3GST
 
 | STRUCTURE OF THE XENOBIOTIC SUBSTRATE BINDING SITE OF A GLUTATHIONE S-TRANSFERASE AS REVEALED BY X-RAY CRYSTALLOGRAPHIC ANALYSIS OF PRODUCT COMPLEXES WITH THE DIASTEREOMERS OF 9-(S-GLUTATHIONYL)-10-HYDROXY-9, 10-DIHYDROPHENANTHRENE | 分子名称: | (9R,10R)-9-(S-GLUTATHIONYL)-10-HYDROXY-9,10-DIHYDROPHENANTHRENE, GLUTATHIONE S-TRANSFERASE, SULFATE ION | 著者 | Ji, X, Ammon, H.L, Armstrong, R.N, Gilliland, G.L. | 登録日 | 1993-06-07 | 公開日 | 1993-10-31 | 最終更新日 | 2023-08-30 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Structure and function of the xenobiotic substrate binding site of a glutathione S-transferase as revealed by X-ray crystallographic analysis of product complexes with the diastereomers of 9-(S-glutathionyl)-10-hydroxy-9,10-dihydrophenanthrene. Biochemistry, 33, 1994
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3GTL
 
 | Backtracked RNA polymerase II complex with 13mer with G<>U mismatch | 分子名称: | DNA (28-MER), DNA (5'-D(*CP*TP*GP*CP*TP*TP*AP*TP*CP*GP*GP*TP*AP*G)-3'), DNA-directed RNA polymerase II subunit RPB1, ... | 著者 | Wang, D, Bushnell, D.A, Huang, X, Westover, K.D, Levitt, M, Kornberg, R.D. | 登録日 | 2009-03-27 | 公開日 | 2009-06-09 | 最終更新日 | 2024-11-06 | 実験手法 | X-RAY DIFFRACTION (3.38 Å) | 主引用文献 | Structural basis of transcription: backtracked RNA polymerase II at 3.4 angstrom resolution. Science, 324, 2009
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1K5A
 
 | Crystal structure of human angiogenin double variant I119A/F120A | 分子名称: | Angiogenin | 著者 | Leonidas, D.D, Shapiro, R, Subbarao, G.V, Russo, A, Acharya, K.R. | 登録日 | 2001-10-10 | 公開日 | 2002-03-20 | 最終更新日 | 2024-11-13 | 実験手法 | X-RAY DIFFRACTION (2.33 Å) | 主引用文献 | Crystallographic studies on the role of the C-terminal segment of human angiogenin in defining enzymatic potency. Biochemistry, 41, 2002
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3MZC
 
 | Human carbonic ahydrase II in complex with a benzenesulfonamide inhibitor | 分子名称: | 4-[(cyclopentylcarbamoyl)amino]benzenesulfonamide, Carbonic anhydrase 2, GLYCEROL, ... | 著者 | Avvaru, B.S, Wagner, J, Robbins, A.H, Mckenna, R. | 登録日 | 2010-05-12 | 公開日 | 2011-03-09 | 最終更新日 | 2023-09-06 | 実験手法 | X-RAY DIFFRACTION (1.498 Å) | 主引用文献 | Selective hydrophobic pocket binding observed within the carbonic anhydrase II active site accommodate different 4-substituted-ureido-benzenesulfonamides and correlate to inhibitor potency. Chem.Commun.(Camb.), 46, 2010
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5BKB
 
 | Crystal structure of AAD-1 in complex with (R)-dichlorprop, Mn(II), and 2-oxoglutarate | 分子名称: | (2R)-2-(2,4-dichlorophenoxy)propanoic acid, (R)-phenoxypropionate/alpha-ketoglutarate-dioxygenase, 2-OXOGLUTARIC ACID, ... | 著者 | Chekan, J.R, Nair, S.K. | 登録日 | 2019-06-02 | 公開日 | 2019-06-12 | 最終更新日 | 2023-09-27 | 実験手法 | X-RAY DIFFRACTION (1.582 Å) | 主引用文献 | Molecular basis for enantioselective herbicide degradation imparted by aryloxyalkanoate dioxygenases in transgenic plants. Proc.Natl.Acad.Sci.USA, 116, 2019
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3WK8
 
 | Crystal structure of soluble epoxide hydrolase in complex with fragment inhibitor | 分子名称: | 6-(trifluoromethyl)-1,3-benzothiazol-2-amine, Bifunctional epoxide hydrolase 2, MAGNESIUM ION, ... | 著者 | Amano, Y, Yamaguchi, T, Tanabe, E. | 登録日 | 2013-10-17 | 公開日 | 2014-04-16 | 最終更新日 | 2024-05-29 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Structural insights into binding of inhibitors to soluble epoxide hydrolase gained by fragment screening and X-ray crystallography. Bioorg.Med.Chem., 22, 2014
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1QQ5
 
 | STRUCTURE OF L-2-HALOACID DEHALOGENASE FROM XANTHOBACTER AUTOTROPHICUS | 分子名称: | FORMIC ACID, PROTEIN (L-2-HALOACID DEHALOGENASE) | 著者 | Ridder, I.S, Rozeboom, H.J, Kalk, K.H, Dijkstra, B.W. | 登録日 | 1999-06-10 | 公開日 | 1999-10-25 | 最終更新日 | 2023-08-16 | 実験手法 | X-RAY DIFFRACTION (1.52 Å) | 主引用文献 | Crystal structures of intermediates in the dehalogenation of haloalkanoates by L-2-haloacid dehalogenase. J.Biol.Chem., 274, 1999
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3GXX
 
 | Structure of the SH2 domain of the Candida glabrata transcription elongation factor Spt6, crystal form B | 分子名称: | Transcription elongation factor SPT6 | 著者 | Dengl, S, Mayer, A, Sun, M, Cramer, P. | 登録日 | 2009-04-03 | 公開日 | 2009-05-26 | 最終更新日 | 2024-11-27 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Structure and in vivo requirement of the yeast Spt6 SH2 domain J.Mol.Biol., 389, 2009
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2GNJ
 
 | PKA three fold mutant model of Rho-kinase with Y-27632 | 分子名称: | (R)-TRANS-4-(1-AMINOETHYL)-N-(4-PYRIDYL) CYCLOHEXANECARBOXAMIDE, cAMP-dependent protein kinase inhibitor alpha, cAMP-dependent protein kinase, ... | 著者 | Bonn, S, Herrero, S, Breitenlechner, C.B, Engh, R.A, Gassel, M, Bossemeyer, D. | 登録日 | 2006-04-10 | 公開日 | 2006-05-23 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (2.28 Å) | 主引用文献 | Structural analysis of protein kinase A mutants with Rho-kinase inhibitor specificity J.Biol.Chem., 281, 2006
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1ZW8
 
 | Solution structure of a ZAP1 zinc-responsive domain provides insights into metalloregulatory transcriptional repression in Saccharomyces cerevisiae | 分子名称: | ZINC ION, Zinc-responsive transcriptional regulator ZAP1 | 著者 | Wang, Z, Feng, L.S, Venkataraman, K, Matskevich, V.A, Parasuram, P, Laity, J.H. | 登録日 | 2005-06-03 | 公開日 | 2006-01-10 | 最終更新日 | 2024-05-22 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution structure of a Zap1 zinc-responsive domain provides insights into metalloregulatory transcriptional repression in Saccharomyces cerevisiae. J.Mol.Biol., 357, 2006
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3WKA
 
 | Crystal structure of soluble epoxide hydrolase in complex with fragment inhibitor | 分子名称: | 6-amino-1-methyl-5-(piperidin-1-yl)pyrimidine-2,4(1H,3H)-dione, Bifunctional epoxide hydrolase 2, MAGNESIUM ION, ... | 著者 | Amano, Y, Yamaguchi, T, Tanabe, E. | 登録日 | 2013-10-18 | 公開日 | 2014-04-16 | 最終更新日 | 2024-05-29 | 実験手法 | X-RAY DIFFRACTION (2.01 Å) | 主引用文献 | Structural insights into binding of inhibitors to soluble epoxide hydrolase gained by fragment screening and X-ray crystallography. Bioorg.Med.Chem., 22, 2014
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2HCT
 
 | Acidic residues at the active sites of CD38 and ADP-ribosyl cyclase determine NAAPD synthesis and hydrolysis activities | 分子名称: | ADP-ribosyl cyclase 1, BETA-NICOTINAMIDE RIBOSE MONOPHOSPHATE | 著者 | Liu, Q, Kriksunov, I.A, Hao, Q, Graeff, R, Lee, H.C. | 登録日 | 2006-06-18 | 公開日 | 2006-08-22 | 最終更新日 | 2024-11-13 | 実験手法 | X-RAY DIFFRACTION (1.95 Å) | 主引用文献 | Acidic residues at the active sites of CD38 and ADP-ribosyl cyclase determine nicotinic acid adenine dinucleotide phosphate (NAADP) synthesis and hydrolysis activities. J.Biol.Chem., 281, 2006
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1QB8
 
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4J03
 
 | Crystal structure of human soluble epoxide hydrolase complexed with fulvestrant | 分子名称: | (7beta,9beta,13alpha,17beta)-7-{9-[(R)-(4,4,5,5,5-pentafluoropentyl)sulfinyl]nonyl}estra-1(10),2,4-triene-3,17-diol, Bifunctional epoxide hydrolase 2, MAGNESIUM ION, ... | 著者 | Morisseau, C, Pakhomova, S, Hwang, S.H, Newcomer, M.E, Hammock, B.D. | 登録日 | 2013-01-30 | 公開日 | 2013-06-05 | 最終更新日 | 2023-09-20 | 実験手法 | X-RAY DIFFRACTION (2.92 Å) | 主引用文献 | Inhibition of soluble epoxide hydrolase by fulvestrant and sulfoxides. Bioorg.Med.Chem.Lett., 23, 2013
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2GNH
 
 | PKA five fold mutant model of Rho-kinase with H1152P | 分子名称: | (S)-2-METHYL-1-[(4-METHYL-5-ISOQUINOLINE)SULFONYL]-HOMOPIPERAZINE, cAMP-dependent protein kinase inhibitor alpha, cAMP-dependent protein kinase, ... | 著者 | Bonn, S, Herrero, S, Breitenlechner, C.B, Engh, R.A, Gassel, M, Bossemeyer, D. | 登録日 | 2006-04-10 | 公開日 | 2006-05-23 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (2.05 Å) | 主引用文献 | Structural analysis of protein kinase A mutants with Rho-kinase inhibitor specificity J.Biol.Chem., 281, 2006
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5BNI
 
 | Porcine CD38 complexed with complexed with a covalent intermediate, ribo-F-ribose-5'-phosphate | 分子名称: | Uncharacterized protein, [(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl [(2R,3R,4S)-4-fluoro-3-hydroxytetrahydrofuran-2-yl]methyl dihydrogen diphosphate | 著者 | Ting, K.Y, Leung, C.F.P, Graeff, R.M, Lee, H.C, Hao, Q, Kotaka, M. | 登録日 | 2015-05-26 | 公開日 | 2016-05-25 | 最終更新日 | 2025-04-09 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Porcine CD38 exhibits prominent secondary NAD(+) cyclase activity. Protein Sci., 25, 2016
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6KH0
 
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1K93
 
 | Crystal structure of the adenylyl cyclase domain of anthrax edema factor (EF) in complex with calmodulin | 分子名称: | CALCIUM ION, CALMODULIN, CALMODULIN-SENSITIVE ADENYLATE CYCLASE, ... | 著者 | Drum, C.L, Yan, S.-Z, Bard, J, Shen, Y.-Q, Lu, D, Soelaiman, S, Grabarek, Z, Bohm, A, Tang, W.-J. | 登録日 | 2001-10-26 | 公開日 | 2002-01-23 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (2.95 Å) | 主引用文献 | Structural basis for the activation of anthrax adenylyl cyclase exotoxin by calmodulin. Nature, 415, 2002
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2H74
 
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2CBD
 
 | STRUCTURE OF NATIVE AND APO CARBONIC ANHYDRASE II AND SOME OF ITS ANION-LIGAND COMPLEXES | 分子名称: | CARBONIC ANHYDRASE II, SULFITE ION, ZINC ION | 著者 | Hakansson, K, Carlsson, M, Svensson, L.A, Liljas, A. | 登録日 | 1992-06-01 | 公開日 | 1993-10-31 | 最終更新日 | 2024-10-30 | 実験手法 | X-RAY DIFFRACTION (1.67 Å) | 主引用文献 | Structure of native and apo carbonic anhydrase II and structure of some of its anion-ligand complexes. J.Mol.Biol., 227, 1992
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2H9G
 
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3W5Y
 
 | MamM-CTD | 分子名称: | Magnetosome protein MamM, SULFATE ION | 著者 | Zeytuni, N, Davidov, G, Zarivach, R. | 登録日 | 2013-02-10 | 公開日 | 2014-04-16 | 最終更新日 | 2023-11-08 | 実験手法 | X-RAY DIFFRACTION (1.95 Å) | 主引用文献 | Cation diffusion facilitators transport initiation and regulation is mediated by cation induced conformational changes of the cytoplasmic domain Plos One, 9, 2014
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3W65
 
 | MamM-CTD D249A and H264A | 分子名称: | Magnetosome protein MamM, SULFATE ION | 著者 | Zeytuni, N, Davidov, G, Zarivach, R. | 登録日 | 2013-02-10 | 公開日 | 2014-04-16 | 最終更新日 | 2023-11-08 | 実験手法 | X-RAY DIFFRACTION (2.37 Å) | 主引用文献 | Cation diffusion facilitators transport initiation and regulation is mediated by cation induced conformational changes of the cytoplasmic domain Plos One, 9, 2014
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1QI1
 
 | Ternary Complex of an NADP Dependent Aldehyde Dehydrogenase | 分子名称: | GLYCERALDEHYDE-3-PHOSPHATE, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, PROTEIN (NADP-DEPENDENT NONPHOSPHORYLATING GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE), ... | 著者 | Cobessi, D, Tete-Favier, F, Marchal, S, Branlant, G, Aubry, A. | 登録日 | 1999-06-02 | 公開日 | 2001-01-10 | 最終更新日 | 2024-12-25 | 実験手法 | X-RAY DIFFRACTION (3 Å) | 主引用文献 | Structural and biochemical investigations of the catalytic mechanism of an NADP-dependent aldehyde dehydrogenase from Streptococcus mutans. J.Mol.Biol., 300, 2000
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3N3J
 
 | Crystal structure of human carbonic anhydrase II in complex with a benzenesulfonamide inhibitor | 分子名称: | 4-({[2-(1-methylethyl)phenyl]carbamoyl}amino)benzenesulfonamide, Carbonic anhydrase 2, GLYCEROL, ... | 著者 | Avvaru, B.S, Wagner, J, Robbins, A.H, McKenna, R. | 登録日 | 2010-05-20 | 公開日 | 2011-03-09 | 最終更新日 | 2023-09-06 | 実験手法 | X-RAY DIFFRACTION (1.5 Å) | 主引用文献 | Selective hydrophobic pocket binding observed within the carbonic anhydrase II active site accommodate different 4-substituted-ureido-benzenesulfonamides and correlate to inhibitor potency. Chem.Commun.(Camb.), 46, 2010
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