1IP0
| NMR STRUCTURE OF HUMAN BETACELLULIN-2 | 分子名称: | BETACELLULIN | 著者 | Miura, K, Doura, H, Aizawa, T, Tada, H, Seno, M, Yamada, H, Kawano, K. | 登録日 | 2001-04-19 | 公開日 | 2002-07-31 | 最終更新日 | 2023-12-27 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution structure of betacellulin, a new member of EGF-family ligands. Biochem.Biophys.Res.Commun., 294, 2002
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1IOX
| NMR Structure of human Betacellulin-2 | 分子名称: | Betacellulin | 著者 | Miura, K, Doura, H, Aizawa, T, Tada, H, Seno, M, Yamada, H, Kawano, K. | 登録日 | 2001-04-18 | 公開日 | 2002-07-24 | 最終更新日 | 2023-12-27 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution structure of betacellulin, a new member of EGF-family ligands. Biochem.Biophys.Res.Commun., 294, 2002
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1LJZ
| NMR structure of an AChR-peptide (Torpedo Californica, alpha-subunit residues 182-202) in complex with alpha-Bungarotoxin | 分子名称: | Acetylcholine receptor protein, alpha-Bungarotoxin | 著者 | Samson, A.O, Scherf, T, Eisenstein, M, Chill, J.H, Anglister, J. | 登録日 | 2002-04-23 | 公開日 | 2002-07-17 | 最終更新日 | 2013-07-24 | 実験手法 | SOLUTION NMR | 主引用文献 | The mechanism for acetylcholine receptor inhibition by alpha-neurotoxins and species-specific resistance to alpha-bungarotoxin revealed by NMR. Neuron, 35, 2002
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1L4W
| NMR structure of an AChR-peptide (Torpedo Californica, alpha-subunit residues 182-202) in complex with alpha-Bungarotoxin | 分子名称: | Acetylcholine receptor protein, alpha-Bungarotoxin | 著者 | Samson, A.O, Scherf, T, Rodriguez, E, Eisenstein, M, Anglister, J. | 登録日 | 2002-03-06 | 公開日 | 2002-07-17 | 最終更新日 | 2022-02-23 | 実験手法 | SOLUTION NMR | 主引用文献 | The mechanism for acetylcholine receptor inhibition by alpha-neurotoxins and species-specific resistance to alpha-bungarotoxin revealed by NMR. Neuron, 35, 2002
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1LO5
| Crystal structure of the D227A variant of Staphylococcal enterotoxin A in complex with human MHC class II | 分子名称: | HLA class II histocompatibility antigen, DR alpha chain, DR-1 beta chain, ... | 著者 | Petersson, K, Thunnissen, M, Forsberg, G, Walse, B. | 登録日 | 2002-05-06 | 公開日 | 2002-12-18 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (3.2 Å) | 主引用文献 | Crystal Structure of a SEA Variant in Complex with MHC Class II Reveals the Ability of SEA to Crosslink MHC Molecules Structure, 10, 2002
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3DN5
| Aldose Reductase in complex with novel biarylic inhibitor | 分子名称: | 3-[5-(3-nitrophenyl)thiophen-2-yl]propanoic acid, Aldose reductase, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE | 著者 | Steuber, H, Klebe, G. | 登録日 | 2008-07-01 | 公開日 | 2009-04-07 | 最終更新日 | 2023-11-01 | 実験手法 | X-RAY DIFFRACTION (1.45 Å) | 主引用文献 | Structure-Based Optimization of Aldose Reductase Inhibitors Originating from Virtual Screening Chemmedchem, 4, 2009
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2K37
| CsmA | 分子名称: | Chlorosome Protein A | 著者 | Pedersen, M, Dittmer, J, Underhaug, J, Miller, M, Nielsen, N.C. | 登録日 | 2008-04-23 | 公開日 | 2008-09-02 | 最終更新日 | 2024-05-08 | 実験手法 | SOLUTION NMR | 主引用文献 | The three-dimensional structure of CsmA: A small antenna protein from the green sulfur bacterium Chlorobium tepidum. Febs Lett., 582, 2008
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2POX
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7P2D
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7XIM
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3CHQ
| Crystal structure of leukotriene a4 hydrolase in complex with N5-[4-(phenylmethoxy)phenyl]-L-glutamine | 分子名称: | (2S)-2-amino-5-oxo-5-[(4-phenylmethoxyphenyl)amino]pentanoic acid, IMIDAZOLE, Leukotriene A-4 hydrolase, ... | 著者 | Thunnissen, M.M.G.M, Adler, M, Whitlow, M. | 登録日 | 2008-03-10 | 公開日 | 2008-04-22 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2.09 Å) | 主引用文献 | Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A4 hydrolase. Bioorg.Med.Chem., 16, 2008
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3CHR
| Crystal structure of leukotriene A4 hydrolase in complex with 4-amino-N-[4-(phenylmethoxy)phenyl]-butanamide | 分子名称: | 4-amino-N-[4-(benzyloxy)phenyl]butanamide, IMIDAZOLE, Leukotriene A-4 hydrolase, ... | 著者 | Thunnissen, M.M.G.M, Adler, M, Whitlow, M. | 登録日 | 2008-03-10 | 公開日 | 2008-04-22 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Synthesis of glutamic acid analogs as potent inhibitors of leukotriene A4 hydrolase. Bioorg.Med.Chem., 16, 2008
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1VST
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6YO6
| Structure of iC3b1 | 分子名称: | hC3Nb1, iC3b1 alpha chain, iC3b1 beta chain | 著者 | Jensen, R.K, Andersen, G.R. | 登録日 | 2020-04-14 | 公開日 | 2021-02-24 | 最終更新日 | 2024-01-24 | 実験手法 | X-RAY DIFFRACTION (6 Å) | 主引用文献 | Complement Receptor 3 Forms a Compact High-Affinity Complex with iC3b. J Immunol., 206, 2021
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4X08
| Structure of H128N/ECP mutant in complex with sulphate anions at 1.34 Angstroms. | 分子名称: | Eosinophil cationic protein, SULFATE ION | 著者 | Blanco, J.A, Garcia, J.M, Salazar, V.A, Sanchez, D, Moussauoi, M, Boix, E. | 登録日 | 2014-11-21 | 公開日 | 2015-10-07 | 最終更新日 | 2024-01-10 | 実験手法 | X-RAY DIFFRACTION (1.34 Å) | 主引用文献 | Structure of H128N/ECP mutant in complex with sulphate anions at 1.34 Angstroms. To Be Published
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5LJM
| Structure of SPATA2 PUB domain | 分子名称: | GLYCEROL, Spermatogenesis-associated protein 2 | 著者 | Elliott, P.R, Komander, D. | 登録日 | 2016-07-18 | 公開日 | 2016-08-24 | 最終更新日 | 2024-05-01 | 実験手法 | X-RAY DIFFRACTION (1.454 Å) | 主引用文献 | SPATA2 Links CYLD to LUBAC, Activates CYLD, and Controls LUBAC Signaling. Mol.Cell, 63, 2016
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6DCV
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6DCW
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3T3P
| A Novel High Affinity Integrin alphaIIbbeta3 Receptor Antagonist That Unexpectedly Displaces Mg2+ from the beta3 MIDAS | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, ... | 著者 | Zhu, J, Zhu, J, Springer, T.A. | 登録日 | 2011-07-25 | 公開日 | 2012-03-28 | 最終更新日 | 2020-07-29 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Structure-Guided Design of a High-Affinity Platelet Integrin alphaIIbbeta3 Receptor Antagonist That Disrupts Mg2+ Binding to the MIDAS Sci Transl Med, 4, 2012
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3T3M
| A Novel High Affinity Integrin alphaIIbbeta3 Receptor Antagonist That Unexpectedly Displaces Mg2+ from the beta3 MIDAS | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, ... | 著者 | Zhu, J, Zhu, J, Springer, T.A. | 登録日 | 2011-07-25 | 公開日 | 2012-03-28 | 最終更新日 | 2023-11-29 | 実験手法 | X-RAY DIFFRACTION (2.6 Å) | 主引用文献 | Structure-Guided Design of a High-Affinity Platelet Integrin alphaIIbbeta3 Receptor Antagonist That Disrupts Mg2+ Binding to the MIDAS Sci Transl Med, 4, 2012
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8GCE
| The Extracellular Domain of Integrin AlphaIIbBeta3 in Intermediate State | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, ... | 著者 | Huo, T, Wu, H, Wang, Z. | 登録日 | 2023-03-01 | 公開日 | 2024-03-06 | 最終更新日 | 2024-10-09 | 実験手法 | ELECTRON MICROSCOPY (3.12 Å) | 主引用文献 | Full-length alpha IIb beta 3 cryo-EM structure reveals intact integrin initiate-activation intrinsic architecture. Structure, 32, 2024
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8GCD
| Full length Integrin AlphaIIbBeta3 in inactive state | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, ... | 著者 | Huo, T, Wu, H, Wang, Z. | 登録日 | 2023-03-01 | 公開日 | 2024-03-06 | 最終更新日 | 2024-10-09 | 実験手法 | ELECTRON MICROSCOPY (2.97 Å) | 主引用文献 | Full-length alpha IIb beta 3 cryo-EM structure reveals intact integrin initiate-activation intrinsic architecture. Structure, 32, 2024
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4UX9
| Crystal structure of JNK1 bound to a MKK7 docking motif | 分子名称: | DUAL SPECIFICITY MITOGEN-ACTIVATED PROTEIN KINASE KINASE 7, MITOGEN-ACTIVATED PROTEIN KINASE 8, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER, ... | 著者 | Kragelj, J, Palencia, A, Nanao, M.H, Maurin, D, Bouvignies, G, Blackledge, M, Ringkjobing-Jensen, M. | 登録日 | 2014-08-20 | 公開日 | 2015-03-25 | 最終更新日 | 2024-01-10 | 実験手法 | X-RAY DIFFRACTION (2.34 Å) | 主引用文献 | Structure and Dynamics of the Mkk7-Jnk Signaling Complex. Proc.Natl.Acad.Sci.USA, 112, 2015
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9XIM
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7O6U
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