6PI3
 
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6PIO
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6PIP
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7RMQ
 | | Crystal structure of cycloviolacin O2 | | 分子名称: | Cycloviolacin O2, D-[I11L]cycloviolacin O2, FORMIC ACID | | 著者 | Huang, Y.H, Du, Q. | | 登録日 | 2021-07-28 | | 公開日 | 2021-09-22 | | 最終更新日 | 2023-11-15 | | 実験手法 | X-RAY DIFFRACTION (1.17 Å) | | 主引用文献 | Enabling Efficient Folding and High-Resolution Crystallographic Analysis of Bracelet Cyclotides.
Molecules, 26, 2021
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6Q1U
 | | Structure of plasmin and peptide complex | | 分子名称: | 1-methyl-1H-1,2,3-triazole, GLY-ARG-ALA-TYR-LYS-SER-LYS-PRO-PRO-ILE-ALA-PHE-PRO-ASP, Plasminogen | | 著者 | Wu, G, Law, R.H.P. | | 登録日 | 2019-08-06 | | 公開日 | 2020-04-15 | | 最終更新日 | 2023-10-11 | | 実験手法 | X-RAY DIFFRACTION (2.3467 Å) | | 主引用文献 | Application and Structural Analysis of Triazole-Bridged Disulfide Mimetics in Cyclic Peptides.
Angew.Chem.Int.Ed.Engl., 59, 2020
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7RJF
 | | MOPD-1 mutant-L47W | | 分子名称: | MALONATE ION, ZINC ION, [L47W]MOPD-1 | | 著者 | Huawu, Y, Conan, K.W, Gordon, J.K, Brett, M.C, Yen-Hua, H, David, J.C. | | 登録日 | 2021-07-20 | | 公開日 | 2021-10-27 | | 最終更新日 | 2023-10-18 | | 実験手法 | X-RAY DIFFRACTION (1.8 Å) | | 主引用文献 | Rational Design of Potent Peptide Inhibitors of the PD-1:PD-L1 Interaction for Cancer Immunotherapy.
J.Am.Chem.Soc., 143, 2021
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2JUE
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5WOV
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5WOW
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5TLR
 | | Solution NMR structure of gHwTx-IV | | 分子名称: | Mu-theraphotoxin-Hs2a | | 著者 | Agwa, A.J, Schroeder, C.I. | | 登録日 | 2016-10-11 | | 公開日 | 2017-02-22 | | 最終更新日 | 2023-06-14 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Spider peptide toxin HwTx-IV engineered to bind to lipid membranes has an increased inhibitory potency at human voltage-gated sodium channel hNaV1.7.
Biochim. Biophys. Acta, 1859, 2017
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8DW5
 | | Complex of Human Transthyretin with 3',5'-Dichlorophenylanthranilic Acid | | 分子名称: | 2-[(3,5-dichlorophenyl)amino]benzoic acid, Transthyretin | | 著者 | Truong, J.Q, Holdsworth, B, Holien, J.K. | | 登録日 | 2022-07-31 | | 公開日 | 2022-08-10 | | 最終更新日 | 2023-10-25 | | 実験手法 | X-RAY DIFFRACTION (1.52 Å) | | 主引用文献 | Structural Analysis of the Complex of Human Transthyretin with 3',5'-Dichlorophenylanthranilic Acid at 1.5 angstrom Resolution.
Molecules, 27, 2022
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6BVY
 | | SFTI-HFRW-4 | | 分子名称: | Trypsin inhibitor 1 HFRW-4 | | 著者 | Schroeder, C.I, White, A. | | 登録日 | 2017-12-14 | | 公開日 | 2018-04-18 | | 最終更新日 | 2023-11-15 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Development of Novel Melanocortin Receptor Agonists Based on the Cyclic Peptide Framework of Sunflower Trypsin Inhibitor-1.
J. Med. Chem., 61, 2018
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6BVX
 | | SFTI-HFRW-2 | | 分子名称: | Trypsin inhibitor 1 HFRW-2 | | 著者 | Schroeder, C.I. | | 登録日 | 2017-12-14 | | 公開日 | 2018-12-19 | | 最終更新日 | 2023-11-15 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Development of Novel Melanocortin Receptor Agonists Based on the Cyclic Peptide Framework of Sunflower Trypsin Inhibitor-1.
J.Med.Chem., 61, 2018
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6BR0
 | | Solution NMR structure for CcoTx-I | | 分子名称: | Beta-theraphotoxin-Cm1a | | 著者 | Agwa, A.J, Schroeder, C.I. | | 登録日 | 2017-11-29 | | 公開日 | 2018-05-16 | | 最終更新日 | 2023-06-14 | | 実験手法 | SOLUTION NMR | | 主引用文献 | 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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6BTV
 | | Solution NMR structures for CcoTx-II | | 分子名称: | Beta-theraphotoxin-Cm1b | | 著者 | Agwa, A.J, Schroeder, C.I. | | 登録日 | 2017-12-07 | | 公開日 | 2018-05-09 | | 最終更新日 | 2023-06-14 | | 実験手法 | SOLUTION NMR | | 主引用文献 | 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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6BVU
 | | SFTI-HFRW-1 | | 分子名称: | Trypsin inhibitor 1 HFRW-1 | | 著者 | Schroeder, C.I. | | 登録日 | 2017-12-13 | | 公開日 | 2018-12-19 | | 最終更新日 | 2023-06-14 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Development of Novel Melanocortin Receptor Agonists Based on the Cyclic Peptide Framework of Sunflower Trypsin Inhibitor-1.
J.Med.Chem., 61, 2018
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6BVW
 | | SFTI-HFRW-3 | | 分子名称: | Trypsin inhibitor 1 HFRW-3 | | 著者 | Schroeder, C.I. | | 登録日 | 2017-12-14 | | 公開日 | 2018-12-19 | | 最終更新日 | 2023-11-15 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Development of Novel Melanocortin Receptor Agonists Based on the Cyclic Peptide Framework of Sunflower Trypsin Inhibitor-1.
J.Med.Chem., 61, 2018
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6D3Z
 | | Protease SFTI complex | | 分子名称: | Plasminogen, Trypsin inhibitor 1 | | 著者 | Law, R.H.P, Wu, G. | | 登録日 | 2018-04-17 | | 公開日 | 2019-01-23 | | 最終更新日 | 2023-10-04 | | 実験手法 | X-RAY DIFFRACTION (2 Å) | | 主引用文献 | Highly Potent and Selective Plasmin Inhibitors Based on the Sunflower Trypsin Inhibitor-1 Scaffold Attenuate Fibrinolysis in Plasma.
J. Med. Chem., 62, 2019
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6DL1
 | | Racemic structure of jatrophidin, an orbitide from Jatropha curcas | | 分子名称: | jatrophidin | | 著者 | Wang, C.K, King, G.J, Ramalho, S.D. | | 登録日 | 2018-05-31 | | 公開日 | 2018-11-14 | | 最終更新日 | 2020-01-01 | | 実験手法 | X-RAY DIFFRACTION (1.029 Å) | | 主引用文献 | Synthesis, Racemic X-ray Crystallographic, and Permeability Studies of Bioactive Orbitides from Jatropha Species.
J. Nat. Prod., 81, 2018
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6D40
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6D3Y
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6DL0
 | | Crystal structure of pohlianin C, an orbitide from Jatropha pohliana | | 分子名称: | pohlianin C | | 著者 | Wang, C.K, King, G.J, Ramalho, S.D. | | 登録日 | 2018-05-31 | | 公開日 | 2018-11-07 | | 最終更新日 | 2023-07-26 | | 実験手法 | X-RAY DIFFRACTION (1.2 Å) | | 主引用文献 | Synthesis, Racemic X-ray Crystallographic, and Permeability Studies of Bioactive Orbitides from Jatropha Species.
J. Nat. Prod., 81, 2018
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6D3X
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2MG9
 | | Truncated EGF-A | | 分子名称: | CALCIUM ION, Low-density lipoprotein receptor | | 著者 | Schroeder, C.I, Rosengren, K. | | 登録日 | 2013-10-30 | | 公開日 | 2014-04-02 | | 実験手法 | SOLUTION NMR | | 主引用文献 | 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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2LZ5
 | | Solution structure of a Novel Alpha-Conotoxin TxIB | | 分子名称: | Conotoxin_TxIB | | 著者 | Luo, S, Zhangsun, D, Wu, Y, Zhu, X, Hu, Y, McIntyre, M, Christensen, S, Akcan, M, Craik, D, McIntosh, J. | | 登録日 | 2012-09-23 | | 公開日 | 2012-12-05 | | 最終更新日 | 2023-06-14 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Characterization of a novel alpha-conotoxin from conus textile that selectively targets alpha6/alpha3beta2beta3 nicotinic acetylcholine receptors.
J.Biol.Chem., 288, 2013
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