3RTY
| Structure of an Enclosed Dimer Formed by The Drosophila Period Protein | 分子名称: | 2,3-DIHYDROXY-1,4-DITHIOBUTANE, Period circadian protein | 著者 | King, H.A, Hoelz, A, Crane, B.R, Young, M.W. | 登録日 | 2011-05-04 | 公開日 | 2011-12-21 | 実験手法 | X-RAY DIFFRACTION (2.85 Å) | 主引用文献 | Structure of an enclosed dimer formed by the Drosophila period protein. J.Mol.Biol., 413, 2011
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4CZ3
| HP24wt derived from the villin headpiece subdomain | 分子名称: | VILLIN-1 | 著者 | Hocking, H, Haese, F, Madl, T, Zacharias, M, Rief, M, Zoldak, G. | 登録日 | 2014-04-16 | 公開日 | 2015-02-18 | 最終更新日 | 2023-06-14 | 実験手法 | SOLUTION NMR | 主引用文献 | A Compact Native 24-Residue Supersecondary Structure Derived from the Villin Headpiece Subdomain. Biophys.J., 108, 2015
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4CZ4
| HP24stab derived from the villin headpiece subdomain | 分子名称: | VILLIN-1 | 著者 | Hocking, H, Haese, F, Madl, T, Zacharias, M, Rief, M, Zoldak, G. | 登録日 | 2014-04-16 | 公開日 | 2015-02-18 | 最終更新日 | 2023-06-14 | 実験手法 | SOLUTION NMR | 主引用文献 | A Compact Native 24-Residue Supersecondary Structure Derived from the Villin Headpiece Subdomain. Biophys.J., 108, 2015
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4B1Q
| NMR structure of the glycosylated conotoxin CcTx from Conus consors | 分子名称: | CONOTOXIN CCTX, alpha-L-galactopyranose-(1-2)-beta-D-galactopyranose-(1-3)-[alpha-L-galactopyranose-(1-4)-2-acetamido-2-deoxy-alpha-D-glucopyranose-(1-6)]2-acetamido-2-deoxy-alpha-D-galactopyranose | 著者 | Hocking, H.G, Gerwig, G.J, Favreau, P, Stocklin, R, Kamerling, J.P, Boelens, R. | 登録日 | 2012-07-12 | 公開日 | 2013-02-06 | 最終更新日 | 2020-07-29 | 実験手法 | SOLUTION NMR | 主引用文献 | Structure of the O-Glycosylated Conopeptide Cctx from Conus Consors Venom. Chemistry, 19, 2013
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2RLQ
| NMR structure of CCP modules 2-3 of complement factor H | 分子名称: | Complement factor H | 著者 | Hocking, H.G, Herbert, A.P, Pangburn, M.K, Kavanagh, D, Barlow, P.N, Uhrin, D. | 登録日 | 2007-07-29 | 公開日 | 2008-02-19 | 最終更新日 | 2024-10-16 | 実験手法 | SOLUTION NMR | 主引用文献 | Structure of the N-terminal region of complement factor H and conformational implications of disease-linked sequence variations. J.Biol.Chem., 283, 2008
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2RLP
| NMR structure of CCP modules 1-2 of complement factor H | 分子名称: | Complement factor H | 著者 | Hocking, H.G, Herbert, A.P, Pangburn, M.K, Kavanagh, D, Barlow, P.N, Uhrin, D. | 登録日 | 2007-07-28 | 公開日 | 2008-02-19 | 最終更新日 | 2022-03-16 | 実験手法 | SOLUTION NMR | 主引用文献 | Structure of the N-terminal region of complement factor H and conformational implications of disease-linked sequence variations. J.Biol.Chem., 283, 2008
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7AST
| Apo Human RNA Polymerase III | 分子名称: | DNA-directed RNA polymerase III subunit RPC1, DNA-directed RNA polymerase III subunit RPC10, DNA-directed RNA polymerase III subunit RPC2, ... | 著者 | Ramsay, E.P, Abascal-Palacios, G, Daiss, J.L, King, H, Gouge, J, Pilsl, M, Beuron, F, Morris, E, Gunkel, P, Engel, C, Vannini, A. | 登録日 | 2020-10-28 | 公開日 | 2020-12-23 | 最終更新日 | 2020-12-30 | 実験手法 | ELECTRON MICROSCOPY (4 Å) | 主引用文献 | Structure of human RNA polymerase III. Nat Commun, 11, 2020
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3ZKT
| SOLUTION STRUCTURE OF THE SOMATOSTATIN SST3 RECEPTOR ANTAGONIST TAU- CONOTOXIN CnVA | 分子名称: | TAU-CNVA | 著者 | Petrel, C, Hocking, H.G, Reynaud, M, Favreau, P, Paolini-Bertrand, M, Peigneur, S, Upert, G, Tytgat, J, Gilles, N, Hartley, O, Boelens, R, Stocklin, R, Servent, D. | 登録日 | 2013-01-24 | 公開日 | 2013-04-24 | 最終更新日 | 2023-06-14 | 実験手法 | SOLUTION NMR | 主引用文献 | Identification, Structural and Pharmacological Characterization of Tau-Cnva, a Conopeptide that Selectively Interacts with Somatostatin Sst3 Receptor. Biochem.Pharmacol, 85, 2013
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2YEN
| Solution structure of the skeletal muscle and neuronal voltage gated sodium channel antagonist mu-conotoxin CnIIIC | 分子名称: | Mu-conotoxin CnIIIC | 著者 | Favreau, P, Benoit, E, Hocking, H.G, Carlier, L, D'hoedt, D, Leipold, E, Markgraf, R, Schlumberger, S, Cordova, M.A, Gaertner, H, Paolini-Bertrand, M, Hartley, O, Tytgat, J, Heinemann, S.H, Bertrand, D, Boelens, R, Stocklin, R, Molgo, J. | 登録日 | 2011-03-28 | 公開日 | 2012-02-08 | 最終更新日 | 2023-06-14 | 実験手法 | SOLUTION NMR | 主引用文献 | A Novel Mu-Conopeptide, Cniiic, Exerts Potent and Preferential Inhibition of Na(V) 1.2/1.4 Channels and Blocks Neuronal Nicotinic Acetylcholine Receptors. Br.J.Pharmacol., 166, 2012
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1YZ5
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