PDB: 19129 件ウェブページステータス検索Chemie searchBIRD

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1EXY	SOLUTION STRUCTURE OF HTLV-1 PEPTIDE BOUND TO ITS RNA APTAMER TARGET 分子名称: HTLV-1 REX PEPTIDE, RNA APTAMER, 33-MER 著者 Jiang, F, Gorin, A, Hu, W, Majumdar, A, Baskerville, S, Xu, W, Ellington, A, Patel, D.J. 登録日 2000-05-05 公開日 2000-05-15 最終更新日 2024-05-22 実験手法 SOLUTION NMR 主引用文献 Anchoring an extended HTLV-1 Rex peptide within an RNA major groove containing junctional base triples. Structure Fold.Des., 7, 1999
5CRX	ASYMMETRIC DNA-BENDING IN THE CRE-LOXP SITE-SPECIFIC RECOMBINATION SYNAPSE 分子名称: DNA (35-MER), PROTEIN (BACTERIOPHAGE P1 CRE GENE) 著者 Guo, F, Gopaul, D.N, Van Duyne, G.D. 登録日 1999-04-21 公開日 1999-07-07 最終更新日 2023-09-20 実験手法 X-RAY DIFFRACTION (2.7 Å) 主引用文献 Asymmetric DNA bending in the Cre-loxP site-specific recombination synapse. Proc.Natl.Acad.Sci.USA, 96, 1999
1GM5	Structure of RecG bound to three-way DNA junction 分子名称: ADENOSINE-5'-DIPHOSPHATE, DNA (5'-(*CP*AP*GP*CP*TP*CP*CP*AP*TP*GP*AP*TP* CP*AP*TP*TP*GP*GP*CP*A)-3'), DNA (5'-(*GP*AP*GP*CP*AP*CP*TP*GP*C)-3'), ... 著者 Singleton, M.R, Scaife, S, Wigley, D.B. 登録日 2001-09-11 公開日 2001-10-03 最終更新日 2011-07-13 実験手法 X-RAY DIFFRACTION (3.24 Å) 主引用文献 Structural Analysis of DNA Replication Fork Reversal by Recg Cell(Cambridge,Mass.), 107, 2001
7RDU	Crystal structure of Campylobacter jejuni keto said reductoisomerase in complex with magnesium and oxidixized and reduced NADPH 分子名称: Ketol-acid reductoisomerase (NADP(+)), MAGNESIUM ION, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, ... 著者 Guddat, L.W, You, L. 登録日 2021-07-11 公開日 2022-07-13 最終更新日 2023-10-18 実験手法 X-RAY DIFFRACTION (2.502 Å) 主引用文献 Multi-faceted approach for the engineering of enzyme variants with improved properties for industrial applications To Be Published
1HBI	CRYSTAL STRUCTURE OF OXYGENATED SCAPHARCA DIMERIC HEMOGLOBIN AT 1.7 ANGSTROMS RESOLUTION 分子名称: HEMOGLOBIN (OXY), OXYGEN MOLECULE, PROTOPORPHYRIN IX CONTAINING FE 著者 Royer Junior, W.E, Condon, P.J. 登録日 1994-06-22 公開日 1994-10-15 最終更新日 2024-02-07 実験手法 X-RAY DIFFRACTION (1.7 Å) 主引用文献 Crystal structure of oxygenated Scapharca dimeric hemoglobin at 1.7-A resolution. J.Biol.Chem., 269, 1994
1HJA	LYS 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH ALPHA-CHYMOTRYPSIN 分子名称: ALPHA-CHYMOTRYPSIN, OVOMUCOID INHIBITOR 著者 Ding, J.-H, James, M.N.G. 登録日 1997-07-09 公開日 1998-01-14 最終更新日 2023-08-09 実験手法 X-RAY DIFFRACTION (2.3 Å) 主引用文献 Crystal Structure of Lys18 Variant of Turkey Ovomucoid Inhibitor Third Domain Complexed with Alpha-Chymotrypsin at 2.3 A To be Published
8UXX	Arp2/3 branch junction complex, BeFx state 分子名称: ADENOSINE-5'-DIPHOSPHATE, ADENOSINE-5'-TRIPHOSPHATE, Actin, ... 著者 Chavali, S.S, Chou, S.Z, Sindelar, C.V. 登録日 2023-11-11 公開日 2024-01-31 最終更新日 2024-03-20 実験手法 ELECTRON MICROSCOPY (3.2 Å) 主引用文献 Cryo-EM structures reveal how phosphate release from Arp3 weakens actin filament branches formed by Arp2/3 complex. Nat Commun, 15, 2024
5KJ3	Connexin 26 WT peptide NMR Structure 分子名称: Gap junction beta-2 protein 著者 Dowd, T.L, Bargiello, T.A. 登録日 2016-06-17 公開日 2016-09-28 最終更新日 2023-06-14 実験手法 SOLUTION NMR 主引用文献 Structural studies of N-terminal mutants of Connexin 26 and Connexin 32 using (1)H NMR spectroscopy. Arch.Biochem.Biophys., 608, 2016
3I7G	MMP-13 in complex with a non zinc-chelating inhibitor 分子名称: 5-(4-chlorophenyl)-N-[(1S)-1-cyclohexyl-2-(methylamino)-2-oxoethyl]furan-2-carboxamide, CALCIUM ION, Collagenase 3, ... 著者 Farrow, N.A. 登録日 2009-07-08 公開日 2009-09-01 最終更新日 2024-02-21 実験手法 X-RAY DIFFRACTION (1.95 Å) 主引用文献 Improving potency and selectivity of a new class of non-Zn-chelating MMP-13 inhibitors. Bioorg.Med.Chem.Lett., 19, 2009
3I7I	MMP-13 in complex with a non zinc-chelating inhibitor 分子名称: CALCIUM ION, Collagenase 3, N-[4-(5-{[(1S)-1-cyclohexyl-2-(methylamino)-2-oxoethyl]carbamoyl}furan-2-yl)phenyl]-1-benzofuran-2-carboxamide, ... 著者 Farrow, N.A, Margarit, S.M. 登録日 2009-07-08 公開日 2009-09-01 最終更新日 2024-02-21 実験手法 X-RAY DIFFRACTION (2.208 Å) 主引用文献 Improving potency and selectivity of a new class of non-Zn-chelating MMP-13 inhibitors. Bioorg.Med.Chem.Lett., 19, 2009
5KE0	Discovery of 1-1H-Pyrazolo 4,3-c pyridine-6-yl urea Inhibitors of Extracellular Signal Regulated Kinase ERK for the Treatment of Cancers 分子名称: 1-[3-(2-methylpyridin-4-yl)-1~{H}-pyrazolo[4,3-c]pyridin-6-yl]-3-(phenylmethyl)urea, Mitogen-activated protein kinase 1, SULFATE ION 著者 Hruza, A, Lim, J. 登録日 2016-06-09 公開日 2016-07-06 最終更新日 2024-03-06 実験手法 X-RAY DIFFRACTION (1.68 Å) 主引用文献 Discovery of 1-(1H-Pyrazolo[4,3-c]pyridin-6-yl)urea Inhibitors of Extracellular Signal-Regulated Kinase (ERK) for the Treatment of Cancers. J.Med.Chem., 59, 2016
3HPV	Crystal Structure Analysis of the 2,3-dioxygenase LapB from Pseudomonas sp. KL28 分子名称: Catechol 2,3-dioxygenase, FE (II) ION 著者 Cho, J.-H, Rhee, S. 登録日 2009-06-05 公開日 2009-10-20 最終更新日 2023-11-01 実験手法 X-RAY DIFFRACTION (2.3 Å) 主引用文献 Crystal structure and functional analysis of the extradiol dioxygenase LapB from a long-chain alkylphenol degradation pathway in Pseudomonas J.Biol.Chem., 284, 2009
5KJG	Connexin 26 G12R mutant NMR structure 分子名称: Gap junction beta-2 protein 著者 Dowd, T.L, Bargiello, T.A. 登録日 2016-06-19 公開日 2016-09-28 最終更新日 2019-12-25 実験手法 SOLUTION NMR 主引用文献 Structural studies of N-terminal mutants of Connexin 26 and Connexin 32 using (1)H NMR spectroscopy. Arch.Biochem.Biophys., 608, 2016
3LO2	Crystal structure of human alpha-defensin 1 (Y21A mutant) 分子名称: (4S)-2-METHYL-2,4-PENTANEDIOL, Neutrophil defensin 1, SULFATE ION, ... 著者 Pazgier, M, Lu, W. 登録日 2010-02-03 公開日 2010-03-09 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (1.56 Å) 主引用文献 Trp-26 imparts functional versatility to human alpha-defensin HNP1. J.Biol.Chem., 285, 2010
3LY8	Crystal structure of mutant D471E of the periplasmic domain of CadC 分子名称: Transcriptional activator cadC 著者 Eichinger, A, Skerra, A. 登録日 2010-02-26 公開日 2011-02-09 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (1.9 Å) 主引用文献 Crystal structure of the sensory domain of Escherichia coli CadC, a member of the ToxR-like protein family. Protein Sci., 20, 2011
3HQ0	Crystal Structure Analysis of the 2,3-dioxygenase LapB from Pseudomonas in complex with a product 分子名称: (2E,4E)-2-hydroxy-6-oxohepta-2,4-dienoic acid, Catechol 2,3-dioxygenase, FE (III) ION 著者 Cho, J.-H, Rhee, S. 登録日 2009-06-05 公開日 2009-10-20 最終更新日 2024-04-03 実験手法 X-RAY DIFFRACTION (2 Å) 主引用文献 Crystal structure and functional analysis of the extradiol dioxygenase LapB from a long-chain alkylphenol degradation pathway in Pseudomonas J.Biol.Chem., 284, 2009
3HPY	Crystal Structure Analysis of the 2,3-dioxygenase LapB from Pseudomonas in the complex with 4-methylcatechol 分子名称: 4-METHYLCATECHOL, Catechol 2,3-dioxygenase, FE (III) ION 著者 Cho, J.-H, Rhee, S. 登録日 2009-06-05 公開日 2009-10-20 最終更新日 2024-04-03 実験手法 X-RAY DIFFRACTION (1.94 Å) 主引用文献 Crystal structure and functional analysis of the extradiol dioxygenase LapB from a long-chain alkylphenol degradation pathway in Pseudomonas J.Biol.Chem., 284, 2009
3LOE	Crystal structure of human alpha-defensin 1 (F28A mutant) 分子名称: GLYCEROL, Neutrophil defensin 1, SULFATE ION 著者 Pazgier, M, Lu, W. 登録日 2010-02-03 公開日 2010-03-09 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (1.56 Å) 主引用文献 Trp-26 imparts functional versatility to human alpha-defensin HNP1. J.Biol.Chem., 285, 2010
3LO1	Crystal structure of human alpha-defensin 1 (Y16A mutant) 分子名称: 2-(2-METHOXYETHOXY)ETHANOL, AZIDE ION, Neutrophil defensin 1 著者 Pazgier, M, Lu, W. 登録日 2010-02-03 公開日 2010-03-09 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (1.6 Å) 主引用文献 Trp-26 imparts functional versatility to human alpha-defensin HNP1. J.Biol.Chem., 285, 2010
3LPL	E. coli pyruvate dehydrogenase complex E1 component E571A mutant 分子名称: 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID, MAGNESIUM ION, PHOSPHATE ION, ... 著者 Furey, W. 登録日 2010-02-05 公開日 2010-03-02 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (2.1 Å) 主引用文献 Communication between thiamin cofactors in the Escherichia coli pyruvate dehydrogenase complex E1 component active centers: evidence for a "direct pathway" between the 4'-aminopyrimidine N1' atoms. J.Biol.Chem., 285, 2010
3LO6	Crystal structure of human alpha-defensin 1 (W26Aba mutant) 分子名称: (4S)-2-METHYL-2,4-PENTANEDIOL, CHLORIDE ION, Neutrophil defensin 1 著者 Pazgier, M, Lu, W. 登録日 2010-02-03 公開日 2010-03-09 最終更新日 2023-11-22 実験手法 X-RAY DIFFRACTION (1.56 Å) 主引用文献 Trp-26 imparts functional versatility to human alpha-defensin HNP1. J.Biol.Chem., 285, 2010
3LQ2	E. coli pyruvate dehydrogenase complex E1 E235A mutant with low TDP concentration 分子名称: 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID, MAGNESIUM ION, PHOSPHATE ION, ... 著者 Furey, W. 登録日 2010-02-08 公開日 2010-03-02 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (1.96 Å) 主引用文献 Communication between thiamin cofactors in the Escherichia coli pyruvate dehydrogenase complex E1 component active centers: evidence for a "direct pathway" between the 4'-aminopyrimidine N1' atoms. J.Biol.Chem., 285, 2010
3LO4	Crystal structure of human alpha-defensin 1 (R24A mutant) 分子名称: CHLORIDE ION, DI(HYDROXYETHYL)ETHER, Neutrophil defensin 1 著者 Pazgier, M, Lu, W. 登録日 2010-02-03 公開日 2010-03-09 最終更新日 2023-09-06 実験手法 X-RAY DIFFRACTION (1.75 Å) 主引用文献 Trp-26 imparts functional versatility to human alpha-defensin HNP1. J.Biol.Chem., 285, 2010
1ULA	APPLICATION OF CRYSTALLOGRAPHIC AND MODELING METHODS IN THE DESIGN OF PURINE NUCLEOSIDE PHOSPHORYLASE INHIBITORS 分子名称: PURINE NUCLEOSIDE PHOSPHORYLASE, SULFATE ION 著者 Ealick, S.E, Rule, S.A, Carter, D.C, Greenhough, T.J, Babu, Y.S, Cook, W.J, Habash, J, Helliwell, J.R, Stoeckler, J.D, Parksjunior, R.E, Chen, S.-F, Bugg, C.E. 登録日 1991-11-05 公開日 1993-01-15 最終更新日 2024-02-14 実験手法 X-RAY DIFFRACTION (2.75 Å) 主引用文献 Application of crystallographic and modeling methods in the design of purine nucleoside phosphorylase inhibitors. Proc.Natl.Acad.Sci.USA, 88, 1991
1ULB	APPLICATION OF CRYSTALLOGRAPHIC AND MODELING METHODS IN THE DESIGN OF PURINE NUCLEOSIDE PHOSPHORYLASE INHIBITORS 分子名称: GUANINE, PURINE NUCLEOSIDE PHOSPHORYLASE, SULFATE ION 著者 Ealick, S.E, Rule, S.A, Carter, D.C, Greenhough, T.J, Babu, Y.S, Cook, W.J, Habash, J, Helliwell, J.R, Stoeckler, J.D, Parksjunior, R.E, Chen, S.-F, Bugg, C.E. 登録日 1991-11-05 公開日 1993-01-15 最終更新日 2024-02-14 実験手法 X-RAY DIFFRACTION (2.75 Å) 主引用文献 Application of crystallographic and modeling methods in the design of purine nucleoside phosphorylase inhibitors. Proc.Natl.Acad.Sci.USA, 88, 1991

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