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Disulphide linked homodimer of designed antimicrobial peptide VG16KRKP
Authors
Datta, A., Bhunia, A.
Assembly
VG16KRKP DIMER
Entity
1. VG16KRKP DIMER (polymer, Thiol state: all disulfide bound), 16 monomers, 1760.116 × 2 Da Detail

VARGWKRKCP LFGKGG


Total weight
3520.232 Da
Max. entity weight
1760.116 Da
Entity Connection
disulfide 1 Detail

IDTypeValue orderAtom ID 1Atom ID 2
1disulfidesing1:CYS9:SG1:CYS9:SG

Exptl. method
solution NMR
Refine. method
distance geometry
Data set
assigned_chemical_shifts
Chem. Shift Complete
Sequence coverage: 100.0 %, Completeness: 81.9 %, Completeness (bb): 85.7 % Detail

Polymer type: polypeptide(L)

Total1H
All81.9 % (86 of 105)81.9 % (86 of 105)
Backbone85.7 % (30 of 35)85.7 % (30 of 35)
Sidechain80.0 % (56 of 70)80.0 % (56 of 70)
Aromatic100.0 % (11 of 11)100.0 % (11 of 11)
Methyl100.0 % (5 of 5)100.0 % (5 of 5)

1. entity

VARGWKRKCP LFGKGG

Sample

Solvent system 90% H2O/10% D2O, Pressure 1 atm, Temperature 298 K, pH 4.5


#NameIsotope labelingTypeConcentration
1VG16KRKP DIMERnatural abundanceprotein1 mM
2D2O[U-2H]solvent10 %
3H2Onatural abundancesolvent90 %
4DSSnatural abundance1 mM

Protein Blocks Logo
Calculated from 20 models in PDB: 2N65, Strand ID: A, B Detail


Release date
2016-03-20
Citation
Designing potent antimicrobial peptides by disulphide linked dimerization and N-terminal lipidation to increase antimicrobial activity and membrane perturbation: Structural insights into lipopolysaccharide binding
Datta, A., Kundu, P., Bhunia, A.
J. Colloid Interface Sci. (2016), 461, 335-345, PubMed 26407061 , DOI 10.1016/j.jcis.2015.09.036 ,
Related entities 1. VG16KRKP DIMER, : 1 : 9 : 3 : 106 entities Detail
Experiments performed 2 experiments Detail
nullKeywords disulphide linked VG16KRKP homodimer