General Information
-
DRAMP ID
- DRAMP29045
-
Peptide Name
- PA2-GNU7
-
Source
- Synthetic construct
-
Family
- Not found
-
Gene
- N/A
-
Sequence
- SQRKLAAKLTSKGGGRLLRPLLQLLKQKLR
-
Sequence Length
- 30
-
UniProt Entry
- No entry found
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Protein Existence
- Synthetic form
Activity Information
-
Biological Activity
- Antimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-
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Target Organism
-
- [Ref.31704464] Gram-positive bacteria: S. aureus (MIC = 2 μM);
- Gram-negative bacteria: P. aeruginosa (MIC = 2 μM), E. coli (MIC = 1 μM), S. typhimurium (MIC = 2 μM);
- Fungi: C.albicans (MIC = 8 μM)
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Hemolytic Activity
-
- [Ref.31678742]PA2-GNU7 was not toxic to human RBCs at the tested concentrations (0 - 65 μM).The haemolysis was less than 2.5 % up to the concentration of 65 μM.
-
Cytotoxicity
-
- Not found
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Binding Target
- Outer membrane proteins (OMPs) like OprF, the major outer membrane porin of P.aeruginosa
Structure Information
-
Linear/Cyclic
- Linear
-
N-terminal Modification
- Free
-
C-terminal Modification
- Free
-
Nonterminal Modifications and Unusual Amino Acids
- None
-
Stereochemistry
- L
-
Structure
- Helix-loop-helix structure
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Structure Description
- ①Molecular modelling showed that the hybrid peptide was predicted to form a helix-loop-helix structure. ②The hybrid peptide PA2-GNU7 was constructed by joining the PA2 peptide (SQRKLAAKLTSK) to GNU7 (RLLRPLLQLLKQKLR) with a short linker (Gly × 3).
-
Helical Wheel Diagram
-
PDB ID
- None
-
Predicted Structure
- There is no predicted structure for DRAMP29045.
Physicochemical Information
-
Formula
- C150H276N50O37
Absent Amino Acids
- CDEFHIMNVWY
Common Amino Acids
- L
Mass
- 3372.15
PI
- 12.49
Basic Residues
- 9
Acidic Residues
- 0
Hydrophobic Residues
- 11
Net Charge
- +9
-
Boman Index
- -6270
Hydrophobicity
- -0.51
Aliphatic Index
- 123.67
Half Life
-
- Mammalian:1.9 hour
- Yeast:>20 hour
- E.coli:>10 hour
Extinction Coefficient Cystines
- 0
Absorbance 280nm
- 0
Polar Residues
- 6
DRAMP29045
Comments Information
Comment
- The specific binding activity of PA2-GNU7 against P. aeruginosa was derived from the binding activity of PA2 peptide.
Literature Information
- ·Literature 1
-
Title
- Development of a novel hybrid antimicrobial peptide for targeted killing of Pseudomonas aeruginosa
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Pubmed ID
- 31678742
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Reference
- Eur J Med Chem. 2020 Jan 1;185:111814. doi: 10.1016/j.ejmech.2019.111814. Epub 2019 Oct 25.
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Author
- Kim H, Jang JH, Kim SC, Cho JH.