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Status:
Available4.6
25 reviewsISBN 10: 0824740629
ISBN 13: 9780824740627
Author: Frank Jordan, Mulchand S Patel
Compiling landmark research from those laying the foundation for medical science's next leap forward, Thiamine: Catalytic Mechanisms in Normal and Disease States fully explores the pathophysiological aspects of a spectrum of diseases associated with TDP-requiring enzymes. Providing brilliant new insights into neurogenerative diseases, this comprehensive volume associates defects in the function of TDP-dependent enzymes with numerous metabolic disorders and disease states, and offers novel aspects of thiamine enzymes in chiral synthesis, as well as new perspectives on the cellular role of thiamine triphosphate and thiamine triphosphates.
Chemical Intermediates in Catalysis by Thiamine Diphosphate
Mechanistic and Structural Studies on Thiamine Biosynthetic Enzymes
Studies on the Structure and Function of Thiamine Pyrophosphokinase
New Perspectives on the Cellular Role of Thiamine Triphosphate and Thiamine Triphosphatase
How Thiamine Works in Enzymes: Time-Resolved NMR Snapshots of TDP-Dependent Enzymes in Action
Thiamine-Dependent Enzymes as Catalysts of C–C Bond-Forming Reactions: The Role of “Orphan” Enzymes
Ligand-Induced Conformational Changes in Thiamine Diphosphate-Dependent Enzymes: Comparison Between Crystal and Solution Structures
Enantioselective Syntheses of Hydroxy Ketones via Benzoylformate Decarboxylase- and Benzaldehyde Lyase-Catalyzed C–C Bond Formation
Benzoylformate Decarboxylase: Lessons in Enzymology
New Concept on the Nature of the Induced Absorption Band of Holotransketolase
Structure of the α-Carbanion/Enamine Reaction Intermediate in the Active Site of Transketolase, Determined by Kinetic Crystallography
Yeast Pyruvate Decarboxylase: New Features of the Structure and Mechanism
Solvent and Carbon Kinetic Isotope Effects on Active-Site and Regulatory-Site Variants of Yeast Pyruvate Decarboxylase
Insights into the Mechanism and Regulation of Bacterial Acetohydroxyacid Synthases
Structure and Properties of Acetohydroxyacid Synthase
Exploring the Substrate Specificity of Benzoylformate Decarboxylase, Pyruvate Decarboxylase, and Benzaldehyde Lyase
Benzoylformate Decarboxylase: Intermediates, Transition States, and Diversions
Structural and Functional Organization of Pyruvate Dehydrogenase Complexes
The Pyruvate Dehydrogenase Multienzyme Complex
Activation and Transfer of Lipoic Acid in Protein Lipoylation in Mammals
Central Organization of Mammalian Pyruvate Dehydrogenase (PD) Complex and Lipoyl Domain-Mediated Activated Function and Control of PD Kinases and Phosphatase 1
Physiological Effects of Replacing the PDH Complex of E. coli by Genetically Engineered Variants or by Pyruvate Oxidase
Structure and Intersubunit Information Transfer in the E. coli Pyruvate Dehydrogenase Multienzyme Complex
Structure, Function, and Regulation of Pyruvate Dehydrogenase Kinase
Three-Dimensional Structures for Components and Domain of the Mammalian Branched-Chain α-Ketoacid Dehydrogenase Complex
Variability of Human Pyruvate Dehydrogenase Complex Deficiency
Kinetic Studies of Human Pyruvate Dehydrogenase and Its Mutants: Interactions with Thiamine Pyrophosphate
The Complexity of Single-Gene Disorders: Lessons from Maple Syrup Urine Disease and Thiamine Responsiveness
Thiamine Pyrophosphate: An Essential Cofactor in the Mammalian Metabolism of 3-Methyl-Branched Fatty Acids
Pathogenesis of Selective Neuronal Loss in Wernicke-Korsakoff Syndrome: Role of Oxidative Stress
Thiamine-Responsive Megaloblastic Anemia Syndrome: Clinical Aspects and Molecular Genetics
Accomplishments and Future Directions
Tags: Frank Jordan, Mulchand S Patel, Thiamine, Catalytic