MYP_136721
Basic Information
SAU-7
Anticancer
Anticancer Antitumor
Anticancer Cytotoxic anticancer activity Cytotoxic
Antimicrobial
Antimicrobial Antibacterial
Antimicrobial Antibacterial Anti-Gram-negative
Antimicrobial Antibacterial Anti-Gram-positive
Antimicrobial Antibiotic activity
Antimicrobial Antifungal
Antiviral
Immunology Innate immune defense Host defense peptide Defense peptide
Immunology Innate immune defense Host defense peptide Host defense activity
Toxicity / Safety Blood cell toxicity Hemolysis Hemolytic
Toxicity / Safety Cytotoxicity Cytotoxic
Toxicity / Safety Negative safety assay result Non-hemolytic
Venom / Toxin General toxin Cytotoxic
Venom / Toxin General toxin Toxic
Standard
13 amino acids
C71H113N15O19
Standard
Sequence
GLFDIIKKIAESF
Physicochemical Analysis
1480.75 Da
6.07
-0.24
-0.45
-0.0183
0.67
0.71
0.30
20.48
127.69
0.1538
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
559.39
-1.87
19.0
19.0
51.0
105.0
2.0
12.0
Structural Visualization
3D PDB MODEL
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2D CHEMICAL STRUCTURE
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Experimental Records
RECORD: Rec_0138881 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
Aurein
32630
Structure & Mods
hydrocarbon-stapled side-chain cyclic peptide [Cyclic]
noncanonical stereochemical modification [Modified]
Acetylation
Amidation
The Ⓧ (position: 9 and 13) in sequence indicates S5 (2-amino-2-methylhept-6-enoic acid). Ⓧ (9) and Ⓧ (13) are cross-linked by hydrocarbon stapling respectively
Bio-Activity Profile
Antifungal
Candida auris 918
>128 μg/mL
MIC
RECORD: Rec_0139673 VERIFIED: YES
Provenance & Taxonomy
Ranoidea raniformis [Animal]
116057
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
Bio-Activity Profile
Antimicrobial Antifungal Anticancer
Escherichia coli
>100 μg/mL
MIC
RECORD: Rec_0142075 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
Aurein
32630
Structure & Mods
hydrocarbon-stapled side-chain cyclic peptide [Cyclic]
noncanonical stereochemical modification [Modified]
Acetylation
Amidation
The Ⓧ (position: 9 and 13) in sequence indicates S5 (2-amino-2-methylhept-6-enoic acid). Ⓧ (9) and Ⓧ (13) are cross-linked by hydrocarbon stapling respectively
Bio-Activity Profile
Antifungal
Candida albicans 904
>128 μg/mL
MIC
RECORD: Rec_0144462 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
Aurein
32630
Structure & Mods
hydrocarbon-stapled side-chain cyclic peptide [Cyclic]
noncanonical stereochemical modification [Modified]
Acetylation
Amidation
The Ⓧ (position: 6 and 10) in sequence indicates S5 (2-amino-2-methylhept-6-enoic acid). Ⓧ (6) and Ⓧ (10) are cross-linked by hydrocarbon stapling respectively
Bio-Activity Profile
Antifungal
Candida auris 919
>128 μg/mL
MIC
RECORD: Rec_0155158 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
Aurein
32630
Structure & Mods
hydrocarbon-stapled side-chain cyclic peptide [Cyclic]
noncanonical stereochemical modification [Modified]
Acetylation
Amidation
The Ⓧ (position: 4 and 8) in sequence indicates S5 (2-amino-2-methylhept-6-enoic acid). Ⓧ (4) and Ⓧ (8) are cross-linked by hydrocarbon stapling respectively
Bio-Activity Profile
Antifungal
Candida krusei ATCC 2340
>128 μg/mL
MIC
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