Model study on the catalytic cycle of glutathione peroxidase utilizing selenocysteine-containing tripeptides : elucidation of the protective bypass mechanism involving selenocysteine selenenic acids
Available in National Diet Library
Find on the publisher's website
NDL Digital Collections
Digital data available
Check on the publisher's website
DOI[10.1246/bcsj.20220156]to the data of the same series
Holdings of Libraries in Japan
This page shows libraries in Japan other than the National Diet Library that hold the material.
Please contact your local library for information on how to use materials or whether it is possible to request materials from the holding libraries.
other
CiNii Research
Search ServiceDigitalYou can check the holdings of institutions and databases with which CiNii Research is linked at the site of CiNii Research.
Bibliographic Record
You can check the details of this material, its authority (keywords that refer to materials on the same subject, author's name, etc.), etc.
- Material Type
- 記事
- Author/Editor
- Ryosuke MasudaSatoru KuwanoShohei Sase
- Publication, Distribution, etc.
- Publication Date
- 2022-07-20
- Publication Date (W3CDTF)
- 2022-07-20
- Periodical title
- Bulletin of the Chemical Society of Japan
- No. or year of volume/issue
- 95(9)
- Volume
- 95(9)
- ISSN (Periodical Title)
- 1348-0634
- ISSN-L (Periodical Title)
- 0009-2673
- Text Language Code
- eng
- DOI
- 10.1246/bcsj.20220156
- Persistent ID (NDL)
- info:ndljp/pid/12686453
- Collection
- Collection (Materials For Handicapped People:1)
- Collection (particular)
- 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会
- Acquisition Basis
- オンライン資料収集制度
- Date Accepted (W3CDTF)
- 2023-03-07T17:43:09+09:00
- Date Captured (W3CDTF)
- 2023-01-20
- Format (IMT)
- application/pdf
- Access Restrictions
- 国立国会図書館内限定公開
- Service for the Digitized Contents Transmission Service
- 図書館・個人送信対象外
- Availability of remote photoduplication service
- 可
- Periodical Title (URI)
- Periodical Title (Persistent ID (NDL))
- info:ndljp/pid/12686450
- Data Provider (Database)
- 国立国会図書館 : 国立国会図書館デジタルコレクション
- Summary, etc.
- コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会
- DOI
- 10.1246/bcsj.20220156
- Access Restrictions
- インターネット公開
- Related Material (URI)
- Is Referenced By
- Efficient oxyselenation and aminoselenation utilizing a selenenyl iodide based on the characteristic thermodynamics of its reaction with olefinsModeling Selenoprotein <i>Se</i>-Nitrosation: Synthesis of a <i>Se</i>-Nitrososelenocysteine with Persistent StabilityStable cysteine sulfenic acid: synthesis by direct oxidation of a thiol, crystallographic analysis, and elucidation of reactivities
- References
- Modeling the Catalytic Cycle of Glutathione Peroxidase by Nuclear Magnetic Resonance Spectroscopic Analysis of Selenocysteine Selenenic AcidsIsolable small-molecule cysteine sulfenic acid[5] Diversity of glutathione peroxidasesA dual attack on the peroxide bond. The common principle of peroxidatic cysteine or selenocysteine residuesPainting argyrins blue: Negishi cross-coupling for synthesis of deep-blue tryptophan analogue β-(1-azulenyl)-l alanine and its incorporation into argyrin CModel study on trapping of protein selenenic acids by utilizing a stable synthetic congenerIdentification of the catalytic site of rat liver glutathione peroxidase as selenocysteineSynthesis and characterization of 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideDiselenides and Iodine: Influence of Solution Equilibria Between Covalent Compounds and Charge – Transfer ComplexesIdentification of selenocysteine in glutathione peroxidase by mass spectroscopySelenium-Catalyzed Reduction of Hydroperoxides in Chemistry and BiologyThe discovery of allyltyrosine based tripeptides as selective inhibitors of the HIV-1 integrase strand-transfer reactionSynthesis of a Stable Selenoaldehyde by Self‐Catalyzed Thermal Dehydration of a Primary‐Alkyl‐Substituted Selenenic AcidSynthesis of selenocysteine-containing dipeptides modeling the active site of thioredoxin reductaseGlutathione peroxidasesFormation of carboxamides by direct condensation of carboxylic acids and amines in alcohols using a new alcohol- and water-soluble condensing agent: DMT-MMOrganoselenium chemistry. Preparation and reactions of 2,4,6-tri-tert-butylbenzeneselenenic acidPreparation of a Selenenic Acid and Isolation of SelenoseleninatesDFT-assisted design and evaluation of bifunctional copper(I) catalysts for the direct intermolecular addition of aldehydes and ketones to alkynesDiscovery and synthesis of novel allylthioaralkylthiopyridazines: their antiproliferative activity against MCF-7 and Hep3B cellsSynthesis of a Stable Primary-Alkyl-Substituted Selenenyl Iodide and Its Hydrolytic Conversion to the Corresponding Selenenic AcidLooking Back at the Early Stages of Redox BiologyIsolation and X‐ray Crystallographic Analysis of a Stable Selenenic AcidThe path of chemical reactions - the IRC approachHighly Efficient Glutathione Peroxidase and Peroxiredoxin Mimetics Protect Mammalian Cells against Oxidative DamageSelenium: Biochemical Role as a Component of Glutathione PeroxidaseSelenomethionine, a potential catalytic antioxidant in biological systemsLate-Stage Functionalization of the Periphery of Oligophenylene Dendrimers with Various Arene Units via Fourfold C–H BorylationModeling of selenocysteine-derived reactive intermediates utilizing a nano-sized molecular cavity as a protective cradleThe glutathione peroxidase family: Discoveries and mechanismThe Refined Structure of the Selenoenzyme Glutathione Peroxidase at 0.2‐nm ResolutionGlutathione peroxidase: A selenoenzymeHEMOGLOBIN CATABOLISMReaction path following in mass-weighted internal coordinatesRedox Chemistry of Selenenic Acids and the Insight It Brings on Transition State Geometry in the Reactions of Peroxyl RadicalsRole of the Chalcogen (S, Se, Te) in the Oxidation Mechanism of the Glutathione Peroxidase Active Site“Stable” selenenic acidsGlutathione Peroxidase-1 in Health and Disease: From Molecular Mechanisms to Therapeutic OpportunitiesIrreversible Inactivation of Glutathione Peroxidase 1 and Reversible Inactivation of Peroxiredoxin II by H <sub>2</sub> O <sub>2</sub> in Red Blood CellsFormulation of the reaction coordinateLoss of selenium from selenoproteins: Conversion of selenocysteine to dehydroalanine in vitroOrganoselenium chemistrySelenocysteine oxidation in glutathione peroxidase catalysis: an MS-supported quantum mechanics studyDual-Reactivity <i>trans</i>-Cyclooctenol Probes for Sulfenylation in Live Cells Enable Temporal Control via Bioorthogonal QuenchingCan dimedone be used to study selenoproteins? An investigation into the reactivity of dimedone toward oxidized forms of selenocysteineOrganoselenium chemistry. Redox chemistry of selenocysteine model systemsA density-functional model of the dispersion interactionA Model Study on the Effect of an Amino Group on the Antioxidant Activity of Glutathione PeroxidaseBiological significance of phospholipid hydroperoxide glutathione peroxidase (PHGPx, GPx4) in mammalian cellsSelenoprotein K form an intermolecular diselenide bond with unusually high redox potentialVersatility of Selenium Catalysis in PHGPx Unraveled by LC/ESI-MS/MSCharacterization of Mammalian SelenoproteomesSelenium Utilization by GPX4 Is Required to Prevent Hydroperoxide-Induced FerroptosisMechanism of the Catalytic Reduction of Hydroperoxides by Ebselen : A Selenium ‐ 77 Nmr StudyUsing dispersion-corrected density functional theory to understand supramolecular binding thermodynamicsContribution of Selenocysteine to the Peroxidase Activity of Selenoprotein SDensity functional calculations on first-row transition metalsProbing the Formation of a Seleninic Acid in Living Cells by the Fluorescence Switching of a Glutathione Peroxidase MimeticGlutathione Peroxidase (GPx)-like Antioxidant Activity of the Organoselenium Drug Ebselen: Unexpected Complications with Thiol Exchange Reactions
- Data Provider (Database)
- 国立情報学研究所 : CiNii Research
- Original Data Provider (Database)
- 雑誌記事索引データベースCrossref科学研究費助成事業データベースCrossrefCrossrefCrossref
- Bibliographic ID (NDL)
- 12686453