• DRAMP ID

    • DRAMP03579
    • Peptide Name

    • Histatin-4 (His-rich; Human, mammals, animals)
    • Source

    • Homo sapiens (Human)
    • Family

    • Not found
    • Gene

    • Not found
    • Sequence

    • RKFHEKHHSHRGYRSNYLYDN
    • Sequence Length

    • 21
    • Protein Existence

    • Protein level
    • Biological Activity

    • Antimicrobial, Antifungal
    • Target Organism

    • No MICs found in DRAMP database
    • Hemolytic Activity

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

      • Not included yet
    • Binding Target

    • Not found
    • Linear/Cyclic

    • Not included yet
    • N-terminal Modification

    • Not included yet
    • C-terminal Modification

    • Not included yet
    • Nonterminal Modifications and Unusual Amino Acids

    • Not included yet
    • Stereochemistry

    • Not included yet
    • Structure

    • Rich
    • Structure Description

    • Not found
    • Helical Wheel Diagram

    • DRAMP03579 helical wheel diagram
    • PDB ID

    • None
    • Predicted Structure

    • There is no predicted structure for DRAMP03579.
    • Formula

    • C121H174N42O33
    • Absent Amino Acids

    • ACIMPQTVW
    • Common Amino Acids

    • H
    • Mass

    • 2744.97
    • PI

    • 9.82
    • Basic Residues

    • 9
    • Acidic Residues

    • 2
    • Hydrophobic Residues

    • 2
    • Net Charge

    • +7
    • Boman Index

    • -101.69
    • Hydrophobicity

    • -2.257
    • Aliphatic Index

    • 18.57
    • Half Life

      • Mammalian:1 hour
      • Yeast:2 min
      • E.coli:2 min
    • Extinction Coefficient Cystines

    • 4470
    • Absorbance 280nm

    • 223.5
    • Polar Residues

    • 8

DRAMP03579

DRAMP03579 chydropathy plot
    • An autoproteolytic product from Histatin 3.

  • ·Literature 1
    • Title

    • Histatins 2 and 4 are autoproteolytic degradation products of human parotid saliva.
    • Reference

    • Oral Microbiol Immunol 1992; 7: 127-128.
    • Author

    • Xu L, Lal K, Pollock JJ.