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Titlebook: Chemistry and Biology of Pteridines and Folates; June E. Ayling,M. Gopal Nair,Charles M. Baugh Book 1993 The Editor(s) (if applicable) and

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书目名称Chemistry and Biology of Pteridines and Folates
编辑June E. Ayling,M. Gopal Nair,Charles M. Baugh
视频videohttp://file.papertrans.cn/225/224783/224783.mp4
丛书名称Advances in Experimental Medicine and Biology
图书封面Titlebook: Chemistry and Biology of Pteridines and Folates;  June E. Ayling,M. Gopal Nair,Charles M. Baugh Book 1993 The Editor(s) (if applicable) and
描述The pteridines in their multitude of forms fulfill many roles in nature ranging from pigments to cofactors for numerous redox and one-carbon transfer reactions. This extraordinary diversity of function is unified by the unique chemistry of the pteridine heterocycle. The International Symposium on the Chemistry and Biology of Pteridines and Folates is a forum for presenting recent and exciting advances in this expanding field. In of ideas results that has often stimulated bringing together various disciplines, a synergy fresh approaches to major problems. The Tenth International Symposium held at Orange Beach, Alabama, March 21-23, 1993, proved no exception by providing new insights into folate enzymology, tetrahydrobiopterin and molybdopterin biosynthesis and function, enzyme synthesis and regulation, along with novel synthetic strategies for producing compounds that will expedite further study. The many outstanding scientific contributions found in the following chapters, which represent the work presented at the Symposium, are a reflection of the significant advances made since the Ninth International Symposium held in Zurich in 1989. Since the 7th International Symposium in St.
出版日期Book 1993
关键词Glutamat; biology; chemistry; enzyme; enzymes; metabolism; research; synthesis
版次1
doihttps://doi.org/10.1007/978-1-4615-2960-6
isbn_softcover978-1-4613-6287-6
isbn_ebook978-1-4615-2960-6Series ISSN 0065-2598 Series E-ISSN 2214-8019
issn_series 0065-2598
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Science+Busines
The information of publication is updating

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https://doi.org/10.1007/978-1-4613-2159-0all yields remained unsatisfactory; ...., . and . were produced in less than a 1% yield by the condensation of biopterin . respectively with D-glucose and D-ribose in DMF in the presence of TsOH at 60 °C for 2 days.. A slighdy improved preparation of the D-Ribofuranoside . was achieved through the sequences shown below (. → .→ . → .)..
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Principles and Practices of Quality Controlion of the phenylalanine hydroxylating system,. plays a unique role as the essential coenzyme for certain hydroxylases such as the enzymes that catalyze the hydroxylation of the aromatic amino acids, phenylalanine, tyrosine and tryptophan..
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,-(,,,-Dimethylaminomethylene)-,,-(2-,-Nitrophenyl. Ethyl)-Biopterin: A Versatile Intermediate for all yields remained unsatisfactory; ...., . and . were produced in less than a 1% yield by the condensation of biopterin . respectively with D-glucose and D-ribose in DMF in the presence of TsOH at 60 °C for 2 days.. A slighdy improved preparation of the D-Ribofuranoside . was achieved through the sequences shown below (. → .→ . → .)..
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Histidines 138 and 143 are Copper Binding Ligands in , Phenylalanine Hydroxylasehe active site. and more recently by X-ray absorption spectroscopy of the copper containing enzyme.. We have used a combination of site directed mutagenesis and pulsed EPR spectroscopy to probe the copper binding site of CV PAH and identify the Cu(II) ligands.
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The Isolation and Characterization of Clones of 4a-Hydroxytetrahydrobiopterin Dehydrataseion of the phenylalanine hydroxylating system,. plays a unique role as the essential coenzyme for certain hydroxylases such as the enzymes that catalyze the hydroxylation of the aromatic amino acids, phenylalanine, tyrosine and tryptophan..
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Estimating Particle Number and Sizein nature xanthopterin (.) and leucopterin (.). In 1933 a third component, isoxanthopterin (.)., was isolated, but his constitution remained also unknown until Robert Purrmann was able to elucidate the structures of all three pigments., which turned out to be derivatives of the pyrazine [2,3-d]pyrimidine (.) ringsystem termed by Wieland...
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