Structural and Chemical Profiling of the Human Cytosolic Sulfotransferases
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Rafael Najmanovich | Alexey Bochkarev | Abdellah Allali-Hassani | Wolfram Tempel | Peter Loppnau | Cheryl H Arrowsmith | Masoud Vedadi | P. Pan | R. Najmanovich | C. Arrowsmith | M. Vedadi | A. Bochkarev | A. Plotnikov | A. Allali-Hassani | P. Loppnau | A. Dong | W. Tempel | Aiping Dong | Aled M Edwards | Alexander N Plotnikov | F. Martín | L. Dombrovski | Patricia W Pan | Ludmila Dombrovski | Fernando Martin | Janet Thonton | A. Edwards | Janet Thonton
[1] L. Pedersen,et al. Crystal structure of SULT2A3, human hydroxysteroid sulfotransferase , 2000, FEBS letters.
[2] R. Weinshilboum,et al. A proposed nomenclature system for the cytosolic sulfotransferase (SULT) superfamily. , 2004, Pharmacogenetics.
[3] K. A. Comer,et al. Human Dehydroepiandrosterone Sulfotransferase , 1995 .
[4] K. S. Arun,et al. Least-Squares Fitting of Two 3-D Point Sets , 1987, IEEE Transactions on Pattern Analysis and Machine Intelligence.
[5] K. A. Comer,et al. Human dehydroepiandrosterone sulfotransferase. Purification, molecular cloning, and characterization. , 1995, Annals of the New York Academy of Sciences.
[6] N. Liyou,et al. Structure of a Human Carcinogen-converting Enzyme, SULT1A1 , 2003, The Journal of Biological Chemistry.
[7] Mei Li,et al. Crystal structure of human sulfotransferase SULT1A3 in complex with dopamine and 3'-phosphoadenosine 5'-phosphate. , 2005, Biochemical and biophysical research communications.
[8] G. Pacifici. Inhibition of human liver and duodenum sulfotransferases by drugs and dietary chemicals: a review of the literature. , 2004, International journal of clinical pharmacology and therapeutics.
[9] Chi‐Huey Wong,et al. Sulfotransferases: structure, mechanism, biological activity, inhibition, and synthetic utility. , 2004, Angewandte Chemie.
[10] Joseph A. Baur,et al. Therapeutic potential of resveratrol: the in vivo evidence , 2006, Nature Reviews Drug Discovery.
[11] R. Shi,et al. Identifying Androsterone (ADT) as a Cognate Substrate for Human Dehydroepiandrosterone Sulfotransferase (DHEA-ST) Important for Steroid Homeostasis , 2004, Journal of Biological Chemistry.
[12] T. Nakayama,et al. Highly conserved mouse and human brain sulfotransferases: molecular cloning, expression, and functional characterization. , 2002, Gene.
[13] Jennifer L. Martin,et al. The Structure of Human SULT1A1 Crystallized with Estradiol , 2005, Journal of Biological Chemistry.
[14] T. P. Dooley. Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs. , 1998, Chemico-biological interactions.
[15] M. Coughtrie,et al. Human Cytosolic Sulfotransferases , 2005 .
[16] H. Glatt,et al. Potent inhibition of estrogen sulfotransferase by hydroxylated metabolites of polyhalogenated aromatic hydrocarbons reveals alternative mechanism for estrogenic activity of endocrine disrupters. , 2002, The Journal of clinical endocrinology and metabolism.
[17] P. Nordlund,et al. Chemical screening methods to identify ligands that promote protein stability, protein crystallization, and structure determination , 2006, Proceedings of the National Academy of Sciences.
[18] R. Weinshilboum,et al. Human SULT1A3 pharmacogenetics: gene duplication and functional genomic studies. , 2004, Biochemical and biophysical research communications.
[19] L. Pedersen,et al. Crystal Structure of the Human Estrogen Sulfotransferase-PAPS Complex , 2002, The Journal of Biological Chemistry.
[20] Sean R. Eddy,et al. Profile hidden Markov models , 1998, Bioinform..
[21] R. Weinshilboum,et al. Catecholestrogen sulfation: possible role in carcinogenesis. , 2002, Biochemical and biophysical research communications.
[22] L. Pedersen,et al. Crystal structure of human catecholamine sulfotransferase. , 1999, Journal of molecular biology.
[23] R. Laskowski. SURFNET: a program for visualizing molecular surfaces, cavities, and intermolecular interactions. , 1995, Journal of molecular graphics.
[24] H. Glatt,et al. Sulfotransferases and acetyltransferases in mutagenicity testing: technical aspects. , 2005, Methods in enzymology.
[25] C. Falany,et al. Expression and characterization of a novel thyroid hormone-sulfating form of cytosolic sulfotransferase from human liver. , 1998, Molecular pharmacology.
[26] M. Zhou,et al. Crystal structure of human dehydroepiandrosterone sulphotransferase in complex with substrate. , 2002, The Biochemical journal.
[27] C. Falany,et al. Bacterial expression and characterization of a cDNA for human liver estrogen sulfotransferase , 1995, The Journal of Steroid Biochemistry and Molecular Biology.
[28] A. Bochkarev,et al. Crystal structures of human sulfotransferases SULT1B1 and SULT1C1 complexed with the cofactor product adenosine‐3′‐ 5′‐diphosphate (PAP) , 2006, Proteins.
[29] C. Bron,et al. Algorithm 457: finding all cliques of an undirected graph , 1973 .
[30] C. Falany,et al. Molecular cloning and expression of novel sulphotransferase-like cDNAs from human and rat brain. , 2000, The Biochemical journal.
[31] T. Leyh,et al. Transition State of the Sulfuryl Transfer Reaction of Estrogen Sulfotransferase* , 2006, Journal of Biological Chemistry.
[32] Jennifer L. Martin,et al. Human SULT1A SULTs , 2005 .
[33] L. Pedersen,et al. Crystal Structure of Human Cholesterol Sulfotransferase (SULT2B1b) in the Presence of Pregnenolone and 3′-Phosphoadenosine 5′-Phosphate , 2003, Journal of Biological Chemistry.
[34] Jennifer L. Martin,et al. Human sulfotransferases and their role in chemical metabolism. , 2006, Toxicological sciences : an official journal of the Society of Toxicology.
[35] H. Glatt,et al. Sulfotransferases in the bioactivation of xenobiotics. , 2000, Chemico-biological interactions.
[36] M. Coughtrie. Catecholamine sulfation in health and disease. , 1998, Advances in pharmacology.
[37] H. Glatt,et al. Potent inhibition of estrogen sulfotransferase by hydroxylated PCB metabolites: a novel pathway explaining the estrogenic activity of PCBs. , 2000, Endocrinology.
[38] A. Hersey,et al. X-ray Crystal Structure of Human Dopamine Sulfotransferase, SULT1A3 , 1999, The Journal of Biological Chemistry.
[39] R D Klausner,et al. The mammalian gene collection. , 1999, Science.
[40] Jennifer L. Martin,et al. Active Site Mutations and Substrate Inhibition in Human Sulfotransferase 1A1 and 1A3* , 2004, Journal of Biological Chemistry.
[41] Jaime Prilusky,et al. Automated analysis of interatomic contacts in proteins , 1999, Bioinform..
[42] R. Duggleby,et al. Analysis of the substrate specificity of human sulfotransferases SULT1A1 and SULT1A3: site-directed mutagenesis and kinetic studies. , 1999, Biochemistry.
[43] Annabel E. Todd,et al. Evolution of function in protein superfamilies, from a structural perspective. , 2001, Journal of molecular biology.
[44] L. Pedersen,et al. Crystallographic analysis of a hydroxylated polychlorinated biphenyl (OH-PCB) bound to the catalytic estrogen binding site of human estrogen sulfotransferase. , 2003, Environmental health perspectives.
[45] E. Brown,et al. Probing the active site of YjeE: a vital Escherichia coli protein of unknown function. , 2004, The Biochemical journal.
[46] Masoud Vedadi,et al. Screening for Ligands Using a Generic and High-Throughput Light-Scattering-Based Assay , 2006, Journal of biomolecular screening.
[47] K. A. Comer,et al. Cloning and expression of human liver dehydroepiandrosterone sulphotransferase. , 1993, The Biochemical journal.
[48] B. Everitt. Cluster Analysis of Subjects, Hierarchical Methods , 2005 .
[49] R. Weinshilboum,et al. Human cytosolic sulfotransferase database mining: identification of seven novel genes and pseudogenes , 2004, The Pharmacogenomics Journal.
[50] A. D. Rodrigues,et al. Sulfotransferase 1E1 is a low km isoform mediating the 3-O-sulfation of ethinyl estradiol. , 2004, Drug metabolism and disposition: the biological fate of chemicals.