Basic Information

IDDRAMP21344
SequenceFLGALWNVFKSVF
Length13
Name[Phe]9-VmCT1-NH2 (Derived from VmCT1)
Sourcesynthetic construct
ActivityAntimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-, Antifungal
Pathogen[Ref.31212183] Gram-positive bacteria: Micrococcus luteus A270 (MIC=0.2 μmol/L), Staphylococcus aureus ATCC 29213 (MIC=0.8 μmol/L), Bacillus megaterium ATCC 10778 (MIC=1.6 μmol/L), Bacillus subtilis ATCC 6633 (MIC=0.8 μmol/L);##Gram-negative bacteria: Escherichia coli SBS 363 (MIC=1.6 μmol/L),Serratia marcescens ATCC 4112 (MIC=0.2 μmol/L);##Fungi: Candida albicans MDM8 (MIC=6.3 μmol/L), Candida tropicalis IOC 4560 (MIC=0.8 μmol/L)
Hemolytic Activity[Ref.31212183] 10% hemolysis at 1.6 μmol/L, 40% hemolysis at 3.1 μmol/L, 60% hemolysis at 6.3 μmol/L, 85% hemolysis at 25 μmol/L for human red blood cells
Cytotoxicity[Ref.31212183] No cytotoxicity information found
N-terminal ModificationFree
C-terminal ModificationAmidation
Linear/Cyclic/BranchedLinear
Uniprot
PDB
3D View
PDB DownloadDownload PDB Predicted by Alphafold2
PubMed ID31212183

Physicochemical Properties

Residues13
SequenceFLGALWNVFKSVF
Molecular Weight1527.805
Grand Average of Hydropathy1.285
Isoelectric Point8.75
Charge at pH 7.40.555
Secondary StructureHelix: 0.615, Turn: 0.231, Sheet: 0.231
Instability Index18.846
Aromaticity0.308

Similar Structure Search

Candidates based on structure

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