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Home > Art, Film & Photography > EC 2.2: EC 2.2.1, Transketolase, 1-Deoxy-D-Xylulose-5-Phosphate Synthase, Formaldehyde Transketolase, 2-Hydroxy-3-Oxoadipate Synthase
EC 2.2: EC 2.2.1, Transketolase, 1-Deoxy-D-Xylulose-5-Phosphate Synthase, Formaldehyde Transketolase, 2-Hydroxy-3-Oxoadipate Synthase

EC 2.2: EC 2.2.1, Transketolase, 1-Deoxy-D-Xylulose-5-Phosphate Synthase, Formaldehyde Transketolase, 2-Hydroxy-3-Oxoadipate Synthase


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About the Book

Chapters: Ec 2.2.1, Transketolase, 1-Deoxy-D-Xylulose-5-Phosphate Synthase, Formaldehyde Transketolase, 2-Hydroxy-3-Oxoadipate Synthase, Fluorothreonine Transaldolase, Acetoin-Ribose-5-Phosphate Transaldolase. Source: Wikipedia. Pages: 24. Not illustrated. Free updates online. Purchase includes a free trial membership in the publisher's book club where you can select from more than a million books without charge. Excerpt: Transketolase - Transketolase is widely expressed in a wide range of organisms including bacteria, plants, and mammals. The following human genes encode proteins with transketolase activity: The entrance to the active site for this enzyme is mainly made up of several arginine, histidine, serine, and aspartate side chains, with a glutamate side chain playing a secondary role. These side chains, specifically Arg359, Arg528, His469, and Ser386, are conserved within each transketolase enzyme and interact with the phosphate group of the donor and acceptor substrates. Because the substrate channel is so narrow, the donor and acceptor substrates cannot be bound simultaneously. Also, the substrates conform into a slightly extended form upon binding in the active site to accommodate this narrow channel. Although this enzyme is able to bind numerous types of substrates, such as phosphorylated and nonphosphorylated monosaccharides including the keto and aldosugars fructose, ribose, etc., it has a high specificity for the stereoconfiguration of the hydroxyl groups of the sugars. These hydroxyl groups at i3 and i4 of the ketose donor must be in the D-threo configuration in order to correctly correspond to the i1 and i2 positions on the aldose acceptor. Also they stabilize the substrate in the active site by interacting with the Asp477, His30, and His263 residues. Disruption of this configuration, both the placement of hydroxyl groups or their stereochemistry, would consequently alter the H-bonding between the resi...More: http://booksllc.net/?id=2679839



Product Details
  • ISBN-13: 9781158688944
  • Publisher: Books LLC
  • Publisher Imprint: Books LLC
  • Height: 152 mm
  • No of Pages: 26
  • Spine Width: 2 mm
  • Weight: 50 gr
  • ISBN-10: 1158688946
  • Publisher Date: 16 Sep 2010
  • Binding: Paperback
  • Language: English
  • Returnable: N
  • Sub Title: EC 2.2.1, Transketolase, 1-Deoxy-D-Xylulose-5-Phosphate Synthase, Formaldehyde Transketolase, 2-Hydroxy-3-Oxoadipate Synthase
  • Width: 229 mm


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EC 2.2: EC 2.2.1, Transketolase, 1-Deoxy-D-Xylulose-5-Phosphate Synthase, Formaldehyde Transketolase, 2-Hydroxy-3-Oxoadipate Synthase

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