Metal-carbon bonds in enzymes and cofactors
Material type:
TextSeries: Publication details: Cambridge RSC 2009Description: xxvii, 510 p. illISBN: - 9781847559159
- 1847559158
- MED QP601.7 M47
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Directorate of Library Services General Collection | Shelf #2 | MED QP601.7.M47 (Browse shelf(Opens below)) | Available | 000000117099 |
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| MED QP572.S7B56 Biochemistry of steroid hormones | MED QP572.S7I8 Hormonal steroids : proceedings of the third International Congress on hormonal steroids Hamburg,7-12 September 1970 | MED QP572.T5T5 Thyroid hormone metabolism :proceedings of an International symposium held in Glasgow 7-9 August 1974 | MED QP601.7.M47 Metal-carbon bonds in enzymes and cofactors | MED QP601.A3.A42 Alcohol and opiates : neurochemical and behavioral mechanisms | MED QP601.H5K3 Biogenesis and physiology of histamine | MED QP601.H5K3 Biogenesis and physiology of histamine |
Organometallic chemistry of B₁₂ coenzymes -- Cobalamin- and corrinoid-dependent enzymes -- Nickel-alkyl bond formation in the active site of methyl-coenzyme M reductase -- Nickel-carbon bonds in acetyl-coenzyme a synthases/carbon monoxide dehydrogenases -- Structure and function of [NiFe]-hydro-genases -- Carbon monoxide and cyanide ligands in the active site of [FeFe]-hydrogenases -- Carbon monoxide as intrinsic ligand to iron in the active site of [Fe]-hydrogenase -- Dual role of heme as cofactor and substrate in the biosynthesis of carbon monoxide -- Copper-carbon bonds in mechanistic and structural probing of proteins as well as in situations where copper is a catalytic or receptor site -- Interaction of cyanide with enzymes containing vanadium, manganese, non-heme iron, and zinc -- Reaction mechanism of the molybdenum hydroxylase xanthine oxidoreductase: evidence against the formation of intermediates having metal-carbon bonds.
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