MYP_125264
Basic Information
TP4-4
Antimicrobial
Antimicrobial Antibacterial
Toxicity / Safety Blood cell toxicity Hemolysis Hemolytic
Standard
25 amino acids
C129H235N43O28
Standard
Sequence
FIIHKKSGGLSKKKAGARKKKRIKK
Physicochemical Analysis
2836.52 Da
12.00
11.84
11.57
0.4735
-1.21
0.52
-0.47
35.19
70.40
0.0400
0.00
0.00
The radar chart summarizes major physicochemical dimensions for quick comparison, while exact numerical values remain listed on the left.
Residue Composition
Amino Acid Composition
Chemical Descriptors
1214.86
-10.84
45.0
41.0
111.0
200.0
2.0
24.0
Structural Visualization
3D PDB MODEL
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2D CHEMICAL STRUCTURE
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Experimental Records
RECORD: Rec_0074447 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
hydrocarbon-stapled side-chain cyclic peptide [Cyclic]
noncanonical stereochemical modification [Modified]
None
Amidation
The Ⓧ (position: 4, 8, 11, 15, 18 and 22) in sequence indicates Fmoc-(R)-2-(4-pentenyl) alanine. Ⓧ (4) and Ⓧ (8), Ⓧ (11) and Ⓧ (15), Ⓧ (18) and Ⓧ (22) are cross-linked by hydrocarbon stapling respectively
Bio-Activity Profile
Antimicrobial Antibacterial
Acinetobacter baumannii
12.5 μM
MBC
RECORD: Rec_0111407 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
hydrocarbon-stapled side-chain cyclic peptide [Cyclic]
noncanonical stereochemical modification [Modified]
None
Amidation
The Ⓧ (position: 4, 8, 11, 15, 18 and 22) in sequence indicates Fmoc-(R)-2-(4-pentenyl) alanine. Ⓧ (4) and Ⓧ (8), Ⓧ (11) and Ⓧ (15), Ⓧ (18) and Ⓧ (22) are cross-linked by hydrocarbon stapling respectively
Bio-Activity Profile
Hemolytic
human red blood cells
100 μM
Hemolysis
RECORD: Rec_0121483 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
hydrocarbon-stapled side-chain cyclic peptide [Cyclic]
noncanonical stereochemical modification [Modified]
None
Amidation
The Ⓧ (position: 4, 8, 11, 15, 18 and 22) in sequence indicates Fmoc-(R)-2-(4-pentenyl) alanine. Ⓧ (4) and Ⓧ (8), Ⓧ (11) and Ⓧ (15), Ⓧ (18) and Ⓧ (22) are cross-linked by hydrocarbon stapling respectively
Bio-Activity Profile
Antimicrobial Antibacterial
Acinetobacter baumannii
12.5 μM
MIC
RECORD: Rec_0150599 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
hydrocarbon-stapled side-chain cyclic peptide [Cyclic]
noncanonical stereochemical modification [Modified]
None
Amidation
The Ⓧ (position: 4, 8, 11, 15, 18 and 22) in sequence indicates Fmoc-(R)-2-(4-pentenyl) alanine. Ⓧ (4) and Ⓧ (8), Ⓧ (11) and Ⓧ (15), Ⓧ (18) and Ⓧ (22) are cross-linked by hydrocarbon stapling respectively
Bio-Activity Profile
Antimicrobial Antibacterial
Staphylococcus aureus
>25 μM
MIC
RECORD: Rec_0312802 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
hydrocarbon-stapled side-chain cyclic peptide [Cyclic]
noncanonical stereochemical modification [Modified]
None
Amidation
The Ⓧ (position: 4, 8, 11, 15, 18 and 22) in sequence indicates Fmoc-(R)-2-(4-pentenyl) alanine. Ⓧ (4) and Ⓧ (8), Ⓧ (11) and Ⓧ (15), Ⓧ (18) and Ⓧ (22) are cross-linked by hydrocarbon stapling respectively
Bio-Activity Profile
Antimicrobial Antibacterial
Staphylococcus aureus
>25 μM
MBC