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Titlebook: Natural Sulfur Compounds; Novel Biochemical an Doriano Cavallini,Gerald E. Gaull,Vincenzo Zappia Book 1980 Plenum Press, New York 1980 Calc

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發(fā)表于 2025-3-21 19:39:27 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Natural Sulfur Compounds
副標(biāo)題Novel Biochemical an
編輯Doriano Cavallini,Gerald E. Gaull,Vincenzo Zappia
視頻videohttp://file.papertrans.cn/662/661946/661946.mp4
圖書封面Titlebook: Natural Sulfur Compounds; Novel Biochemical an Doriano Cavallini,Gerald E. Gaull,Vincenzo Zappia Book 1980 Plenum Press, New York 1980 Calc
描述The third International Meeting on "Low Molecular Weight Sulfur Containing Natural Products,"sponsored by the International Union of Pure and Applied Chemistry, was held in the historical building of the Accademia Nazionale dei Lincei, Rome, Italy, June 18-21, 1979. The symposium was held in order to exchange knowledge in the intriguing and complex field of sulfur biochemistry. This theme brought together scientists from many speciali- zed areas from organic and physical chemistry to biology and medicine. The interdisciplinary nature of the meeting gave to the participants the opportunity to discuss pro- blems of common interest approached from different scienti- fic standpoints. This volume contains 47 contributions presented at the meeting which mainly deal with new structural and metabolic aspects of sulfur biochemistry. An important aspect of such a scientific meeting is the rapid publication of the proceedings. Through the cooperation of the authors in providing "camera ready" copies of their manuscripts, the good efforts of the Orga- nizing Committee, and the Plenum Press Publishing Co., it has been possible to publish this book within a few months of the meeting.
出版日期Book 1980
關(guān)鍵詞Calcium; Glutamat; Glutamin; Oxidation; amino acid; biochemistry; biology; catalysis; chemistry; metabolism; m
版次1
doihttps://doi.org/10.1007/978-1-4613-3045-5
isbn_softcover978-1-4613-3047-9
isbn_ebook978-1-4613-3045-5
copyrightPlenum Press, New York 1980
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Antagonists of Folic Acid and Vitamin B6 in Regulation of S-Adenosylmethionine and S-Adenosylhomocyzone) and related compounds is due to the inhibition of SAM decarboxylase (EC 4.1.1.50) in malignant tissue. The antitumor activity of cycloleucine (the conformational analogue of L-methionine) was suggested to be due to inhibition of L-methionine conversion to SAM catalyzed by SAM synthetase (EC 2.5.1.6)..
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Methylase Mechanisms: Steric Constraints and Modes of Catalysis,ith more recent results of our chemical mechanism studies. Ultimately, we would like to use this information in the design of potent, specific multisubstrate adduct (“transition state analog”) inhibitors (3) of these reactions.
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Adenosylmethionine as a Precursor for Nucleic Acids Modification,e transfer of both the adenosyl moiety and of the 3-amino-3-carboxypropyl group have been described in very few instances.: the acceptor molecules are enzyme proteins for the adenosyl moiety., and transfer RNA (tRNA) for the 3-amino-3-carboxypropyl group..
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Involvement of S-Adenosylmethionine in Brain Phospholipid Metabolism,hway, first demonstrated in liver by Bremer and Greenberg. and successively described in this tissue by several authors, has not been however unequivocally demonstrated in brain, and conflicting data have been produced in this connection..
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Homocysteine Biosynthesis in Plants,s eventually to inorganic sulfate. Plants complete the cycle of sulfur by reductive assimilation of inorganic sulfate to methionine (and cysteine) (Siegel, 1975), and are thus the ultimate source of methionine in most animal diets.
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