related]

  • 33. Actomyosin interaction at low ATP concentrations.
    Maffei M, Longa E, Sabatini A, Vacca A, Iotti S.
    Eur Biophys J; 2017 Mar 05; 46(2):195-202. PubMed ID: 28039513
    [Abstract] [Full Text] [Related]

  • 34. The mechanism of ATP hydrolysis by smooth muscle myosin and subfragments using steady state titration and 18O exchange.
    Dash PK, Hackney DD.
    Biochem Int; 1991 Dec 05; 25(6):1013-22. PubMed ID: 1839764
    [Abstract] [Full Text] [Related]

  • 35. Prodan fluorescence reflects differences in nucleotide-induced conformational states in the myosin head and allows continuous visualization of the ATPase reactions.
    Hiratsuka T.
    Biochemistry; 1998 May 19; 37(20):7167-76. PubMed ID: 9585528
    [Abstract] [Full Text] [Related]

  • 36. Actin-induced local conformational change in the myosin molecule. II. Conformational change around the S2 thiol group related to the essential intermediate of ATP hydrolysis.
    Kameyama T.
    J Biochem; 1980 Feb 19; 87(2):581-6. PubMed ID: 6987217
    [Abstract] [Full Text] [Related]

  • 37. Some characteristics of beta-naphthyl triphosphate as a substrate of heavy meromyosin. F-actin-inactivated hydrolysis showing initial burst.
    Fujisaki H, Asai H.
    J Biochem; 1978 Feb 19; 83(2):403-7. PubMed ID: 344308
    [Abstract] [Full Text] [Related]

  • 38. [Effect of Ca2+ on the motility of myosin head in the F-actin-HMM complex].
    Borovikov IuS, Wrotek M, Aksenova NB, Lebedeva NN, Kankol I.
    Biokhimiia; 1988 Jan 19; 53(1):97-100. PubMed ID: 3282547
    [Abstract] [Full Text] [Related]

  • 39. Novel mode of cooperative binding between myosin and Mg2+ -actin filaments in the presence of low concentrations of ATP.
    Tokuraku K, Kurogi R, Toya R, Uyeda TQ.
    J Mol Biol; 2009 Feb 13; 386(1):149-62. PubMed ID: 19100745
    [Abstract] [Full Text] [Related]

  • 40. Analysis of the bound nucleotide in the acto-heavy meromyosin in vitro motility assay.
    Kellermayer MS.
    Physiol Chem Phys Med NMR; 1996 Feb 13; 28(3):143-51. PubMed ID: 9091891
    [Abstract] [Full Text] [Related]


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