Basic Information

IDDRAMP29106
SequenceRKKRRQRRRLNLKALLAVAKKIL
Length23
Namet Mastoparan-C(tMP-C, Tat (49-57)-Mastoparan-C)
SourceSynthetic construct
ActivityAntimicrobial, Antibacterial,Anti-Gram+, Anti-Gram-, Anti-cancer,Antifungal
Pathogen[Ref.29904274]Gram-positive bacteria:Staphylococcus aureus NCTC 10788(MIC=4 µM); Staphylococcus aureus NCTC 10788(MBC=4 µM); Staphylococcus aureus ATCC 12493(MRSA,MIC=4 µM); Staphylococcus aureus ATCC 12493(MRSA,MBC=8 µM); Enterococcus faecalis NCTC 12697(MIC=8 µM); Enterococcus faecalis NCTC 12697(MBC=16 µM);##Gram-negative bacteria:Escherichia coli NCTC 10418(MIC=2 µM); Escherichia coli NCTC 10418(MBC=2 µM); Pseudomonas aeruginosa ATCC 27853(MIC=4 µM); Pseudomonas aeruginosa ATCC 27853(MBC=4 µM);##Fungi:Candida albicans NCTC 1467(MIC=2 µM); Candida albicans NCTC 1467(MBC=2 µM);##Cancer:Human squamous lung carcinoma NCI-H157(IC50=2.79 µM);Human breast adenocarcinoma MDA-MB-435S(IC50=3.86 µM);Human prostate adenocarcinoma PC-3(IC50=3.86 µM);Human glioblastoma U251-MG(IC50=3.36 µM); Human breast adenocarcinoma MCF-7(IC50=3.70 µM).
Hemolytic Activity[Ref.29904274]50% hemolysis against horse erythrocytes at 77.94 µM.
Cytotoxicity[Ref.29904274]Cytotoxicity:Human microvascular endothelial cells HMEC-1(IC50=9.18 µM).
N-terminal ModificationFree
C-terminal ModificationAmidation
Linear/Cyclic/BranchedLinear
Uniprot P01516, Q76PP9
PDB
3D View
PDB DownloadDownload PDB Predicted by Alphafold2
PubMed ID29904274

Physicochemical Properties

Residues23
SequenceRKKRRQRRRLNLKALLAVAKKIL
Molecular Weight2829.533
Grand Average of Hydropathy-0.887
Isoelectric Point12
Charge at pH 7.410.545
Secondary StructureHelix: 0.304, Turn: 0.043, Sheet: 0.348
Instability Index107.817
Aromaticity0

Similar Structure Search

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