General Information
-
DRAMP ID
- DRAMP04186
-
Peptide Name
- L5K5W1 (L5K5Wn model peptide)
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Source
- Synthetic construct (De novo design)
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Family
- Not found
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Gene
- Not found
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Sequence
- WLKKLLKKLLK
-
Sequence Length
- 11
-
UniProt Entry
- No entry found
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Protein Existence
- Synthetic
Activity Information
-
Biological Activity
- Antimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-
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Target Organism
-
- Gram-positive bacteria: Bacillus subtilis ATCC 6633 (MIC=2 µg/mL), Staphylococcus aureus ATCC 6538p (MIC=2 µg/mL), Staphylococcus epidermis ATCC 12228 (MIC=2 µg/mL), Micrococcus luteus ATCC 10240 (MIC=4 µg/mL), MRSA-TK784 (MIC=8 µg/mL).
- Gram-negative bacteria: Escherichia coli ATCC 25922 (MIC=4 µg/mL), Shigella dysenteriae ATCC 9752 (MIC=2 µg/mL), Salmonella typhimurium ATCC 14028 (MIC=2 µg/mL), Klebsiella pneumoniae ATCC 10031 (MIC=2 µg/mL), Pseudomonas aeruginosa ATCC 27853 (MIC=8 µg/mL).
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Hemolytic Activity
-
- 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
- Not found
Structure Information
-
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 DRAMP04186.
Physicochemical Information
-
Formula
- C71H127N17O12
Absent Amino Acids
- ACDEFGHIMNPQRSTVY
Common Amino Acids
- KL
Mass
- 1410.9
PI
- 10.6
Basic Residues
- 5
Acidic Residues
- 0
Hydrophobic Residues
- 6
Net Charge
- +5
-
Boman Index
- -0.82
Hydrophobicity
- -0.127
Aliphatic Index
- 177.27
Half Life
-
- Mammalian:2.8 hour
- Yeast:3 min
- E.coli:2 min
Extinction Coefficient Cystines
- 5500
Absorbance 280nm
- 550
Polar Residues
- 0
DRAMP04186
Comments Information
Function
- Has antibacterial activity against the Gram-positive, Gram-negative bacteria and a multi-drug resistant strain.
Chemical modification
- C-terminal amidation.
Literature Information
- ·Literature 1
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Title
- Structural characterization of de novo designed L5K5W model peptide isomers with potent antimicrobial and varied hemolytic activities.
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Pubmed ID
- 23344198
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Reference
- Molecules. 2013 Jan 11;18(1):859-876.
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Author
- Kim SJ, Kim JS, Lee YS, Sim DW, Lee SH, Bahk YY, Lee KH, Kim EH, Park SJ, Lee BJ, Won HS.