cis-trans Isomerization in BiochemistryChristophe Dugave John Wiley & Sons, 13 груд. 2006 р. - 368 стор. Collating the knowledge from over 20,000 publications in chemistry, biology and nanotechnology, this handbook is the first to comprehensively present the state of the art in one ready reference. A team of international authors connects the various disciplines involved, covering cis-trans isomerization of double bonds and pseudo-double bonds, as well as other cis-trans isomerizations. For biochemists, organic chemists, physicochemists, photochemists, polymer and medicinal chemists. |
Зміст
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| 7 | |
| 15 | |
4 Retinal Binding Proteins | 53 |
5 NonRetinal Chromophoric Proteins | 77 |
6 Fatty Acids and Phospholipids | 95 |
7 In Silico Dynamic Studies of CisTrans Isomerization in Organic and Biological Systems | 113 |
8 Chemical Aspects of the Restricted Rotation of Esters Amides and Related Compounds | 143 |
9 Amide CisTrans Isomerization in Peptides and Proteins | 167 |
10 Enzymes Catalyzing Peptide Bond CisTrans Isomerizations | 195 |
11 Tailoring the CisTrans Isomerization of Amides | 225 |
12 Peptidyl Prolyl Isomerases New Targets for Novel Therapeutics? | 261 |
13 Other CisTrans Isomerizations in Organic Molecules and Biomolecules | 295 |
14 CisTrans Isomerism in Metal Complexes | 321 |
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Загальні терміни та фрази
absorption all-trans amide peptide bonds amino acid analogs archaeal rhodopsins atoms b-turn bacteriorhodopsin barrier binding Biochem Biochemistry Biol biological Biophys catalysis catalytic cell chain Chem chemical chemistry chromophore cis conformation cis isomer cis-trans isomerization complex compounds cyclophilin dihedral angles dipeptide domain double bond effect electronic energy enzyme excited excited-state fatty acid Fischer FKBP fluorescence folding formation function geometry H-bonds hFKBP12 hydrogen bond inhibition inhibitors interaction intermediate Kandori kcal mol–1 kinetic kJ mol–1 Lett ligands lipid mechanism membrane moiety molecular molecules motif Natl Acad ofthe parvulins pathway peptide bond photoisomerization Phys Pin1 polypeptide PPIase activity Proc proline prolyl bond protein protonated Schiff base quantum yield Raman reaction receptor residues retinal rhodopsin rotation Schiff base secondary amide peptide side-chain solvent species spectra spectroscopy stabilize steric structure substituents substrate tion trans conformation trans isomer transition triplet WPro