Search

Connecting hydrophobic surfaces in cyclic peptides increases membrane permeability
Authors
Hoang, H.N.
Assembly
Cyclic peptide ALA-MEA-PRO-ILE-PRO-ITZ
Entity
1. Cyclic peptide ALA-MEA-PRO-ILE-PRO-ITZ (polymer, Thiol state: not present), 6 monomers, 753.9506 Da Detail

AXPIPX


Formula weight
753.9506 Da
Source organism
Homo sapiens
Exptl. method
solution NMR
Data set
assigned_chemical_shifts
Chem. Shift Complete
Sequence coverage: 66.7 %, Completeness: 25.0 %, Completeness (bb): 100.0 % Detail

Polymer type: polypeptide(L)

Total1H
All25.0 % (6 of 24)25.0 % (6 of 24)
Backbone100.0 % (6 of 6)100.0 % (6 of 6)
Sidechain 0.0 % (0 of 18) 0.0 % (0 of 18)
Methyl 0.0 % (0 of 3) 0.0 % (0 of 3)

1. entity 1

AXPIPX

Sample

Solvent system chloroform, Pressure 1.0 atm, Temperature 298 K, pH 7.0, Details 1.0 mM compound 10 Cyclic peptide ALA-MEA-PRO-ILE-PRO-ITZ, chloroform


#NameIsotope labelingTypeConcentration
1compound 10 Cyclic peptide ALA-MEA-PRO-ILE-PRO-ITZnatural abundance1.0 mM

Release date
2021-08-30
Citation
Connecting Hydrophobic Surfaces in Cyclic Peptides Increases Membrane Permeability
Hoang, H.N., Hill, T.A., Fairlie, D.P.
Angew. Chem Int Ed Engl. (2021), 60, 8385-8390, PubMed 33185961 , DOI 10.1002/anie.202012643 ,
Entries sharing articles BMRB: 2 entries Detail
  BMRB: 30838 released on 2023-10-01
    Title Connecting hydrophobic surfaces in cyclic peptides increases membrane permeability
  BMRB: 30840 released on 2021-08-30
    Title Connecting hydrophobic surfaces in cyclic peptides increases membrane permeability
Experiments performed 1 experiments Detail
Chemical shift validation 3 contents Detail
Keywords PEPTIDE BINDING PROTEIN, cyclic peptides