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September 18, 2003Journal of the American Chemical Society213 citations

Structure of Antibacterial Peptide Microcin J25:  A 21-Residue Lariat Protoknot

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MBMarvin J. BayroJMJayanta MukhopadhyayGSG.V.T. Swapna

Key Points

  • To resolve and correct the covalent and three-dimensional structure of the antibacterial peptide microcin J25 (MccJ25).
  • Structural analysis and characterization of the 21-residue peptide microcin J25 to determine its covalent connectivity and folding conformation.
  • Microcin J25 is not a simple 21-residue cycle as previously reported, but rather a 21-residue lariat protoknot composed of an 8-residue cyclic segment and a 13-residue linear segment threaded through the ring.
  • The peptide represents the first identified example of a lariat protoknot architecture formed by a backbone-side chain amide linkage.

Abstract

The antibacterial peptide microcin J25 (MccJ25) inhibits bacterial transcription by binding within, and obstructing, the nucleotide-uptake channel of bacterial RNA polymerase. Published covalent and three-dimensional structures indicate that MccJ25 is a 21-residue cycle. Here, we show that the published covalent and three-dimensional structures are incorrect, and that MccJ25 in fact is a 21-residue "lariat protoknot", consisting of an 8-residue cyclic segment followed by a 13-residue linear segment that loops back and threads through the cyclic segment. MccJ25 is the first example of a lariat protoknot involving a backbone-side chain amide linkage.

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Cite This Study

Bayro et al. (2003) studied this question.

synapsesocial.com/papers/69dd7c6580eea7d3f699cea6https://doi.org/10.1021/ja036677e
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