PDB: 183105 件ウェブページステータス検索Chemie searchBIRD

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3WVZ	Crystal structure of Hikeshi, a new nuclear transport receptor of Hsp70 分子名称: Protein Hikeshi 著者 Song, J, Kose, S, Watanabe, A, Son, S.Y, Choi, S, Hong, R.H, Yamashita, E, Park, I.Y, Imamoto, N, Lee, S.J. 登録日 2014-06-12 公開日 2015-03-25 最終更新日 2024-03-20 実験手法 X-RAY DIFFRACTION (1.88 Å) 主引用文献 Structural and functional analysis of Hikeshi, a new nuclear transport receptor of Hsp70s Acta Crystallogr.,Sect.D, 71, 2015
1HLY	SOLUTION STRUCTURE OF HONGOTOXIN 1 分子名称: HONGOTOXIN 1 著者 Pragl, B, Koschak, A, Trieb, M, Obermair, G, Kaufmann, W.A, Gerster, U, Blanc, E, Hahn, C, Prinz, H, Schutz, G, Darbon, H, Gruber, H.J, Knaus, H.G. 登録日 2000-12-04 公開日 2003-09-30 最終更新日 2022-02-23 実験手法 SOLUTION NMR 主引用文献 Synthesis, characterization, and application of cy-dye- and alexa-dye-labeled hongotoxin(1) analogues. The first high affinity fluorescence probes for voltage-gated K+ channels. BIOCONJUG.CHEM., 13, 2002
3RF2	Crystal Structure of 30S Ribosomal Protein S8 from Aquifex Aeolicus 分子名称: 30S ribosomal protein S8, SULFATE ION 著者 Menichelli, E, Williamson, J.R. 登録日 2011-04-05 公開日 2011-11-16 最終更新日 2024-02-21 実験手法 X-RAY DIFFRACTION (2.16 Å) 主引用文献 The Structure of Aquifex aeolicus Ribosomal Protein S8 Reveals a Unique Subdomain that Contributes to an Extremely Tight Association with 16S rRNA. J.Mol.Biol., 415, 2012
4QUM	Crystal structure of PTPN3 (PTPH1) in complex with a dually phosphorylated MAPK12 peptide 分子名称: Mitogen-activated protein kinase 12, Tyrosine-protein phosphatase non-receptor type 3 著者 Chen, K.E, Meng, T.C, Wang, A.H.J. 登録日 2014-07-10 公開日 2014-12-10 最終更新日 2023-12-06 実験手法 X-RAY DIFFRACTION (2.516 Å) 主引用文献 Reciprocal allosteric regulation of p38 gamma and PTPN3 involves a PDZ domain-modulated complex formation. Sci.Signal., 7, 2014
4MHF	Crystal structure of a TRAP periplasmic solute binding protein from Polaromonas sp. JS666 (Bpro_3107), target EFI-510173, with bound alpha/beta D-Glucuronate, space group P21 分子名称: TRAP dicarboxylate transporter, DctP subunit, alpha-D-glucopyranuronic acid, ... 著者 Vetting, M.W, Toro, R, Bhosle, R, Al Obaidi, N.F, Morisco, L.L, Wasserman, S.R, Sojitra, S, Zhao, S, Stead, M, Washington, E, Scott Glenn, A, Chowdhury, S, Evans, B, Hammonds, J, Hillerich, B, Love, J, Seidel, R.D, Imker, H.J, Jacobson, M.P, Gerlt, J.A, Almo, S.C, Enzyme Function Initiative (EFI) 登録日 2013-08-29 公開日 2013-09-18 最終更新日 2020-07-29 実験手法 X-RAY DIFFRACTION (1.46 Å) 主引用文献 Experimental strategies for functional annotation and metabolism discovery: targeted screening of solute binding proteins and unbiased panning of metabolomes. Biochemistry, 54, 2015
3S2Y	Crystal structure of a chromate/uranium reductase from Gluconacetobacter hansenii 分子名称: CHLORIDE ION, Chromate reductase, FLAVIN MONONUCLEOTIDE, ... 著者 Jin, H, Zhang, Y, Buchko, G.W, Li, P, Squier, T.C, Robinson, H, Varnum, S.M, Long, P.E. 登録日 2011-05-17 公開日 2012-05-30 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (2.244 Å) 主引用文献 Structure Determination and Functional Analysis of a Chromate Reductase from Gluconacetobacter hansenii. Plos One, 7, 2012
1L3Q	H. rufescens abalone shell Lustrin A consensus repeat, FPGKNVNCTSGE, pH 7.4, 1-H NMR structure 分子名称: Lustrin A 著者 Evans, J.S, Wustman, B.A, Zhang, B, Morse, D.E. 登録日 2002-02-28 公開日 2002-03-15 最終更新日 2024-05-22 実験手法 SOLUTION NMR 主引用文献 Model peptide studies of sequence regions in the elastomeric biomineralization protein, Lustrin A. I. The C-domain consensus-PG-, -NVNCT-motif Biopolymers, 63, 2002
3OE4	Rat catechol O-methyltransferase in complex with a catechol-type, purine-containing bisubstrate inhibitor - humanized form 分子名称: Catechol O-methyltransferase, MAGNESIUM ION, N-[(E)-3-[(2R,3S,4R,5R)-3,4-dihydroxy-5-purin-9-yl-oxolan-2-yl]prop-2-enyl]-2,3-dihydroxy-5-nitro-benzamide 著者 Ehler, A, Schlatter, D, Stihle, M, Benz, J, Rudolph, M.G. 登録日 2010-08-12 公開日 2011-03-16 最終更新日 2024-04-03 実験手法 X-RAY DIFFRACTION (1.49 Å) 主引用文献 Molecular Recognition at the Active Site of Catechol-O-methyltransferase (COMT): Adenine Replacements in Bisubstrate Inhibitors Chemistry, 17, 2011
2WV3	Neuroplastin-55 binds to and signals through the fibroblast growth factor receptor 分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, NEUROPLASTIN 著者 Soroka, V, Owczarek, S, Kastrup, J.S, Berezin, V, Bock, E, Gajhede, M. 登録日 2009-10-13 公開日 2009-12-15 最終更新日 2020-07-29 実験手法 X-RAY DIFFRACTION (1.95 Å) 主引用文献 Neuroplastin-55 Binds to and Signals Through the Fibroblast Growth Factor Receptor Faseb J., 24, 2010
4TQ5	Structure of a UbiA homolog from Archaeoglobus fulgidus 分子名称: octyl beta-D-glucopyranoside, prenyltransferase 著者 Huang, H, Levin, E.J, Bai, Y, Zhou, M, New York Consortium on Membrane Protein Structure (NYCOMPS) 登録日 2014-06-10 公開日 2014-07-16 最終更新日 2023-12-27 実験手法 X-RAY DIFFRACTION (3.2023 Å) 主引用文献 Structure of a Membrane-Embedded Prenyltransferase Homologous to UBIAD1. Plos Biol., 12, 2014
3OZT	Rat catechol O-methyltransferase in complex with a catechol-type, 4-oxo-pyridinyl-containing inhibitor - humanized form 分子名称: Catechol O-methyltransferase, MAGNESIUM ION, N-[(E)-3-[(2R,3S,4R,5R)-3,4-dihydroxy-5-(4-oxopyridin-1-yl)oxolan-2-yl]prop-2-enyl]-2,3-dihydroxy-5-nitro-benzamide 著者 Ehler, A, Schlatter, D, Stihle, M, Benz, J, Rudolph, M.G. 登録日 2010-09-27 公開日 2011-03-16 最終更新日 2024-04-03 実験手法 X-RAY DIFFRACTION (1.48 Å) 主引用文献 Molecular Recognition at the Active Site of Catechol-O-methyltransferase (COMT): Adenine Replacements in Bisubstrate Inhibitors Chemistry, 17, 2011
3WZ7	Endothiapepsin in complex with Gewald reaction-derived inhibitor (6) 分子名称: DIMETHYL SULFOXIDE, Endothiapepsin, N-benzyl-2-({N-[2-(1H-indol-3-yl)ethyl]glycyl}amino)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide 著者 Kuhnert, M, Steuber, H, Diederich, W.E. 登録日 2014-09-19 公開日 2015-08-05 最終更新日 2023-11-08 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 Tracing binding modes in hit-to-lead optimization: chameleon-like poses of aspartic protease inhibitors Angew.Chem.Int.Ed.Engl., 54, 2015
1KCN	Structure of e109 Zeta Peptide, an Antagonist of the High-Affinity IgE Receptor 分子名称: e109 zeta peptide 著者 Nakamura, G.R, Reynolds, M.E, Chen, Y.M, Starovasnik, M.A, Lowman, H.B. 登録日 2001-11-09 公開日 2002-03-06 最終更新日 2022-02-23 実験手法 SOLUTION NMR 主引用文献 Stable "zeta" peptides that act as potent antagonists of the high-affinity IgE receptor. Proc.Natl.Acad.Sci.USA, 99, 2002
2VQ9	RNASE ZF-3E 分子名称: CHLORIDE ION, RNASE 1 著者 Kazakou, K, Holloway, D.E, Prior, S.H, Subramanian, V, Acharya, K.R. 登録日 2008-03-12 公開日 2008-06-17 最終更新日 2023-12-13 実験手法 X-RAY DIFFRACTION (1.85 Å) 主引用文献 Ribonuclease A Homologues of the Zebrafish: Polymorphism, Crystal Structures of Two Representatives and Their Evolutionary Implications J.Mol.Biol., 380, 2008
2VQ8	RNASE ZF-1A 分子名称: CHLORIDE ION, RNASE ZF-1A 著者 Kazakou, K, Holloway, D.E, Prior, S.H, Subramanian, V, Acharya, K.R. 登録日 2008-03-12 公開日 2008-06-17 最終更新日 2023-12-13 実験手法 X-RAY DIFFRACTION (1.35 Å) 主引用文献 Ribonuclease A Homologues of the Zebrafish: Polymorphism, Crystal Structures of Two Representatives and Their Evolutionary Implications. J.Mol.Biol., 380, 2008
1KCO	Structure of e131 Zeta Peptide, a Potent Antagonist of the High-Affinity IgE Receptor 分子名称: e131 Zeta Peptide 著者 Nakamura, G.R, Reynolds, M.E, Chen, Y.M, Starovasnik, M.A, Lowman, H.B. 登録日 2001-11-09 公開日 2002-03-06 最終更新日 2022-02-23 実験手法 SOLUTION NMR 主引用文献 Stable "zeta" peptides that act as potent antagonists of the high-affinity IgE receptor. Proc.Natl.Acad.Sci.USA, 99, 2002
3OE5	Rat catechol O-methyltransferase in complex with a catechol-type, pyridylsulfanyl-containing inhibitor - humanized form 分子名称: Catechol O-methyltransferase, MAGNESIUM ION, N-[(E)-3-[(2R,3S,4R,5S)-3,4-dihydroxy-5-pyridin-4-ylsulfanyl-oxolan-2-yl]prop-2-enyl]-2,3-dihydroxy-5-nitro-benzamide 著者 Ehler, A, Schlatter, D, Stihle, M, Benz, J, Rudolph, M.G. 登録日 2010-08-12 公開日 2011-03-16 最終更新日 2024-04-03 実験手法 X-RAY DIFFRACTION (1.52 Å) 主引用文献 Molecular Recognition at the Active Site of Catechol-O-methyltransferase (COMT): Adenine Replacements in Bisubstrate Inhibitors Chemistry, 17, 2011
3THR	Crystal structure of rat native liver Glycine N-methyltransferase complexed with 5-methyltetrahydrofolate monoglutamate 分子名称: 5-METHYL-5,6,7,8-TETRAHYDROFOLIC ACID, Glycine N-methyltransferase, TRIS(HYDROXYETHYL)AMINOMETHANE 著者 Luka, Z, Pakhomova, S, Loukachevitch, L.V, Newcomer, M.E, Wagner, C. 登録日 2011-08-19 公開日 2011-11-16 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Differences in folate-protein interactions result in differing inhibition of native rat liver and recombinant glycine N-methyltransferase by 5-methyltetrahydrofolate. Biochim.Biophys.Acta, 1824, 2011
3SQH	Crystal structure of prethrombin-2 mutant S195A in the the open form 分子名称: Thrombin light chain, heavy chain 著者 Pozzi, N, Chen, Z, Di Cera, E. 登録日 2011-07-05 公開日 2011-11-30 最終更新日 2023-09-13 実験手法 X-RAY DIFFRACTION (2.2 Å) 主引用文献 Crystal structures of prethrombin-2 reveal alternative conformations under identical solution conditions and the mechanism of zymogen activation. Biochemistry, 50, 2011
3WW0	Crystal structure of F97A mutant, a new nuclear transport receptor of Hsp70 分子名称: Protein Hikeshi 著者 Song, J, Kose, S, Watanabe, A, Son, S.Y, Choi, S, Hong, R.H, Yamashita, E, Park, I.Y, Imamoto, N, Lee, S.J. 登録日 2014-06-12 公開日 2015-03-25 最終更新日 2024-03-20 実験手法 X-RAY DIFFRACTION (2.5 Å) 主引用文献 Structural and functional analysis of Hikeshi, a new nuclear transport receptor of Hsp70s Acta Crystallogr.,Sect.D, 71, 2015
2WNM	Solution structure of Gp2 分子名称: GENE 2 著者 Camara, B, Liu, M, Shadrinc, A, Liu, B, Simpson, P, Weinzierl, R, Severinovc, K, Cota, E, Matthews, S, Wigneshweraraj, S.R. 登録日 2009-07-13 公開日 2010-02-16 最終更新日 2024-05-15 実験手法 SOLUTION NMR 主引用文献 T7 Phage Protein Gp2 Inhibits the Escherichia Coli RNA Polymerase by Antagonizing Stable DNA Strand Separation Near the Transcription Start Site. Proc.Natl.Acad.Sci.USA, 107, 2010
1IY7	Crystal Structure of CPA and sulfamide-based inhibitor complex 分子名称: Carboxypeptidase A, PHENYLALANINE-N-SULFONAMIDE, ZINC ION 著者 Kim, S.J, Woo, J.R, Park, J.D, Kim, D.H, Ryu, S.E. 登録日 2002-07-24 公開日 2003-01-28 最終更新日 2023-12-27 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Sulfamide-Based Inhibitors for Carboxypeptidase A. Novel Type Transition State Analogue Inhibitors for Zinc Proteases J.Med.Chem., 45, 2002
1IOZ	Crystal Structure of the C-HA-RAS Protein Prepared by the Cell-Free Synthesis 分子名称: GUANOSINE-5'-DIPHOSPHATE, TRANSFORMING PROTEIN P21/H-RAS-1 著者 Kigawa, T, Yamaguchi-Nunokawa, E, Kodama, K, Matsuda, T, Yabuki, T, RIKEN Structural Genomics/Proteomics Initiative (RSGI) 登録日 2001-04-18 公開日 2001-10-03 最終更新日 2023-12-27 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Selenomethionine incorporation into a protein by cell-free synthesis J.STRUCT.FUNCT.GENOM., 2, 2001
4CIU	Crystal structure of E. coli ClpB 分子名称: ADENOSINE-5'-DIPHOSPHATE, CHAPERONE PROTEIN CLPB 著者 Kopp, J, Sinning, I, Bukau, B, Kummer, E, Mogk, A. 登録日 2013-12-16 公開日 2014-05-14 最終更新日 2019-05-22 実験手法 X-RAY DIFFRACTION (3.5 Å) 主引用文献 Head-to-Tail Interactions of the Coiled-Coil Domains Regulate Clpb Cooperation with Hsp70 in Protein Disaggregation Elife, 3, 2014
3OZS	Rat catechol O-methyltransferase in complex with a catechol-type, trifluoromethyl-imidazolyl-containing inhibitor - humanized form 分子名称: Catechol O-methyltransferase, MAGNESIUM ION, N-[(E)-3-[(2R,3S,4R,5R)-3,4-dihydroxy-5-[4-(trifluoromethyl)imidazol-1-yl]oxolan-2-yl]prop-2-enyl]-2,3-dihydroxy-5-nitro-benzamide 著者 Ehler, A, Schlatter, D, Stihle, M, Benz, J, Rudolph, M.G. 登録日 2010-09-27 公開日 2011-03-16 最終更新日 2024-04-03 実験手法 X-RAY DIFFRACTION (1.44 Å) 主引用文献 Molecular Recognition at the Active Site of Catechol-O-methyltransferase (COMT): Adenine Replacements in Bisubstrate Inhibitors Chemistry, 17, 2011

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