S. Matsuda

发表

On the origins of triterpenoid skeletal diversity.

Ran Xu, G. Fazio, S. Matsuda, 2004, Phytochemistry.

Studies on the Substrate Binding Segments and Catalytic Action of Lanosterol Synthase. Affinity Labeling with Carbocations Derived from Mechanism-Based Analogs of 2,3-Oxidosqualene and Site-Directed Mutagenesis Probes

E. Corey, S. Matsuda, Hengmiao Cheng, 1997 .

An Arabidopsis oxidosqualene cyclase catalyzes iridal skeleton formation by Grob fragmentation.

W. K. Wilson, Q. Xiong, S. Matsuda, 2006, Angewandte Chemie.

Arabidopsis thaliana Squalene Epoxidase 1 Is Essential for Root and Seed Development*

B. Bartel, S. Matsuda, Jeanne M Rasbery, 2007, Journal of Biological Chemistry.

Synergistic activation by Ras and 14-3-3 protein of a mitogen-activated protein kinase kinase kinase named Ras-dependent extracellular signal-regulated kinase kinase stimulator.

K. Irie, K. Matsumoto, S. Kuroda, 1994, The Journal of biological chemistry.

An Oxysterol-derived Positive Signal for 3-Hydroxy- 3-methylglutaryl-CoA Reductase Degradation in Yeast*

R. Gardner, S. Matsuda, R. Hampton, 2001, The Journal of Biological Chemistry.

Stereochemistry and mechanism of the biosynthesis of leukotriene A4 from 5(S)-hydroperoxy-6(E),8,11,14(Z)-eicosatetraenoic acid. Evidence for an organoiron intermediate

E. Corey, S. Wright, S. Matsuda, 1989 .

Cloning and heterologous expression of the Trypanosoma brucei lanosterol synthase gene.

F. Buckner, S. Matsuda, L. Nguyen, 2000, Molecular and biochemical parasitology.

Structure of the human Lanosterol synthase gene and its analysis as a candidate for holoprosencephaly (HPE1).

S. Antonarakis, C. Rossier, M. Muenke, 1999 .

Cloning and Functional Characterization of a β-Pinene Synthase from Artemisia annua That Shows a Circadian Pattern of Expression1

Shan Lu, Ran Xu, S. Matsuda, 2002, Plant Physiology.

Alternative pathways of sterol synthesis in yeast Use of C27 sterol tracers to study aberrant double-bond migrations and evaluate their relative importance

W. K. Wilson, Ran Xu, S. Matsuda, 2002, Steroids.

Protostadienol biosynthesis and metabolism in the pathogenic fungus Aspergillus fumigatus.

W. K. Wilson, Q. Xiong, S. Matsuda, 2009, Organic letters.

Arabidopsis thaliana LUP1 converts oxidosqualene to multiple triterpene alcohols and a triterpene diol.

M. Meyer, S. Matsuda, M. J. Segura, 2000, Organic letters.

Mutagenesis Approaches to Deduce StructureFunction Relationships in Terpene Synthases

S. Matsuda, M. J. Segura, E. Jackson, 2003 .

Molecular cloning of the human gene encoding lanosterol synthase from a liver cDNA library.

E. Corey, D. R. Liu, S. Matsuda, 1995, Biochemical and biophysical research communications.

Isolation of an Arabidopsis thaliana gene encoding cycloartenol synthase by functional expression in a yeast mutant lacking lanosterol synthase by the use of a chromatographic screen.

E. Corey, B. Bartel, S. Matsuda, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Cloning and functional characterization of a Trypanosoma brucei lanosterol 14α-demethylase gene ☆

F. Buckner, S. Matsuda, L. Nguyen, 2001 .

Cholesterol Import by Aspergillus fumigatus and Its Influence on Antifungal Potency of Sterol Biosynthesis Inhibitors

W. K. Wilson, Q. Xiong, J. Tarrand, 2005, Antimicrobial Agents and Chemotherapy.

Structure of the human Lanosterol Synthase gene and its analysis as a candidate for holoprosencephaly (HPE1)

S. Antonarakis, C. Rossier, M. Muenke, 1999, Human Genetics.

Catalytic enatioselective synthesis of (3S)-2,3-oxidosqualene

E. Corey, K. Yi, S. Matsuda, 1992 .

New Insights Regarding the Cyclization Pathway for Sterol Biosynthesis from (S)-2,3-Oxidosqualene

E. Corey, S. Matsuda, S. Sarshar, 1995 .

Mixed bioengineering-chemical synthesis approach for the efficient preparation of Δ7-dafachronic acid.

S. Matsuda, Z. Ball, Matias I. Kinzurik, 2014, Organic letters.

Metabolic engineering to produce sesquiterpenes in yeast.

S. Matsuda, B. Jackson, Elizabeth A Hart-Wells, 2003, Organic letters.

Intermediacy of 8-(R)-HPETE in the conversion of arachidonic acid to pre-clavulone a by Clavularia viridis. Implications for the biosynthesis of marine prostanoids

E. Corey, S. Matsuda, M. d'Alarcao, 1987 .

Mechanistic insights into triterpene synthesis from quantum mechanical calculations. Detection of systematic errors in B3LYP cyclization energies.

W. K. Wilson, Q. Xiong, S. Matsuda, 2006, Organic & biomolecular chemistry.

chy1, an Arabidopsis Mutant with Impaired β-Oxidation, Is Defective in a Peroxisomal β-Hydroxyisobutyryl-CoA Hydrolase*

B. Bartel, K. Krukenberg, S. Matsuda, 2001, The Journal of Biological Chemistry.

An oxidosqualene cyclase makes numerous products by diverse mechanisms: a challenge to prevailing concepts of triterpene biosynthesis.

W. K. Wilson, Carl S. Onak, Q. Xiong, 2007, Journal of the American Chemical Society.

Biosynthetic diversity in plant triterpene cyclization.

B. Bartel, S. Matsuda, Jeanne M Rasbery, 2006, Current opinion in plant biology.

The molecular cloning of 8-epicedrol synthase from Artemisia annua.

S. Matsuda, L. Hua, 1999, Archives of biochemistry and biophysics.

A genomics approach to the early stages of triterpene saponin biosynthesis in Medicago truncatula.

Hideyuki Suzuki, R. Dixon, Ran Xu, 2002, The Plant journal : for cell and molecular biology.

Functional Cloning of an Arabidopsis thalianacDNA Encoding Cycloeucalenol Cycloisomerase*

S. Matsuda, J. Giner, E. A. Hart, 2000, The Journal of Biological Chemistry.

Are Isoursenol and γ-Amyrin Rare Triterpenes in Nature or Simply Overlooked by Usual Analytical Methods?

W. K. Wilson, S. Matsuda, Hui Shan, 2015, Organic letters.

Lanosterol biosynthesis in plants.

Q. Xiong, M. Kolesnikova, S. Matsuda, 2006, Archives of biochemistry and biophysics.

Oxidosqualene cyclase inhibitors as antimicrobial agents.

J. C. Hinshaw, I. Coppens, P. Garnier, 2003, Journal of medicinal chemistry.

Cloning and analysis of Trypanosoma cruzi lanosterol 14α-demethylase

S. Boyle, F. Buckner, C. Verlinde, 2003 .

A putative precursor of isomalabaricane triterpenoids from lanosterol synthase mutants.

W. K. Wilson, S. Matsuda, Hui Shan, 2006, Organic letters.

Biosynthesis of 8-R-HPETE and preclavulone-A from arachidonate in several species of caribbean coral. A widespread route to marine prostanoids.

E. Corey, S. Matsuda, R. Nagata, 1988 .

Generality of marine prostanoid biosynthesis by the 2-oxidopentadienylcation pathway

E. Corey, S. Matsuda, 1987 .

Structure and reactivity of the dammarenyl cation: configurational transmission in triterpene synthesis.

W. K. Wilson, Q. Xiong, M. Ceruti, 2005, The Journal of organic chemistry.

Oxidosqualene Cyclase Residues that Promote Formation of Cycloartenol, Lanosterol, and Parkeol

W. K. Wilson, M. Meyer, S. Matsuda, 2000 .

Methodology for the Preparation of Pure Recombinant S. cerevisiae Lanosterol Synthase Using a Baculovirus Expression System. Evidence That Oxirane Cleavage and A-Ring Formation Are Concerted in the Biosynthesis of Lanosterol from 2,3-Oxidosqualene

E. Corey, S. Matsuda, Hengmiao Cheng, 1997 .

Molecular cloning of a Schizosaccharomyces pombe cDNA encoding lanosterol synthase and investigation of conserved tryptophan residues.

E. Corey, S. Matsuda, C. H. Baker, 1996, Biochemical and biophysical research communications.

Enzyme redesign: two mutations cooperate to convert cycloartenol synthase into an accurate lanosterol synthase.

T. Schulz-Gasch, S. Matsuda, Silvia Lodeiro, 2005, Journal of the American Chemical Society.

Directed evolution experiments reveal mutations at cycloartenol synthase residue His477 that dramatically alter catalysis.

M. Meyer, S. Matsuda, Silvia Lodeiro, 2002, Organic letters.

Directed Evolution To Investigate Steric Control of Enzymatic Oxidosqualene Cyclization. An Isoleucine-to-Valine Mutation in Cycloartenol Synthase Allows Lanosterol and Parkeol Biosynthesis

W. K. Wilson, S. Matsuda, L. Hua, 1999 .

Cloning and characterization of the Arabidopsis thaliana lupeol synthase gene.

W. K. Wilson, B. Bartel, S. Matsuda, 1998, Phytochemistry.

A Tyrosine-to-Threonine Mutation Converts Cycloartenol Synthase to an Oxidosqualene Cyclase that Forms Lanosterol as Its Major Product

S. Matsuda, Andy Wilson, J. Herrera, 2000 .

Mutagenesis approaches to deduce structure-function relationships in terpene synthases.

S. Matsuda, B. Jackson, M. J. Segura, 2003, Natural product reports.

An effective strategy for exploring unknown metabolic pathways by genome mining.

M. Kolesnikova, S. Matsuda, D. A. Castillo, 2013, Journal of the American Chemical Society.

Product profile of PEN3: the last unexamined oxidosqualene cyclase in Arabidopsis thaliana.

W. K. Wilson, Pietro Morlacchi, A. Bhaduri, 2009, Organic letters.

Genome mining to identify new plant triterpenoids.

Ran Xu, G. Fazio, S. Matsuda, 2004, Journal of the American Chemical Society.

Cloning and characterization of Ginkgo biloba levopimaradiene synthase which catalyzes the first committed step in ginkgolide biosynthesis.

S. Matsuda, J. Pang, H. G. Schepmann, 2001, Archives of biochemistry and biophysics.

A new irreversible inhibitor of soybean lipoxygenase: relevance to mechanism

E. Corey, S. Matsuda, M. d'Alarcao, 1986 .

Steric bulk at cycloartenol synthase position 481 influences cyclization and deprotonation.

M. Meyer, S. Matsuda, J. Pang, 2000, Organic letters.

Steric bulk at position 454 in Saccharomyces cerevisiae lanosterol synthase influences B-ring formation but not deprotonation.

S. Matsuda, L. Hua, B. M. Joubert, 2000, Organic letters.

Characterization of a Family of IAA-Amino Acid Conjugate Hydrolases from Arabidopsis*

B. Bartel, S. Matsuda, Bonnie Bartel, 2002, The Journal of Biological Chemistry.

Cloning and analysis of Trypanosoma cruzi lanosterol 14alpha-demethylase.

S. Boyle, F. Buckner, C. Verlinde, 2003, Molecular and biochemical parasitology.

Stereochemistry of water addition in triterpene synthesis: the structure of arabidiol.

W. K. Wilson, Allie C. Obermeyer, Q. Xiong, 2007, Organic letters.

Oxidosqualene Cyclase Second‐Sphere Residues Profoundly Influence the Product Profile

T. Schulz-Gasch, M. Stahl, S. Matsuda, 2004, ChemBioChem.

Directed evolution to generate cycloartenol synthase mutants that produce lanosterol.

M. Meyer, Ran Xu, S. Matsuda, 2002, Organic letters.

Trypanosome and animal lanosterol synthases use different catalytic motifs.

F. Buckner, S. Matsuda, B. M. Joubert, 2001, Organic letters.

Cloning and characterization of the Dictyostelium discoideum cycloartenol synthase cDNA

W. K. Wilson, M. Meyer, W. Gu, 2000, Lipids.

Molecular cloning, characterization, and overexpression of ERG7, the Saccharomyces cerevisiae gene encoding lanosterol synthase.

E. Corey, B. Bartel, S. Matsuda, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Cloning and Functional Characterization of a -Pinene Synthase from Artemisia annua That Shows a Circadian Pattern of Expression

Ran Xu, S. Matsuda, Xiao-Ya Chen, 2002 .

Purification of the 2,3-oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae

E. Corey, S. Matsuda, 1991 .

Umbelliferone aminoalkyl derivatives as inhibitors of oxidosqualene cyclases from Saccharomyces cerevisiae, Tripanosoma cruzi, and Pneumocystis carinii

S. Oliaro-Bosso, F. Viola, G. Cravotto, 2004, Lipids.

Enzymatic synthesis of an indole diterpene by an oxidosqualene cyclase: mechanistic, biosynthetic, and phylogenetic implications.

W. K. Wilson, A. Ganesan, Q. Xiong, 2003, Journal of the American Chemical Society.

Relaxing effects of 15-lipoxygenase products of arachidonic acid on rat aorta.

E. Corey, B. Wróblewska, S. Matsuda, 1987, The Journal of pharmacology and experimental therapeutics.

Enzymatic cyclization of dioxidosqualene to heterocyclic triterpenes.

W. K. Wilson, S. Matsuda, Hui Shan, 2005, Journal of the American Chemical Society.

chy1, an Arabidopsis mutant with impaired beta-oxidation, is defective in a peroxisomal beta-hydroxyisobutyryl-CoA hydrolase.

B. Bartel, K. Krukenberg, S. Matsuda, 2001, The Journal of biological chemistry.

Astertarone A Synthase from Chinese Cabbage Does Not Produce the C4-Epimer: Mechanistic Insights.

W. K. Wilson, S. Matsuda, Megan K Moore, 2018, Organic letters.

Arabidopsis camelliol C synthase evolved from enzymes that make pentacycles.

W. K. Wilson, Allie C. Obermeyer, M. Kolesnikova, 2007, Organic letters.