DOI: 10.1038/31978. Crystal structure of the tetramerization domain of the Shaker potassium channel

Crystal structure of the tetramerization domain of the Shaker potassium channel

10.1038/31978

Crossref journal-article

Springer Science and Business Media LLC

Nature (297)

Bibliography

Kreusch, A., Pfaffinger, P. J., Stevens, C. F., & Choe, S. (1998). Crystal structure of the tetramerization domain of the Shaker potassium channel. Nature, 392(6679), 945â948.

Authors 4

Andreas Kreusch (first)
Paul J. Pfaffinger (additional)
Charles F. Stevens (additional)
Senyon Choe (additional)

References 30 Referenced 249

Noda, M. et al. Primary structure of Electrophorus electricus sodium channel deduced from cDNA sequence. Nature 312, 121–127 (1984). (10.1038/312121a0) / Nature by M Noda (1984)
Tanabe, T. et al. Primary structure of the receptor for calcium channel blockers from skeletal muscle. Nature 328, 313– 318 (1987). (10.1038/328313a0) / Nature by T Tanabe (1987)
Papazian, D. M., Schwarz, T. L., Tempel, B. L., Jan, Y. N. & Jan, Y. L. Cloning of genomic and complementary DNA from Shaker, a putative potassium channel gene form Drosophila. Science 237, 749–753 ( 1987). (10.1126/science.2441470) / Science by DM Papazian (1987)
MacKinnon, R. Determination of the subunit stoichiometry of a voltage-activated potassium channel. Nature 350, 232– 235 (1991). (10.1038/350232a0) / Nature by R MacKinnon (1991)
Li, M., Unwin, N., Stauffer, K. A., Jan, L. Y. & Jan, Y. N. Images of purified Shaker potassium channels. Curr. Biol. 4, 110– 115 (1994). (10.1016/S0960-9822(94)00026-6) / Curr. Biol. by M Li (1994)
Miller, C. 1990: Annus mirabilis of potassium channels. Science 252, 1092–1095 (1991). (10.1126/science.252.5009.1092) / Science by C Miller (1991)
Shen, N. V., Chen, X., Boyer, M. M. & Pfaffinger, P. J. Deletion analysis of K+ channel assembly. Neuron 11, 67–76 (1993). (10.1016/0896-6273(93)90271-R) / Neuron by NV Shen (1993)
Li, M., Jan, Y. N. & Jan, L. Y. Specification of subunit assembly by the hydrophilic amino-terminal domain of the Shaker potassium channel. Science 257, 1225–1230 (1992). (10.1126/science.1519059) / Science by M Li (1992)
Schwarz, T. L., Tempel, B. L., Papazian, D. M., Jan, Y. N. & Jan, L. Y. Multiple potassium-channel components are produced by alternative splicing at the Shaker locus in Drosophila . Nature 331, 137–142 (1988). (10.1038/331137a0) / Nature by TL Schwarz (1988)
Wei, A. et al. K+ current diversity is produced by an extended gene family conserved in Drosophila and mouse. Science 248, 599–603 (1990). (10.1126/science.2333511) / Science by A Wei (1990)
Stühmer, W. et al. Molecular basis of functional diversity of voltage-gated potassium channels in mammalian brain. EMBO J. 8, 3235–3244 (1989). (10.1002/j.1460-2075.1989.tb08483.x) / EMBO J. by W Stühmer (1989)
Holm, L. & Sander, C. Protein structure comparison by alignments of distance matrices. J. Mol. Biol. 233, 123–138 (1993). (10.1006/jmbi.1993.1489) / J. Mol. Biol. by L Holm (1993)
Murzin, A. G., Brenner, S. E., Hubbard, S. T. & Chothia, C. “SCOP”: a structural classification of proteins database for the investigation of sequences and structures. J. Mol. Biol. 247, 536–540 (1995). / J. Mol. Biol. by AG Murzin (1995)
Hol, W. G., van Duijnen, P. T. & Berendsen, H. J. The alpha-helix dipole and the properties of proteins. Nature 273, 443–446 (1978). (10.1038/273443a0) / Nature by WG Hol (1978)
Hoshi, T., Zagotta, W. N. & Aldrich, R. W. Biophysical and molecular mechanisms of Shaker potassium channel inactivation. Science 250, 533– 538 (1990). (10.1126/science.2122519) / Science by T Hoshi (1990)
MacKinnon, R., Aldrich, R. W. & Lee, A. W. Functional stoichiometry of Shaker potassium channel inactivation. Science 262, 757– 759 (1993). (10.1126/science.7694359) / Science by R MacKinnon (1993)
Foster, C. D., Chung, S., Zagotta, W. N., Aldrich, R. W. & Levitan, I. B. Apeptide derived from the ShakerB K+ channel produces short and long blocks of reconstituted Ca2+-dependent K+ channels. Neuron 9, 229–236 ( 1992). (10.1016/0896-6273(92)90162-7) / Neuron by CD Foster (1992)
Toro, L., Stefani, E. & Latorre, R. Internal blockade of a Ca2+-activated K+ channel by ShakerB inactivating “ball” peptide. Neuron 9, 237–245 (1992). (10.1016/0896-6273(92)90163-8) / Neuron by L Toro (1992)
Antz, C. et al. NMR structure of inactivation gates from mammalian voltage-dependent potassium channels. Nature 385, 272– 274 (1997). (10.1038/385272a0) / Nature by C Antz (1997)
Isacoff, E. Y., Jan, Y. N. & Jan, L. Y. Putative receptor for the cytoplasmic inactivation gate in the Shaker K+ channel. Nature 353 , 86–90 (1991). (10.1038/353086a0) / Nature by EY Isacoff (1991)
Liu, T., Holmgren, M., Jurman, M. E. & Yellen, G. Gated access to the pore of a voltage-dependent K+ channel. Neuron 19, 175–184 (1997). (10.1016/S0896-6273(00)80357-8) / Neuron by T Liu (1997)
Mannuzzu, L. M., Moronne, M. M. & Isacoff, E. Y. Direct physical measure of conformational rearrangement underlying potassium channel gating. Science 271, 213–216 (1996). (10.1126/science.271.5246.213) / Science by LM Mannuzzu (1996)
Otwinowski, Z. in Data Collection and Processing (eds Swayer, L., Isaac, N. & Bailey, S.) 56–62 (SERC Daresbury Laboratory, Warrington, UK, 1993). / Data Collection and Processing by Z Otwinowski (1993)
Hendrickson, W. A. Determination of macromolecular structures from anomalous diffraction of synchrotron radiation. Science 254, 51– 58 (1991). (10.1126/science.1925561) / Science by WA Hendrickson (1991)
Collaborative Computational Project, Number4. The CCP4 Suite: Programs for Crystallography. Acta Crystallogr. D 50, 670– 673 (1994). / Acta Crystallogr. D by Number4 Collaborative Computational Project (1994)
Jones, T. A., Zou, J. Y., Cowan, S. W. & Kjelgard, M. W. Improved methods for building protein models in electron density maps and the location of errors in these models. Acta Crystallogr. A 47, 110–119 (1991). (10.1107/S0108767390010224) / Acta Crystallogr. A by TA Jones (1991)
Brunger, A. T. X-PLOR Version 3.8(Dept of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT, 1996).
Navaza, J. AMoRe: an automated package for molecular replacement. Acta Crystallogr. A 50, 157–163 ( 1994). (10.1107/S0108767393007597) / Acta Crystallogr. A by J Navaza (1994)
Evans, S. V. SETOR: hardware lighted three-dimensional solid model representations of macromolecules. J. Mol. Graph. 11, 134– 138 (1993). (10.1016/0263-7855(93)87009-T) / J. Mol. Graph. by SV Evans (1993)
Nicholls, A., Sharp, K. & Honig, B. Protein folding and association: insights from the interfacial and thermodynamic properties of hydrocarbons. Proteins Struc. Funct. Genet. 11, 281–296 ( 1991). (10.1002/prot.340110407) / Proteins Struc. Funct. Genet. by A Nicholls (1991)

Dates

Type	When
Created	23 years, 1 month ago (July 26, 2002, 4:37 a.m.)
Deposited	2 years, 3 months ago (May 16, 2023, 9:14 p.m.)
Indexed	3 weeks, 3 days ago (Aug. 7, 2025, 5:03 p.m.)
Issued	27 years, 5 months ago (April 1, 1998)
Published	27 years, 5 months ago (April 1, 1998)
Published Print	27 years, 5 months ago (April 1, 1998)

Funders 0

None

BibTeX

@article{Kreusch_1998, title={Crystal structure of the tetramerization domain of the Shaker potassium channel}, volume={392}, ISSN={1476-4687}, url={http://dx.doi.org/10.1038/31978}, DOI={10.1038/31978}, number={6679}, journal={Nature}, publisher={Springer Science and Business Media LLC}, author={Kreusch, Andreas and Pfaffinger, Paul J. and Stevens, Charles F. and Choe, Senyon}, year={1998}, month=apr, pages={945–948} }

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