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Titlebook: Bioinorganic Chemistry of Copper; Kenneth D. Karlin,Zoltán Tyeklár Book 1993 Springer Science+Business Media Dordrecht 1993 Alanin.Inorgan

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ok is highly interdisciplinary in its approach--theoutstandinglist of contributors includes coordination chemists,biochemists,biophysicists, and molecular biologists. Chapters aregrouped intomajor areas of research interest in inorganic copperchemistry,spectroscopy, oxygen chemistry, biochemistry, a
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Investigation of Type 1 Copper Site Geometry by Spectroscopy and Molecular Redesignis observed for 11 different cupredoxins. These findings suggest that all cupredoxins have a highly conserved Cu(His).Cys geometry including (i) a trigonal planar array for the three Cu ligands and (ii) a ..-C.-. in the Cu-cysteinate moiety.
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Three-Dimensional Structure of the Oxygenated Form of the Hemocyanin Subunit II of , at Atomic Resole oxygenated form of these proteins is characterized by absorption maxima at about 340 and 580 nm, while the deoxygenated form is colorless. A major interesting question that can be addressed after determining the structure of hemocyanin using single crystal x-ray diffraction methods is: How does the protein bind molecular oxygen?
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Cambridge, Keynes and the Apostles,p of primary, secondary and tertiary structures, and synthesized either . or ., can fold, itself into the predicted three dimensional structure under certain conditions. A zinc-binding site has also been introduced into a designed protein5. These studies have demonstrated that protein design in indeed achievable.
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https://doi.org/10.1007/978-1-349-01939-7articulate methane monooxygenase (pMMO) found in the membrane fraction of the cells appears to be expressed in all types of methanotrophic bacteria [3–6]. Only the sMMO has been purified and extensively characterized [7–11].
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hnsHopkins University Copper Symposium, held inAugust 1992. Researchersin chemistry, biochemistry, molecularbiology, and medicinalchemistry will find it to be an essentialreference on its subject.978-94-011-6877-9978-94-011-6875-5
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