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By Carey F., Sundberg R.

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Reproduced with the permission of Ref. G-G-E-L-W-K-L-H-E-E-L-L-K-K-F-E-E-L-L-K-L-H-E-E-R-L-K-K-L-CONH 2 72 = = histidine imidazole ~= metalloporphyrin Fig. 27. The preparation of a supramolecularpeptide nanostructureby the selectivecomplexation of four metalloporphyrins[67]. (Reproducedwith the permissionof Ref. 1) peptide chains of different lengths (hence layers of different thicknesses), the authors have been able to level cleverly the surface using aminopeptidases that hydrolyze from the N-terminus the longer chain, producing a flatter surface (Fig.

3 Final Comment . . . . . . . . . . . . . . . . 92 4 References . . . . . . . . . . . . . . . . . 93 Topics in Current Chemistry, Vol. -D. 1 Introduction The significance of cytochrome P450 catalyzed reactions has now been recognized for more than 30 years [1] as one of nature's most common and sophisticated methods to oxidize endogeneous compounds in procaryotic and eucaryotic organisms. Accordingly, P450 enzymes can be isolated from bacteria [2] plants [3] and different tissues of mammals [4], where numerous isozymes participate highly specifically in the metabolism of compounds as diverse as steroids, fatty acids and alkaloids.

5 Benzylic H y d r o x y l a t i o n s . . . . . . . . . . . . 6 A r o m a t i c H y d r o x y l a t i o n s . . . . . . . . . . . 7 O x i d a t i o n s I n v o l v i n g H e t e r o a t o m P a r t i c i p a t i o n . . . . . 40 40 46 55 58 63 65 66 2 Active Site Analogues of Cytochrome P450 . . . . . . . 5 Introduction .............................. Thiolate Coordinating Iron Porphyrins .............. P450 A n a l o g u e s with S u b s t r a t e R e c o g n i t i o n Sites .

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