1TR6
| NMR solution structure of omega-conotoxin [K10]GVIA, a cyclic cysteine knot peptide | Descriptor: | Omega-conotoxin GVIA | Authors: | Mould, J, Yasuda, T, Schroeder, C.I, Beedle, A.M, Doering, C.J, Zamponi, G.W, Adams, D.J, Lewis, R.J. | Deposit date: | 2004-06-21 | Release date: | 2004-07-13 | Last modified: | 2011-10-05 | Method: | SOLUTION NMR | Cite: | The alpha2delta auxiliary subunit reduces affinity of omega-conotoxins for recombinant N-type (Cav2.2) calcium channels J.Biol.Chem., 279, 2004
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6BTV
| Solution NMR structures for CcoTx-II | Descriptor: | Beta-theraphotoxin-Cm1b | Authors: | Agwa, A.J, Schroeder, C.I. | Deposit date: | 2017-12-07 | Release date: | 2018-05-09 | Last modified: | 2023-06-14 | Method: | SOLUTION NMR | Cite: | Gating modifier toxins isolated from spider venom: Modulation of voltage-gated sodium channels and the role of lipid membranes. J. Biol. Chem., 293, 2018
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6BR0
| Solution NMR structure for CcoTx-I | Descriptor: | Beta-theraphotoxin-Cm1a | Authors: | Agwa, A.J, Schroeder, C.I. | Deposit date: | 2017-11-29 | Release date: | 2018-05-16 | Last modified: | 2023-06-14 | Method: | SOLUTION NMR | Cite: | Gating modifier toxins isolated from spider venom: Modulation of voltage-gated sodium channels and the role of lipid membranes. J. Biol. Chem., 293, 2018
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2MH1
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7A64
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4NE9
| PCSK9 in complex with LDLR peptide | Descriptor: | 2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, Low-density lipoprotein receptor, ... | Authors: | Liu, S. | Deposit date: | 2013-10-28 | Release date: | 2014-09-10 | Last modified: | 2020-07-29 | Method: | X-RAY DIFFRACTION (2.6 Å) | Cite: | Design and synthesis of truncated EGF-A peptides that restore LDL-R recycling in the presence of PCSK9 in vitro. Chem.Biol., 21, 2014
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6PX7
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6PX8
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8FEY
| Solution structure of Pmu1a | Descriptor: | Pmu1a toxin | Authors: | Daly, N.L, Wilson, D.T. | Deposit date: | 2022-12-07 | Release date: | 2023-03-29 | Last modified: | 2023-08-02 | Method: | SOLUTION NMR | Cite: | Pmu1a, a novel spider toxin with dual inhibitory activity at pain targets hNa V 1.7 and hCa V 3 voltage-gated channels. Febs J., 290, 2023
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2N8E
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