PDB: 37044 件ウェブページステータス検索Chemie searchBIRD

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1UJ0	Crystal Structure of STAM2 SH3 domain in complex with a UBPY-derived peptide 分子名称: PHOSPHATE ION, deubiquitinating enzyme UBPY, signal transducing adaptor molecule (SH3 domain and ITAM motif) 2 著者 Kaneko, T, Kumasaka, T, Ganbe, T, Sato, T, Miyazawa, K, Kitamura, N, Tanaka, N. 登録日 2003-07-24 公開日 2003-12-23 最終更新日 2023-12-27 実験手法 X-RAY DIFFRACTION (1.7 Å) 主引用文献 Structural insight into modest binding of a non-PXXP ligand to the signal transducing adaptor molecule-2 Src homology 3 domain. J.Biol.Chem., 278, 2003
1W11	UROKINASE TYPE PLASMINOGEN ACTIVATOR 分子名称: N-(BENZYLSULFONYL)-D-SERYL-N-{4-[AMINO(IMINO)METHYL]BENZYL}-L-ALANINAMIDE, SULFATE ION, UROKINASE-TYPE PLASMINOGEN ACTIVATOR 著者 Jacob, U. 登録日 2004-06-15 公開日 2008-05-20 最終更新日 2019-10-09 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Crystals of Urokinase Type Plasminogen Activator Complexes Reveal the Binding Mode of Peptidomimetic Inhibitors. J.Mol.Biol., 328, 2003
1W1F	SH3 DOMAIN OF HUMAN LYN TYROSINE KINASE 分子名称: TYROSINE-PROTEIN KINASE LYN 著者 Bauer, F, Schweimer, K, Hoffmann, S, Roesch, P, Sticht, H. 登録日 2004-06-17 公開日 2005-07-06 最終更新日 2024-05-15 実験手法 SOLUTION NMR 主引用文献 Structural Characterization of Lyn-SH3 Domain in Complex with a Herpesviral Protein Reveals an Extended Recognition Motif that Enhances Binding Affinity. Protein Sci., 14, 2005
1W20	Structure of Neuraminidase from English duck subtype N6 complexed with 30 mM sialic acid (NANA, Neu5Ac), crystal soaked for 3 hours at 291 K 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 Rudino-Pinera, E, Tunnah, P, Crennell, S.J, Webster, R.G, Laver, W.G, Garman, E.F. 登録日 2004-06-24 公開日 2006-01-25 最終更新日 2023-12-13 実験手法 X-RAY DIFFRACTION (2.08 Å) 主引用文献 The Crystal Structure of Type a Influenza Virus Neuraminidase of the N6 Subtype Reveals the Existence of Two Separate Neu5Ac Binding Sites To be Published
1W2R	Solution structure of CR2 SCR 1-2 by X-ray scattering 分子名称: COMPLEMENT RECEPTOR TYPE 2 PRECURSOR, 著者 Gilbert, H.E, Hannan, J.P, Holers, V.M, Perkins, S.J. 登録日 2004-07-08 公開日 2005-09-29 最終更新日 2024-05-08 実験手法 SOLUTION SCATTERING 主引用文献 Solution Structure of the Complex between Cr2 Scr 1-2 and C3D of Human Complement: An X-Ray Scattering and Sedimentation Modelling Study. J.Mol.Biol., 346, 2005
1W6I	plasmepsin II-pepstatin A complex 分子名称: PEPSTATIN, PLASMEPSIN 2 PRECURSOR 著者 Lindberg, J, Johansson, P.-O, Rosenquist, A, Kvarnstroem, I, Vrang, L, Samuelsson, B, Unge, T. 登録日 2004-08-18 公開日 2006-07-05 最終更新日 2018-01-17 実験手法 X-RAY DIFFRACTION (2.7 Å) 主引用文献 Structural Study of a Novel Inhibitor with Bulky P1 Side Chain in Complex with Plasmepsin II -Implications for Drug Design To be Published
1WAV	CRYSTAL STRUCTURE OF FORM B MONOCLINIC CRYSTAL OF INSULIN 分子名称: INSULIN, PHENOL, ZINC ION 著者 Liang, D.-C, Ding, J.-H, Chang, W.-R, Wan, Z.-L. 登録日 1996-02-28 公開日 1997-02-28 最終更新日 2024-06-05 実験手法 X-RAY DIFFRACTION (2.5 Å) 主引用文献 Molecular replacement study on form-B monoclinic crystal of insulin. Sci.China, Ser.C: Life Sci., 39, 1996
1W13	UROKINASE TYPE PLASMINOGEN ACTIVATOR 分子名称: N-(BENZYLSULFONYL)-D-SERYL-N-(4-{[AMINO(IMINO)METHYL]AMINO}BENZYL)-L-ALANINAMIDE, SULFATE ION, UROKINASE-TYPE PLASMINOGEN ACTIVATOR 著者 Jacob, U. 登録日 2004-06-15 公開日 2008-05-20 最終更新日 2019-05-22 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Crystals of Urokinase Type Plasminogen Activator Complexes Reveal the Binding Mode of Peptidomimetic Inhibitors. J.Mol.Biol., 328, 2003
1W2L	Cytochrome c domain of caa3 oxygen oxidoreductase 分子名称: 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, ACETATE ION, CYTOCHROME OXIDASE SUBUNIT II, ... 著者 Srinivasan, V, Rajendran, C, Sousa, F.L, Melo, A.M.P, Saraiva, L.M, Pereira, M.M, Santana, M, Teixeira, M, Michel, H. 登録日 2004-07-06 公開日 2005-01-19 最終更新日 2019-05-22 実験手法 X-RAY DIFFRACTION (1.3 Å) 主引用文献 Structure at 1.3 A resolution of Rhodothermus marinus caa(3) cytochrome c domain. J. Mol. Biol., 345, 2005
1W84	p38 Kinase crystal structure in complex with small molecule inhibitor 分子名称: 3-(2-PYRIDIN-4-YLETHYL)-1H-INDOLE, MITOGEN-ACTIVATED PROTEIN KINASE 14 著者 Tickle, J, Jhoti, H, Cleasby, A, Devine, L. 登録日 2004-09-16 公開日 2005-02-08 最終更新日 2024-05-08 実験手法 X-RAY DIFFRACTION (2.2 Å) 主引用文献 Identification of novel p38alpha MAP kinase inhibitors using fragment-based lead generation. J. Med. Chem., 48, 2005
1W6Z	High Energy Tetragonal Lysozyme X-ray Structure 分子名称: CHLORIDE ION, HOLMIUM (III) ATOM, LYSOZYME C 著者 Jakoncic, J, Aslantas, M, Honkimaki, V, Di Michiel, M, Stojanoff, V. 登録日 2004-08-25 公開日 2004-11-10 最終更新日 2023-12-13 実験手法 X-RAY DIFFRACTION (1.65 Å) 主引用文献 Anomalous Diffraction at Ultra-High Energy for Protein Crystallography. J.Appl.Crystallogr., 39, 2006
1W92	The structure of carbomonoxy murine neuroglobin reveals a heme- sliding mechanism for affinity regulation 分子名称: CARBON MONOXIDE, NEUROGLOBIN, PROTOPORPHYRIN IX CONTAINING FE 著者 Vallone, B, Nienhaus, K, Matthes, A, Brunori, M, Nienhaus, G.U. 登録日 2004-10-05 公開日 2004-11-02 最終更新日 2023-12-13 実験手法 X-RAY DIFFRACTION (1.7 Å) 主引用文献 The Structure of Carbonmonoxy Neuroglobin Reveals a Heme-Sliding Mechanism for Control of Ligand Affinity Proc.Natl.Acad.Sci.USA, 101, 2004
1W6H	Novel plasmepsin II-inhibitor complex 分子名称: N-((3S,4S)-5-[(4-BROMOBENZYL)OXY]-3-HYDROXY-4-{[N-(PYRIDIN-2-YLCARBONYL)-L-VALYL]AMINO}PENTANOYL)-L-ALANYL-L-LEUCINAMIDE, PLASMEPSIN 2 著者 Lindberg, J, Johansson, P.-O, Rosenquist, A, Kvarnstroem, I, Vrang, L, Samuelsson, B, Unge, T. 登録日 2004-08-18 公開日 2006-07-05 最終更新日 2018-01-17 実験手法 X-RAY DIFFRACTION (2.24 Å) 主引用文献 Structural Study of a Novel Inhibitor with Bulky P1 Side Chain in Complex with Plasmepsin II -Implications for Drug Design To be Published
1WAK	X-ray structure of SRPK1 分子名称: 1,2-ETHANEDIOL, SERINE/THREONINE-PROTEIN KINASE SPRK1 著者 Ngo, J.C, Gullingsrud, J, Chakrabarti, S, Nolen, B, Aubol, B.E, Fu, X.D, Adams, J.A, Mccammon, J.A, Ghosh, G. 登録日 2004-10-26 公開日 2006-07-11 最終更新日 2024-05-08 実験手法 X-RAY DIFFRACTION (1.73 Å) 主引用文献 Sr Protein Kinase 1 is Resilient to Inactivation. Structure, 15, 2007
5BYZ	ERK5 in complex with small molecule 分子名称: 4-({5-fluoro-4-[2-methyl-1-(propan-2-yl)-1H-imidazol-5-yl]pyrimidin-2-yl}amino)-N-[2-(piperidin-1-yl)ethyl]benzamide, GLYCEROL, Mitogen-activated protein kinase 7 著者 Chen, H, Tucker, J, Wang, X, Gavine, P.R, Philips, C, Augustin, M.A, Schreiner, P, Steinbacher, S, Preston, M, Ogg, D. 登録日 2015-06-11 公開日 2016-05-04 最終更新日 2024-05-08 実験手法 X-RAY DIFFRACTION (1.65 Å) 主引用文献 Discovery of a novel allosteric inhibitor-binding site in ERK5: comparison with the canonical kinase hinge ATP-binding site. Acta Crystallogr D Struct Biol, 72, 2016
1VHB	BACTERIAL DIMERIC HEMOGLOBIN FROM VITREOSCILLA STERCORARIA 分子名称: HEMOGLOBIN, PROTOPORPHYRIN IX CONTAINING FE 著者 Tarricone, C, Galizzi, A, Coda, A, Ascenzi, P, Bolognesi, M. 登録日 1997-02-19 公開日 1998-02-25 最終更新日 2024-02-14 実験手法 X-RAY DIFFRACTION (1.83 Å) 主引用文献 Unusual structure of the oxygen-binding site in the dimeric bacterial hemoglobin from Vitreoscilla sp. Structure, 5, 1997
1VIP	ANTICOAGULANT CLASS II PHOSPHOLIPASE A2 FROM THE VENOM OF VIPERA RUSSELLI RUSSELLI 分子名称: PHOSPHOLIPASE A2, SULFATE ION 著者 Carredano, E, Westerlund, B, Persson, B, Saarinen, M, Ramaswamy, S, Eaker, D, Eklund, H. 登録日 1997-02-27 公開日 1997-06-16 最終更新日 2023-08-09 実験手法 X-RAY DIFFRACTION (2.2 Å) 主引用文献 The three-dimensional structures of two toxins from snake venom throw light on the anticoagulant and neurotoxic sites of phospholipase A2. Toxicon, 36, 1998
1VPI	PHOSPHOLIPASE A2 INHIBITOR FROM VIPOXIN 分子名称: PHOSPHOLIPASE A2 INHIBITOR 著者 Devedjiev, Y.D, Popov, A.N. 登録日 1996-12-17 公開日 1997-12-24 最終更新日 2023-08-09 実験手法 X-RAY DIFFRACTION (1.76 Å) 主引用文献 X-ray structure at 1.76 A resolution of a polypeptide phospholipase A2 inhibitor. J.Mol.Biol., 266, 1997
1VJ9	Urokinase Plasminogen Activator B-Chain-JT464 Complex 分子名称: N-(BENZYLSULFONYL)-L-SERYL-N~1~-{4-[AMINO(IMINO)METHYL]BENZYL}-O-BENZYL-L-SERINAMIDE, SULFATE ION, plasminogen activator, ... 著者 Schweinitz, A, Steinmetzer, T, Banke, I.J, Arlt, M.J.E, Stuerzebecher, A, Schuster, O, Geissler, A, Giersiefen, H, Zeslawska, E, Jacob, U, Kruger, A, Stuerzebecher, J. 登録日 2004-02-03 公開日 2004-06-22 最終更新日 2023-08-23 実験手法 X-RAY DIFFRACTION (2.4 Å) 主引用文献 Design of novel and selective inhibitors of urokinase-type plasminogen activator with improved pharmacokinetic properties for use as antimetastatic agents J.Biol.Chem., 279, 2004
1VIH	NMR STUDY OF VIGILIN, REPEAT 6, MINIMIZED AVERAGE STRUCTURE 分子名称: VIGILIN 著者 Musco, G, Stier, G, Joseph, C, Morelli, M.A.C, Nilges, M, Gibson, T.J, Pastore, A. 登録日 1995-11-29 公開日 1996-04-03 最終更新日 2024-05-22 実験手法 SOLUTION NMR 主引用文献 Three-dimensional structure and stability of the KH domain: molecular insights into the fragile X syndrome. Cell(Cambridge,Mass.), 85, 1996
1W10	Urokinase type plasminogen activator 分子名称: N-(ISOBUTOXYCARBONYL)-D-SERYL-N-((1S)-4-{[AMINO(IMINO)METHYL]AMINO}-1-FORMYLBUTYL)-L-ALANINAMIDE, SULFATE ION, UROKINASE-TYPE PLASMINOGEN ACTIVATOR 著者 Jacob, U. 登録日 2004-06-15 公開日 2008-05-20 最終更新日 2019-09-18 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Crystals of urokinase type plasminogen activator complexes reveal the binding mode of peptidomimetic inhibitors. J.Mol.Biol., 328, 2003
3S3I	p38 kinase crystal structure in complex with small molecule inhibitor 分子名称: 3-(3-tert-butyl[1,2,4]triazolo[4,3-a]pyridin-7-yl)-N-cyclopropyl-4-methylbenzamide, Mitogen-activated protein kinase 14 著者 Segarra, V, Aiguade, J, Roca, R, Fisher, M, Lamers, M. 登録日 2011-05-18 公開日 2012-04-04 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 Novel triazolopyridylbenzamides as potent and selective p38 alpha inhibitors. Bioorg.Med.Chem.Lett., 22, 2012
5CKW	Crystal structure of LegK4_AMPPNP Kinase 分子名称: CALCIUM ION, LegK4, MAGNESIUM ION, ... 著者 Flayhan, A, Terradot, L. 登録日 2015-07-15 公開日 2015-10-14 最終更新日 2024-01-10 実験手法 X-RAY DIFFRACTION (2.49 Å) 主引用文献 The structure of Legionella pneumophila LegK4 type four secretion system (T4SS) effector reveals a novel dimeric eukaryotic-like kinase. Sci Rep, 5, 2015
1W12	UROKINASE TYPE PLASMINOGEN ACTIVATOR 分子名称: N-((1S)-4-{[AMINO(IMINO)METHYL]AMINO}-1-FORMYLBUTYL)-2-{(3R)-3-[(BENZYLSULFONYL)AMINO]-2-OXO-5-PHENYL-2,3-DIHYDRO-1H-1,4-BENZODIAZEPIN-1-YL}ACETAMIDE, UROKINASE-TYPE PLASMINOGEN ACTIVATOR 著者 Jacob, U. 登録日 2004-06-15 公開日 2008-05-20 最終更新日 2019-05-22 実験手法 X-RAY DIFFRACTION (2.4 Å) 主引用文献 Crystals of Urokinase Type Plasminogen Activator Complexes Reveal the Binding Mode of Peptidomimetic Inhibitors. J.Mol.Biol., 328, 2003
1W21	Structure of Neuraminidase from English duck subtype N6 complexed with 30 mM sialic acid (NANA, Neu5Ac), crystal soaked for 43 hours at 291 K. 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 Rudino-Pinera, E, Tunnah, P, Crennell, S.J, Webster, R.G, Laver, W.G, Garman, E.F. 登録日 2004-06-25 公開日 2006-01-25 最終更新日 2023-12-13 実験手法 X-RAY DIFFRACTION (2.08 Å) 主引用文献 The Crystal Structure of Type a Influenza Virus Neuraminidase of the N6 Subtype Reveals the Existence of Two Separate Neu5Ac Binding Sites To be Published

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