• DRAMP ID

    • DRAMP02573
    • Peptide Name

    • Penaeidin-3a (Pen-3a; shrimps, Arthropods, animals)
    • Source

    • Litopenaeus vannamei (Whiteleg shrimp) (Penaeus vannamei)
    • Family

    • Belongs to the penaeidin family
    • Gene

    • Not found
    • Sequence

    • QVYKGGYTRPIPRPPPFVRPLPGGPIGPYNGCPVSCRGISFSQARSCCSRLGRCCHVGKGYS
    • Sequence Length

    • 62
    • Protein Existence

    • Protein level
    • Biological Activity

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

      • Gram-positive bacteria: Aerococcus viridans (MIC=0.3-0.6 µM), Micrococcus luteus (MIC=1.25-2.5 µM), Bacillus megaterium (MIC=2.5-5 µM), Enterococcus fecalis (MIC>20 µM), Saphylococcus aureus (MIC>40 µM);
      • Gram-negative bacteria: Escherichia coli 363 (MI=10-20 µM), Vibrio vulnificus (MIC>20 µM), Salmonella thyphimurium (MIC>40 µM), Klebsiella pneumoniae (MIC>40 µM).
      • Fungi: Fusarium oxysporum (MIC=5-10 µM), Botrytis cinerea (MIC=5-10 µM), Neurospora crassa (MIC=1.25-2.5 µM), Aspergillus fumigatus (MIC>20 µM).
    • 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

    • Chitin-binding
    • Linear/Cyclic

    • Cyclic
    • N-terminal Modification

    • pyroglutamic acid
    • C-terminal Modification

    • Amidation
    • Nonterminal Modifications and Unusual Amino Acids

    • Disulfide bonds between Cys32 and Cys47,Cys36 and Cys54,Cys48 and Cys55. O-glycosylated on Thr8
    • Stereochemistry

    • L
    • Structure

    • Not found
    • Structure Description

    • Not found
    • Helical Wheel Diagram

    • DRAMP02573 helical wheel diagram
    • PDB ID

    • None
    • Predicted Structure

    • There is no predicted structure for DRAMP02573.
    • Formula

    • C291H456N90O77S6
    • Absent Amino Acids

    • DEMW
    • Common Amino Acids

    • GP
    • Mass

    • 6639.74
    • PI

    • 9.89
    • Basic Residues

    • 10
    • Acidic Residues

    • 0
    • Hydrophobic Residues

    • 12
    • Net Charge

    • +10
    • Boman Index

    • -95.84
    • Hydrophobicity

    • -0.377
    • Aliphatic Index

    • 51.77
    • Half Life

      • Mammalian:0.8 hour
      • Yeast:10 min
      • E.coli:>10 hour
    • Extinction Coefficient Cystines

    • 6335
    • Absorbance 280nm

    • 103.85
    • Polar Residues

    • 28

DRAMP02573

DRAMP02573 chydropathy plot
    • Function

    • Posesses antibacterial and antifungal activity. Presents chitin-binding activity.
    • Tissue specificity

    • Higher expression in hemocytes and to a lesser extent in heart, testis, gills, intestine, lymphonoid organ and hepatopancreas. Traces in eyes and subcuticular epithelium. Not present in the brain.
    • Developmental stage

    • Expression decreases 3 hours after microbial challenge to return to control levels after 12 hours and slightly increases after 24 hours.
    • PTM

    • C-terminal amidation and contains three disulfide bonds 32-47; 36-54; 48-55.
  • ·Literature 1
    • Title

    • Penaeidins, a new family of antimicrobial peptides isolated from the shrimp Penaeus vannamei (Decapoda).
    • Reference

    • J Biol Chem. 1997 Nov 7;272(45):28398-28406.
    • Author

    • Destoumieux D, Bulet P, Loew D, Van Dorsselaer A, Rodriguez J, Bachère E.
  • ·Literature 2
    • Title

    • Recombinant expression and range of activity of penaeidins, antimicrobial peptides from penaeid shrimp.
    • Reference

    • Eur J Biochem. 1999 Dec;266(2):335-346.
    • Author

    • Destoumieux D, Bulet P, Strub JM, Van Dorsselaer A, Bachère E.
  • ·Literature 3
    • Title

    • Solution structure of the recombinant penaeidin-3, a shrimp antimicrobial peptide.
    • Reference

    • J Biol Chem. 2003 Sep 19;278(38):36859-36867.
    • Author

    • Yang Y, Poncet J, Garnier J, Zatylny C, Bachère E, Aumelas A.