MYP_136721
SAU-7
Anticancer
Anticancer
▸
Antitumor
Anticancer
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Cytotoxic anticancer activity
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Cytotoxic
Antimicrobial
Antimicrobial
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Antibacterial
Antimicrobial
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Antibacterial
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Anti-Gram-negative
Antimicrobial
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Antibacterial
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Anti-Gram-positive
Antimicrobial
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Antibiotic activity
Antimicrobial
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Antifungal
Immunology
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Innate immune defense
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Host defense peptide
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Defense peptide
Immunology
▸
Innate immune defense
▸
Host defense peptide
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Host defense activity
Toxicity / Safety
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Blood cell toxicity
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Hemolysis
▸
Hemolytic
Toxicity / Safety
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Cytotoxicity
▸
Cytotoxic
Toxicity / Safety
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Negative safety assay result
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Non-hemolytic
Venom / Toxin
▸
General toxin
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Cytotoxic
Venom / Toxin
▸
General toxin
▸
Toxic
Standard
13 amino acids
C71H113N15O19
Standard
GLFDIIKKIAESF
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.
Amino Acid Composition
559.39
-1.87
19.0
19.0
51.0
105.0
2.0
12.0
3D PDB MODEL
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2D CHEMICAL STRUCTURE
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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
Showing 5 records on this page · Page 12 of 37