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6NM3

NMR structure of WW295

Summary for 6NM3
Entry DOI10.2210/pdb6nm3/pdb
NMR InformationBMRB: 30558
DescriptorWW295 peptide (1 entity in total)
Functional Keywordsantimicrobial protein
Biological sourcesynthetic construct
Total number of polymer chains1
Total formula weight1273.55
Authors
Wang, G.,Zarena, D. (deposition date: 2019-01-10, release date: 2020-07-15, Last modification date: 2024-11-13)
Primary citationLakshmaiah Narayana, J.,Mishra, B.,Lushnikova, T.,Wu, Q.,Chhonker, Y.S.,Zhang, Y.,Zarena, D.,Salnikov, E.S.,Dang, X.,Wang, F.,Murphy, C.,Foster, K.W.,Gorantla, S.,Bechinger, B.,Murry, D.J.,Wang, G.
Two distinct amphipathic peptide antibiotics with systemic efficacy.
Proc.Natl.Acad.Sci.USA, 117:19446-19454, 2020
Cited by
PubMed Abstract: Antimicrobial peptides are important candidates for developing new classes of antibiotics because of their potency against antibiotic-resistant pathogens. Current research focuses on topical applications and it is unclear how to design peptides with systemic efficacy. To address this problem, we designed two potent peptides by combining database-guided discovery with structure-based design. When bound to membranes, these two short peptides with an identical amino acid composition can adopt two distinct amphipathic structures: A classic horizontal helix (horine) and a novel vertical spiral structure (verine). Their horizontal and vertical orientations on membranes were determined by solid-state N NMR data. While horine was potent primarily against gram-positive pathogens, verine showed broad-spectrum antimicrobial activity. Both peptides protected greater than 80% mice from infection-caused deaths. Moreover, horine and verine also displayed significant systemic efficacy in different murine models comparable to conventional antibiotics. In addition, they could eliminate resistant pathogens and preformed biofilms. Significantly, the peptides showed no nephrotoxicity to mice after intraperitoneal or intravenous administration for 1 wk. Our study underscores the significance of horine and verine in fighting drug-resistant pathogens.
PubMed: 32723829
DOI: 10.1073/pnas.2005540117
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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