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Structural and Functional Insights of Wilson Disease Copper-Transporting ATPase

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Abstract

Wilson disease is an autosomal recessive disorder of copper metabolism. The gene for this disorder has been cloned and identified to encode a copper-transporting ATPase (ATP7B), a member of a large family of cation transporters, the P-type ATPases. In addition to the core elements common to all P-type ATPases, the Wilson copper-transporting ATPase has a large cytoplasmic N-terminus comprised six heavy metal associated (HMA) domains, each of which contains the copper-binding sequence motif GMT/HCXXC. Extensive studies addressing the functional, regulatory, and structural aspects of heavy metal transport by heavy metal transporters in general, have offered great insights into copper transport by Wilson copper-transporting ATPase. The findings from these studies have been used together with homology modeling of the Wilson disease copper-transporting ATPases based on the X-ray structure of the sarcoplasmic reticulum (SR) calcium-ATPase, to present a hypothetical model of the mechanism of copper transport by copper-transporting ATPases.

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REFERENCES

  • Baker, D., and Sali, A. (2001). Science 294, 93–96.

    Google Scholar 

  • Beard, S. J., Hashim, R., Membrillo-Hernandez, J., Hughes, M. N., and Poole, R. K. (1997). Mol. Microbiol. 25, 883–891.

    Google Scholar 

  • Bissig, K. D., Wunderli-Ye, H., Duda, P. W., and Solioz, M. (2001). Biochem. J. 357, 217–223.

    Google Scholar 

  • Bowmaker, G. A., Clark, G. R., Seadon, J. K., and Dance, I. G. (1984). Polyhedron 3, 535–544.

    Google Scholar 

  • Bull, P. C., Thomas, G. R., Rommens, J. M., Forbes, J. R., and Cox, D. W. (1993). Nat. Genet. 5, 327–337.

    Google Scholar 

  • Clark-Baldwin, K., Tierney, D. L., Govindaswamy, N., Gruff, E. S., Kim, C., Berg, J., Koch, S. A., and Penner-Hahn, J. E. (1998). J. Am. Chem. Soc. 120, 8401–8409.

    Google Scholar 

  • Coucouvanis, D., Murphy, C. N., and Kanodia, S. K. (1980). Inorg. Chem. 19, 2993–2998.

    Google Scholar 

  • Dance, I. G. (1986). Polyhedron 5, 1037–1104.

    Google Scholar 

  • Danks, D. M. (1995). In Metabolic Basis of Inherited Disease (Scriver, C. R., Beaudet, A. I., Sly, W. S., and Valle, D., eds.), McGraw-Hill, New York, pp. 2211–2235.

  • DiDonato, M., Hsu, H. F., Narindrasorasak, S., Que, L., Jr., and Sarkar, B. (2000). Biochemistry 39, 1890–1896.

    Google Scholar 

  • DiDonato, M., Narindrasorasak, S., Forbes, J. R., Cox, D.W., and Sarkar, B. (1997). J. Biol. Chem. 272, 33279–33282. ATP7B Structure and Function 349

    Google Scholar 

  • DiDonato, M., Zhang, J., Que, L., Jr., and arkar, B. (2002). J. Biol. Chem. 31, 31.

    Google Scholar 

  • Fatemi, N., and Sarkar, B. (in press). Inorg. Chim. Acta.

  • Fiser, A., and Sali, A. (in press). Methods Enzymol.

  • Forbes, J. R., and Cox, D. W. (1998). Am. J. Hum. Genet. 63, 1663–1674.

    Google Scholar 

  • Forbes, J. R., and Cox, D. W. (2000). Hum. Mol. Genet. 9, 1927–1935.

    Google Scholar 

  • Forbes, J. R., Hsi, G., and Cox, D.W. (1999). J. Biol. Chem. 274, 12408–12413.

    Google Scholar 

  • Fujisawa, K., Imai, S., Kitajima, M., and Moro-oka, Y. (1998). Inorg. Chem. 37, 168–169.

    Google Scholar 

  • Gitschier, J., Moffat, B., Reilly, D., Wood, W. I., and Fairbrother, W. J. (1998). Nat. Struct. Biol. 5, 47–54]

    Google Scholar 

  • Goodyer, I. D., Jones, E. E., Monaco, A. P., and Francis, M. J. (1999). Hum. Mol. Genet. 8, 1473–1478.

    Google Scholar 

  • Guex, N., and Peitsch, M. C. (1997). Electrophoresis 18, 2714–2723.

    Google Scholar 

  • Hisano, T., Hata, Y., Fujii, T., Liu, J. Q., Kurihara, T., Esaki, N., and Soda, K. (1996). J. Biol. Chem. 271, 20322–20330.

    Google Scholar 

  • Hou, Z.-J., Narindrasorasak, S., Bhushan, B., Sarkar, B., and Mitra, B. (2001). J. Biol. Chem. 276, 40858–40863.

    Google Scholar 

  • Jones, D. T., Taylor, W. R., and Thornton, J. M. (1992). Nature 358, 86–89.

    Google Scholar 

  • Kau, L.-S., Spira-Solomon, D. J., Penner-Hahn, J. E., Hodgson, K. O., and Solomon, E. I. (1987). J. Am. Chem. Soc. 109, 6433–6442.

    Google Scholar 

  • Koch, S. A., Millar, M., and O'sullivan, T. (1984). Inorg. Chem. 23, 122–124.

    Google Scholar 

  • Lutsenko, S., Petrukhin, K., Cooper, M. J., Gilliam, C. T., and Kaplan, J. H. (1997). J. Biol. Chem. 272, 18939–18944.

    Google Scholar 

  • Marti-Renom, M. A., Stuart, A. C., Fiser, A., Sanchez, R., Melo, F., and Sali, A. (2000). Annu. Rev. Biophys. Biomol. Struct. 29, 291–325.

    Google Scholar 

  • Mense, M., Dunbar, L. A., Blostein, R., and Caplan, M. J. (2000). J. Biol. Chem. 275, 1749–1756.

    Google Scholar 

  • O'Halloran, T. V. (1993). Science 261, 715–725.

    Google Scholar 

  • Petris, M. J., Mercer, J. F., Culvenor, J. G., Lockhart, P., Gleeson, P. A., and Camakaris, J. (1996). EMBO J. 15, 6084–6095.

    Google Scholar 

  • Petrukhin, K., Fischer, S. G., Pirastu, M., Tanzi, R. E., Chernov, I., Devoto, M., Brzustowicz, L. M., Cayanis, E., Vitale, E., Russo, J. J., Matseoane, D., Boukhgalter, B., Wasco, W., Figus, A. L., Loudianos, J., Cao, A., Sternlieb, I., Evgrafov, O., Parano, E., Pavone, L., Warburton, D., Ott, J., Penchaszadeh, G. K., Scheinberg, I. H., and Gilliam, T. C. (1993). Nat. Genet. 5, 338–343.

    Google Scholar 

  • Pickering, I. J., George, G. N., Dameron, C. T., Kurz, B., Winge, D. R., and Dance, I. G. (1993). J. Am. Chem. Soc. 115, 9498–9505.

    Google Scholar 

  • Pufahl, R. A., Singer, C. P., Peariso, K. L., Lin, S. J., Schmidt, P. J., Fahrni, C. J., Culotta, V. C., Penner-Hahn, J. E., and O'Halloran, T. V. (1997). Science 278, 853–856.

    Google Scholar 

  • Ralle, M., Cooper, M. J., Lutsenko, S., and Blackburn, N. J. (1998). J. Am. Chem. Soc. 120, 13525–13526.

    Google Scholar 

  • Rensing, C., Fan, B., Sharma, R., Mitra, B., and Rosen, B. P. (2000). Proc. Natl. Acad. Sci. U.S.A. 97, 652–656.

    Google Scholar 

  • Rensing, C., Mitra, B., and Rosen, B. P. (1997). Proc. Natl. Acad. Sci. U.S.A. 94, 14326–14331.

    Google Scholar 

  • Rensing, C., Sun, Y., Mitra, B., and Rosen, B. P. (1998). J. Biol. Chem. 273, 32614–32617.

    Google Scholar 

  • Rice, W. J., Young, H. S., Martin, D. W., Sachs, J. R., and Stokes, D. L. (2001). Biophys. J. 80, 2187–2197.

    Google Scholar 

  • Roberts, E. A., and Cox, D. W. (1998). Baillieres Clin. Gastroenterol. 12, 237–256.

    Google Scholar 

  • Roelofsen, H., Wolters, H., Van Luyn, M. J., Miura, N., Kuipers, F., and Vonk, R. J. (2000). Gastroenterology 119, 782–793.

    Google Scholar 

  • Rost, B. (1999). Protein Eng. 12, 85–94.

    Google Scholar 

  • Sali, A., and Kuriyan, J. (1999). Trends Cell Biol. 9, 20–24.

    Google Scholar 

  • Sanchez, R., and Sali, A. (1997). Curr. Opin. Struct. Biol. 7, 206–214.

    Google Scholar 

  • Sanchez, R., and Sali, A. (1998). Proc. Natl. Acad. Sci.U.S.A.95, 13597–13602.

    Google Scholar 

  • Saqi, M. A., Russell, R. B., and Sternberg, M. J. (1998). Protein Eng. 11, 627–630.

    Google Scholar 

  • Sass-Kortsak, A. (1975). Pediatr. Clin. North. Am. 22, 963–984.

    Google Scholar 

  • Scarborough, G. A. (2000). J. Exp. Biol. 203(Pt. 1), 147–154.

    Google Scholar 

  • Scheinberg, I. H., and Sternlieb, I. (1984). Wilson's Disease, Saunders, Philadelphia, PA.

  • Schiff, L. A., Nibert, M. L., and Fields, B. N. (1988). Proc. Natl. Acad. Sci. U.S.A. 85, 4195–4199.

    Google Scholar 

  • Sharma, R., Rensing, C., Rosen, B. P., and Mitra, B. (2000). J. Biol. Chem. 275, 3873–3878.

    Google Scholar 

  • Silver, S., Nucifora, G., Chu, L., and Misra, T. K. (1989). Trends Biochem. Sci. 14, 76–80.

    Google Scholar 

  • Sippl, M. J. (1990). J. Mol. Biol. 213, 859–883.

    Google Scholar 

  • Sippl, M. J. (1993). J. Comput-Aided Mol. Des. 7, 473–501.

    Google Scholar 

  • Srinivasan, C., Posewitz, M. C., George, G. N., and Winge, D. R. (1998). Biochemistry 37, 7572–7577.

    Google Scholar 

  • Stokes, D. L., and Green, N. M. (2000). Biophys. J. 78, 1765–1776.

    Google Scholar 

  • Strausak, D., La Fontaine, S., Hill, J., Firth, S. D., Lockhart, P. J., and Mercer, J. F. (1999). J. Biol. Chem. 274, 11170–11177.

    Google Scholar 

  • Sweadner, K. J., and Donnet, C. (2001). Biochem. J. 356, 685–704.

    Google Scholar 

  • Tanzi, R. E., Petrukhin, K., Chernov, I., Pellequer, J. L., Wasco, W., Ross, B., Romano, D. M., Parano, E., Pavone, L., Brzustowicz, L. M., Devoto, M., Peppercorn, J., Bush, A. I., Sternlieb, I., Pirastu, M., Gusella, J. F., Evgrafov, O., Penchaszadeh, G. K., Honig, B., Edelman, I. S., Soares, M. B., Scheinberg, I. H., and Gilliam, T. C. (1993). Nat. Genet. 5, 344–350.

    Google Scholar 

  • Toyoshima, C., Nakasako, M., Nomura, H., and Ogawa, H. (2000). Nature 405, 647–655.

    Google Scholar 

  • Tsivkovskii, R., Eisses, J. F., Kaplan, J. H., and Lutsenko, S. (2001a). J. Biol. Chem. 24, 24.

    Google Scholar 

  • Tsivkovskii, R., MacArthur, B. C., and Lutsenko, S. (2001b). J. Biol. Chem. 276, 2234–2242.

    Google Scholar 

  • Voskoboinik, I., Greenough, M., La Fontaine, S., Mercer, J. F., and Camakaris, J. (2001). Biochem. Biophys. Res. Commun. 281, 966–970.

    Google Scholar 

  • Wilson, S. A. K. (1912). Brain 34, 295–508.

    Google Scholar 

  • Wingfield, P. T., and Pain, R. H. (1996). In Current Protocols in Protein Science (Coligan, J. E., Dunn, B. M., Ploegh, H. L., Speicher, D.W., and Wingfield, P.T., eds.), Wiley, NewYork, Vol. 1, pp. 7.6.1–7.6.23.

  • Yamaguchi, Y., Heiny, M. E., and Gitlin, J. D. (1993). Biochem. Biophys. Res. Commun. 197, 271–277.

    Google Scholar 

  • Yamaguchi, Y., Heiny, M. E., Suzuki, M., and Gitlin, J. D. (1996). Proc. Natl. Acad. Sci. U.S.A. 93, 14030–14035.

    Google Scholar 

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Correspondence to Bibudhendra Sarkar.

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Fatemi, N., Sarkar, B. Structural and Functional Insights of Wilson Disease Copper-Transporting ATPase. J Bioenerg Biomembr 34, 339–349 (2002). https://doi.org/10.1023/A:1021245902195

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