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2M2G

Solution structure of the antimicrobial peptide [Aba3,16]BTD-2

Summary for 2M2G
Entry DOI10.2210/pdb2m2g/pdb
Related2M1P 2M2H 2M2S 2M2X 2M2Y 2lye
NMR InformationBMRB: 18913
Related PRD IDPRD_000998
Descriptor[Aba3,16]BTD-2 (1 entity in total)
Functional Keywordstheta-defensin, cyclic peptides, cyclic cystine ladder, disulfide bond, antimicrobial peptide, antimicrobial protein
Total number of polymer chains1
Total formula weight2054.59
Authors
Conibear, A.C.,Rosengren, K.,Daly, N.L.,Troiera Henriques, S.,Craik, D.J. (deposition date: 2012-12-20, release date: 2013-02-27, Last modification date: 2023-06-14)
Primary citationConibear, A.C.,Rosengren, K.J.,Daly, N.L.,Henriques, S.T.,Craik, D.J.
The cyclic cystine ladder in theta-defensins is important for structure and stability, but not antibacterial activity.
J.Biol.Chem., 288:10830-10840, 2013
Cited by
PubMed Abstract: θ-Defensins are ribosomally synthesized cyclic peptides found in the leukocytes of some primate species and have promising applications as antimicrobial agents and scaffolds for peptide drugs. The cyclic cystine ladder motif, comprising a cyclic peptide backbone and three parallel disulfide bonds, is characteristic of θ-defensins. In this study, we explore the role of the cyclic peptide backbone and cystine ladder in the structure, stability, and activity of θ-defensins. θ-Defensin analogues with different numbers and combinations of disulfide bonds were synthesized and characterized in terms of their NMR solution structures, serum and thermal stabilities, and their antibacterial and membrane-binding activities. Whereas the structures and stabilities of the peptides were primarily dependent on the number and position of the disulfide bonds, their antibacterial and membrane-binding properties were dependent on the cyclic backbone. The results provide insights into the mechanism of action of θ-defensins and illustrate the potential of θ-defensin analogues as scaffolds for peptide drug design.
PubMed: 23430740
DOI: 10.1074/jbc.M113.451047
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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