Basic Information

IDDRAMP18584
SequenceKWCFCVCYRGICRCRCRG
Length18
Name[Arg13]ccTP (ccTP peptide derivative)
SourceSynthetic construct
ActivityAntimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-, Anitifungal
Pathogen[Ref.10673369]Gram-positive bacteria: Staphylococcus aureus (MIC=1.3 μM in low-salt; MIC=0.9 μM in high-salt), Micrococcus luteus (MIC=0.5 μM in low-salt; MIC=0.5 μM in high-salt), Enterococcus faecalis (MIC=1.9 μM in low-salt; MIC=1.3 μM in high-salt);##Gram-negative bacteria: Escherichia coli (MIC=10.4 μM in low-salt; MIC=0.9 μM in high-salt), Pseudomonas aeruginosa (MIC=6.2 μM in low-salt; MIC=10.4 μM in high-salt), Primula vulgaris (MIC=16.4 μM in low-salt; MIC=28.9 μM in high-salt), Klebsiella oxytoca (MIC=4.0 μM in low-salt; MIC=7.6 μM in high-salt);##Fungi: Candida albicans (MIC=24.2 μM in low-salt; MIC=30.2 μM in high-salt), Candida kefyr (MIC=1.1 μM in low-salt; MIC=4.3 μM in high-salt), Candida tropicalis (MIC=12.4 μM in low-salt; MIC=3.9 μM in high-salt).
Hemolytic Activity[Ref.10673369] EC25=590 μM against human red blood cells
CytotoxicityNo cytotoxicity information found
N-terminal ModificationNo specific N-terminal
C-terminal ModificationNo specific C-terminal
Linear/Cyclic/BranchedCyclic
Uniprot
PDB
3D View
PDB DownloadDownload PDB Predicted by Alphafold2
PubMed ID10673369

Physicochemical Properties

Residues18
SequenceKWCFCVCYRGICRCRCRG
Molecular Weight2212.736
Grand Average of Hydropathy0.089
Isoelectric Point9.216
Charge at pH 7.44.405
Secondary StructureHelix: 0.278, Turn: 0.111, Sheet: 0.000
Instability Index-18.289
Aromaticity0.167

Similar Structure Search

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