The scientist’s investigation covers issues in Biochemistry, Enzyme, Stereochemistry, Microbiology and Enzyme inhibitor. His work on Reductase and Acetylcholinesterase as part of general Enzyme research is often related to Farnesyl-diphosphate farnesyltransferase and Ascaris suum, thus linking different fields of science. His Stereochemistry study combines topics in areas such as Ring and Biosynthesis.
Kazuro Shiomi combines subjects such as Type three secretion system and In vivo with his study of Microbiology. His work focuses on many connections between Enzyme inhibitor and other disciplines, such as Peptide sequence, that overlap with his field of interest in Depsipeptide and Organic chemistry. Kazuro Shiomi studied Antibiotics and Residue that intersect with Streptomyces.
Kazuro Shiomi focuses on Stereochemistry, Biochemistry, Microbiology, Antibiotics and Streptomyces. His research links Chitinase with Stereochemistry. His is doing research in Enzyme, Reductase, Fermentation, In vitro and Biological activity, both of which are found in Biochemistry.
The Enzyme inhibitor and Acetylcholinesterase research Kazuro Shiomi does as part of his general Enzyme study is frequently linked to other disciplines of science, such as Farnesyl-diphosphate farnesyltransferase, therefore creating a link between diverse domains of science. The Microbiology study which covers Bacteria that intersects with Antimicrobial. The concepts of his Streptomyces study are interwoven with issues in Staphylococcus aureus and Imipenem.
His main research concerns Stereochemistry, Biochemistry, Microbiology, Streptomyces and Moiety. His Stereochemistry research is multidisciplinary, incorporating perspectives in Combinatorial chemistry, Streptomyces griseus and Cytotoxicity. His study ties his expertise on Bacteria together with the subject of Biochemistry.
His studies in Bacteria integrate themes in fields like Stem rot, Cell wall, Peptide and Enzyme. His study on Antibiotics is often connected to Antiparasitic as part of broader study in Microbiology. He works mostly in the field of Streptomyces, limiting it down to topics relating to Staphylococcus aureus and, in certain cases, Enterococcus.
His primary areas of study are Stereochemistry, Biochemistry, Microbiology, Lactam and Moiety. His Stereochemistry research incorporates themes from Bioisostere and Streptomyces griseus. His study focuses on the intersection of Biochemistry and fields such as Bacteria with connections in the field of Antimicrobial.
His Microbiology research is multidisciplinary, incorporating elements of Diaminopimelic acid and 16S ribosomal RNA. While the research belongs to areas of Lactam, he spends his time largely on the problem of Staphylococcus aureus, intersecting his research to questions surrounding Streptomyces, Enterococcus and Combinatorial chemistry. His work carried out in the field of Moiety brings together such families of science as Polyene and Chromatography, Silica gel.
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Structural and Computational Analysis of the Quinone-binding Site of Complex II (Succinate-Ubiquinone Oxidoreductase) A MECHANISM OF ELECTRON TRANSFER AND PROTON CONDUCTION DURING UBIQUINONE REDUCTION
Rob Horsefield;Victoria Yankovskaya;Graham Sexton;William Whittingham.
Journal of Biological Chemistry (2006)
Atpenins, potent and specific inhibitors of mitochondrial complex II (succinate-ubiquinone oxidoreductase)
Hiroko Miyadera;Kazuro Shiomi;Hideaki Ui;Yuichi Yamaguchi.
Proceedings of the National Academy of Sciences of the United States of America (2003)
An anthelmintic compound, nafuredin, shows selective inhibition of complex I in helminth mitochondria
Satoshi Ōmura;Hiroko Miyadera;Hideaki Ui;Kazuro Shiomi.
Proceedings of the National Academy of Sciences of the United States of America (2001)
Structures of Human Acetylcholinesterase Bound to Dihydrotanshinone I and Territrem B Show Peripheral Site Flexibility
Jonah Cheung;Ebony N. Gary;Kazuro Shiomi;Terrone L. Rosenberry.
ACS Medicinal Chemistry Letters (2013)
Argadin, a new chitinase inhibitor, produced by Clonostachys sp. FO-7314.
Noriko Arai;Kazuro Shiomi;Yuuichi Yamaguchi;Rokuro Masuma.
Chemical & Pharmaceutical Bulletin (2000)
Potent Antimalarial Activities of Polyether Antibiotic, X-206
Kazuhiko Otoguro;Akiko Kohana;Chizu Manabe;Aki Ishiyama.
The Journal of Antibiotics (2001)
High-resolution structures of a chitinase complexed with natural product cyclopentapeptide inhibitors: mimicry of carbohydrate substrate.
Douglas R. Houston;Kazuro Shiomi;Noriko Arai;Satoshi Ōmura.
Proceedings of the National Academy of Sciences of the United States of America (2002)
Specificity and Affinity of Natural Product Cyclopentapeptide Inhibitors against A. fumigatus, Human, and Bacterial Chitinases
Francesco V. Rao;Douglas R. Houston;Rolf G. Boot;Johannes M.F.G. Aerts.
Chemistry & Biology (2004)
Inhibition of farnesyl-protein transferase by gliotoxin and acetylgliotoxin
Didier Van Der Pyl;Junji Inokoshi;Kazuro Shiomi;Hong Yang.
The Journal of Antibiotics (1992)
Structure of aureobasidin A.
Katsushige Ikai;Kazutoh Takesako;Kazuro Shiomi;Makoto Moriguchi.
The Journal of Antibiotics (1991)
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