Peptide record

TPDB13460

Antibacterial Anticancer Antifungal Toxicity standard
25 amino acids
Basic Information
3D PDB MODEL
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TPDB13460
Antibacterial Anticancer Antifungal Toxicity
Anti-infective peptides Cancer-related peptides Toxicity and safety peptides
AntiBP3 Peptipedia CancerPPD 2.0 dbACP Antifungipept CAFPdb dbAMP ToxinPred 3.0
standard
No
A 25-aa standard natural multi-activity (Antibacterial, Anticancer, Antifungal, and other sources) peptide sequence curated from AntiBP3, Peptipedia, CancerPPD 2.0, and other sources, with an available 3D structural model.
Sequence
GLWSKIKDAAKTAGKAALGFVNEMV
Physicochemical Analysis
C118H193N31O33S1
RCQHPY
A
2606.08
10.16
4
2
13
+2
2.58
0.180
90.00
Mammalian: 30 hour Yeast: >20 hour E.coli: >10 hour
5500
211.05
3
Residue Composition
number
5
A
0
R
1
N
1
D
0
C
1
E
0
Q
3
G
0
H
1
I
2
L
4
K
1
M
1
F
0
P
1
S
1
T
1
W
0
Y
2
V
Amino Acid Distribution
A: 5 R: 0 N: 1 D: 1 C: 0 E: 1 Q: 0 G: 3 H: 0 I: 1 L: 2 K: 4 M: 1 F: 1 P: 0 S: 1 T: 1 W: 1 Y: 0 V: 2
Chemical Descriptors
25
C118H193N31O33S1
2606.08
10.16
+2
2.58
0.180
Evidence Records 14 records
Evidence 1 Activity

Activity

MIC
Antibacterial
16 µM

Target

Staphylococcus aureus NCTC 10788

Source & Reference

dbAMP

Other

Source Activity Label Source Definition
Antibacterial
dbAMP classified as Antibacterial under the Anti-bacterial function class.
Broad spectrum, active against S. aureus NCTC 10788 (MIC 16 uM), MRSA NCTC 12493 (MIC 32 uM), E. faecalis NCTC 12697 (MIC 16 uM), Gram- E. coli NCTC 1041
Evidence 2 Activity

Activity

MIC
Antibacterial
16 µM

Target

Enterococcus faecalis NCTC 12697

Source & Reference

dbAMP

Other

d spectrum, active against S. aureus NCTC 10788 (MIC 16 uM), MRSA NCTC 12493 (MIC 32 uM), E. faecalis NCTC 12697 (MIC 16 uM), Gram- E. coli NCTC 10418 (MIC 8 uM), P. aeruginosa ATCC 27853 (MIC 16 uM), K. pneumoniae
Evidence 3 Activity

Activity

MIC
Antibacterial
8 µM

Target

Escherichia coli NCTC 10418

Source & Reference

dbAMP

Other

10788 (MIC 16 uM), MRSA NCTC 12493 (MIC 32 uM), E. faecalis NCTC 12697 (MIC 16 uM), Gram- E. coli NCTC 10418 (MIC 8 uM), P. aeruginosa ATCC 27853 (MIC 16 uM), K. pneumoniae ATCC 43816 (MIC 8 uM), and C. albica
Evidence 4 Activity

Activity

MIC
Antibacterial
16 µM

Target

Pseudomonas aeruginosa ATCC 27853

Source & Reference

dbAMP

Other

493 (MIC 32 uM), E. faecalis NCTC 12697 (MIC 16 uM), Gram- E. coli NCTC 10418 (MIC 8 uM), P. aeruginosa ATCC 27853 (MIC 16 uM), K. pneumoniae ATCC 43816 (MIC 8 uM), and C. albicans NCYC 1467 (MIC 64 uM). MBC is usual
Evidence 5 Activity

Activity

MIC
Antibacterial
8 µM

Target

Klebsiella pneumoniae ATCC 43816

Source & Reference

dbAMP

Other

7 (MIC 16 uM), Gram- E. coli NCTC 10418 (MIC 8 uM), P. aeruginosa ATCC 27853 (MIC 16 uM), K. pneumoniae ATCC 43816 (MIC 8 uM), and C. albicans NCYC 1467 (MIC 64 uM). MBC is usually 2 fold higher than MIC.
Evidence 6 Activity

Activity

MIC
Antibacterial
64 µM

Target

Candida albicans NCYC 1467

Source & Reference

dbAMP

Other

MIC 8 uM), P. aeruginosa ATCC 27853 (MIC 16 uM), K. pneumoniae ATCC 43816 (MIC 8 uM), and C. albicans NCYC 1467 (MIC 64 uM). MBC is usually 2 fold higher than MIC.
Evidence 7 Activity

Activity

MIC
Antifungal
16 µM

Target

Staphylococcus aureus NCTC 10788

Source & Reference

dbAMP CAFPdb Antifungipept

Other

Source Activity Label Source Definition
Antifungal
dbAMP classified under the Anti-fungal function class.
Broad spectrum, active against S. aureus NCTC 10788 (MIC 16 uM), MRSA NCTC 12493 (MIC 32 uM), E. faecalis NCTC 12697 (MIC 16 uM), Gram- E. coli NCTC 1041
Evidence 8 Activity

Activity

MIC
Antifungal
16 µM

Target

Enterococcus faecalis NCTC 12697

Source & Reference

dbAMP CAFPdb Antifungipept

Other

d spectrum, active against S. aureus NCTC 10788 (MIC 16 uM), MRSA NCTC 12493 (MIC 32 uM), E. faecalis NCTC 12697 (MIC 16 uM), Gram- E. coli NCTC 10418 (MIC 8 uM), P. aeruginosa ATCC 27853 (MIC 16 uM), K. pneumoniae
Evidence 9 Activity

Activity

MIC
Antifungal
8 µM

Target

Escherichia coli NCTC 10418

Source & Reference

dbAMP CAFPdb Antifungipept

Other

10788 (MIC 16 uM), MRSA NCTC 12493 (MIC 32 uM), E. faecalis NCTC 12697 (MIC 16 uM), Gram- E. coli NCTC 10418 (MIC 8 uM), P. aeruginosa ATCC 27853 (MIC 16 uM), K. pneumoniae ATCC 43816 (MIC 8 uM), and C. albica
Evidence 10 Activity

Activity

MIC
Antifungal
16 µM

Target

Pseudomonas aeruginosa ATCC 27853

Source & Reference

dbAMP CAFPdb Antifungipept

Other

493 (MIC 32 uM), E. faecalis NCTC 12697 (MIC 16 uM), Gram- E. coli NCTC 10418 (MIC 8 uM), P. aeruginosa ATCC 27853 (MIC 16 uM), K. pneumoniae ATCC 43816 (MIC 8 uM), and C. albicans NCYC 1467 (MIC 64 uM). MBC is usual
Evidence 11 Activity

Activity

MIC
Antifungal
8 µM

Target

Klebsiella pneumoniae ATCC 43816

Source & Reference

dbAMP CAFPdb Antifungipept

Other

7 (MIC 16 uM), Gram- E. coli NCTC 10418 (MIC 8 uM), P. aeruginosa ATCC 27853 (MIC 16 uM), K. pneumoniae ATCC 43816 (MIC 8 uM), and C. albicans NCYC 1467 (MIC 64 uM). MBC is usually 2 fold higher than MIC.
Evidence 12 Activity

Activity

MIC
Antifungal
64 µM

Target

Candida albicans NCYC 1467

Source & Reference

dbAMP CAFPdb Antifungipept

Other

MIC 8 uM), P. aeruginosa ATCC 27853 (MIC 16 uM), K. pneumoniae ATCC 43816 (MIC 8 uM), and C. albicans NCYC 1467 (MIC 64 uM). MBC is usually 2 fold higher than MIC.
Evidence 13 Activity

Activity

IC50
Toxicity
51.04 µM
Cytotoxic
IC50 | 51.04 | µM | target cell: Human microvascular endothelial cells HMEC-1

Target

Human microvascular endothelial cells HMEC-1

Source & Reference

NA
DBAASP
A Novel Dermaseptin Isolated from the Skin Secretion of Phyllomedusa tarsius and Its Cationicity-Enhanced Analogue Exhibiting Effective Antimicrobial and Anti-Proliferative Activities. | Biomolecules | 2019
Evidence 14 Activity

Activity

50% Hemolysis
Toxicity
210 µM
Hemolytic Cytotoxic
50% Hemolysis | 210 | µM | target cell: Horse erythrocytes

Target

Horse erythrocytes

Source & Reference

NA
DBAASP
A Novel Dermaseptin Isolated from the Skin Secretion of Phyllomedusa tarsius and Its Cationicity-Enhanced Analogue Exhibiting Effective Antimicrobial and Anti-Proliferative Activities. | Biomolecules | 2019