General Information
Activity Information
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Biological Activity
- Antimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-
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Target Organism
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- Gram-negative bacterium: Salmonella typhimurium ATCC 14028;
- Gram-positive bacteria: Enterococcus faecalis, Listeria monocytogenes type 1 clinical isolate, Streptococcus pyogenes clinical isolate.
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Hemolytic Activity
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- No hemolysis information or data found in the reference(s) presented in this entry
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Cytotoxicity
-
- Not included yet
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Binding Target
- Lipopolysaccharide (LPS)-binding
Structure Information
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Linear/Cyclic
- Not included yet
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N-terminal Modification
- Not included yet
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C-terminal Modification
- Not included yet
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Nonterminal Modifications and Unusual Amino Acids
- Not included yet
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Stereochemistry
- Not included yet
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Structure
- Not found
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Structure Description
- Not found
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Helical Wheel Diagram
-
PDB ID
- None
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Predicted Structure
- There is no predicted structure for DRAMP03359.
Physicochemical Information
-
Formula
- C177H282N62O46S9
Absent Amino Acids
- EFHIMVY
Common Amino Acids
- C
Mass
- 4303.11
PI
- 9.08
Basic Residues
- 7
Acidic Residues
- 1
Hydrophobic Residues
- 6
Net Charge
- +6
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Boman Index
- -97.06
Hydrophobicity
- -0.74
Aliphatic Index
- 25.79
Half Life
-
- Mammalian:5.5 hour
- Yeast:3 min
- E.coli:2 min
Extinction Coefficient Cystines
- 11500
Absorbance 280nm
- 310.81
Polar Residues
- 15
DRAMP03359
Comments Information
Function
- Antimicrobial peptide that defense response to Gram-negative bacterium and Gram-positive bacterium.
MOA
- CRS peptides were able to bind LPS and to reduce its immunostimulatory activity, leading to a substantial reduction in cellular activation.
Literature Information
- ·Literature 1
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Title
- Increased diversity of intestinal antimicrobial peptides by covalent dimer formation.
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Pubmed ID
- 15235601
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Reference
- Nat Immunol. 2004 Aug;5(8):836-843.
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Author
- Hornef MW, Pütsep K, Karlsson J, Refai E, Andersson M.