The Organic Chemistry of Biological PathwaysIntended for advanced undergraduates and graduate students in all areas of biochemistry, The Organic Chemistry of Biological Pathways provides an accurate treatment of the major biochemical pathways from the perspective of mechanistic organic chemistry. |
Mitä ihmiset sanovat - Kirjoita arvostelu
Yhtään arvostelua ei löytynyt.
Sisältö
Common Mechanisms in Biological Chemistry 1 | 11 |
Common Mechanisms in Biological Chemistry 1 | 18 |
Problems | 37 |
Biomolecules | 43 |
Lipid Metabolism | 93 |
Carbohydrate Metabolism | 161 |
Amino Acid Metabolism | 221 |
Nucleotide Metabolism | 305 |
References | 332 |
Biosynthesis of Some Natural Products | 339 |
A Summary of Biological Transformations | 409 |
Appendixes | 429 |
B Using the KEGG and BRENDA Databases | 436 |
Abbreviations Used in This Book | 474 |
Muita painoksia - Näytä kaikki
The Organic Chemistry of Biological Pathways, Second Edition John McMurry,Tadhg Begley Esikatselu ei käytettävissä - 2015 |
Yleiset termit ja lausekkeet
3-phosphate 5-Phospho acetyl CoA active addition reaction alcohol amino acids aspartate atom base begins biological biosynthesis bond carbon carbonyl group catabolism catalyzed CH2OH CH₂OPO32 CH3 CH3 CH3 H CH3O CO₂ CO₂ CO₂ H CO₂H coenzyme complex compounds conversion cycle cysteine decarboxylation deprotonated diphosphate double bond electron enolate enzyme example Fe(II final followed formation fructose give glucose Glutamate glyceraldehyde 3-phosphate H CH3 H H H H H3C H NH3 H₂N H₂O H3C CH3 H3C H H3C H3C hydrogen hydrolysis hydroxylation imine initial intermediate involves isomerization ketone lipoamide mechanism methyl molecules monophosphate NAD+ Note nucleophilic nucleophilic addition O₂C occurs OH CH₂OPO32 OH H OH OH OH organic oxidation oxygen pathway phosphate protein proton pyruvate reaction reduction residue ribose ring SCOA serine shown in Figure step stereoisomers structure substrate synthase thioester tion transfer undergoes yield