PDB: 243083 件ウェブページステータス検索Chemie searchBIRD

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1DF5	INTERACTIONS BETWEEN HIV-1 GP41 CORE AND DETERGENTS AND THEIR IMPLICATIONS FOR MEMBRANE FUSION 分子名称: HIV-1 ENVELOPE GLYCOPROTEIN GP41 著者 Shu, W, Ji, H, Lu, M. 登録日 1999-11-17 公開日 1999-11-24 最終更新日 2024-02-07 実験手法 X-RAY DIFFRACTION (2.7 Å) 主引用文献 Interactions between HIV-1 gp41 core and detergents and their implications for membrane fusion. J.Biol.Chem., 275, 2000
1EWS	THE THREE-DIMENSIONAL SOLUTION STRUCTURE OF THE RABBIT KIDNEY DEFENSIN, RK-1 分子名称: RK-1 DEFENSIN 著者 McManus, A.M, Dawson, N.F, Wade, J.D, Craik, D.J. 登録日 2000-04-26 公開日 2001-05-02 最終更新日 2024-11-20 実験手法 SOLUTION NMR 主引用文献 Three-dimensional structure of RK-1: a novel alpha-defensin peptide. Biochemistry, 39, 2000
1EBW	HIV-1 protease in complex with the inhibitor BEA322 分子名称: HIV-1 PROTEASE, N,N-[2,5-O-[DIBENZYL]-GLUCARYL]-DI-[ISOLEUCYL-AMIDO-METHANE] 著者 Unge, T. 登録日 2000-01-25 公開日 2002-06-26 最終更新日 2024-02-07 実験手法 X-RAY DIFFRACTION (1.81 Å) 主引用文献 Optimization of P1-P3 groups in symmetric and asymmetric HIV-1 protease inhibitors Eur.J.Biochem., 270, 2003
1YP0	Structure of the steroidogenic factor-1 ligand binding domain bound to phospholipid and a SHP peptide motif 分子名称: DI-PALMITOYL-3-SN-PHOSPHATIDYLETHANOLAMINE, Nuclear receptor subfamily 0, group B, ... 著者 Li, Y, Choi, M, Cavey, G, Daugherty, J, Suino, K, Kovach, A, Bingham, N, Kliewer, S, Xu, H. 登録日 2005-01-28 公開日 2005-04-19 最終更新日 2024-02-14 実験手法 X-RAY DIFFRACTION (1.5 Å) 主引用文献 Crystallographic identification and functional characterization of phospholipids as ligands for the orphan nuclear receptor steroidogenic factor-1. Mol.Cell, 17, 2005
1E21	Ribonuclease 1 des1-7 Crystal Structure at 1.9A 分子名称: RIBONUCLEASE 1 著者 Pous, J, Mallorqui-Fernandez, G, Peracaula, R, Terzyan, S.S, Futami, J, Tada, H, Yamada, H, Seno, M, De Llorens, R, Gomis-Ruth, F.X, Coll, M. 登録日 2000-05-15 公開日 2001-05-03 最終更新日 2024-11-06 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 Three-Dimensional Crystal Structure of Human Rnase 1Dn7 at 1.9A Resolution Acta Crystallogr.,Sect.D, 57, 2001
1EC2	HIV-1 protease in complex with the inhibitor BEA428 分子名称: HIV-1 PROTEASE, N,N-[2,5-O-[DI-4-PYRIDIN-3-YL-BENZYL]-GLUCARYL]-DI-[VALYL-AMIDO-METHANE] 著者 Unge, T. 登録日 2000-01-25 公開日 2002-06-26 最終更新日 2024-02-07 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Optimization of P1-P3 groups in symmetric and asymmetric HIV-1 protease inhibitors Eur.J.Biochem., 270, 2003
2H5S	SA2-13 penam sulfone complexed to wt SHV-1 beta-lactamase 分子名称: (3R)-4-[(4-CARBOXYBUTANOYL)OXY]-N-[(1E)-3-OXOPROP-1-EN-1-YL]-3-SULFINO-D-VALINE, CYCLOHEXYL-HEXYL-BETA-D-MALTOSIDE, SHV-1 beta-lactamase 著者 van den Akker, F, Padayatti, P.S. 登録日 2006-05-27 公開日 2006-10-17 最終更新日 2024-11-13 実験手法 X-RAY DIFFRACTION (1.28 Å) 主引用文献 Rational Design of a beta-Lactamase Inhibitor Achieved via Stabilization of the trans-Enamine Intermediate: 1.28 A Crystal Structure of wt SHV-1 Complex with a Penam Sulfone. J.Am.Chem.Soc., 128, 2006
3TKW	Crystal structure of HIV protease model precursor/Darunavir complex 分子名称: (3R,3AS,6AR)-HEXAHYDROFURO[2,3-B]FURAN-3-YL(1S,2R)-3-[[(4-AMINOPHENYL)SULFONYL](ISOBUTYL)AMINO]-1-BENZYL-2-HYDROXYPROPYLCARBAMATE, CHLORIDE ION, GLYCEROL, ... 著者 Agniswamy, J, Sayer, J, Weber, I, Louis, J. 登録日 2011-08-29 公開日 2012-04-25 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (1.55 Å) 主引用文献 Terminal interface conformations modulate dimer stability prior to amino terminal autoprocessing of HIV-1 protease. Biochemistry, 51, 2012
4JO3	Crystal structure of rabbit mAb R20 Fab in complex with V3 C-terminus of HIV-1 Consensus B gp120 分子名称: SULFATE ION, gp120, monoclonal anti-HIV-1 gp120 V3 antibody R20 heavy chain, ... 著者 Pan, R.M, Kong, X.P. 登録日 2013-03-16 公開日 2013-07-31 最終更新日 2024-11-27 実験手法 X-RAY DIFFRACTION (2.6 Å) 主引用文献 Rabbit Anti-HIV-1 Monoclonal Antibodies Raised by Immunization Can Mimic the Antigen-Binding Modes of Antibodies Derived from HIV-1-Infected Humans. J.Virol., 87, 2013
2ZIC	Crystal structure of Streptococcus mutans dextran glucosidase 分子名称: 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, CALCIUM ION, Dextran glucosidase, ... 著者 Hondoh, H, Saburi, W, Mori, H, Okuyama, M, Nakada, T, Matsuura, Y, Kimura, A. 登録日 2008-02-14 公開日 2008-06-24 最終更新日 2023-11-01 実験手法 X-RAY DIFFRACTION (2.2 Å) 主引用文献 Substrate recognition mechanism of alpha-1,6-glucosidic linkage hydrolyzing enzyme, dextran glucosidase from Streptococcus mutans. J.Mol.Biol., 378, 2008
1SLN	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN FIBROBLAST STROMELYSIN-1 INHIBITED WITH THE N-CARBOXY-ALKYL INHIBITOR L-702,842 分子名称: CALCIUM ION, N-(R-CARBOXY-ETHYL)-ALPHA-(S)-(2-PHENYLETHYL)GLYCYL-L-ARGININE-N-PHENYLAMIDE, STROMELYSIN-1, ... 著者 Becker, J.W. 登録日 1995-08-03 公開日 1996-12-17 最終更新日 2024-02-14 実験手法 X-RAY DIFFRACTION (2.27 Å) 主引用文献 Stromelysin-1: three-dimensional structure of the inhibited catalytic domain and of the C-truncated proenzyme. Protein Sci., 4, 1995
1I7M	HUMAN S-ADENOSYLMETHIONINE DECARBOXYLASE WITH COVALENTLY BOUND PYRUVOYL GROUP AND COMPLEXED WITH 4-AMIDINOINDAN-1-ONE-2'-AMIDINOHYDRAZONE 分子名称: 1,4-DIAMINOBUTANE, 4-AMIDINOINDAN-1-ONE-2'-AMIDINOHYDRAZONE, S-ADENOSYLMETHIONINE DECARBOXYLASE ALPHA CHAIN, ... 著者 Tolbert, W.D, Ekstrom, J.L, Mathews, I.I, Secrist III, J.A, Pegg, A.E, Ealick, S.E. 登録日 2001-03-09 公開日 2001-08-22 最終更新日 2024-10-09 実験手法 X-RAY DIFFRACTION (2.24 Å) 主引用文献 The structural basis for substrate specificity and inhibition of human S-adenosylmethionine decarboxylase. Biochemistry, 40, 2001
5AMA	Crystal structure of the Angiotensin-1 converting enzyme N-domain in complex with amyloid-beta 1-16 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, ANGIOTENSIN-CONVERTING ENZYME, ... 著者 Masuyer, G, Larmuth, K.M, Douglas, R.G, Sturrock, E.D, Acharya, K.R. 登録日 2015-03-10 公開日 2016-01-13 最終更新日 2024-11-13 実験手法 X-RAY DIFFRACTION (1.8 Å) 主引用文献 The Kinetic and Structural Characterisation of Amyloid-Beta Metabolism by Human Angiotensin-1- Converting Enzyme (Ace) FEBS J., 283, 2016
2M9R	3D NMR structure of a complex between the amyloid beta peptide (1-40) and the polyphenol epsilon-viniferin glucoside 分子名称: (2S,3S)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-6-yl beta-D-glucopyranoside, Amyloid beta A4 protein 著者 Monti, J, Richard, T. 登録日 2013-06-19 公開日 2013-09-11 最終更新日 2024-05-01 実験手法 SOLUTION NMR 主引用文献 3D NMR structure of a complex between the amyloid beta peptide (1-40) and the polyphenol epsilon-viniferin glucoside: Implications in Alzheimer's disease. Biochim.Biophys.Acta, 1830, 2013
1KKT	Structure of P. citrinum alpha 1,2-mannosidase reveals the basis for differences in specificity of the ER and Golgi Class I enzymes 分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, Mannosyl-oligosaccharide alpha-1,2-mannosidase, ... 著者 Lobsanov, Y.D, Vallee, F, Imberty, A, Yoshida, T, Yip, P, Herscovics, A, Howell, P.L. 登録日 2001-12-10 公開日 2002-01-23 最終更新日 2024-11-13 実験手法 X-RAY DIFFRACTION (2.2 Å) 主引用文献 Structure of Penicillium citrinum alpha 1,2-mannosidase reveals the basis for differences in specificity of the endoplasmic reticulum and Golgi class I enzymes. J.Biol.Chem., 277, 2002
1DW6	Structural and kinetic analysis of drug resistant mutants of HIV-1 protease 分子名称: HIV-1 PROTEASE, N-[(2R)-2-({N~5~-[amino(iminio)methyl]-L-ornithyl-L-valyl}amino)-4-methylpentyl]-L-phenylalanyl-L-alpha-glutamyl-L-alanyl-L-norleucinamide 著者 Mahalingam, B, Louis, J.M, Reed, C.C, Adomat, J.M, Krouse, J, Wang, Y.F, Harrison, R.W, Weber, I.T. 登録日 2000-01-24 公開日 2000-07-26 最終更新日 2024-02-07 実験手法 X-RAY DIFFRACTION (1.88 Å) 主引用文献 Structural and kinetic analysis of drug resistant mutants of HIV-1 protease. Eur.J.Biochem., 263, 1999
2M9S	3D NMR structure of a complex between the amyloid beta peptide (1-40) and the polyphenol epsilon-viniferin glucoside 分子名称: (2S,3S)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-6-yl beta-D-glucopyranoside, Amyloid beta A4 protein 著者 Monti, J, Richard, T. 登録日 2013-06-19 公開日 2013-09-11 最終更新日 2024-05-01 実験手法 SOLUTION NMR 主引用文献 3D NMR structure of a complex between the amyloid beta peptide (1-40) and the polyphenol epsilon-viniferin glucoside: Implications in Alzheimer's disease. Biochim.Biophys.Acta, 1830, 2013
4I5C	The Jak1 kinase domain in complex with inhibitor 分子名称: 1,2-ETHANEDIOL, 3-oxo-3-[(3R)-3-(pyrrolo[2,3-b][1,2,3]triazolo[4,5-d]pyridin-1(6H)-yl)piperidin-1-yl]propanenitrile, Tyrosine-protein kinase JAK1 著者 Fong, R, Lupardus, P.J. 登録日 2012-11-28 公開日 2013-05-22 最終更新日 2024-10-30 実験手法 X-RAY DIFFRACTION (2.1 Å) 主引用文献 Novel triazolo-pyrrolopyridines as inhibitors of Janus kinase 1. Bioorg.Med.Chem.Lett., 23, 2013
3GXG	Crystal structure of Putative phosphatase (DUF442) (YP_001181608.1) from SHEWANELLA PUTREFACIENS CN-32 at 1.60 A resolution 分子名称: 1,2-ETHANEDIOL, ACETATE ION, CHLORIDE ION, ... 著者 Joint Center for Structural Genomics (JCSG) 登録日 2009-04-02 公開日 2009-07-07 最終更新日 2024-11-20 実験手法 X-RAY DIFFRACTION (1.6 Å) 主引用文献 Crystal structure of Putative phosphatase (DUF442) (YP_001181608.1) from SHEWANELLA PUTREFACIENS CN-32 at 1.60 A resolution To be published
4JQI	Structure of active beta-arrestin1 bound to a G protein-coupled receptor phosphopeptide 分子名称: 1,2-ETHANEDIOL, Beta-arrestin-1, CHLORIDE ION, ... 著者 Shukla, A.K, Manglik, A, Kruse, A.C, Xiao, K, Reis, R.I, Tseng, W.C, Staus, D.P, Hilger, D, Uysal, S, Huang, L.H, Paduch, M, Shukla, P.T, Koide, A, Koide, S, Weis, W.I, Kossiakoff, A.A, Kobilka, B.K, Lefkowitz, R.J. 登録日 2013-03-20 公開日 2013-04-17 最終更新日 2024-10-16 実験手法 X-RAY DIFFRACTION (2.6 Å) 主引用文献 Structure of active beta-arrestin-1 bound to a G-protein-coupled receptor phosphopeptide. Nature, 497, 2013
1XJQ	ADP Complex OF HUMAN PAPS SYNTHETASE 1 分子名称: ADENOSINE-5'-DIPHOSPHATE, Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthetase 1 著者 Harjes, S, Bayer, P, Scheidig, A.J. 登録日 2004-09-24 公開日 2005-08-30 最終更新日 2023-08-23 実験手法 X-RAY DIFFRACTION (2.06 Å) 主引用文献 The crystal structure of human PAPS synthetase 1 reveals asymmetry in substrate binding J.Mol.Biol., 347, 2005
1XLC	MECHANISM FOR ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE INVOLVING RING OPENING FOLLOWED BY A 1,2-HYDRIDE SHIFT 分子名称: D-XYLOSE ISOMERASE, MAGNESIUM ION, Xylitol 著者 Collyer, C.A, Henrick, K, Blow, D.M. 登録日 1991-10-09 公開日 1993-07-15 最終更新日 2024-02-14 実験手法 X-RAY DIFFRACTION (2.5 Å) 主引用文献 Mechanism for aldose-ketose interconversion by D-xylose isomerase involving ring opening followed by a 1,2-hydride shift. J.Mol.Biol., 212, 1990
1DLB	HELICAL INTERACTIONS IN THE HIV-1 GP41 CORE REVEALS STRUCTURAL BASIS FOR THE INHIBITORY ACTIVITY OF GP41 PEPTIDES 分子名称: HIV-1 ENVELOPE GLYCOPROTEIN GP41 著者 Shu, W, Liu, J, Ji, H, Rading, L, Jiang, S, Lu, M. 登録日 1999-12-09 公開日 1999-12-15 最終更新日 2024-02-07 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Helical interactions in the HIV-1 gp41 core reveal structural basis for the inhibitory activity of gp41 peptides. Biochemistry, 39, 2000
1DD2	BIOTIN CARBOXYL CARRIER DOMAIN OF TRANSCARBOXYLASE (TC 1.3S) 分子名称: TRANSCARBOXYLASE 1.3S SUBUNIT 著者 Reddy, D.V, Shenoy, B.C, Carey, P.R, Sonnichsen, F.D. 登録日 1999-11-06 公開日 2000-03-24 最終更新日 2024-05-22 実験手法 SOLUTION NMR 主引用文献 High resolution solution structure of the 1.3S subunit of transcarboxylase from Propionibacterium shermanii. Biochemistry, 39, 2000
3RKJ	Crystal Structure of New Delhi Metallo-Beta-Lactamase-1 from Klebsiella pnueumoniae 分子名称: Beta-lactamase NDM-1, GLYCEROL, SULFATE ION 著者 Kim, Y, Tesar, C, Jedrzejczak, R, Binkowski, T.A, Babnigg, G, Sacchettini, J, Joachimiak, A, Midwest Center for Structural Genomics (MCSG), Structures of Mtb Proteins Conferring Susceptibility to Known Mtb Inhibitors (MTBI) 登録日 2011-04-18 公開日 2011-05-18 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Structure of Apo- and Monometalated Forms of NDM-1 A Highly Potent Carbapenem-Hydrolyzing Metallo-beta-Lactamase Plos One, 6, 2011

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