5NN3
 
 | Crystal structure of human lysosomal acid-alpha-glucosidase, GAA | 分子名称: | 1,2-ETHANEDIOL, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Roig-Zamboni, V, Cobucci-Ponzano, B, Iacono, R, Ferrara, M.C, Germany, S, Parenti, G, Bourne, Y, Moracci, M. | 登録日 | 2017-04-08 | 公開日 | 2017-10-25 | 最終更新日 | 2024-11-20 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Structure of human lysosomal acid alpha-glucosidase-a guide for the treatment of Pompe disease. Nat Commun, 8, 2017
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5UF7
 
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6TC3
 
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5ECL
 
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1U27
 
 | Triglycine variant of the ARNO Pleckstrin Homology Domain in complex with Ins(1,3,4,5)P4 | 分子名称: | Cytohesin 2, INOSITOL-(1,3,4,5)-TETRAKISPHOSPHATE | 著者 | Cronin, T.C, DiNitto, J.P, Czech, M.P, Lambright, D.G. | 登録日 | 2004-07-16 | 公開日 | 2005-02-01 | 最終更新日 | 2023-08-23 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Structural determinants of phosphoinositide selectivity in splice variants of Grp1 family PH domains Embo J., 23, 2004
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6AX4
 
 | Plk-1 polo-box domain in complex with histidine N(tau)-cyclized Macrocycle 5b. | 分子名称: | AMYLAMINE, Serine/threonine-protein kinase PLK1, histidine N(tau)-cyclized Macrocycle 5b | 著者 | Grant, R.A, Hymel, D, Yaffe, M.B, Burke, T.R. | 登録日 | 2017-09-06 | 公開日 | 2018-09-12 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (1.45 Å) | 主引用文献 | Histidine N( tau )-cyclized macrocycles as a new genre of polo-like kinase 1 polo-box domain-binding inhibitors. Bioorg. Med. Chem. Lett., 28, 2018
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2RSV
 
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7HF1
 
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4OY2
 
 | Crystal structure of TAF1-TAF7, a TFIID subcomplex | 分子名称: | 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, Transcription initiation factor TFIID subunit 1, Transcription initiation factor TFIID subunit 7, ... | 著者 | Bhattacharya, S, Lou, X, Rajashankar, K, Jacobson, R.H, Webb, P. | 登録日 | 2014-02-10 | 公開日 | 2014-06-25 | 最終更新日 | 2024-11-20 | 実験手法 | X-RAY DIFFRACTION (2.9 Å) | 主引用文献 | Structural and functional insight into TAF1-TAF7, a subcomplex of transcription factor II D. Proc.Natl.Acad.Sci.USA, 111, 2014
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5ECH
 
 | Crystal Structure of FIN219-FIP1 complex with JA and ATP | 分子名称: | ADENOSINE-5'-TRIPHOSPHATE, GLUTATHIONE, Glutathione S-transferase U20, ... | 著者 | Chen, C.Y, Cheng, Y.S. | 登録日 | 2015-10-20 | 公開日 | 2016-11-02 | 最終更新日 | 2023-11-08 | 実験手法 | X-RAY DIFFRACTION (2.14 Å) | 主引用文献 | Structural basis of jasmonate-amido synthetase FIN219 in complex with glutathione S-transferase FIP1 during the JA signal regulation Proc. Natl. Acad. Sci. U.S.A., 114, 2017
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3LDJ
 
 | Crystal structure of aprotinin in complex with sucrose octasulfate: unusual interactions and implication for heparin binding | 分子名称: | 1,3,4,6-tetra-O-sulfo-beta-D-fructofuranose-(2-1)-2,3,4,6-tetra-O-sulfonato-alpha-D-glucopyranose, ACETATE ION, Pancreatic trypsin inhibitor | 著者 | Yang, I.S, Kim, T.G, Park, B.S, Kim, K.H. | 登録日 | 2010-01-13 | 公開日 | 2010-09-15 | 最終更新日 | 2025-05-07 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Crystal structures of aprotinin and its complex with sucrose octasulfate reveal multiple modes of interactions with implications for heparin binding. Biochem.Biophys.Res.Commun., 2010
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1O86
 
 | Crystal Structure of Human Angiotensin Converting Enzyme in complex with lisinopril. | 分子名称: | ANGIOTENSIN CONVERTING ENZYME, CHLORIDE ION, GLYCINE, ... | 著者 | Natesh, R, Schwager, S.L.U, Sturrock, E.D, Acharya, K.R. | 登録日 | 2002-11-25 | 公開日 | 2003-02-07 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Crystal Structure of the Human Angiotensin-Converting Enzyme-Lisinopril Complex Nature, 421, 2003
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7HFY
 
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7HF6
 
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3F67
 
 | Crystal Structure of Putative Dienelactone Hydrolase from Klebsiella pneumoniae subsp. pneumoniae MGH 78578 | 分子名称: | 1,2-ETHANEDIOL, ACETIC ACID, FORMIC ACID, ... | 著者 | Kim, Y, Li, H, Bearden, J, Joachimiak, A, Midwest Center for Structural Genomics (MCSG) | 登録日 | 2008-11-05 | 公開日 | 2008-11-25 | 最終更新日 | 2024-11-13 | 実験手法 | X-RAY DIFFRACTION (1.74 Å) | 主引用文献 | Crystal Structure of Putative Dienelactone Hydrolase from Klebsiella pneumoniae subsp. pneumoniae MGH 78578 To be Published
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6HVU
 
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1KNT
 
 | THE 1.6 ANGSTROMS STRUCTURE OF THE KUNITZ-TYPE DOMAIN FROM THE ALPHA3 CHAIN OF THE HUMAN TYPE VI COLLAGEN | 分子名称: | COLLAGEN TYPE VI, SULFATE ION | 著者 | Arnoux, B, Merigeau, K, Saludjian, P, Norris, F, Norris, K, Bjorn, S, Olsen, O, Petersen, L, Ducruix, A. | 登録日 | 1994-08-18 | 公開日 | 1994-11-01 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (1.6 Å) | 主引用文献 | The 1.6 A structure of Kunitz-type domain from the alpha 3 chain of human type VI collagen. J.Mol.Biol., 246, 1995
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5FL4
 
 | Three dimensional structure of human carbonic anhydrase IX in complex with 5-(1-naphthalen-1-yl-1,2,3-triazol-4-yl)thiophene-2-sulfonamide | 分子名称: | 5-(1-naphthalen-1-yl-1,2,3-triazol-4-yl)thiophene-2-sulfonamide, ACETIC ACID, CARBONIC ANHYDRASE 9, ... | 著者 | Leitans, J, Tars, K, Zalubovskis, R. | 登録日 | 2015-10-21 | 公開日 | 2015-11-11 | 最終更新日 | 2024-11-13 | 実験手法 | X-RAY DIFFRACTION (1.82 Å) | 主引用文献 | An Efficient Expression and Crystallization System of the Cancer Asociated Carbonic Anhydrase Isoform Ix. J.Med.Chem., 58, 2015
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4O78
 
 | Crystal structure of the first bromodomain of human BRD4 in complex with GW612286X | 分子名称: | 1,2-ETHANEDIOL, Bromodomain-containing protein 4, CHLORIDE ION, ... | 著者 | Zhu, J.-Y, Ember, S.W, Watts, C, Schonbrunn, E. | 登録日 | 2013-12-24 | 公開日 | 2014-03-05 | 最終更新日 | 2023-09-20 | 実験手法 | X-RAY DIFFRACTION (1.34 Å) | 主引用文献 | Acetyl-lysine Binding Site of Bromodomain-Containing Protein 4 (BRD4) Interacts with Diverse Kinase Inhibitors. Acs Chem.Biol., 9, 2014
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3FJD
 
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9K9N
 
 | Cryo-EM structure of MjHKU4r-CoV-1 receptor-binding domain complexed with human CD26 | 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, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Sun, J.Q. | 登録日 | 2024-10-27 | 公開日 | 2025-09-03 | 実験手法 | ELECTRON MICROSCOPY (2.61 Å) | 主引用文献 | Rational design of human CD26 receptor for a strong neutralizing ability against MjHKU4r-CoV-1 and MERS-CoV Hlife, 2025
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5UIQ
 
 | Crystal structure of IRAK4 in complex with compound 9 | 分子名称: | 2-[(propan-2-yl)oxy]benzamide, Interleukin-1 receptor-associated kinase 4 | 著者 | Han, S, Chang, J.S. | 登録日 | 2017-01-14 | 公開日 | 2017-05-24 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (2.64 Å) | 主引用文献 | Discovery of Clinical Candidate 1-{[(2S,3S,4S)-3-Ethyl-4-fluoro-5-oxopyrrolidin-2-yl]methoxy}-7-methoxyisoquinoline-6-carboxamide (PF-06650833), a Potent, Selective Inhibitor of Interleukin-1 Receptor Associated Kinase 4 (IRAK4), by Fragment-Based Drug Design. J. Med. Chem., 60, 2017
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5UIS
 
 | Crystal structure of IRAK4 in complex with compound 12 | 分子名称: | 4-{[(3R)-piperidin-3-yl]oxy}-6-[(propan-2-yl)oxy]quinoline-7-carboxamide, Interleukin-1 receptor-associated kinase 4 | 著者 | Han, S, Chang, J.S. | 登録日 | 2017-01-14 | 公開日 | 2017-05-24 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Discovery of Clinical Candidate 1-{[(2S,3S,4S)-3-Ethyl-4-fluoro-5-oxopyrrolidin-2-yl]methoxy}-7-methoxyisoquinoline-6-carboxamide (PF-06650833), a Potent, Selective Inhibitor of Interleukin-1 Receptor Associated Kinase 4 (IRAK4), by Fragment-Based Drug Design. J. Med. Chem., 60, 2017
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1KZV
 
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7HQS
 
 | PanDDA analysis group deposition -- Crystal Structure of FatA in complex with Z56912586 | 分子名称: | 1,3-benzothiazol-2-amine, Oleoyl-acyl carrier protein thioesterase 1, chloroplastic, ... | 著者 | Kot, E, Ni, X, Tomlinson, C.W.E, Fearon, D, Aschenbrenner, J.C, Fairhead, M, Koekemoer, L, Marx, M.L, Wright, N.D, Mulholland, N.P, Montgomery, M.G, von Delft, F. | 登録日 | 2024-12-23 | 公開日 | 2025-08-13 | 実験手法 | X-RAY DIFFRACTION (1.617 Å) | 主引用文献 | PanDDA analysis group deposition To Be Published
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