Nonproteinogenic Amino Acid Building Blocks for Nonribosomal Peptide and Hybrid Polyketide Scaffolds

被引:288
作者
Walsh, Christopher T. [1 ]
Brien, Robert V. O. [2 ]
Khosla, Chaitan [2 ,3 ]
机构
[1] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[2] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[3] Stanford Univ, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
biosynthesis; nonproteinogenic amino acids; nonribosomal peptides; polyketides; BIOSYNTHETIC GENE-CLUSTER; LIPOPEPTIDE ANTIBIOTIC FRIULIMICIN; CYSTEINE PROTEASE INHIBITORS; BIOACTIVE MARINE METABOLITES; SPONGE MICROCIONA-EURYPA; TRANSFER-RNA-SYNTHETASES; SYRINGAE PV.-SYRINGAE; IN-VITRO; ESCHERICHIA-COLI; GLYCOPEPTIDE ANTIBIOTICS;
D O I
10.1002/anie.201208344
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Freestanding nonproteinogenic amino acids have long been recognized for their antimetabolite properties and tendency to be uncovered to reactive functionalities by the catalytic action of target enzymes. By installing them regiospecifically into biogenic peptides and proteins, it may be possible to usher a new era at the interface between small molecule and large molecule medicinal chemistry. Site-selective protein functionalization offers uniquely attractive strategies for posttranslational modification of proteins. Last, but not least, many of the amino acids not selected by nature for protein incorporation offer rich architectural possibilities in the context of ribosomally derived polypeptides. This Review summarizes the biosynthetic routes to and metabolic logic for the major classes of the noncanonical amino acid building blocks that end up in both nonribosomal peptide frameworks and in hybrid nonribosomal peptide-polyketide scaffolds.
引用
收藏
页码:7098 / 7124
页数:27
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