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Carbonic Anhydrase: Mechanism, Regulation, Links to Disease, and Industrial Applications (Hardcover, 2014 ed.) Loot Price: R5,209
Discovery Miles 52 090
You Save: R346 (6%)
Carbonic Anhydrase: Mechanism, Regulation, Links to Disease, and Industrial Applications (Hardcover, 2014 ed.): Susan C. Frost,...

Carbonic Anhydrase: Mechanism, Regulation, Links to Disease, and Industrial Applications (Hardcover, 2014 ed.)

Susan C. Frost, Robert McKenna

Series: Subcellular Biochemistry, 75

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List price R5,555 Loot Price R5,209 Discovery Miles 52 090 | Repayment Terms: R488 pm x 12* You Save R346 (6%)

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The study of carbonic anhydrase has spanned multiple generations of scientists. Carbonic anhydrase was first discovered in 1932 by Meldrum and Roughton. Inhibition by sulfanilamide was shown in 1940 by Mann and Keilin. Even Hans Krebs contributed to early studies with a paper in 1948 showing the relationship of 25 different sulfonamides to CA inhibition. It was he who pointed out the importance of both the charged and uncharged character of these compounds for physiological experiments. The field of study that focuses on carbonic anhydrase (CA) has exploded in recent years with the identification of new families and isoforms. The CAs are metalloenzymes which are comprised of 5 structurally different families: the alpha, beta, gamma, and delta, and epsilon classes. The alpha class is found primarily in animals with several isoforms associated with human disease. The beta CAs are expressed primarily in plants and are the most divergent. The gamma CAs are the most ancient. These are structurally related to the beta CAs, but have a mechanism more similar to the alpha CAs. The delta CAs are found in marine algae and diflagellates. The epsilon class is found in prokaryotes in which it is part of the carboxysome shell perhaps supplying RuBisCO with CO2 for carbon fixation. With the excitement surrounding the discovery of disease-related CAs, scientists have redoubled their efforts to better understand structure-function relationships, to design high affinity, isotype-specific inhibitors, and to delineate signaling systems that play regulatory roles over expression and activity. We have designed the book to cover basic information of mechanism, structure, and function of the CA families. The authors included in this book bring to light the newest data with regard to the role of CA in physiology and pathology, across phylums, and in unique environmental niches.

General

Imprint: Springer
Country of origin: Netherlands
Series: Subcellular Biochemistry, 75
Release date: November 2013
First published: 2014
Editors: Susan C. Frost • Robert McKenna
Dimensions: 235 x 155 x 25mm (L x W x T)
Format: Hardcover
Pages: 430
Edition: 2014 ed.
ISBN-13: 978-9400773585
Categories: Books > Medicine > Pre-clinical medicine: basic sciences > Medical genetics
Books > Medicine > General issues > Medical equipment & techniques > Medical research
Books > Science & Mathematics > Biology, life sciences > Biochemistry > Proteins
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LSN: 9400773587
Barcode: 9789400773585

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