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Pseudoprolines with substitution in position 2 of the proline ring are named Ser/Thr/Cys-(ψR1,R2 Pro). Due to the preference for a cis-amide bond [ 10 ] with the preceding residue of C2-substituted pseudoprolines, their incorporation results in a kink conformation of the peptide backbone, thus preventing peptide aggregation, self-association ...
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A deficiency of the latter enzyme leads to higher levels of proline and a buildup of the intermediate breakdown product pyrroline-5-carboxylate, causing the signs and symptoms of hyperprolinemia type II.Hyperprolinemia is inherited in an autosomal recessive pattern, which means two copies of the gene in each cell are altered.
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Furthermore, proline is rarely found in α and β structures as it would reduce the stability of such structures, because its side chain α-nitrogen can only form one nitrogen bond. Additionally, proline is the only amino acid that does not form a red-purple colour when developed by spraying with ninhydrin for uses in chromatography. Proline ...
Proline: Pro or P hydroxylation: Serine: Ser or S Phosphorylation, O-linked glycosylation, N-acetylation (N-terminus) Threonine: Thr or T Phosphorylation, O-linked glycosylation, N-acetylation (N-terminus) Tryptophan: Trp or W mono- or di-oxidation, formation of kynurenine, tryptophan tryptophylquinone: Tyrosine: Tyr or Y sulfation ...
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A prominent example of proline catalysis is the addition of acetone or hydroxyacetone to a diverse set of aldehydes catalyzed by 20-30% proline catalyst loading with high (>99%) enantioselectivity yielding diol products. [37] As refined by List and Notz, the aforementioned reaction produces diol products as follows: [38]
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