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Titlebook: Membrane Protein Protocols; Expression, Purifica Barry S. Selinsky Book 2003 Humana Press 2003

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书目名称Membrane Protein Protocols
副标题Expression, Purifica
编辑Barry S. Selinsky
视频video
概述Includes supplementary material:
丛书名称Methods in Molecular Biology
图书封面Titlebook: Membrane Protein Protocols; Expression, Purifica Barry S. Selinsky Book 2003 Humana Press 2003
描述Knowledge of the three-dimensional structure of a protein is absolutely required for the complete understanding of its function. The spatial orientation of amino acids in the active site of an enzyme demonstrates how substrate specificity is defined, and assists the medicinal chemist in the design of s- cific, tight-binding inhibitors. The shape and contour of a protein surface hints at its interaction with other proteins and with its environment. Structural ana- sis of multiprotein complexes helps to define the role and interaction of each individual component, and can predict the consequences of protein mutation or conditions that promote dissociation and rearrangement of the complex. Determining the three-dimensional structure of a protein requires milligram quantities of pure material. Such quantities are required to refine crystallization conditions for X-ray analysis, or to overcome the sensitivity limitations of NMR spectroscopy. Historically, structural determination of proteins was limited to those expressed naturally in large amounts, or derived from a tissue or cell source inexpensive enough to warrant the use of large quantities of cells. H- ever, with the advent of the
出版日期Book 2003
版次1
doihttps://doi.org/10.1385/159259400X
isbn_softcover978-1-61737-376-3
isbn_ebook978-1-59259-400-9Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2003
The information of publication is updating

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Dihydroorotate Dehydrogenase of , 5′-position of dihydroorotate by a cysteine or a serine residue in the enzyme, a hydride ion is transferred to FMN from the 6-position of the substrate (.,.). The first half reaction is common to all DHODs, but different types of DHODs deviate from each other in quaternary structure, subcellular lo
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Isolation of the Melanocortin 5 Receptorvariably tests for ligand-specific stimulation of adenylyl cyclase activity to confirm that hormone binding stimulates a G-protein coupled receptor to dissociate from a G.. These experiments have produced important information about binding and have begun the process toward developing both agonists
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Book 2003e the sensitivity limitations of NMR spectroscopy. Historically, structural determination of proteins was limited to those expressed naturally in large amounts, or derived from a tissue or cell source inexpensive enough to warrant the use of large quantities of cells. H- ever, with the advent of the
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