Basic Information

IDDRAMP21241
SequenceGFIFHIIKGLFHAGKMIHGLV
Length21
NameEpinecidin-1 (Derived from Epinecidin)
SourceSynthetic construct
ActivityAntimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-
Pathogen[Ref.23598079] Gram-positive bacteria : Micrococcus luteus(MIC=6.25 mg/L), Staphylococcus aureus(MIC=50 mg/L), Streptococcus pneumoniae(MIC=50 mg/L), Streptococcus agalactiae(MIC>=100 mg/L), Staphylococcus sp.(MIC=6.25 mg/L);##Gram-negative bacteria : Grouper Vibrio alginolyticus(MIC=6.25 mg/L), Vibrio harveyi(MIC=6.25 mg/L), Vibrio vulnificus(MIC=50 mg/L)
Hemolytic Activity[Ref.23598079] 0% hemolysis at 25 mg/L , 10% hemolysis at 50 mg/L , 15% hemolysis at 100 mg/L , 30% hemolysis at 200 mg/L , 50% hemolysis at 400 mg/L against sheep red blood cells
Cytotoxicity[Ref.23598079] No cytotoxicity information found.
N-terminal ModificationFree
C-terminal ModificationFree
Linear/Cyclic/BranchedLinear
Uniprot
PDB
3D View
PDB DownloadDownload PDB Predicted by Alphafold2
PubMed ID23598079

Physicochemical Properties

Residues21
SequenceGFIFHIIKGLFHAGKMIHGLV
Molecular Weight2335.855
Grand Average of Hydropathy1.09
Isoelectric Point10.003
Charge at pH 7.41.662
Secondary StructureHelix: 0.476, Turn: 0.190, Sheet: 0.190
Instability Index34.781
Aromaticity0.143

Similar Structure Search

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