The repeating segments of the F-actin cross-linking gelation factor (ABP-120) have an immunoglobulin-like fold (original) (raw)
References
Eichinger, L. et al. Mechanical perturbation elicits a phenotypic difference between Dictyostelium wild-type cells and cytoskeletal mutants. Biophys. J.70, 1054–1060 (1996). ArticleCAS Google Scholar
Cunningham, C.C. et al. Actin-binding protein requirement for cortical stability and efficient locomotion. Science255, 325–327 (1992). ArticleCAS Google Scholar
Noegel, A.A., Rapp, S., Lottspeich, F., Schleicher, M. & Stewart, M. The Dictyostelium gelation factor shares a putative actin binding site with α-actinins and dystrophin and also has a rod repetitive segment containing six 100-residue motifs that appear to have cross-beta conformation. J. Cell Biol.109, 607–618 (1989). ArticleCAS Google Scholar
Yan, Y. et al. Crystal structure of the repetitive segments of spectrin. Science262, 2027–2030 (1993). ArticleCAS Google Scholar
Davison, M.D., Baron, M.D., Critchley, D.R. & Wootton, J.C. Structural analysis of homologous repeated repetitive segments in α-actinin and spectrin. Int. J. Biol. Macromol.11, 81–90 (1989). ArticleCAS Google Scholar
Gorlin, J.B. et al. Human endothelial actin-binding protein (ABP-280, nonmuscle filamin): A molecular leaf spring. J. Cell Biol.111, 1089–1105 (1990). ArticleCAS Google Scholar
Hartwig, J.H. in Protein profile vol. 2, p.739–747, Academic Press, N.Y. (1995) Google Scholar
Stendahl, O.I., Hartwig, J.H., Brotschi, E.A. & Stossel, T.P. Distribution of actin-binding protein and myosin in macrophages during spreading and phagocytosis. J. Cell. Biol.84, 215–224 (1980). ArticleCAS Google Scholar
Carboni, J.M. & Condeelis, J.S. Ligand-induced changes in the location of actin, myosin, 95 K (α-actinin), and 120 K protein in amoebae of Dictyostelium discoideum. J. Cell Biol.100, 1884–1893 (1985). ArticleCAS Google Scholar
Condeelis, J. et al. Actin polymerisation and pseudopod extension during amoeboid chemotaxis. Cell Motil. Cytoskel.10 77–90. ArticleCAS Google Scholar
Condeelis, J., Vahey, M., Carboni, J.M., DeMey, J. & Ogihara, S. Properties of the 120,000- and 95,000-dalton actin-binding proteins from Dictyostelium discoideum and their possible functions in assembling the cytoplasmic matrix. J. Cell Biol.99, 119s–126s (1984). ArticleCAS Google Scholar
Kay, L.E., Torchia, D.A. & Bax, A. Backbone dynamics of proteins as studied by 15N inverse detected heteronuclear NMR spectroscopy: Application to staphylococcal nuclease. Biochemistry28, 8972–8979 (1989). ArticleCAS Google Scholar
Farrow, N.A. et al. Backbone dynamics of a free and a phosphopeptide-complexed Src homology 2 repetitive segment studied by 15N NMR relaxation. Biochemistry33, 5984–6003 (1994). ArticleCAS Google Scholar
Clore, G.M., Driscoll, P.C., Wingfield, P.T. & Gronenborn, A.M. Analysis of the backbone dynamics of interleukin 1β using two-dimensional inverse detected he teronuclear 15N-1H NMR spectroscopy. Biochemistry27, 7387–7401 (1990). Article Google Scholar
Clubb, R.T. et al. Backbone dynamics of the oligomerization repetitive segment of p53 determind from 15N NMR relaxation measurements. Protein Sci3, 855–862 (1995). Google Scholar
Zink, T. et al. Structure and dynamics of the human granulocyte colony-stimulating factor determined by NMR spectroscopy. Loop mobility in a four-helix-bundle protein. Biochemistry33, 8453–8463 (1994). ArticleCAS Google Scholar
Wüthrich, K. NMR of proteins and nucleic acids. New York: Wiley (1986). Book Google Scholar
Spera, S. & Bax, A. 1991. Empirical correlation between protein backbone conformation and Cα and Cβ 13C nuclear magnetic resonance chemical shifts. J. Am. Chem. Soc.113, 5490–5492 (1991). ArticleCAS Google Scholar
Wishart, D.S., Sykes, B.D. & Richards, F.M. Relationship between nuclear magnetic resonance chemical shift and protein secondary structure. J. Mol. Biol.222, 311–333 (1991). ArticleCAS Google Scholar
Holak, T.A., Gondol, D., Otlewski, J. & Wilusz, T. Determination of the complete 3-dimensional structure of the trypsin-inhibitor from squash seeds in aqueous-solution by nuclear magnetic-resonance and a combination of distance geometry and dynamical simulated annealing. J. Mol. Biol.210, 635–648 (1989). ArticleCAS Google Scholar
Brünger, A.T. & Nilges, M. Computational challenges for macromolecular structure determination by X-ray crystallography and solution nmr spectroscopy. Q. Rev. Biophys.26, 49–125 (1993). Article Google Scholar
Harpaz, Y. & Chothia, C. Many of the immunoglobulin superfamily domains in cell adhesion molecules and surface receptors belong to a new structural set which is close to that containing variable domains. J. Mol. Biol.238, 528–539 (1994). ArticleCAS Google Scholar
Bork, P., Holm, L. & Sander, C. The immunoglobulin fold, structural classi fication, sequence patterns and common core. J. Mol. Biol.242, 309–320 (1994). CAS Google Scholar
Tabor, S. Protein expression using the T7 RNA polymerase/promoter system. In Current Protocols in Molecular Biology (Ausubel, F.A. et al. eds.), Greene Publishing and Wiley Interscience, New York, 16.2.1–16.2.11 (1990). Google Scholar
Hoffman, D.W. & Spicer, L.D. Isotopic labeling of specific amino acid types as an aid to NMR spectrum assignment of the methione represser protein. In Techniques in protein chemistry II. Villafranca, J.J., Ed., San Diego: Academic Press. 409–419 (1991). Google Scholar
Muchmore, D.C., Mclntosh, L.P., Russell, C.B., Anderson, D.E. & Dahlquist, T.W. Expression and nitrogen-15 labeling of proteins for proton and nitrogen-15 nuclear magnetic resonance. Meth. Enzym.177, 44–73 (1989). ArticleCAS Google Scholar
Clore, G.M. et al. Overcoming the overlap problem in the assignment of 1H NMR spectra of larger proteins by use of three-dimensional heteronuclear 1H-15N Hart man-Hahn-multiple quantum coherence and nuclear Overhauser-multiple quantum coherence spectroscopy: application to interleukin 1β. Biochemistry28, 6150–6156 (1989). Article Google Scholar
Bax, A. & Davis, D.G. MLEV-17-Based two-dimensional homonuclear magneti zation transfer spectroscopy. J. Magn. Reson.65, 355–360 (1985). CAS Google Scholar
Jeener, J., Meier, B.H., Bachman, P. & Ernst, R.R. Investigation of exchange processes by two-dimensional NMR spectroscopy. J. Chem. Phys.71, 4546–4553 (1979). ArticleCAS Google Scholar
Guèron, M., Plateau, P. & Decorps, M. Solvent signal suppression in NMR. Prog. NMR Spectrosc.23, 135–209 (1991). Article Google Scholar
Jahnke, W., Baur, M., Gemmecker, G. & Kessler, H. Improved accuracy of NMR structures by a modified NOESY-HSQC experiment. J. Magn. Reson.B 106, 86–88 (1995). Article Google Scholar
Muhandiram, D.R., Farrow, N., Xu, G.Y., Smallcombe, S.J. & Kay, L.E. A gradient 13C NOESY-HSQC experiment for recording NOESY spectra of 13C- labeled proteins dissolved in H2O.J. Magn. Reson.B102, 317–321 (1993). Article Google Scholar
Mori, S., Abeygunawardana, C., Johnson, M.N. & van Zijl, P.C.M. Improved sensitivity of HSQC spectra of exchanging protons at short interscan delays using a new fast HSQC (FHSQC) detection scheme that avoids water saturation. J. Magn. Reson. B108, 94–98 (1995). ArticleCAS Google Scholar
Farrow, N.A. et al. Backbone dynamics of a free and a phosphopeptide-complexed Src homology 2 domain studied by 15N NMR relaxation. Biochemistry33, 5984–6003 (1994). ArticleCAS Google Scholar
Cieslar, C., Ross, A., Zink, T. & Holak, T.A. Efficiency in multidimensional NMR by optimized recording of time point-phase pairs in evolution periods and their selective linear transformation. J. Magn. Reson. B101, 97–101 (1993). ArticleCAS Google Scholar
Grzesiek, S. & Bax, A. Improved 3D triple-resonance NMR techniques applied to a 31 kDa protein. J. Magn. Reson.96, 432–440 (1992). CAS Google Scholar
Sklendr,V., Piotto, M., Leppik, R. & Saudek, V. Gradient-tailored water suppression for 1H-15NHSQC experiments optimized to retain full sensitivity. J. Magn. Reson. A102, 241–245 (1993). Article Google Scholar
Grzesiek, S. & Bax, A. Correlating backbone amide and side chain resonances in larger proteins by multiple relayed triple resonance NMR. J. Am. Chem. Soc.114, 6291–6293. ArticleCAS Google Scholar
Kay, L.E., Xu, G-Y., Singer, A.U., Muhandiram, D.R. & Foreman-Kay, J.D. A gradient-enhanced HCCH-TOCSY experiment for recording side-chain 1H and 13C correlations in H2O samples of proteins. J. Magn. Reson. B101, 333–337 (1993). ArticleCAS Google Scholar
Hyberts, S.G., Mäki, W. & Wagner, G. Stereospecific assignments of side-chain protons and characterization of torsion angles in Eglin c. Eur. J. Biochem.164, 625–635 (1987). ArticleCAS Google Scholar
Wagner, G. et al. Protein structures in solution by NMR and distance geometry. The polypeptide fold of the basic trypsin inhibitor determined using two different algorithms, DISGEO and DISMAN. J. Mol. Biol.196, 611–639 (1988). Article Google Scholar
Vuister, G.W. & Bax, A. Quantitative J correlation: a new approach for measuring homonuclear three bond J(HN-Hα) coupling constants in 15N-enriched proteins. J. Am. Chem. Soc.115, 7772–7777 (1993). ArticleCAS Google Scholar
Seip, S., Balbach, J. & Kessler, H. Determination of backbone conformation of isotopically enriched proteins based on coupling constants. J. Magn. Reson. B104, 172–179 (1994). ArticleCAS Google Scholar
Marion, D. & Wüthrich, K. Application of phase sensitive two dimensional correlated spectroscopy (COSY ) for measurements of 1H-1H spin-spin coupling constants in proteins. Biochem. Biophys. Res. Commun.113, 967–974 (1983). ArticleCAS Google Scholar
Nicholls, A., Sharp, K. & Honig, B. Protein folding and association: insights from the interfacial and thermodynamic properties of hydrocarbons. Proteins11, 281–296 (1991). ArticleCAS Google Scholar
Insight II, Release 95.0, Biosym/MSI, San Diego (1995).