MYP_152608
Basic Information
Dermaseptin-PP
Anticancer
Anticancer Cytotoxic anticancer activity Cytotoxic
Antimicrobial
Antimicrobial Antifungal
Toxicity / Safety Blood cell toxicity Hemolysis Hemolytic
Toxicity / Safety Cytotoxicity Cytotoxic
Venom / Toxin General toxin Cytotoxic
Wound healing/Regeneration Wound healing
Standard
26 amino acids
C123H214N32O30S
Standard
Sequence
ALWKDMLKGIGKLAGKAALGAVKTLV
Physicochemical Analysis
2653.28 Da
10.18
3.79
3.60
0.1458
0.64
0.71
0.26
-5.24
131.54
0.0385
5500.00
5500.00
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
994.24
-5.29
35.0
35.0
93.0
186.0
2.0
25.0
Structural Visualization
3D PDB MODEL
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2D CHEMICAL STRUCTURE
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Experimental Records
RECORD: Rec_0059572 VERIFIED: YES
Provenance & Taxonomy
Phyllomedusa palliata [Animal]
Dermaseptin
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
APD analysis reveals that this sequence is similar (85.71%) to Dermaseptin-B3 L=A=K: 19%; G: 15%. GRAVY: 0.638; mol Wt: 2653.3; mol formula: C123H215N32O30S1; mol ex coeff: 5550. Chemical modification: Reduction of disulfide bonds and alkylation of cysteines indicate that disulfide bonds are important for peptide stability rather than activity
Bio-Activity Profile
Antimicrobial Antifungal Anticancer Wound healing
Enterococcus faecalis NCTC 1269
4 μM
MIC
RECORD: Rec_0083433 VERIFIED: YES
Provenance & Taxonomy
Phyllomedusa palliata [Animal]
Dermaseptin
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
None
None
Bio-Activity Profile
Antimicrobial Anticancer
PC-3
4.15 μM
IC50
RECORD: Rec_0092748 VERIFIED: YES
Provenance & Taxonomy
Phyllomedusa palliata [Animal]
Dermaseptin
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
APD analysis reveals that this sequence is similar (85.71%) to Dermaseptin-B3 L=A=K: 19%; G: 15%. GRAVY: 0.638; mol Wt: 2653.3; mol formula: C123H215N32O30S1; mol ex coeff: 5550. Chemical modification: Reduction of disulfide bonds and alkylation of cysteines indicate that disulfide bonds are important for peptide stability rather than activity
Bio-Activity Profile
Antimicrobial Antifungal Anticancer Wound healing
PC-3
4.15 μM
IC50
RECORD: Rec_0114049 VERIFIED: YES
Provenance & Taxonomy
Phyllomedusa palliata [Animal]
Dermaseptin
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
APD analysis reveals that this sequence is similar (85.71%) to Dermaseptin-B3 L=A=K: 19%; G: 15%. GRAVY: 0.638; mol Wt: 2653.3; mol formula: C123H215N32O30S1; mol ex coeff: 5550. Chemical modification: Reduction of disulfide bonds and alkylation of cysteines indicate that disulfide bonds are important for peptide stability rather than activity
Bio-Activity Profile
Antimicrobial Antifungal Anticancer Wound healing
MCF-7
2.92 μM
IC50
RECORD: Rec_0127595 VERIFIED: YES
Provenance & Taxonomy
Phyllomedusa palliata [Animal]
Dermaseptin
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
APD analysis reveals that this sequence is similar (85.71%) to Dermaseptin-B3 L=A=K: 19%; G: 15%. GRAVY: 0.638; mol Wt: 2653.3; mol formula: C123H215N32O30S1; mol ex coeff: 5550. Chemical modification: Reduction of disulfide bonds and alkylation of cysteines indicate that disulfide bonds are important for peptide stability rather than activity
Bio-Activity Profile
Antimicrobial Antifungal Anticancer Wound healing
U251 MG cells
2.47 μM
IC50
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