• DRAMP ID

    • DRAMP18322
    • Peptide Name

    • Hominicin (Bacteriocin)
    • Source

    • Staphylococcus hominis MBBL 2-9
    • Family

    • Not found
    • Gene

    • Not found
    • Sequence

    • ITPATPFTPAIITEITAAVIA
    • Sequence Length

    • 21
    • UniProt Entry

    • No entry found
    • Protein Existence

    • Protein level
    • Biological Activity

    • Antimicrobial, Antibacterial, Anti-Gram+
    • Target Organism

      • [Ref.20654578] Gram-positive bacteria: Staphylococcus aureus (MIC=0.06 µg/ml), MRSA (MIC=0.96 µg/ml), VISA (MIC=3.82 µg/ml).
    • Hemolytic Activity

      • No hemolysis information or data found in the reference(s) presented in this entry
    • Cytotoxicity

    • No cytotoxicity information found in the reference(s) presented
    • Binding Target

    • Not found
    • Linear/Cyclic

    • Linear
    • N-terminal Modification

    • Free
    • C-terminal Modification

    • Free
    • Nonterminal Modifications and Unusual Amino Acids

    • 1-DmIle(N,N-dimethyl Ile)-I; 2,5,8,15-DHB(dehydrated threonine)-T;21-Dmp(N2, N2-dimethyl-1,2-propanediamine)-A
    • Stereochemistry

    • L
    • Structure

    • Not found
    • Structure Description

    • NMR played a critical role in establishing the peptide primary structure. While the N-terminal residue is an N,N-dimethyl Ile (DmIle), the C-terminus is a N2, N2-dimethyl-1,2-propanediamine (Dmp). In addition, threonines are dehydrated into Dhb. In this sense, this peptide may be classified as a class I variant bacteriocin.
    • Helical Wheel Diagram

    • DRAMP18322 helical wheel diagram
    • PDB ID

    • None
    • Predicted Structure

    • There is no predicted structure for DRAMP18322.
    • Formula

    • C99H163N21O29
    • Absent Amino Acids

    • CDGHKLMNQRSWY
    • Common Amino Acids

    • AIT
    • Mass

    • 2111.51
    • PI

    • 4
    • Basic Residues

    • 0
    • Acidic Residues

    • 1
    • Hydrophobic Residues

    • 12
    • Net Charge

    • -1
    • Boman Index

    • 2101
    • Hydrophobicity

    • 1.271
    • Aliphatic Index

    • 130.48
    • Half Life

      • Mammalian:20 hour
      • Yeast:30 min
      • E.coli:>10 hour
    • Extinction Coefficient Cystines

    • 0
    • Absorbance 280nm

    • 0
    • Polar Residues

    • 5

DRAMP18322

DRAMP18322 chydropathy plot
    • Function

    • Hominicin exhibited heat stability up to 121 degrees C for 15min and activity under both acidic and basic conditions (from pH 2.0 to 10.0). Hominicin exhibited distinct structural and attractive biochemical characteristics with a high bactericidal activity against MRSA and VISA, heat-tolerance and pH stability.
  • ·Literature 1
    • Title

    • Characterization and structure identification of an antimicrobial peptide, hominicin, produced by Staphylococcus hominis MBBL 2-9.
    • Reference

    • Biochem Biophys Res Commun. 2010 Aug 20;399(2):133-138.
    • Author

    • Kim PI, Sohng JK, Sung C, Joo HS, Kim EM, Yamaguchi T, Park D, Kim BG.