Basic Information

IDDRAMP21263
SequenceLLKLLLKLLLKLL
Length13
NameKL10A0 (De novo synthesis)
SourceSynthetic construct
ActivityAntimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-
Pathogen[Ref.26385363] Gram-positive bacteria : Staphylococcus aureus ATCC 29213(MIC>128 μM), Staphylococcus epidermidis ATCC 12228(MIC>128 μM), Streptococcus faecalis ATCC 29212(MIC>128 μM), Bacillus subtilis CMCC 63501(MIC>128 μM);##Gram-negative bacteria : Escherichia coli ATCC25922(MIC>128 μM), Escherichia coli K88(MIC>128 μM), Escherichia coli CVCC 1515(MIC>128 μM), Escherichia coli UB1005(MIC>128 μM), Bacterium pyocyaneum ATCC 27853(MIC>128 μM), Salmonella typhimurium ATCC 14028(MIC>128 μM), Salmonella pullorum C79–13(MIC>128 μM)
Hemolytic Activity[Ref.26385363] MHC5=2 μM against human red blood cells
Cytotoxicity[Ref.26385363] The cell viability of HEK293 cells induced by KL10A0 is 93.9%, 93.3%, 81.9%, 77.2%, 75.6%, 67.8%, 51.9% and 19.4% at peptide concentrations of 1, 2, 4, 8, 16, 32, 64 and 128 μM. The cell viability of HEK293 cells induced by control Melitti
N-terminal ModificationFree
C-terminal ModificationAmidation
Linear/Cyclic/BranchedLinear
Uniprot
PDB
3D View
PDB DownloadDownload PDB Predicted by Alphafold2
PubMed ID26385363

Physicochemical Properties

Residues13
SequenceLLKLLLKLLLKLL
Molecular Weight1534.108
Grand Average of Hydropathy2.023
Isoelectric Point10.302
Charge at pH 7.42.55
Secondary StructureHelix: 0.769, Turn: 0.000, Sheet: 0.769
Instability Index-29.954
Aromaticity0

Similar Structure Search

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