Basic Information

IDDRAMP03933
SequenceIIYCNRRTGKCQRM
Length14
NameI14M (truncated isoform of thanatin, residue 8-21)
SourceSynthetic construct
ActivityAntimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-, Antifungal
PathogenGram-positive bacteria: Aerococcus viridans (MIC=1.2-2.5 µM), Micrococcus luteus (MIC=5-10 µM), Bacillus megaterium (MIC=10-20 µM);##Gram-negative bacteria: Escherichia coli D22 (MIC=20-40 µM), Escherichia coli D31 (MIC=20-40 µM), Klebsiella pneumoniae (MIC=20-40 µM).##Fungi: Neurospora crassa (MIC=20-40 µM), Botrytis cinerea (MIC=10-20 µM), Alternaria brassicicola (MIC=5-10 µM), Fusarium culmorum (MIC=20-40 µM).
Hemolytic ActivityNo hemolysis information or data found in the reference(s) presented in this entry
CytotoxicityNot included yet
N-terminal ModificationNot included yet
C-terminal ModificationNot included yet
Linear/Cyclic/BranchedNot included yet
Uniprot
PDB
3D View
PDB DownloadDownload PDB Predicted by Alphafold2
PubMed ID8577744

Physicochemical Properties

Residues14
SequenceIIYCNRRTGKCQRM
Molecular Weight1742.102
Grand Average of Hydropathy-0.779
Isoelectric Point10.099
Charge at pH 7.43.503
Secondary StructureHelix: 0.214, Turn: 0.143, Sheet: 0.071
Instability Index32.686
Aromaticity0.071

Similar Structure Search

Candidates based on structure

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