MYP_125527
GF-17
Anticancer
Anticancer
▸
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
Antiviral
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Anti-Filovirus
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Antiviral
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Anti-HIV
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Antiviral
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Antiviral mechanism
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Reproductive biology
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Contraceptive activity
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Spermicidal
Toxicity / Safety
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Blood cell toxicity
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Hemolysis
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Hemolytic
Toxicity / Safety
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Cytotoxicity
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Cytotoxic
Venom / Toxin
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General toxin
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Cytotoxic
Standard
17 amino acids
C97H164N30O22
Standard
GFKRIVQRIKDFLRNLV
2102.53 Da
11.72
3.76
3.55
0.2211
-0.09
0.97
-0.19
23.91
125.88
0.1176
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
890.14
-5.57
32.0
26.0
74.0
149.0
2.0
18.0
3D PDB MODEL
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2D CHEMICAL STRUCTURE
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RECORD: Rec_0318781
VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
Cathelicidin
32630
Structure & Mods
Single-chain peptide backbone represented as a linear sequence entry [Linear]
canonical L-amino-acid peptide [L]
Amidation
Bio-Activity Profile
Antimicrobial
Antibacterial
Anti-Gram-positive
Anti-Gram-negative
Staphylococcus aureus UAMS1
3.1 μM
MIC
RECORD: Rec_0330758
VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
Cathelicidin
32630
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
Amidation
Bio-Activity Profile
Antimicrobial
Antibacterial
Anti-Gram-positive
Anti-Gram-negative
E. faecium V284-17
2 μM
MIC
RECORD: Rec_0348496
VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
Cathelicidin
32630
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
None
Amidation
Bio-Activity Profile
Anti-EBOV
Entry inhibition
Ebola Virus (EBOV) | Hela cells
10.1 μM
IC50
Mammalian: 30 h; Yeast: >20 h; E. coli: >10 h
RECORD: Rec_0348680
VERIFIED: YES
Provenance & Taxonomy
Synthetic construct based on Derivative of [Synthetic]
32630
Structure & Mods
linear peptide [Linear]
mixed L/D amino-acid peptide [Mixed]
Amidation
FK-16 (residues 17-32 of LL-37) was identified as the major antimicrobial peptide of human cathelicidin LL-37 by NMR-trim. GF-17 = G + FK-16: mol wt 2102.5. Chemical modification: Both GF-17 and FK-16 are C-terminally amidated. SAR: FK-16 and GF-17 have similar antibacterial activity, indicating the N-terminal glycine has a minimal effect (Wang et al., 2019); 17BIPHE2 was designed based on the 3D structure of GF-17d3, which contains three D-amino acids at positions 20, 24, and 28 (numbered as in LL-37) (Wang et al., 2014). 17BIPHE2 is active against the ESKAPE pathogens (MIC 3.1-6.2 uM). Both GF-17 and 17BIPHE2 inhibited Zika virus (He et al., 2018). Updated 4/2013; 10/2013; Jan2014; 4/2016; 4/2017;3/2018; 6/2019; 8/2021; 11/2023; 8/2024; ref link updare 10/2024
Bio-Activity Profile
Antimicrobial
Anticancer
Spermicidal
the ESKAPE pathogens
3.1-6.2 μM
MIC
RECORD: Rec_0351400
VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
Cathelicidin
32630
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
Amidation
Bio-Activity Profile
Antimicrobial
Antibacterial
Anti-Gram-positive
Anti-Gram-negative
Staphylococcus aureus USA300
2-4 μM
MIC
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