-
-
-
Sequence
- FIIⓧKKSⓧGLⓧKKKⓧGAⓧKKKⓧIKK
-
-
Original Sequence
- FIHHIIGGLFSAGKAIHRLIRRRRR
-
Source
- Synthetic construct
-
-
Biological Activity
- Antimicrobial, Antibacterial, Anti-Gram+, Anti-Gram-
-
- Function: Antibacterial activity against Gram-positive and Gram-negative bacteria.
-
Target Organism
-
- [Ref.36877022]Gram-positive bacteria: Staphylococcus aureus(MIC>25 μM; MBC>25 μM);
- Gram-negative bacteria:Acinetobacter baumannii(MIC=12.5 μM; MBC=12.5 μM).
-
Hemolytic Activity
-
- [Ref.36877022]It shows 15% hemolysis against human red blood cells at the concentration greater than 100 μM.
-
Cytotoxicity
-
No cytotoxicity information found in the reference(s) presented
-
Linear/Cyclic
- Cyclic (Stapled)
-
N-terminal Modification
- Free
-
C-terminal Modification
- Amidation
-
Special Amino Acid and Stapling Position
- ①The Ⓧ (position: 4, 8, 11, 15, 18 and 22) in sequence indicates Fmoc-(R)-2-(4-pentenyl) alanine. ②Ⓧ (4) and Ⓧ (8), Ⓧ (11) and Ⓧ (15), Ⓧ (18) and Ⓧ (22) are cross-linked by hydrocarbon stapling respectively.
-
-
Secondary Structure
- No specific results about the strcture presented in the forms of tables, graphs or words
-
Structure Description
- No other descriptive information about the structure found in the literature
-
-
There is no predicted structure for DRAMP29350.
- Literature 1
-
Title
- Rational Design of Stapled Antimicrobial Peptides to Enhance Stability and In Vivo Potency against Polymicrobial Sepsis.
-
-
Reference
- Microbiol Spectr. 2023 Mar 6;11(2):e0385322.
-
Author
- Yeh JC, Hazam PK, Hsieh CY, Hsu PH, Lin WC, Chen YR, Li CC, Chen JY.